Protein ID | Hirsu2|2490 |
Gene name | |
Location | Contig_16:7415..9530 |
Strand | + |
Gene length (bp) | 2115 |
Transcript length (bp) | 2046 |
Coding sequence length (bp) | 2046 |
Protein length (aa) | 682 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF01529 | DHHC | DHHC palmitoyltransferase | 1.5E-35 | 468 | 593 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q4I2M7|ERFB_GIBZE | Palmitoyltransferase ERF2 OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ERF2 PE=3 SV=1 | 27 | 676 | 0.0E+00 |
sp|Q7SFL7|ERFB_NEUCR | Palmitoyltransferase erf2 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ptr-2 PE=3 SV=1 | 28 | 681 | 0.0E+00 |
sp|Q5B3W7|ERFB_EMENI | Palmitoyltransferase erf2 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=erf2 PE=3 SV=2 | 97 | 666 | 9.0E-167 |
sp|Q4WWN2|ERFB_ASPFU | Palmitoyltransferase erf2 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=erf2 PE=3 SV=1 | 21 | 662 | 3.0E-163 |
sp|Q6C890|ERFB_YARLI | Palmitoyltransferase ERF2 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=ERF2 PE=3 SV=2 | 311 | 598 | 8.0E-69 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q4I2M7|ERFB_GIBZE | Palmitoyltransferase ERF2 OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ERF2 PE=3 SV=1 | 27 | 676 | 0.0E+00 |
sp|Q7SFL7|ERFB_NEUCR | Palmitoyltransferase erf2 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ptr-2 PE=3 SV=1 | 28 | 681 | 0.0E+00 |
sp|Q5B3W7|ERFB_EMENI | Palmitoyltransferase erf2 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=erf2 PE=3 SV=2 | 97 | 666 | 9.0E-167 |
sp|Q4WWN2|ERFB_ASPFU | Palmitoyltransferase erf2 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=erf2 PE=3 SV=1 | 21 | 662 | 3.0E-163 |
sp|Q6C890|ERFB_YARLI | Palmitoyltransferase ERF2 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=ERF2 PE=3 SV=2 | 311 | 598 | 8.0E-69 |
sp|Q6BHT4|ERFB_DEBHA | Palmitoyltransferase ERF2 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=ERF2 PE=3 SV=2 | 352 | 640 | 2.0E-60 |
sp|O74384|ERFB_SCHPO | Palmitoyltransferase erf2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=erf2 PE=1 SV=1 | 344 | 628 | 3.0E-53 |
sp|Q6FSS4|ERFB_CANGA | Palmitoyltransferase ERF2 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=ERF2 PE=3 SV=1 | 350 | 630 | 5.0E-50 |
sp|P59268|ZDHC9_MOUSE | Palmitoyltransferase ZDHHC9 OS=Mus musculus GN=Zdhhc9 PE=2 SV=1 | 342 | 625 | 5.0E-50 |
sp|Q06551|ERFB_YEAST | Palmitoyltransferase ERF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ERF2 PE=1 SV=1 | 350 | 655 | 5.0E-50 |
sp|Q5R5J8|ZDHC9_PONAB | Palmitoyltransferase ZDHHC9 OS=Pongo abelii GN=ZDHHC9 PE=2 SV=1 | 342 | 625 | 6.0E-50 |
sp|Q9Y397|ZDHC9_HUMAN | Palmitoyltransferase ZDHHC9 OS=Homo sapiens GN=ZDHHC9 PE=1 SV=2 | 342 | 625 | 6.0E-50 |
sp|Q58DA8|ZDHC9_BOVIN | Palmitoyltransferase ZDHHC9 OS=Bos taurus GN=ZDHHC9 PE=2 SV=1 | 342 | 625 | 7.0E-50 |
sp|Q750R7|ERFB_ASHGO | Palmitoyltransferase ERF2 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=ERF2 PE=3 SV=1 | 289 | 640 | 2.0E-46 |
sp|Q9SB58|ZDH19_ARATH | Protein S-acyltransferase 8 OS=Arabidopsis thaliana GN=PAT08 PE=1 SV=2 | 342 | 630 | 1.0E-45 |
sp|Q8IZN3|ZDH14_HUMAN | Probable palmitoyltransferase ZDHHC14 OS=Homo sapiens GN=ZDHHC14 PE=1 SV=1 | 344 | 625 | 1.0E-45 |
sp|Q8BQQ1|ZDH14_MOUSE | Probable palmitoyltransferase ZDHHC14 OS=Mus musculus GN=Zdhhc14 PE=1 SV=1 | 344 | 625 | 2.0E-45 |
sp|Q6CQB5|ERFB_KLULA | Palmitoyltransferase ERF2 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ERF2 PE=3 SV=1 | 337 | 593 | 2.0E-42 |
sp|Q9NUE0|ZDH18_HUMAN | Palmitoyltransferase ZDHHC18 OS=Homo sapiens GN=ZDHHC18 PE=2 SV=2 | 342 | 625 | 1.0E-39 |
sp|Q5Y5T5|ZDHC8_MOUSE | Probable palmitoyltransferase ZDHHC8 OS=Mus musculus GN=Zdhhc8 PE=1 SV=1 | 356 | 626 | 1.0E-39 |
sp|Q2THW8|ZDHC8_CANLF | Probable palmitoyltransferase ZDHHC8 OS=Canis lupus familiaris GN=ZDHHC8 PE=2 SV=1 | 356 | 626 | 2.0E-39 |
