Symbol:
BTK
Name:
Bruton tyrosine kinase
RGD ID:
14174315
Description:
ENCODES a protein that exhibits protein tyrosine kinase activity (ortholog); INVOLVED IN cellular response to molecule of fungal origin (ortholog); cellular response to reactive oxygen species (ortholog); eosinophil homeostasis (ortholog); PARTICIPATES IN erythropoietin signaling pathway; FasL mediated signaling pathway; Fc epsilon receptor mediated signaling pathway; ASSOCIATED WITH Adenoviridae Infections (ortholog); agammaglobulinemia (ortholog); agammaglobulinemia 1 (ortholog); FOUND IN perinuclear region of cytoplasm (ortholog)
Type:
protein-coding
RefSeq Status:
VALIDATED
Previously known as:
Bruton agammaglobulinemia tyrosine kinase; tyrosine-protein kinase BTK
RGD Orthologs
Alliance Orthologs
More Info
more info ...
More Info
Latest Assembly:
Sscrofa11.1 - Pig Sscrofa11.1 Assembly
Position:
JBrowse:
View Region in Genome Browser (JBrowse)
Model
BTK Pig agammaglobulinemia 1 ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Autosomal recessive agammaglobulinemia 1 ClinVar PMID:10092645|PMID:11206059|PMID:11410123|PMID:11445810|PMID:11472359|PMID:11668622|PMID:11742281|PMID:12217331|PMID:14974089|PMID:15661032|PMID:16862044|PMID:16951917|PMID:17327079|PMID:17765309|PMID:18518992|PMID:19039656|PMID:19419768|PMID:19904586|PMID:20529312|PMID:23424595|PMID:25741868|PMID:27512878|PMID:27980540|PMID:28492532|PMID:29424453|PMID:29503650|PMID:30072168|PMID:30564228|PMID:7678697|PMID:7809124|PMID:7849697|PMID:7849721|PMID:7880320|PMID:8090769|PMID:8162056|PMID:8380905|PMID:8594569|PMID:8695804|PMID:8939985|PMID:9143921|PMID:9188445|PMID:9445504|PMID:9524120|PMID:9545398|PMID:9880544 BTK Pig autistic disorder ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Autism ClinVar PMID:21681106|PMID:30208311 BTK Pig autosomal hemophilia A ISO RGD:1342660 8554872 ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA A ClinVar PMID:31690835 BTK Pig common variable immunodeficiency ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Common variable immunodeficiency ClinVar PMID:11472359|PMID:18241230|PMID:25741868|PMID:28492532 BTK Pig deafness-dystonia-optic neuronopathy syndrome ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Deafness dystonia syndrome ClinVar BTK Pig developmental and epileptic encephalopathy 9 ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 9 ClinVar PMID:28492532 BTK Pig diffuse large B-cell lymphoma ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Diffuse large B cell lymphoma ClinVar PMID:24869598|PMID:25082755|PMID:25189416|PMID:25741868|PMID:27199251|PMID:28049639|PMID:28212557|PMID:28418267|PMID:28492532|PMID:29496671|PMID:29875397|PMID:30018078|PMID:32455989|PMID:33154951|PMID:36029036 BTK Pig Fabry disease ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Fabry disease ClinVar PMID:10666480|PMID:12175777|PMID:15661032|PMID:16862044|PMID:19419768|PMID:28492532|PMID:31795557 BTK Pig factor VIII deficiency ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Factor 8 deficiency, congenital ClinVar PMID:31690835 BTK Pig genetic disease ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:28492532|PMID:33584693|PMID:36790564 BTK Pig isolated growth hormone deficiency type III ISO RGD:1342660 8554872 ClinVar Annotator: match by term: BTK-related condition | ClinVar Annotator: match by term: X-linked agammaglobulinemia more ... ClinVar PMID:10092645|PMID:10373551|PMID:10612838|PMID:10666480|PMID:10678660|PMID:10737994|PMID:10754312|PMID:10844531|PMID:10859027|PMID:10887125|PMID:11027452|PMID:11102984|PMID:11206059|PMID:11410123|PMID:11438999|PMID:11445810|PMID:11472359|PMID:11527964|PMID:11555397|PMID:11564824|PMID:11668622|PMID:11742281|PMID:11809909|PMID:11892085|PMID:11956200|PMID:12175777|PMID:12204007|PMID:12217331|PMID:1240516|PMID:12405164|PMID:12655572|PMID:12768435|PMID:14974089|PMID:15024743|PMID:15112668|PMID:15358621|PMID:15661032|PMID:15821893|PMID:16159644|PMID:16160918|PMID:16199547|PMID:16297664|PMID:16712653|PMID:16729790|PMID:16751014|PMID:16862044|PMID:16913189|PMID:16943681|PMID:16951917|PMID:17045652|PMID:17327079|PMID:17576681|PMID:17765309|PMID:18241230|PMID:18518992|PMID:18677443|PMID:19039656|PMID:19302039|PMID:19419768|PMID:19763152|PMID:19904586|PMID:20307669|PMID:20529312|PMID:20721470|PMID:20723125|PMID:21039741|PMID:21397315|PMID:21520333|PMID:21984432|PMID:22378381|PMID:22406018|PMID:22736418|PMID:23335184|PMID:23424595|PMID:24001798|PMID:24033266|PMID:24383975|PMID:24477949|PMID:24586880|PMID:24658450|PMID:24869597|PMID:24869598|PMID:24885015|PMID:25082755|PMID:25189416|PMID:25270678|PMID:25525159|PMID:25640679|PMID:25741868|PMID:25777788|PMID:26915675|PMID:26931785|PMID:26960951|PMID:27199251|PMID:27512878|PMID:27535475|PMID:27577878|PMID:27593100|PMID:27980540|PMID:28049639|PMID:28212557|PMID:28359783|PMID:28418267|PMID:28492532|PMID:2896233|PMID:29202590|PMID:29424453|PMID:29496671|PMID:29503650|PMID:29658452|PMID:29709555|PMID:29875397|PMID:29921932|PMID:30018078|PMID:30072168|PMID:30240888|PMID:30290665|PMID:30311057|PMID:30564228|PMID:30697212|PMID:30882382|PMID:31795557|PMID:32067425|PMID:32117230|PMID:32441320|PMID:32455989|PMID:32477911|PMID:32492159|PMID:32499645|PMID:32552675|PMID:32581362|PMID:32888943|PMID:33013854|PMID:33042921|PMID:33154951|PMID:33224144|PMID:33225392|PMID:33226337|PMID:33377626|PMID:33584693|PMID:33815962|PMID:34029777|PMID:34177947|PMID:34182127|PMID:34249912|PMID:34262886|PMID:3486747|PMID:34975878|PMID:35196427|PMID:35382780|PMID:35482138|PMID:36029036|PMID:36790564|PMID:4697357|PMID:7554467|PMID:7627183|PMID:7633420|PMID:7633429|PMID:7678697|PMID:7711734|PMID:7809124|PMID:7849697|PMID:7849721|PMID:7880320|PMID:7897635|PMID:8013627|PMID:8090769|PMID:8162018|PMID:8162056|PMID:8164701|PMID:8164707|PMID:8332900|PMID:8332901|PMID:8380905|PMID:8562928|PMID:8594569|PMID:8644706|PMID:8695804|PMID:8723128|PMID:8834236|PMID:8851194|PMID:8938104|PMID:8939985|PMID:9106525|PMID:9143921|PMID:9188445|PMID:9192269|PMID:9260159|PMID:9445504|PMID:9524120|PMID:9536098|PMID:9545398|PMID:9880544 BTK Pig primary immunodeficiency disease ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Inherited Immunodeficiency Diseases ClinVar