Symbol:
DPAGT1
Name:
dolichyl-phosphate N-acetylglucosaminephosphotransferase 1
RGD ID:
13848982
Description:
ENCODES a protein that exhibits glycosyltransferase activity (inferred); phosphotransferase activity, for other substituted phosphate groups (inferred); transferase activity (inferred); INVOLVED IN dolichol-linked oligosaccharide biosynthetic process (inferred); protein glycosylation (inferred); protein N-linked glycosylation (inferred); ASSOCIATED WITH acute intermittent porphyria (ortholog); acute porphyria (ortholog); CD3epsilon deficiency (ortholog); FOUND IN Golgi apparatus (ortholog)
Type:
protein-coding
RefSeq Status:
MODEL
Previously known as:
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
RGD Orthologs
Alliance Orthologs
More Info
more info ...
More Info
Latest Assembly:
Sscrofa11.1 - Pig Sscrofa11.1 Assembly
Position:
Pig Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl Sscrofa11.1 Ensembl 9 46,310,872 - 46,316,858 (-) Ensembl Sscrofa11.1 susScr11 Sscrofa11.1 Sscrofa11.1 9 46,308,824 - 46,316,905 (-) NCBI Sscrofa11.1 Sscrofa11.1 susScr11 Sscrofa11.1 Sscrofa10.2 9 51,346,007 - 51,352,208 (-) NCBI Sscrofa10.2 Sscrofa10.2 susScr3
JBrowse:
View Region in Genome Browser (JBrowse)
Model
DPAGT1 Pig acute intermittent porphyria ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Acute intermittent porphyria | ClinVar Annotator: match by term: PBGD more ... ClinVar PMID:18414213|PMID:25741868|PMID:28492532 DPAGT1 Pig acute porphyria ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Acute Porphyria ClinVar PMID:18414213|PMID:25741868|PMID:28492532 DPAGT1 Pig CD3epsilon deficiency ISO RGD:1349923 8554872 ClinVar Annotator: match by term: CD3epsilon deficiency ClinVar PMID:14602880|PMID:15546002|PMID:1635567|PMID:17277165|PMID:24216686|PMID:24910257|PMID:25373860|PMID:26822028|PMID:28492532|PMID:8490660 DPAGT1 Pig chromosome 11 partial duplication syndrome ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Distal trisomy 11q ClinVar PMID:25741868 DPAGT1 Pig congenital disorder of glycosylation ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Carbohydrate-deficient glycoprotein syndrome | ClinVar Annotator: match by term: Congenital more ... ClinVar PMID:12872255|PMID:18414213|PMID:22304930|PMID:22742743|PMID:23806237|PMID:25741868|PMID:28492532|PMID:30117111|PMID:31589614|PMID:33743358 DPAGT1 Pig congenital disorder of glycosylation Ij ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1J ClinVar