sp|Q59QL0|ERFB_CANAL | Palmitoyltransferase ERF2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ERF2 PE=3 SV=2 | 350 | 592 | 2.0E-39 |
sp|Q2THX0|ZDHC8_PANTR | Probable palmitoyltransferase ZDHHC8 OS=Pan troglodytes GN=ZDHHC8 PE=2 SV=1 | 356 | 626 | 2.0E-39 |
sp|Q9ULC8|ZDHC8_HUMAN | Probable palmitoyltransferase ZDHHC8 OS=Homo sapiens GN=ZDHHC8 PE=1 SV=3 | 356 | 626 | 2.0E-39 |
sp|Q5Y5T2|ZDH18_MOUSE | Palmitoyltransferase ZDHHC18 OS=Mus musculus GN=Zdhhc18 PE=1 SV=4 | 342 | 625 | 2.0E-39 |
sp|Q5R838|ZDHC5_PONAB | Palmitoyltransferase ZDHHC5 OS=Pongo abelii GN=ZDHHC5 PE=2 SV=1 | 356 | 626 | 5.0E-39 |
sp|Q9FLM3|ZDH23_ARATH | Probable protein S-acyltransferase 6 OS=Arabidopsis thaliana GN=PAT06 PE=2 SV=1 | 342 | 634 | 6.0E-39 |
sp|Q2TGJ1|ZDH18_RAT | Palmitoyltransferase ZDHHC18 OS=Rattus norvegicus GN=Zdhhc18 PE=2 SV=1 | 342 | 625 | 6.0E-39 |
sp|Q8VDZ4|ZDHC5_MOUSE | Palmitoyltransferase ZDHHC5 OS=Mus musculus GN=Zdhhc5 PE=1 SV=1 | 356 | 626 | 7.0E-39 |
sp|Q0WQK2|ZDHC9_ARATH | Probable protein S-acyltransferase 7 OS=Arabidopsis thaliana GN=PAT07 PE=1 SV=1 | 342 | 639 | 2.0E-38 |
sp|Q2THW7|ZDHC5_RAT | Palmitoyltransferase ZDHHC5 OS=Rattus norvegicus GN=Zdhhc5 PE=1 SV=1 | 356 | 626 | 2.0E-38 |
sp|Q2THW9|ZDHC5_CANLF | Palmitoyltransferase ZDHHC5 OS=Canis lupus familiaris GN=ZDHHC5 PE=2 SV=1 | 356 | 626 | 3.0E-38 |
sp|Q9C0B5|ZDHC5_HUMAN | Palmitoyltransferase ZDHHC5 OS=Homo sapiens GN=ZDHHC5 PE=1 SV=2 | 356 | 626 | 7.0E-38 |
sp|Q2THX1|ZDHC5_PANTR | Palmitoyltransferase ZDHHC5 OS=Pan troglodytes GN=ZDHHC5 PE=2 SV=1 | 356 | 626 | 8.0E-38 |
sp|E1BLT8|ZDHC5_BOVIN | Palmitoyltransferase ZDHHC5 OS=Bos taurus GN=ZDHHC5 PE=3 SV=1 | 358 | 626 | 9.0E-38 |
sp|Q9M306|ZDH10_ARATH | Probable protein S-acyltransferase 5 OS=Arabidopsis thaliana GN=PAT05 PE=1 SV=2 | 342 | 619 | 3.0E-36 |
sp|Q9M1K5|ZDH13_ARATH | Probable protein S-acyltransferase 4 OS=Arabidopsis thaliana GN=PAT04 PE=2 SV=1 | 342 | 640 | 1.0E-35 |
sp|Q8VYS8|ZDH24_ARATH | Probable protein S-acyltransferase 9 OS=Arabidopsis thaliana GN=PAT09 PE=2 SV=1 | 341 | 630 | 1.0E-34 |
sp|Q5PNZ1|ZDH21_ARATH | Probable protein S-acyltransferase 3 OS=Arabidopsis thaliana GN=PAT03 PE=2 SV=1 | 323 | 681 | 1.0E-30 |
sp|B3DN87|ZDH12_ARATH | Probable protein S-acyltransferase 1 OS=Arabidopsis thaliana GN=PAT01 PE=2 SV=1 | 342 | 631 | 1.0E-27 |
sp|O80685|ZDHC4_ARATH | Probable protein S-acyltransferase 2 OS=Arabidopsis thaliana GN=PAT02 PE=2 SV=3 | 342 | 670 | 1.0E-24 |
sp|Q550R7|ZDHC1_DICDI | Putative ZDHHC-type palmitoyltransferase 1 OS=Dictyostelium discoideum GN=DDB_G0276997 PE=3 SV=3 | 369 | 537 | 1.0E-23 |
sp|Q557H5|ZDHC3_DICDI | Putative ZDHHC-type palmitoyltransferase 3 OS=Dictyostelium discoideum GN=DDB_G0273477 PE=3 SV=1 | 454 | 533 | 7.0E-21 |
sp|Q5FWL7|ZDH15_XENLA | Palmitoyltransferase ZDHHC15 OS=Xenopus laevis GN=zdhhc15 PE=2 SV=1 | 468 | 622 | 8.0E-20 |
sp|Q9UIJ5|ZDHC2_HUMAN | Palmitoyltransferase ZDHHC2 OS=Homo sapiens GN=ZDHHC2 PE=2 SV=1 | 460 | 618 | 2.0E-19 |
sp|Q8BGJ0|ZDH15_MOUSE | Palmitoyltransferase ZDHHC15 OS=Mus musculus GN=Zdhhc15 PE=1 SV=1 | 467 | 618 | 3.0E-19 |
sp|P59267|ZDHC2_MOUSE | Palmitoyltransferase ZDHHC2 OS=Mus musculus GN=Zdhhc2 PE=2 SV=1 | 460 | 618 | 3.0E-19 |
sp|Q2TGJ4|ZDH15_RAT | Palmitoyltransferase ZDHHC15 OS=Rattus norvegicus GN=Zdhhc15 PE=2 SV=1 | 467 | 618 | 3.0E-19 |
sp|Q96MV8|ZDH15_HUMAN | Palmitoyltransferase ZDHHC15 OS=Homo sapiens GN=ZDHHC15 PE=2 SV=1 | 467 | 618 | 3.0E-19 |
sp|Q9JKR5|ZDHC2_RAT | Palmitoyltransferase ZDHHC2 OS=Rattus norvegicus GN=Zdhhc2 PE=2 SV=1 | 460 | 618 | 5.0E-19 |
sp|Q9C533|ZDHC1_ARATH | Probable protein S-acyltransferase 22 OS=Arabidopsis thaliana GN=PAT22 PE=2 SV=2 | 457 | 609 | 2.0E-18 |
sp|Q8WVZ1|ZDH19_HUMAN | Probable palmitoyltransferase ZDHHC19 OS=Homo sapiens GN=ZDHHC19 PE=2 SV=2 | 381 | 547 | 3.0E-18 |
sp|Q500Z2|ZDH20_ARATH | Probable protein S-acyltransferase 15 OS=Arabidopsis thaliana GN=PAT15 PE=2 SV=1 | 468 | 618 | 1.0E-17 |
sp|Q555N7|ZDHC4_DICDI | Putative ZDHHC-type palmitoyltransferase 4 OS=Dictyostelium discoideum GN=DDB_G0274251 PE=3 SV=1 | 464 | 589 | 2.0E-17 |