PMID:11809909|PMID:12405164|PMID:15661032|PMID:16862044|PMID:17576681|PMID:19419768|PMID:25741868|PMID:28492532|PMID:32499645|PMID:32581362|PMID:7627183|PMID:7849697|PMID:9536098|PMID:9545398 BTK Pig ROLANDIC EPILEPSY, INTELLECTUAL DISABILITY, AND SPEECH DYSPRAXIA, X-LINKED ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked ClinVar PMID:28492532 BTK Pig syndromic X-linked intellectual disability Lubs type ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type ClinVar PMID:25741868 BTK Pig X-linked agammaglobulinemia ISO RGD:1342660 8554872 ClinVar Annotator: match by term: X-linked agammaglobulinemia ClinVar PMID:10092645|PMID:10373551|PMID:10678660|PMID:10737994|PMID:10754312|PMID:10844531|PMID:10859027|PMID:10887125|PMID:11102984|PMID:11206059|PMID:11410123|PMID:11445810|PMID:11472359|PMID:11527964|PMID:11555397|PMID:11564824|PMID:11586956|PMID:11668622|PMID:11742281|PMID:11809909|PMID:12204007|PMID:12217331|PMID:12405164|PMID:12655572|PMID:12768435|PMID:14974089|PMID:15024743|PMID:15112668|PMID:15661032|PMID:16053733|PMID:16159644|PMID:16160918|PMID:16199547|PMID:16712653|PMID:16751014|PMID:16862044|PMID:16913189|PMID:16951917|PMID:17045652|PMID:17164954|PMID:17327079|PMID:17576681|PMID:17765309|PMID:18241230|PMID:18518992|PMID:18677443|PMID:19039656|PMID:19419768|PMID:19904586|PMID:20529312|PMID:21397315|PMID:23335184|PMID:23424595|PMID:24001798|PMID:24033266|PMID:24383975|PMID:24820629|PMID:24885015|PMID:25142992|PMID:25525159|PMID:25741868|PMID:25777788|PMID:26915675|PMID:26981933|PMID:27512878|PMID:27577878|PMID:27980540|PMID:28492532|PMID:2896233|PMID:29424453|PMID:29503650|PMID:29921932|PMID:30072168|PMID:30240888|PMID:30290665|PMID:30311057|PMID:30564228|PMID:30627929|PMID:30697212|PMID:31803177|PMID:32499645|PMID:32581362|PMID:32888943|PMID:33042921|PMID:33224144|PMID:33377626|PMID:34029777|PMID:3486747|PMID:34975878|PMID:4697357|PMID:7554467|PMID:7627183|PMID:7633420|PMID:7633429|PMID:7678697|PMID:7711734|PMID:7809124|PMID:7849697|PMID:7849721|PMID:7880320|PMID:8090769|PMID:8162018|PMID:8162056|PMID:8164701|PMID:8164707|PMID:8332900|PMID:8332901|PMID:8380905|PMID:8594569|PMID:8644706|PMID:8695804|PMID:8938104|PMID:8939985|PMID:9106525|PMID:9143921|PMID:9188445|PMID:9260159|PMID:9445504|PMID:9524120|PMID:9536098|PMID:9545398|PMID:9880544 BTK Pig X-Linked Hypogammaglobulinemia ISO RGD:1342660 8554872 ClinVar Annotator: match by term: Hypogammaglobulinemia, X-linked ClinVar PMID:8758136
Imported Annotations - SMPDB
Imported Annotations - PID (archival)
BTK (Sus scrofa - pig)
BTK (Homo sapiens - human)
Human Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCh38 X 101,349,450 - 101,390,796 (-) NCBI GRCh38 GRCh38 hg38 GRCh38 GRCh38.p14 Ensembl X 101,349,338 - 101,390,796 (-) Ensembl GRCh38 hg38 GRCh38 GRCh37 X 100,604,438 - 100,645,784 (-) NCBI GRCh37 GRCh37 hg19 GRCh37 Build 36 X 100,491,098 - 100,527,838 (-) NCBI NCBI36 Build 36 hg18 NCBI36 Build 34 X 100,410,586 - 100,447,327 NCBI Celera X 101,123,894 - 101,160,669 (-) NCBI Celera Cytogenetic Map X q22.1 NCBI HuRef X 90,410,583 - 90,447,505 (-) NCBI HuRef CHM1_1 X 100,497,918 - 100,534,692 (-) NCBI CHM1_1 T2T-CHM13v2.0 X 99,793,571 - 99,834,908 (-) NCBI T2T-CHM13v2.0