PMID:12872255|PMID:16199547|PMID:17576681|PMID:18414213|PMID:22304930|PMID:22492991|PMID:22742743|PMID:22786653|PMID:23249953|PMID:23430862|PMID:23591138|PMID:23806237|PMID:24033266|PMID:24759841|PMID:25326635|PMID:25500013|PMID:25741868|PMID:26467025|PMID:28454995|PMID:28492532|PMID:28662078|PMID:28712839|PMID:30117111|PMID:30388443|PMID:31127727|PMID:31153949|PMID:31589614|PMID:33743358|PMID:9536098 DPAGT1 Pig congenital myasthenic syndrome 13 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Congenital myasthenic syndrome 13 | ClinVar Annotator: match by term: more ... ClinVar PMID:12872255|PMID:16199547|PMID:17576681|PMID:18414213|PMID:22742743|PMID:22786653|PMID:23249953|PMID:23430862|PMID:23591138|PMID:23806237|PMID:24033266|PMID:24759841|PMID:25500013|PMID:25741868|PMID:26467025|PMID:28454995|PMID:28492532|PMID:28662078|PMID:28712839|PMID:30117111|PMID:30388443|PMID:31127727|PMID:31153949|PMID:31589614|PMID:33743358|PMID:9536098 DPAGT1 Pig Dwarfism ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Short stature ClinVar PMID:32581362 DPAGT1 Pig Familial Atrial Fibrillation 14 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Atrial fibrillation, familial, 14 ClinVar PMID:28492532 DPAGT1 Pig genetic disease ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Inborn genetic diseases ClinVar PMID:17576681|PMID:22742743|PMID:23806237|PMID:25741868|PMID:26467025|PMID:28492532|PMID:30117111|PMID:31589614|PMID:33743358|PMID:9536098 DPAGT1 Pig glycogen storage disease Ib ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Glucose-6-phosphate transport defect ClinVar PMID:28492532 DPAGT1 Pig immunodeficiency 17 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Immunodeficiency 17 | ClinVar Annotator: match by term: Immunodeficiency 17, more ... ClinVar PMID:14602880|PMID:15546002|PMID:1635567|PMID:17277165|PMID:24216686|PMID:24910257|PMID:25373860|PMID:26822028|PMID:28492532|PMID:8490660 DPAGT1 Pig immunodeficiency 18 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Immunodeficiency 18 ClinVar PMID:14602880|PMID:15546002|PMID:1635567|PMID:17277165|PMID:24216686|PMID:24910257|PMID:25373860|PMID:26822028|PMID:28492532|PMID:8490660 DPAGT1 Pig immunodeficiency 19 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Immunodeficiency 19 ClinVar PMID:14602880|PMID:15546002|PMID:1635567|PMID:17277165|PMID:24216686|PMID:24910257|PMID:25373860|PMID:26822028|PMID:28492532|PMID:8490660 DPAGT1 Pig inflammatory bowel disease 28 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Inflammatory bowel disease 28 ClinVar PMID:14602880|PMID:15546002|PMID:1635567|PMID:17277165|PMID:24216686|PMID:24910257|PMID:25373860|PMID:26822028|PMID:28492532|PMID:8490660 DPAGT1 Pig isolated microphthalmia 5 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Isolated