sp|Q94C49|ZDH18_ARATH | Probable protein S-acyltransferase 13 OS=Arabidopsis thaliana GN=PAT13 PE=2 SV=1 | 394 | 594 | 3.0E-17 |
sp|Q5AGV7|PFA4_CANAL | Palmitoyltransferase PFA4 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PFA4 PE=3 SV=1 | 375 | 596 | 4.0E-17 |
sp|Q5Y5T1|ZDH20_MOUSE | Probable palmitoyltransferase ZDHHC20 OS=Mus musculus GN=Zdhhc20 PE=1 SV=1 | 467 | 608 | 5.0E-17 |
sp|Q93VV0|ZDHC6_ARATH | Probable protein S-acyltransferase 16 OS=Arabidopsis thaliana GN=PAT16 PE=2 SV=1 | 467 | 618 | 6.0E-17 |
sp|Q6CPU8|PFA3_KLULA | Palmitoyltransferase PFA3 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=PFA3 PE=3 SV=1 | 405 | 589 | 1.0E-16 |
sp|Q810M5|ZDH19_MOUSE | Probable palmitoyltransferase ZDHHC19 OS=Mus musculus GN=Zdhhc19 PE=1 SV=1 | 389 | 547 | 2.0E-16 |
sp|Q0VC89|ZDH20_BOVIN | Probable palmitoyltransferase ZDHHC20 OS=Bos taurus GN=ZDHHC20 PE=2 SV=1 | 467 | 608 | 5.0E-16 |
sp|Q9NXF8|ZDHC7_HUMAN | Palmitoyltransferase ZDHHC7 OS=Homo sapiens GN=ZDHHC7 PE=1 SV=2 | 342 | 603 | 1.0E-15 |
sp|Q6FXC6|SWF1_CANGA | Palmitoyltransferase SWF1 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=SWF1 PE=3 SV=1 | 463 | 526 | 1.0E-15 |
sp|Q7S7C5|PFA3_NEUCR | Palmitoyltransferase pfa3 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ptr-3 PE=3 SV=3 | 468 | 601 | 1.0E-15 |
sp|Q923G5|ZDHC7_RAT | Palmitoyltransferase ZDHHC7 OS=Rattus norvegicus GN=Zdhhc7 PE=1 SV=1 | 390 | 603 | 2.0E-15 |
sp|Q91WU6|ZDHC7_MOUSE | Palmitoyltransferase ZDHHC7 OS=Mus musculus GN=Zdhhc7 PE=1 SV=1 | 390 | 603 | 2.0E-15 |
sp|Q75AW7|PFA3_ASHGO | Palmitoyltransferase PFA3 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=PFA3 PE=3 SV=2 | 468 | 590 | 3.0E-15 |
sp|Q9LIE4|ZDHC8_ARATH | Probable protein S-acyltransferase 20 OS=Arabidopsis thaliana GN=PAT20 PE=3 SV=2 | 470 | 591 | 3.0E-15 |
sp|Q3EC11|ZDHC2_ARATH | Probable protein S-acyltransferase 23 OS=Arabidopsis thaliana GN=PAT23 PE=2 SV=2 | 470 | 597 | 3.0E-15 |
sp|Q9D270|ZDH21_MOUSE | Probable palmitoyltransferase ZDHHC21 OS=Mus musculus GN=Zdhhc21 PE=1 SV=2 | 396 | 575 | 3.0E-15 |
sp|Q6CJC5|SWF1_KLULA | Palmitoyltransferase SWF1 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=SWF1 PE=3 SV=1 | 470 | 526 | 3.0E-15 |
sp|Q9ESG8|ZDH16_MOUSE | Probable palmitoyltransferase ZDHHC16 OS=Mus musculus GN=Zdhhc16 PE=1 SV=2 | 450 | 613 | 4.0E-15 |
sp|Q5W0Z9|ZDH20_HUMAN | Probable palmitoyltransferase ZDHHC20 OS=Homo sapiens GN=ZDHHC20 PE=1 SV=1 | 467 | 589 | 4.0E-15 |
sp|P42836|PFA3_YEAST | Palmitoyltransferase PFA3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PFA3 PE=1 SV=1 | 470 | 589 | 4.0E-15 |
sp|A2VDT6|ZDH21_BOVIN | Probable palmitoyltransferase ZDHHC21 OS=Bos taurus GN=ZDHHC21 PE=2 SV=1 | 396 | 575 | 7.0E-15 |
sp|O60069|SWF1_SCHPO | Palmitoyltransferase swf1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=swf1 PE=3 SV=1 | 470 | 589 | 8.0E-15 |
sp|Q4WZL8|PFA3_ASPFU | Palmitoyltransferase pfa3 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=pfa3 PE=3 SV=1 | 402 | 601 | 9.0E-15 |
sp|Q6BP23|SWF1_DEBHA | Palmitoyltransferase SWF1 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=SWF1 PE=3 SV=1 | 376 | 526 | 2.0E-14 |
sp|Q5RB84|ZDH21_PONAB | Probable palmitoyltransferase ZDHHC21 OS=Pongo abelii GN=ZDHHC21 PE=2 SV=1 | 396 | 575 | 2.0E-14 |
sp|Q8IVQ6|ZDH21_HUMAN | Palmitoyltransferase ZDHHC21 OS=Homo sapiens GN=ZDHHC21 PE=2 SV=1 | 396 | 575 | 2.0E-14 |
sp|C8VCL4|PFA3_EMENI | Palmitoyltransferase pfa3 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=pfa3 PE=3 SV=2 | 468 | 601 | 2.0E-14 |
sp|Q8VYP5|ZDH14_ARATH | Probable protein S-acyltransferase 14 OS=Arabidopsis thaliana GN=PAT14 PE=2 SV=1 | 397 | 602 | 2.0E-14 |
sp|Q8L5Y5|ZDH17_ARATH | Probable protein S-acyltransferase 19 OS=Arabidopsis thaliana GN=PAT19 PE=2 SV=1 | 470 | 591 | 2.0E-14 |
sp|Q4IA62|PFA3_GIBZE | Palmitoyltransferase PFA3 OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=PFA3 PE=3 SV=1 | 468 | 596 | 3.0E-14 |