Btk (Mus musculus - house mouse)
Mouse Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCm39 X 133,443,083 - 133,484,366 (-) NCBI GRCm39 GRCm39 mm39 GRCm39 Ensembl X 133,443,085 - 133,484,319 (-) Ensembl GRCm39 Ensembl GRCm38 X 134,542,334 - 134,583,628 (-) NCBI GRCm38 GRCm38 mm10 GRCm38 GRCm38.p6 Ensembl X 134,542,336 - 134,583,570 (-) Ensembl GRCm38 mm10 GRCm38 MGSCv37 X 131,076,880 - 131,117,679 (-) NCBI GRCm37 MGSCv37 mm9 NCBIm37 MGSCv36 X 129,888,761 - 129,929,466 (-) NCBI MGSCv36 mm8 Celera X 117,421,885 - 117,462,725 (-) NCBI Celera Cytogenetic Map X E3 NCBI cM Map X 56.18 NCBI
Btk (Rattus norvegicus - Norway rat)
Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCr8 X 102,016,070 - 102,055,448 (-) NCBI GRCr8 mRatBN7.2 X 97,722,796 - 97,762,315 (-) NCBI mRatBN7.2 mRatBN7.2 mRatBN7.2 Ensembl X 97,722,802 - 97,761,853 (-) Ensembl mRatBN7.2 Ensembl UTH_Rnor_SHR_Utx X 99,397,016 - 99,436,088 (-) NCBI Rnor_SHR UTH_Rnor_SHR_Utx UTH_Rnor_SHRSP_BbbUtx_1.0 X 102,907,749 - 102,946,794 (-) NCBI Rnor_SHRSP UTH_Rnor_SHRSP_BbbUtx_1.0 UTH_Rnor_WKY_Bbb_1.0 X 100,410,180 - 100,449,237 (-) NCBI Rnor_WKY UTH_Rnor_WKY_Bbb_1.0 Rnor_6.0 X 105,360,922 - 105,390,580 (-) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_6.0 Ensembl X 105,360,922 - 105,390,580 (-) Ensembl Rnor6.0 rn6 Rnor6.0 Rnor_5.0 X 105,250,666 - 105,279,934 (-) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 RGSC_v3.4 X 121,998,935 - 122,030,289 (-) NCBI RGSC3.4 RGSC_v3.4 rn4 RGSC3.4 RGSC_v3.1 X 122,072,367 - 122,103,722 (-) NCBI Celera X 98,764,036 - 98,794,122 (-) NCBI Celera Cytogenetic Map X q32 NCBI
Btk (Chinchilla lanigera - long-tailed chinchilla)
Chinchilla Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl ChiLan1.0 Ensembl NW_004955503 7,482,793 - 7,515,120 (-) Ensembl ChiLan1.0 ChiLan1.0 NW_004955503 7,483,819 - 7,515,085 (-) NCBI ChiLan1.0 ChiLan1.0
BTK (Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl NHGRI_mPanPan1-v2 X 100,948,666 - 100,985,544 (-) NCBI NHGRI_mPanPan1-v2 NHGRI_mPanPan1 X 100,952,265 - 100,989,149 (-) NCBI NHGRI_mPanPan1 Mhudiblu_PPA_v0 X 90,551,874 - 90,588,786 (-) NCBI Mhudiblu_PPA_v0 Mhudiblu_PPA_v0 panPan3 PanPan1.1 X 100,684,017 - 100,720,868 (-) NCBI panpan1.1 PanPan1.1 panPan2 PanPan1.1 Ensembl X 100,684,017 - 100,725,187 (-) Ensembl panpan1.1 panPan2
BTK (Canis lupus familiaris - dog)
Dog Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl CanFam3.1 X 75,270,952 - 75,302,663 (-) NCBI CanFam3.1 CanFam3.1 canFam3 CanFam3.1 CanFam3.1 Ensembl X 75,270,979 - 75,302,562 (-) Ensembl CanFam3.1 canFam3 CanFam3.1 ROS_Cfam_1.0 X 76,691,359 - 76,723,087 (-) NCBI ROS_Cfam_1.0 ROS_Cfam_1.0 Ensembl X 76,691,367 - 76,723,042 (-) Ensembl ROS_Cfam_1.0 Ensembl UMICH_Zoey_3.1 X 74,255,464 - 74,287,205 (-) NCBI UMICH_Zoey_3.1 UNSW_CanFamBas_1.0 X 75,915,885 - 75,947,610 (-) NCBI UNSW_CanFamBas_1.0 UU_Cfam_GSD_1.0 X 75,678,325 - 75,710,045 (-) NCBI UU_Cfam_GSD_1.0
Btk (Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
BTK (Chlorocebus sabaeus - green monkey)
Btk (Heterocephalus glaber - naked mole-rat)
.