microphthalmia 5 ClinVar PMID:28492532 DPAGT1 Pig long QT syndrome 10 ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Long QT syndrome 10 ClinVar PMID:28492532 DPAGT1 Pig RASopathy ISO RGD:1349923 8554872 ClinVar Annotator: match by term: RASopathy ClinVar PMID:22742743|PMID:28492532 DPAGT1 Pig schizophrenia ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Schizophrenia ClinVar PMID:21681106|PMID:30208311 DPAGT1 Pig Tubular Aggregate Myopathies ISO RGD:1349923 8554872 ClinVar Annotator: match by term: Myopathy with tubular aggregates ClinVar PMID:25741868|PMID:38124360
DPAGT1 (Sus scrofa - pig)
Pig Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl Sscrofa11.1 Ensembl 9 46,310,872 - 46,316,858 (-) Ensembl Sscrofa11.1 susScr11 Sscrofa11.1 Sscrofa11.1 9 46,308,824 - 46,316,905 (-) NCBI Sscrofa11.1 Sscrofa11.1 susScr11 Sscrofa11.1 Sscrofa10.2 9 51,346,007 - 51,352,208 (-) NCBI Sscrofa10.2 Sscrofa10.2 susScr3
DPAGT1 (Homo sapiens - human)
Human Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCh38 11 119,093,874 - 119,101,853 (-) NCBI GRCh38 GRCh38 hg38 GRCh38 GRCh38.p14 Ensembl 11 119,096,025 - 119,108,331 (-) Ensembl GRCh38 hg38 GRCh38 GRCh37 11 118,967,220 - 118,972,563 (-) NCBI GRCh37 GRCh37 hg19 GRCh37 Build 36 11 118,472,423 - 118,477,995 (-) NCBI NCBI36 Build 36 hg18 NCBI36 Build 34 11 118,472,422 - 118,477,995 NCBI Celera 11 116,124,628 - 116,130,198 (-) NCBI Celera Cytogenetic Map 11 q23.3 NCBI HuRef 11 114,906,662 - 114,912,231 (-) NCBI HuRef CHM1_1 11 118,853,515 - 118,859,087 (-) NCBI CHM1_1 T2T-CHM13v2.0 11 119,114,257 - 119,122,234 (-) NCBI T2T-CHM13v2.0
Dpagt1 (Mus musculus - house mouse)
Mouse Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCm39 9 44,237,314 - 44,247,374 (+) NCBI GRCm39 GRCm39 mm39 GRCm39 Ensembl 9 44,237,316 - 44,245,197 (+) Ensembl GRCm39 Ensembl GRCm38 9 44,325,857 - 44,333,895 (+) NCBI GRCm38 GRCm38 mm10 GRCm38 GRCm38.p6 Ensembl 9 44,326,019 - 44,333,900 (+) Ensembl GRCm38 mm10 GRCm38 MGSCv37 9 44,134,928 - 44,141,683 (+) NCBI GRCm37 MGSCv37 mm9 NCBIm37 MGSCv36 9 44,077,840 - 44,084,595 (+) NCBI MGSCv36 mm8 Celera 9 41,581,588 - 41,588,325 (+) NCBI Celera Cytogenetic Map 9 A5.2 NCBI cM Map 9 24.84 NCBI
Dpagt1 (Rattus norvegicus - Norway rat)