sp|Q4PE27|PFA4_USTMA | Palmitoyltransferase PFA4 OS=Ustilago maydis (strain 521 / FGSC 9021) GN=PFA4 PE=3 SV=2 | 468 | 618 | 3.0E-14 |
sp|Q6BMV2|PFA3_DEBHA | Palmitoyltransferase PFA3 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=PFA3 PE=3 SV=2 | 468 | 605 | 4.0E-14 |
sp|Q52T38|ZDH22_ARATH | Protein S-acyltransferase 24 OS=Arabidopsis thaliana GN=PAT24 PE=2 SV=1 | 402 | 597 | 9.0E-14 |
sp|Q14AK4|ZDH11_MOUSE | Probable palmitoyltransferase ZDHHC11 OS=Mus musculus GN=Zdhhc11 PE=2 SV=2 | 468 | 598 | 9.0E-14 |
sp|Q5A861|SWF1_CANAL | Palmitoyltransferase SWF1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=SWF1 PE=3 SV=1 | 468 | 526 | 1.0E-13 |
sp|Q7Z8U2|AKR1_ASPOR | Palmitoyltransferase akr1 OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=akr1 PE=3 SV=2 | 381 | 594 | 1.0E-13 |
sp|Q8I0G4|ZDHC4_CAEEL | Zinc finger DHHC domain-containing protein 4 OS=Caenorhabditis elegans GN=dhhc-4 PE=3 SV=1 | 467 | 608 | 1.0E-13 |
sp|Q4WC37|PFA4_ASPFU | Palmitoyltransferase pfa4 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=pfa4 PE=3 SV=2 | 367 | 581 | 1.0E-13 |
sp|Q4R7E2|ZDH16_MACFA | Probable palmitoyltransferase ZDHHC16 OS=Macaca fascicularis GN=ZDHHC16 PE=2 SV=1 | 450 | 613 | 1.0E-13 |
sp|Q5M757|ZDH15_ARATH | Probable protein S-acyltransferase 12 OS=Arabidopsis thaliana GN=PAT12 PE=2 SV=1 | 394 | 589 | 2.0E-13 |
sp|Q969W1|ZDH16_HUMAN | Probable palmitoyltransferase ZDHHC16 OS=Homo sapiens GN=ZDHHC16 PE=2 SV=1 | 450 | 613 | 2.0E-13 |
sp|Q4X251|AKR1_ASPFU | Palmitoyltransferase akr1 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=akr1 PE=3 SV=2 | 383 | 598 | 2.0E-13 |
sp|Q5FVR1|ZDHC4_RAT | Probable palmitoyltransferase ZDHHC4 OS=Rattus norvegicus GN=Zdhhc4 PE=2 SV=1 | 470 | 590 | 2.0E-13 |
sp|Q58CU4|ZDH16_BOVIN | Probable palmitoyltransferase ZDHHC16 OS=Bos taurus GN=ZDHHC16 PE=2 SV=1 | 450 | 613 | 2.0E-13 |
sp|P0CS68|PFA4_CRYNJ | Palmitoyltransferase PFA4 OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=PFA4 PE=3 SV=2 | 458 | 618 | 4.0E-13 |
sp|P0CS69|PFA4_CRYNB | Palmitoyltransferase PFA4 OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=PFA4 PE=3 SV=1 | 458 | 618 | 4.0E-13 |
sp|J9VJ99|PFA4_CRYNH | Palmitoyltransferase PFA4 OS=Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) GN=PFA4 PE=1 SV=2 | 458 | 618 | 5.0E-13 |
sp|Q3EBC2|ZDHC5_ARATH | Probable protein S-acyltransferase 17 OS=Arabidopsis thaliana GN=PAT17 PE=2 SV=1 | 413 | 526 | 6.0E-13 |
sp|Q7S3M5|AKR1_NEUCR | Palmitoyltransferase akr1 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ptr-1 PE=3 SV=2 | 370 | 522 | 7.0E-13 |
sp|Q6FW70|PFA3_CANGA | Palmitoyltransferase PFA3 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=PFA3 PE=3 SV=1 | 434 | 542 | 9.0E-13 |
sp|Q8R0N9|ZDHC1_MOUSE | Probable palmitoyltransferase ZDHHC1 OS=Mus musculus GN=Zdhhc1 PE=2 SV=2 | 469 | 601 | 1.0E-12 |
sp|Q6CUB5|PFA4_KLULA | Palmitoyltransferase PFA4 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=PFA4 PE=3 SV=1 | 468 | 546 | 1.0E-12 |
sp|E9PTT0|ZDH17_RAT | Palmitoyltransferase ZDHHC17 OS=Rattus norvegicus GN=Zdhhc17 PE=1 SV=1 | 383 | 596 | 1.0E-12 |
sp|Q6BLY8|PFA4_DEBHA | Palmitoyltransferase PFA4 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=PFA4 PE=3 SV=2 | 375 | 589 | 1.0E-12 |
sp|Q4WN54|SWF1_ASPFU | Palmitoyltransferase swf1 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=swf1 PE=3 SV=1 | 466 | 589 | 1.0E-12 |
sp|Q80TN5|ZDH17_MOUSE | Palmitoyltransferase ZDHHC17 OS=Mus musculus GN=Zdhhc17 PE=1 SV=2 | 451 | 596 | 1.0E-12 |
sp|Q9NPG8|ZDHC4_HUMAN | Probable palmitoyltransferase ZDHHC4 OS=Homo sapiens GN=ZDHHC4 PE=2 SV=1 | 470 | 590 | 1.0E-12 |
sp|Q6DR03|ZDHC3_ARATH | Protein S-acyltransferase 21 OS=Arabidopsis thaliana GN=PAT21 PE=2 SV=1 | 359 | 591 | 1.0E-12 |
sp|Q9D6H5|ZDHC4_MOUSE | Probable palmitoyltransferase ZDHHC4 OS=Mus musculus GN=Zdhhc4 PE=2 SV=1 | 470 | 602 | 2.0E-12 |