Click on a value in the shaded box below the category label to view a detailed expression data table for that system.
alimentary part of gastrointestinal system
10
4
23
3
2
5
14
12
23
3
6
3
Too many to show, limit is 500. Download them if you would like to view them all.
Ensembl Acc Id:
ENSSSCT00000013662 ⟹ ENSSSCP00000013290
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 Ensembl X 82,981,515 - 83,014,573 (-) Ensembl
Ensembl Acc Id:
ENSSSCT00000025835 ⟹ ENSSSCP00000025530
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 Ensembl X 82,981,515 - 83,014,573 (-) Ensembl
Ensembl Acc Id:
ENSSSCT00000097469 ⟹ ENSSSCP00000077524
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 Ensembl X 82,981,518 - 83,014,463 (-) Ensembl
RefSeq Acc Id:
NM_001243576 ⟹ NP_001230505
RefSeq Status:
VALIDATED
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 X 82,981,512 - 83,014,475 (-) NCBI
Sequence:
CTTCCTCTCTGGACTGTAAGAATATGTCTCCAGGGCCAGTGTCTTCTGACATCGAGTCCCACCTTCAAAGTCCTGGCATCTCAATGCATCCAGGAAGCTACCTGCATTAAAGTCAGGACTGAGCATAC AGTGAGCTCCAGAAAGAAGAAGCTATGGCTGCGGTGATACTGGAGAGCATCTTTCTGAAACGATCTCAGCAGGAAAAGAAAACATCACCTTTGAACTTCAAGAAGCGCCTCTTTCTCTTGACCGTGCA AAAACTTTCCTACTATGAGTATGACTTTGAACGTGGGAGAAGAGGCAGTAAGAAGGGTTCAATAGATGTTGAGAAGATCACCTGCGTTGAAACAGTTGTTCCTGAGAAAAATCCTCCCCCTGAAAGAC AGATTCCGAGAAGGGGTGAAGAGTCCAGTGAAATGGAGCAGATTTCAATTATTGAAAGGTTCCCTTACCCCTTCCAGGTTGTATATGATGAAGGGCCTCTCTACGTCTTCTCCCCAACTGAAGAACTG AGAAAGCGTTGGATTCACCAGCTCAAAAGTGTAATCCGGTACAACAGTGATCTGGTACAGAAATACCACCCTTGCTTCTGGATTGATGGGCAGTATCTCTGCTGCTCTCAGACAGCCAAAAATGCTAT GGGCTGCCAAATTTTGGAGAACAGAAATGGAAGCTTAAAACCTGGGAGTTCACACCGAAAGACGAAAAAGCCTCTTCCTCCCACACCTGAGGAGGACCAGATCTTAAAAAAGCCACTGCCCCCTGAGC CAACAGCAGCACCGGTCTCGACAAGTGAGCTGAAAAAGGTTGTAGCCCTTTATGATTACATGCCAATGAATGCAAATGATCTACAGCTGCGGAAGGGCGACGAGTATTTTATCCTGGAGGAGAGCAAC TTACCCTGGTGGCGAGCCCGGGACAAAAATGGGCAGGAAGGCTACATCCCTAGTAACTATGTAACCGAAGCAGAAGACTCCATAGAAATGTATGAGTGGTATTCCAAACACATGACTCGGAGTCAAGC TGAGCAACTGCTAAAGCAAGAGGGCAAAGAAGGAGGCTTCATTGTCAGAGACTCCAGCAAAGCTGGAAAATATACTGTGTCTGTGTTTGCTAAAGCCACAGGGGAACCTCAAGGGGTGATACGTCATT ATGTTGTGTGTTCCACACCTCAGAGCCAGTATTATCTGGCTGAGAAGCACCTTTTCAGCACCATCCCTGAGCTCATTAACTACCACCAGCATAATTCTGCAGGACTCATATCTAGGCTCAAATATCCA