Rat Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl GRCr8 8 53,560,869 - 53,567,625 (+) NCBI GRCr8 mRatBN7.2 8 44,664,055 - 44,671,102 (+) NCBI mRatBN7.2 mRatBN7.2 mRatBN7.2 Ensembl 8 44,664,071 - 44,671,087 (+) Ensembl mRatBN7.2 Ensembl UTH_Rnor_SHR_Utx 8 50,160,306 - 50,166,698 (+) NCBI Rnor_SHR UTH_Rnor_SHR_Utx UTH_Rnor_SHRSP_BbbUtx_1.0 8 48,439,022 - 48,445,414 (+) NCBI Rnor_SHRSP UTH_Rnor_SHRSP_BbbUtx_1.0 UTH_Rnor_WKY_Bbb_1.0 8 46,309,400 - 46,315,792 (+) NCBI Rnor_WKY UTH_Rnor_WKY_Bbb_1.0 Rnor_6.0 8 48,657,779 - 48,664,531 (+) NCBI Rnor6.0 Rnor_6.0 rn6 Rnor6.0 Rnor_6.0 Ensembl 8 48,657,795 - 48,664,860 (+) Ensembl Rnor6.0 rn6 Rnor6.0 Rnor_5.0 8 47,276,761 - 47,283,502 (+) NCBI Rnor5.0 Rnor_5.0 rn5 Rnor5.0 RGSC_v3.4 8 47,305,087 - 47,311,488 NCBI RGSC3.4 RGSC_v3.4 rn4 RGSC3.4 Celera 8 44,250,639 - 44,257,040 (+) NCBI Celera Cytogenetic Map 8 q22 NCBI
Dpagt1 (Chinchilla lanigera - long-tailed chinchilla)
Chinchilla Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl ChiLan1.0 Ensembl NW_004955412 20,205,381 - 20,217,871 (-) Ensembl ChiLan1.0 ChiLan1.0 NW_004955412 20,205,381 - 20,217,874 (-) NCBI ChiLan1.0 ChiLan1.0
DPAGT1 (Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl NHGRI_mPanPan1-v2 9 119,801,299 - 119,807,961 (-) NCBI NHGRI_mPanPan1-v2 NHGRI_mPanPan1 11 120,904,998 - 120,911,981 (-) NCBI NHGRI_mPanPan1 Mhudiblu_PPA_v0 11 113,934,705 - 113,940,535 (-) NCBI Mhudiblu_PPA_v0 Mhudiblu_PPA_v0 panPan3 PanPan1.1 11 117,863,866 - 117,870,198 (-) NCBI panpan1.1 PanPan1.1 panPan2 PanPan1.1 Ensembl 11 117,863,866 - 117,870,204 (-) Ensembl panpan1.1 panPan2
DPAGT1 (Canis lupus familiaris - dog)
Dog Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl CanFam3.1 5 14,760,518 - 14,765,306 (+) NCBI CanFam3.1 CanFam3.1 canFam3 CanFam3.1 CanFam3.1 Ensembl 5 14,760,784 - 14,764,967 (+) Ensembl CanFam3.1 canFam3 CanFam3.1 Dog10K_Boxer_Tasha 5 14,813,227 - 14,818,301 (+) NCBI Dog10K_Boxer_Tasha ROS_Cfam_1.0 5 14,703,570 - 14,708,640 (+) NCBI ROS_Cfam_1.0 ROS_Cfam_1.0 Ensembl 5 14,704,093 - 14,708,640 (+) Ensembl ROS_Cfam_1.0 Ensembl UMICH_Zoey_3.1 5 14,841,611 - 14,846,682 (+) NCBI UMICH_Zoey_3.1 UNSW_CanFamBas_1.0 5 14,745,627 - 14,750,704 (+) NCBI UNSW_CanFamBas_1.0 UU_Cfam_GSD_1.0 5 14,786,006 - 14,791,077 (+) NCBI UU_Cfam_GSD_1.0
Dpagt1 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl HiC_Itri_2 NW_024404947 101,127,692 - 101,133,021 (-) NCBI HiC_Itri_2 SpeTri2.0 Ensembl NW_004936542 4,048,979 - 4,054,105 (-) Ensembl SpeTri2.0 SpeTri2.0 Ensembl SpeTri2.0 NW_004936542 4,049,107 - 4,054,100 (-) NCBI SpeTri2.0 SpeTri2.0 SpeTri2.0
DPAGT1 (Chlorocebus sabaeus - green monkey)
Green Monkey Assembly Chr Position (strand) Source Genome Browsers JBrowse NCBI UCSC Ensembl ChlSab1.1 1 110,469,312 - 110,474,859 (-) NCBI ChlSab1.1 ChlSab1.1 chlSab2 ChlSab1.1 Ensembl 1 110,469,794 - 110,474,440 (-) Ensembl ChlSab1.1 ChlSab1.1 Ensembl chlSab2 Vero_WHO_p1.0 NW_023666043 15,559,397 - 15,564,905 (+) NCBI Vero_WHO_p1.0 Vero_WHO_p1.0