sp|Q9H8X9|ZDH11_HUMAN | Probable palmitoyltransferase ZDHHC11 OS=Homo sapiens GN=ZDHHC11 PE=2 SV=1 | 468 | 604 | 2.0E-12 |
sp|Q04629|SWF1_YEAST | Palmitoyltransferase SWF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SWF1 PE=1 SV=2 | 470 | 614 | 2.0E-12 |
sp|Q5B0V6|AKR1_EMENI | Palmitoyltransferase akr1 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=akr1 PE=3 SV=2 | 381 | 606 | 2.0E-12 |
sp|Q5Y5T3|ZDH23_MOUSE | Palmitoyltransferase ZDHHC23 OS=Mus musculus GN=Zdhhc23 PE=2 SV=1 | 448 | 574 | 2.0E-12 |
sp|P0C7U3|ZH11B_HUMAN | Probable palmitoyltransferase ZDHHC11B OS=Homo sapiens GN=ZDHHC11B PE=3 SV=1 | 468 | 539 | 3.0E-12 |
sp|P0CS66|AKR1_CRYNJ | Palmitoyltransferase AKR1 OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=AKR1 PE=3 SV=1 | 400 | 597 | 3.0E-12 |
sp|P0CS67|AKR1_CRYNB | Palmitoyltransferase AKR1 OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=AKR1 PE=3 SV=1 | 400 | 597 | 3.0E-12 |
sp|Q9M115|ZDH16_ARATH | Protein S-acyltransferase 18 OS=Arabidopsis thaliana GN=PAT18 PE=2 SV=2 | 464 | 595 | 3.0E-12 |
sp|Q4I8B6|AKR1_GIBZE | Palmitoyltransferase AKR1 OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=AKR1 PE=3 SV=1 | 470 | 591 | 3.0E-12 |
sp|Q8IUH5|ZDH17_HUMAN | Palmitoyltransferase ZDHHC17 OS=Homo sapiens GN=ZDHHC17 PE=1 SV=2 | 451 | 596 | 4.0E-12 |
sp|Q8WTX9|ZDHC1_HUMAN | Probable palmitoyltransferase ZDHHC1 OS=Homo sapiens GN=ZDHHC1 PE=2 SV=1 | 469 | 635 | 5.0E-12 |
sp|Q5FC64|ZDHCS_CAEEL | Palmitoyltransferase spe-10 OS=Caenorhabditis elegans GN=spe-10 PE=1 SV=1 | 467 | 589 | 6.0E-12 |
sp|Q5ADN9|PFA3_CANAL | Palmitoyltransferase PFA3 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PFA3 PE=3 SV=1 | 468 | 590 | 7.0E-12 |
sp|Q76IC6|ZDH23_RAT | Palmitoyltransferase ZDHHC23 OS=Rattus norvegicus GN=Zdhhc23 PE=1 SV=2 | 448 | 574 | 7.0E-12 |
sp|Q86A83|ZDHC2_DICDI | Putative ZDHHC-type palmitoyltransferase 2 OS=Dictyostelium discoideum GN=DDB_G0274739 PE=2 SV=2 | 468 | 546 | 1.0E-11 |
sp|Q8R173|ZDHC3_MOUSE | Palmitoyltransferase ZDHHC3 OS=Mus musculus GN=Zdhhc3 PE=1 SV=1 | 400 | 524 | 1.0E-11 |
sp|Q9NYG2|ZDHC3_HUMAN | Palmitoyltransferase ZDHHC3 OS=Homo sapiens GN=ZDHHC3 PE=1 SV=2 | 400 | 524 | 1.0E-11 |
sp|Q58DT3|ZDHC4_BOVIN | Probable palmitoyltransferase ZDHHC4 OS=Bos taurus GN=ZDHHC4 PE=2 SV=1 | 470 | 590 | 1.0E-11 |
sp|Q7RWM9|SWF1_NEUCR | Palmitoyltransferase SWF1 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=swf-1 PE=3 SV=1 | 402 | 526 | 2.0E-11 |
sp|Q74ZZ2|SWF1_ASHGO | Palmitoyltransferase SWF1 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=SWF1 PE=3 SV=1 | 470 | 526 | 4.0E-11 |
sp|Q7SCY6|PFA4_NEUCR | Palmitoyltransferase pfa4 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ptr-4 PE=3 SV=1 | 367 | 562 | 5.0E-11 |
sp|Q6FVE6|PFA4_CANGA | Palmitoyltransferase PFA4 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=PFA4 PE=3 SV=1 | 469 | 527 | 5.0E-11 |
sp|Q4P6L3|AKR1_USTMA | Palmitoyltransferase AKR1 OS=Ustilago maydis (strain 521 / FGSC 9021) GN=AKR1 PE=3 SV=1 | 363 | 517 | 5.0E-11 |
sp|Q9UVH3|AKR1_MORAP | Palmitoyltransferase AKR1 (Fragment) OS=Mortierella alpina PE=3 SV=1 | 470 | 595 | 1.0E-10 |
sp|Q75CB4|PFA4_ASHGO | Palmitoyltransferase PFA4 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=PFA4 PE=3 SV=2 | 469 | 528 | 2.0E-10 |
sp|Q5BD15|PFA4_EMENI | Palmitoyltransferase pfa4 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=pfa4 PE=3 SV=1 | 367 | 534 | 2.0E-10 |
sp|Q2HJ95|ZDHC6_BOVIN | Palmitoyltransferase ZDHHC6 OS=Bos taurus GN=ZDHHC6 PE=2 SV=1 | 465 | 532 | 2.0E-10 |
sp|Q5BC23|SWF1_EMENI | Palmitoyltransferase swf1 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=swf1 PE=3 SV=1 | 470 | 589 | 2.0E-10 |
sp|Q9CPV7|ZDHC6_MOUSE | Palmitoyltransferase ZDHHC6 OS=Mus musculus GN=Zdhhc6 PE=2 SV=1 | 389 | 522 | 3.0E-10 |
sp|Q5REH2|ZDHC6_PONAB | Palmitoyltransferase ZDHHC6 OS=Pongo abelii GN=ZDHHC6 PE=3 SV=1 | 467 | 522 | 4.0E-10 |
sp|Q9H6R6|ZDHC6_HUMAN | Palmitoyltransferase ZDHHC6 OS=Homo sapiens GN=ZDHHC6 PE=1 SV=1 | 467 | 522 | 4.0E-10 |