GTGTCTCAACAAAACAAGAATGCGCCGTCCACTGCAGGCCTGGGCTACGGATCATGGGAAATTGATCCAAAAGACCTGACCTTCTTGAAGGAGCTGGGGACTGGACAATTTGGAGTAGTGAAGTATGG GAAATGGAGGGGCCAGTATGATGTGGCCATCAAGATGATCAAAGAAGGCTCCATGTCTGAGGATGAGTTCATTGAAGAAGCCAAAGTCATGATGAATCTTTCCCACGAGAAGCTGGTGCAGCTGTATG GTGTCTGCACCAAACAGCGCCCCATCTTCATCATCACTGAGTACATGGCCAATGGCTGCCTCCTGAACTACCTGAGGGAGATGCGCCACCGCTTCCAGACTCAGCAGCTGCTGGAGATGTGCAAGGAT GTCTGTGAAGCTATGGAATACCTGGAGTCAAAGCAGTTCCTCCACCGAGACCTGGCGGCTCGGAACTGTTTGGTGAATGACCAAGGAGTTGTTAAAGTATCAGACTTTGGCCTATCCAGGTATGTTCT GGATGATGAATACACAAGCTCAGTAGGCTCCAAATTTCCAGTCCGGTGGTCTCCACCAGAAGTCCTCATGTATAGCAAGTTCAGCAGCAAATCTGATATTTGGGCTTTTGGGGTGTTGATGTGGGAAA TTTACTCTCTGGGGAAGATGCCATATGAGAGATTTACCAACAGCGAAACAGCTGAACACATTGCCCAAGGCCTACGTCTCTACAGGCCTCATCTAGCTTCAGAGAGGGTCTATACCATCATGTACAGC TGCTGGCATGAGAAAGCAGATGAACGTCCCACTTTCAAAATTCTTCTGAGCAACATTCTAGATGTCATGGATGAAGAATCCTGAGCTCACCAATAAGTTTCTTGGTTCCACTCCTCGCCTCCGCAAGC CCCAATTTCACTTTCTCTGAGGAAATCCCAGGCTTACAGGCCCTGGAGCCTTTGCACCCTCGCTGAATACACAAAGGCCCCTCTCTACATCTAGGAATGCCTCTCTTTTTCCTGGGATAGTACCTTCT GAGGGCAAGGAATTATTGTGCCTGGTATTTTCCCCCAGAGAGGACATTTCCTAAGAGTATTAAGACAGACTGAATTGGGAATAGAAACGTTTTGGGGGGAGGGAGGGATGTAAATAGCCTCACAAGGG GTCCAACCGCTCTCTAGGTAGGCAATAGAACTTGAGGGGAGGGAGGTAGAATTTGGCAGGAATGAAACGGTGTTATAAAAATGGGAGGGGAGGGTGTTTTGATAAAATAAAATTACTGGAAAGCAAAA AAAAAAAAAAAAAAAAAAAAAAAAAA
hide sequence
RefSeq Acc Id:
NP_001230505 ⟸ NM_001243576
- UniProtKB:
A0A8D1AME0 (UniProtKB/TrEMBL), A0A8W4FDY6 (UniProtKB/TrEMBL)
- Sequence:
MAAVILESIFLKRSQQEKKTSPLNFKKRLFLLTVQKLSYYEYDFERGRRGSKKGSIDVEKITCVETVVPEKNPPPERQIPRRGEESSEMEQISIIERFPYPFQVVYDEGPLYVFSPTEELRKRWIHQL KSVIRYNSDLVQKYHPCFWIDGQYLCCSQTAKNAMGCQILENRNGSLKPGSSHRKTKKPLPPTPEEDQILKKPLPPEPTAAPVSTSELKKVVALYDYMPMNANDLQLRKGDEYFILEESNLPWWRARD KNGQEGYIPSNYVTEAEDSIEMYEWYSKHMTRSQAEQLLKQEGKEGGFIVRDSSKAGKYTVSVFAKATGEPQGVIRHYVVCSTPQSQYYLAEKHLFSTIPELINYHQHNSAGLISRLKYPVSQQNKNA PSTAGLGYGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEYL ESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASERVYTIMYSCWHEKADE RPTFKILLSNILDVMDEES
hide sequence
Ensembl Acc Id:
ENSSSCP00000025530 ⟸ ENSSSCT00000025835
Ensembl Acc Id:
ENSSSCP00000013290 ⟸ ENSSSCT00000013662
Ensembl Acc Id:
ENSSSCP00000077524 ⟸ ENSSSCT00000097469