sp|O14345|PFA3_SCHPO | Palmitoyltransferase pfa3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=pfa3 PE=3 SV=1 | 468 | 593 | 5.0E-10 |
sp|Q09701|AKR1_SCHPO | Palmitoyltransferase akr1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=akr1 PE=3 SV=1 | 469 | 527 | 7.0E-10 |
sp|Q8IYP9|ZDH23_HUMAN | Palmitoyltransferase ZDHHC23 OS=Homo sapiens GN=ZDHHC23 PE=1 SV=3 | 470 | 574 | 7.0E-10 |
sp|Q12006|PFA4_YEAST | Palmitoyltransferase PFA4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PFA4 PE=1 SV=1 | 470 | 544 | 8.0E-10 |
sp|Q7XA86|ZDH11_ARATH | Protein S-acyltransferase 10 OS=Arabidopsis thaliana GN=PAT10 PE=1 SV=1 | 470 | 540 | 1.0E-09 |
sp|Q8T2Q0|ZDHC6_DICDI | Putative ZDHHC-type palmitoyltransferase 6 OS=Dictyostelium discoideum GN=DDB_G0275149 PE=2 SV=1 | 452 | 541 | 1.0E-09 |
sp|Q4WUK1|PFA5_ASPFU | Palmitoyltransferase pfa5 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=pfa5 PE=3 SV=2 | 469 | 567 | 1.0E-09 |
sp|Q6BP97|PFA5_DEBHA | Palmitoyltransferase PFA5 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=PFA5 PE=3 SV=2 | 470 | 602 | 2.0E-09 |
sp|Q8VC90|ZDH12_MOUSE | Probable palmitoyltransferase ZDHHC12 OS=Mus musculus GN=Zdhhc12 PE=2 SV=1 | 454 | 619 | 2.0E-09 |
sp|Q5B433|PFA5_EMENI | Palmitoyltransferase pfa5 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=pfa5 PE=3 SV=2 | 469 | 573 | 4.0E-09 |
sp|Q9LIH7|ZDHC7_ARATH | Protein S-acyltransferase 11 OS=Arabidopsis thaliana GN=PAT11 PE=2 SV=1 | 470 | 544 | 4.0E-09 |
sp|Q6CG20|SWF1_YARLI | Palmitoyltransferase SWF1 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=SWF1 PE=3 SV=1 | 408 | 517 | 7.0E-09 |
sp|Q554E7|ZDHC5_DICDI | Putative ZDHHC-type palmitoyltransferase 5 OS=Dictyostelium discoideum GN=DDB_G0275097 PE=3 SV=1 | 470 | 524 | 2.0E-08 |
sp|Q6DGF5|ZDH12_RAT | Probable palmitoyltransferase ZDHHC12 OS=Rattus norvegicus GN=Zdhhc12 PE=2 SV=1 | 465 | 619 | 2.0E-08 |
sp|Q4IMZ7|PFA4_GIBZE | Palmitoyltransferase PFA4 OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=PFA4 PE=3 SV=1 | 468 | 560 | 4.0E-08 |
sp|Q6C7Q0|PFA4_YARLI | Palmitoyltransferase PFA4 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=PFA4 PE=3 SV=1 | 469 | 589 | 6.0E-08 |
sp|Q96GR4|ZDH12_HUMAN | Probable palmitoyltransferase ZDHHC12 OS=Homo sapiens GN=ZDHHC12 PE=2 SV=2 | 465 | 619 | 2.0E-07 |
sp|Q5NVB9|ZDH13_PONAB | Palmitoyltransferase ZDHHC13 OS=Pongo abelii GN=ZDHHC13 PE=2 SV=1 | 470 | 532 | 2.0E-07 |
sp|Q6UX98|ZDH24_HUMAN | Probable palmitoyltransferase ZDHHC24 OS=Homo sapiens GN=ZDHHC24 PE=1 SV=1 | 469 | 590 | 2.0E-07 |
sp|Q4R690|ZDH13_MACFA | Palmitoyltransferase ZDHHC13 OS=Macaca fascicularis GN=ZDHHC13 PE=2 SV=1 | 470 | 532 | 3.0E-07 |
sp|Q8IUH4|ZDH13_HUMAN | Palmitoyltransferase ZDHHC13 OS=Homo sapiens GN=ZDHHC13 PE=1 SV=3 | 470 | 535 | 4.0E-07 |
sp|Q54VH7|ZDHC8_DICDI | Putative ZDHHC-type palmitoyltransferase 8 OS=Dictyostelium discoideum GN=DDB_G0280329 PE=2 SV=1 | 477 | 527 | 7.0E-07 |
sp|Q6IR37|ZDH24_MOUSE | Probable palmitoyltransferase ZDHHC24 OS=Mus musculus GN=Zdhhc24 PE=2 SV=2 | 469 | 594 | 1.0E-06 |
sp|Q6C4W5|PFA3_YARLI | Palmitoyltransferase PFA3 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=PFA3 PE=3 SV=1 | 467 | 596 | 1.0E-06 |
sp|Q9CWU2|ZDH13_MOUSE | Palmitoyltransferase ZDHHC13 OS=Mus musculus GN=Zdhhc13 PE=1 SV=2 | 470 | 533 | 1.0E-06 |
sp|Q552M6|ZDHC7_DICDI | Putative ZDHHC-type palmitoyltransferase 7 OS=Dictyostelium discoideum GN=DDB_G0276017 PE=2 SV=1 | 470 | 610 | 1.0E-06 |
sp|A0PK84|ZDH22_MOUSE | Palmitoyltransferase ZDHHC22 OS=Mus musculus GN=Zdhhc22 PE=2 SV=1 | 478 | 535 | 2.0E-06 |
sp|Q03289|PFA5_YEAST | Palmitoyltransferase PFA5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PFA5 PE=1 SV=1 | 470 | 612 | 2.0E-06 |
sp|Q2TGI8|ZDH22_RAT | Palmitoyltransferase ZDHHC22 OS=Rattus norvegicus GN=Zdhhc22 PE=2 SV=1 | 478 | 535 | 2.0E-06 |
sp|Q6C7D1|PFA5_YARLI | Palmitoyltransferase PFA5 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=PFA5 PE=3 SV=1 | 468 | 530 | 3.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016409 | palmitoyltransferase activity | Yes |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | No |
GO:0016740 | transferase activity | No |
GO:0003824 | catalytic activity | No |
GO:0003674 | molecular_function | No |
GO:0016746 | acyltransferase activity | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Golgi apparatus | Transmembrane domain | 0.1493 | 0.1074 | 0.036 | 0.4931 | 0.1558 | 0.0039 | 0.4268 | 0.2567 | 0.7139 | 0.0073 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 369 | 391 | 22 |
2 | 396 | 418 | 22 |
3 | 516 | 538 | 22 |
4 | 558 | 580 | 22 |
Orthofinder run ID | 4 |
Orthogroup | 2108 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
Protein | >Hirsu2|2490 MEHPDSDEQPMARADAADGPPSARHPRPVSVVSSRIADVASEAAGDARPPRYGSSPPPKGPDLASRPDIRPDTAQ TGASPKAAWPAPQARRTSYASGLPAKRGSIASVSNASAGRAPSLTTKTHVPSITSNAFFHPMSSQKLQAQRAAVS RPAAALRRPSQPQPHLADLDDAATDLGGSVVNENIVAHHRQLSGADNQRARAPSRGTEMTEHENFDRVTGNTSPS HGHNPNGSQPDSVRPLRRTSNPRPRLSVTAERGFKDLGSLPSPIKSSRSFRSSFLLPNRSDHGQASQNRSTEGAE KLSSSNSSPRLRPVDSLGQPAPPSAKAQAQVGRGTPARPEGRVYQYFDGNTVFCLGGRWQNTKHRPINVATGLLV LVPCVLFYVFEASWLWHNVSPAIPITFAYLTYICLSSFLHASVSDPGILPRNLHRFPPLYEQEDLLRVGPPTNDW TLIKSVEGSTAAMEVPVKHCRTCNIWRPPRAHHCRLCDNCIETHDHHCVWLNNCVGKRNYRFFFTFVTSATLLAA YLVATSLAQVLLYMDREHVSFSRAIDHFRVPFALAILGFFEFLYPAALMGYHLFLMARGETTREFMNSHKFAKKQ RYRAFSQGGIARNLLAVLCRPRPPTYYRFKNRYRHGDQRLGSRRHHHARKNSQGLEMDAVQPGGSSRGFQGPVAL REPSRG* |
Coding | >Hirsu2|2490 ATGGAGCACCCAGACTCGGACGAACAGCCCATGGCTCGCGCCGACGCCGCCGACGGTCCGCCGTCCGCGCGCCAC CCCCGGCCCGTCAGCGTCGTTTCGTCCCGCATCGCCGACGTCGCCAGCGAAGCCGCCGGCGATGCGAGACCGCCG CGCTACGGCTCGAGCCCGCCGCCCAAGGGTCCCGACCTTGCCTCGCGCCCCGACATCCGCCCCGACACGGCCCAG ACGGGAGCCTCGCCCAAGGCCGCCTGGCCCGCTCCTCAGGCCCGGCGCACGAGCTACGCCTCCGGCTTGCCCGCC AAGAGAGGCAGCATCGCCAGCGTGTCCAACGCATCCGCCGGCCGCGCCCCCAGCCTGACGACCAAGACGCACGTC CCCTCCATCACCTCCAACGCCTTCTTCCATCCCATGAGCTCGCAGAAGCTGCAGGCCCAGCGCGCTGCCGTCTCG AGGCCCGCCGCCGCCCTCCGCCGCCCCTCGCAGCCGCAACCCCATCTCGCCGACCTGGACGATGCCGCCACCGAC CTGGGCGGCAGCGTCGTCAACGAGAATATCGTCGCCCATCACCGCCAGCTGAGCGGCGCCGACAACCAGCGCGCG CGCGCGCCCTCGCGCGGCACCGAGATGACCGAGCACGAGAACTTCGATCGCGTCACGGGAAACACGAGCCCCTCG CACGGCCACAACCCCAACGGCAGCCAGCCGGATAGTGTCCGGCCGCTGCGCCGCACCTCGAACCCCCGCCCCCGT CTCAGCGTCACGGCCGAAAGAGGTTTCAAGGATCTCGGGAGTCTGCCGAGCCCCATCAAATCCTCGCGCTCCTTC CGCTCCAGCTTTCTCCTCCCCAACCGCAGCGACCACGGCCAGGCCAGCCAGAACCGGAGCACCGAGGGCGCCGAG AAGCTCTCGTCCAGCAACTCGTCTCCTCGCCTGCGGCCCGTCGACTCCCTCGGCCAGCCCGCGCCGCCGTCCGCC AAGGCCCAGGCCCAGGTTGGGCGCGGCACCCCGGCTCGGCCGGAGGGCCGCGTCTACCAGTACTTCGATGGCAAC ACCGTCTTCTGCCTCGGCGGCCGCTGGCAAAACACCAAACACAGGCCCATCAACGTCGCGACCGGCCTCCTGGTC CTGGTGCCCTGTGTGCTCTTCTACGTCTTCGAGGCCTCCTGGTTGTGGCACAACGTCTCGCCCGCCATCCCAATC ACCTTTGCCTACCTGACCTACATCTGCCTCTCCTCCTTCCTGCACGCCTCCGTCTCGGATCCCGGAATCCTCCCT CGCAACCTTCACCGGTTCCCCCCCCTCTACGAGCAGGAGGACCTGCTGCGCGTCGGGCCGCCCACCAACGACTGG ACGCTCATCAAGTCGGTCGAGGGAAGCACGGCGGCCATGGAGGTGCCCGTCAAGCACTGTCGCACCTGCAACATC TGGCGGCCGCCCCGCGCCCACCACTGCCGCCTCTGCGACAACTGCATCGAGACGCACGACCACCACTGCGTCTGG CTCAACAACTGTGTCGGGAAGCGCAACTATCGCTTCTTCTTCACCTTTGTCACGTCGGCCACCCTGCTGGCCGCC TACCTCGTCGCCACCAGTCTGGCCCAGGTGCTCCTGTACATGGATCGCGAGCACGTTTCCTTCTCCAGGGCCATC GACCACTTCCGCGTGCCCTTCGCCCTCGCCATCCTCGGCTTCTTCGAGTTCCTCTACCCGGCCGCCCTGATGGGC TACCACCTGTTCCTGATGGCGCGAGGCGAGACGACGCGCGAGTTCATGAACTCGCACAAGTTCGCCAAGAAGCAG CGATACCGCGCCTTCAGCCAGGGCGGCATCGCGAGAAACCTGCTTGCCGTCCTCTGCCGTCCGCGCCCGCCGACC TACTACCGCTTCAAGAACCGGTACCGGCACGGCGACCAGCGGCTCGGCTCCCGGCGACACCACCACGCCAGGAAG AATTCTCAGGGGCTCGAGATGGACGCGGTCCAGCCCGGCGGCTCGTCCCGAGGATTCCAAGGCCCGGTAGCGCTA AGAGAGCCGAGCCGAGGATGA |
Transcript | >Hirsu2|2490 ATGGAGCACCCAGACTCGGACGAACAGCCCATGGCTCGCGCCGACGCCGCCGACGGTCCGCCGTCCGCGCGCCAC CCCCGGCCCGTCAGCGTCGTTTCGTCCCGCATCGCCGACGTCGCCAGCGAAGCCGCCGGCGATGCGAGACCGCCG CGCTACGGCTCGAGCCCGCCGCCCAAGGGTCCCGACCTTGCCTCGCGCCCCGACATCCGCCCCGACACGGCCCAG ACGGGAGCCTCGCCCAAGGCCGCCTGGCCCGCTCCTCAGGCCCGGCGCACGAGCTACGCCTCCGGCTTGCCCGCC AAGAGAGGCAGCATCGCCAGCGTGTCCAACGCATCCGCCGGCCGCGCCCCCAGCCTGACGACCAAGACGCACGTC CCCTCCATCACCTCCAACGCCTTCTTCCATCCCATGAGCTCGCAGAAGCTGCAGGCCCAGCGCGCTGCCGTCTCG AGGCCCGCCGCCGCCCTCCGCCGCCCCTCGCAGCCGCAACCCCATCTCGCCGACCTGGACGATGCCGCCACCGAC CTGGGCGGCAGCGTCGTCAACGAGAATATCGTCGCCCATCACCGCCAGCTGAGCGGCGCCGACAACCAGCGCGCG CGCGCGCCCTCGCGCGGCACCGAGATGACCGAGCACGAGAACTTCGATCGCGTCACGGGAAACACGAGCCCCTCG CACGGCCACAACCCCAACGGCAGCCAGCCGGATAGTGTCCGGCCGCTGCGCCGCACCTCGAACCCCCGCCCCCGT CTCAGCGTCACGGCCGAAAGAGGTTTCAAGGATCTCGGGAGTCTGCCGAGCCCCATCAAATCCTCGCGCTCCTTC CGCTCCAGCTTTCTCCTCCCCAACCGCAGCGACCACGGCCAGGCCAGCCAGAACCGGAGCACCGAGGGCGCCGAG AAGCTCTCGTCCAGCAACTCGTCTCCTCGCCTGCGGCCCGTCGACTCCCTCGGCCAGCCCGCGCCGCCGTCCGCC AAGGCCCAGGCCCAGGTTGGGCGCGGCACCCCGGCTCGGCCGGAGGGCCGCGTCTACCAGTACTTCGATGGCAAC ACCGTCTTCTGCCTCGGCGGCCGCTGGCAAAACACCAAACACAGGCCCATCAACGTCGCGACCGGCCTCCTGGTC CTGGTGCCCTGTGTGCTCTTCTACGTCTTCGAGGCCTCCTGGTTGTGGCACAACGTCTCGCCCGCCATCCCAATC ACCTTTGCCTACCTGACCTACATCTGCCTCTCCTCCTTCCTGCACGCCTCCGTCTCGGATCCCGGAATCCTCCCT CGCAACCTTCACCGGTTCCCCCCCCTCTACGAGCAGGAGGACCTGCTGCGCGTCGGGCCGCCCACCAACGACTGG ACGCTCATCAAGTCGGTCGAGGGAAGCACGGCGGCCATGGAGGTGCCCGTCAAGCACTGTCGCACCTGCAACATC TGGCGGCCGCCCCGCGCCCACCACTGCCGCCTCTGCGACAACTGCATCGAGACGCACGACCACCACTGCGTCTGG CTCAACAACTGTGTCGGGAAGCGCAACTATCGCTTCTTCTTCACCTTTGTCACGTCGGCCACCCTGCTGGCCGCC TACCTCGTCGCCACCAGTCTGGCCCAGGTGCTCCTGTACATGGATCGCGAGCACGTTTCCTTCTCCAGGGCCATC GACCACTTCCGCGTGCCCTTCGCCCTCGCCATCCTCGGCTTCTTCGAGTTCCTCTACCCGGCCGCCCTGATGGGC TACCACCTGTTCCTGATGGCGCGAGGCGAGACGACGCGCGAGTTCATGAACTCGCACAAGTTCGCCAAGAAGCAG CGATACCGCGCCTTCAGCCAGGGCGGCATCGCGAGAAACCTGCTTGCCGTCCTCTGCCGTCCGCGCCCGCCGACC TACTACCGCTTCAAGAACCGGTACCGGCACGGCGACCAGCGGCTCGGCTCCCGGCGACACCACCACGCCAGGAAG AATTCTCAGGGGCTCGAGATGGACGCGGTCCAGCCCGGCGGCTCGTCCCGAGGATTCCAAGGCCCGGTAGCGCTA AGAGAGCCGAGCCGAGGATGA |
Gene | >Hirsu2|2490 ATGGAGCACCCAGACTCGGACGAACAGCCCATGGCTCGCGCCGACGCCGCCGACGGTCCGCCGTCCGCGCGCCAC CCCCGGCCCGTCAGCGTCGTTTCGTCCCGCATCGCCGACGTCGCCAGCGAAGCCGCCGGCGATGCGAGACCGCCG CGCTACGGCTCGAGCCCGCCGCCCAAGGGTCCCGACCTTGCCTCGCGCCCCGACATCCGCCCCGACACGGCCCAG ACGGGAGCCTCGCCCAAGGCCGCCTGGCCCGCTCCTCAGGCCCGGCGCACGAGCTACGCCTCCGGCTTGCCCGCC AAGAGAGGCAGCATCGCCAGCGTGTCCAACGCATCCGCCGGCCGCGCCCCCAGCCTGACGACCAAGACGCACGTC CCCTCCATCACCTCCAACGCCTTCTTCCATCCCATGAGCTCGCAGAAGCTGCAGGCCCAGCGCGCTGCCGTCTCG AGGCCCGCCGCCGCCCTCCGCCGCCCCTCGCAGCCGCAACCCCATCTCGCCGACCTGGACGATGCCGCCACCGAC CTGGGCGGCAGCGTCGTCAACGAGAATATCGTCGCCCATCACCGCCAGCTGAGCGGCGCCGACAACCAGCGCGCG CGCGCGCCCTCGCGCGGCACCGAGATGACCGAGCACGAGAACTTCGATCGCGTCACGGGAAACACGAGCCCCTCG CACGGCCACAACCCCAACGGCAGCCAGCCGGATAGTGTCCGGCCGCTGCGCCGCACCTCGAACCCCCGCCCCCGT CTCAGCGTCACGGCCGAAAGAGGTTTCAAGGATCTCGGGAGTCTGCCGAGCCCCATCAAATCCTCGCGCTCCTTC CGCTCCAGCTTTCTCCTCCCCAACCGCAGCGACCACGGCCAGGCCAGCCAGAACCGGAGCACCGAGGGCGCCGAG AAGCTCTCGTCCAGCAACTCGTCTCCTCGCCTGCGGCCCGTCGACTCCCTCGGCCAGCCCGCGCCGCCGTCCGCC AAGGCCCAGGCCCAGGTTGGGCGCGGCACCCCGGCTCGGCCGGAGGGCCGCGTCTACCAGTACTTCGATGGCAAC ACCGTCTTCTGCCTCGGCGGCCGCTGGCAAAACACCAAACACAGGCCCATCAACGTCGCGACCGGCCTCCTGGTC CTGGTGCCCTGTGTGCTCTTCTACGTCTTCGAGGCCTCCTGGTTGTGGCACAACGTCTCGCCCGCCATCCCAATC ACCTTTGCCTACCTGACCTACATCTGCCTCTCCTCCTTCCTGCACGCCTCCGTCTCGGATCCCGGAGTAAGTGGC ACGCCCCTCGCCTGTCAGCTTGGATGCCCGTCGTCGAGGAGTGGCTAACGTGACGGACAGATCCTCCCTCGCAAC CTTCACCGGTTCCCCCCCCTCTACGAGCAGGAGGACCTGCTGCGCGTCGGGCCGCCCACCAACGACTGGACGCTC ATCAAGTCGGTCGAGGGAAGCACGGCGGCCATGGAGGTGCCCGTCAAGCACTGTCGCACCTGCAACATCTGGCGG CCGCCCCGCGCCCACCACTGCCGCCTCTGCGACAACTGCATCGAGACGCACGACCACCACTGCGTCTGGCTCAAC AACTGTGTCGGGAAGCGCAACTATCGCTTCTTCTTCACCTTTGTCACGTCGGCCACCCTGCTGGCCGCCTACCTC GTCGCCACCAGTCTGGCCCAGGTGCTCCTGTACATGGATCGCGAGCACGTTTCCTTCTCCAGGGCCATCGACCAC TTCCGCGTGCCCTTCGCCCTCGCCATCCTCGGCTTCTTCGAGTTCCTCTACCCGGCCGCCCTGATGGGCTACCAC CTGTTCCTGATGGCGCGAGGCGAGACGACGCGCGAGTTCATGAACTCGCACAAGTTCGCCAAGAAGCAGCGATAC CGCGCCTTCAGCCAGGGCGGCATCGCGAGAAACCTGCTTGCCGTCCTCTGCCGTCCGCGCCCGCCGACCTACTAC CGCTTCAAGAACCGGTACCGGCACGGCGACCAGCGGCTCGGCTCCCGGCGACACCACCACGCCAGGAAGAATTCT CAGGGGCTCGAGATGGACGCGGTCCAGCCCGGCGGCTCGTCCCGAGGATTCCAAGGCCCGGTAGCGCTAAGAGAG CCGAGCCGAGGATGA |