Dpagt1 (Heterocephalus glaber - naked mole-rat)
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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:
ENSSSCT00000016476 ⟹ ENSSSCP00000016033
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 Ensembl 9 46,310,877 - 46,316,858 (-) Ensembl
Ensembl Acc Id:
ENSSSCT00000103127 ⟹ ENSSSCP00000078582
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 Ensembl 9 46,310,872 - 46,316,673 (-) Ensembl
RefSeq Acc Id:
XM_003129927 ⟹ XP_003129975
Type:
CODING
Position:
Pig Assembly Chr Position (strand) Source Sscrofa11.1 9 46,308,824 - 46,316,905 (-) NCBI
Sequence:
AGTTGCTCTGCTAACTAGACCCGGGCGGAAACAGTAAGTAGGTAGATGCAGTGAGGCAGAACCAAGGTTGACTTTACTGAGGCTCCTGAGAGTTCCCAGGGCGGCTCAGGTTGGAGTTGTTGGTTTTG CTCAGGCCAGTGTCGGAAAACTCAGCCTGTGGGGAGCGGCCACTTCTTACTGCTAGGGACCGTTAGCTAAGGAGGCGGCCGAGAGGGCCGCCTGGCCAGTTACCATGTGGGCCTTCCCGGAGTTGCCG ATGCCGCTGTTGGTGAATTTGATCGGCTCGCTGCTGGGATTTGTGGCCACACTCACCCTCATCCCTGCCTTCCGTGGCCACTTCATCGCCGCGCGTCTCTGCGGCCAGGATCTCAACAAATCCAACCG GCAGCAAATCCCAGAATCCCAGGGAGTGATCAGCGGTGCTGTTTTCCTTATCATCCTCTTCTGCTTCATCCCTTTCCCTTTCCTGAACTGCTTTGTGGAGGAGCACTGTAAAGCCTTCCCCCACCATG AATTTGTGGCCCTGATAGGTGCGCTCCTTGCCATCTGCTGCATGATTTTCCTGGGCTTCGCGGATGATGTTTTGAATCTGCGCTGGCGCCATAAGCTGCTGCTGCCCACAGCTGCCTCACTACCTCTC CTCATGGTCTATTTCACCAACTTTGGCAACACGACCATCGTGGTACCCAAGCCCTTCCGCCCAATTCTTGGCCTGCATCTGGACTTGGGAATCCTGTACTATGTCTACATGGGGCTGCTGGCAGTGTT CTGTACCAATGCCATCAATATTCTAGCAGGAATTAATGGCCTAGAGGCTGGCCAGTCGCTAGTCATTTCTGCTTCCATCATTGTCTTCAACCTGGTAGAGCTGGAAGGTGATTATCGGGATGATCACG TCTTTTCCCTCTACTTCATGATACCTTTTTTCTTCACCACTTTGGGATTGCTCTACCATAACTGGTACCCATCCCGGGTGTTTGTGGGAGATACCTTCTGCTACTTTGCTGGCATGACCTTTGCCGTG GTGGGCATCTTGGGACACTTCAGCAAGACTATGCTACTCTTCTTCATGCCTCAGGTGTTCAACTTCCTCTACTCACTGCCTCAGCTCCTGCATATCATCCCCTGCCCGCGCCACCGTATGCCCAGACT CAATACCAAGACAGGCAAACTGGAGATGAGCTATTCCAAGTTCAAGACCAAGAGCCTCTCTTTCTTGGGCACCTTTATTCTAAAGGTAGCAGAGAGCCTCCGGCTAGTGACCGTGCGCCAGAGTGAGA ATGAGGATGGTGCCTTCACAGAGTGTAACAACATGACCCTCATCAACTTGCTACTCAAAGTCTTTGGGCCCATGCATGAGAGAAATCTCACCCTGTTCCTGCTACTGCTGCAGGTCGTGGGCAGTGCT GTCACCTTCTCCATTCGTTACCAGCTTGTCCGACTCTTCTATGATGTCTGAGTCGCCTAATCATTGCCTTTTGCTTCATAACCACTAGGGTCCCTGACTCAGGCTCAGCTCTTCTGGACCAAGACTGC CTCCTGGTCCAAGCCTCTCCCACCCTTCATTCTCCAGATTTTGTCCTCAGCATTTCCTTTCCCCTATGATTATTGACATCCTTGGGCCTTTCTTGCCCTCTAGGGCTGTTGATTGAACTTTGCTTATG GCTTTCTTCAACTTGCCACTCTCCCTCTCCATCCCACTTTTGCAGCCACCTAAGCAGGGAATACTGTAGCTTTTATGCAGTTACCCACAACTCTGACACTCAAGGAATATGCTGGGCCTGGGGATAGA ACCCTGGCTGCGGATAGGGTCACAGGCTTGAGGATGACTTGACATTTGACTATAATTAAGTATTCTGATGATTCAGAGCAGACTGGGGGGCCAGGTGCTCCCAGTGGCAACAATAAAAAGTTGTTTTT TCTTGTTGTTTCTGTAGGTGTATTTCCTATGTGGGCATTTTAAGGTAGATTGGGAGTGTTGGTGGAGGCATTTCCTCTAAGAGTTTGCCTATCTCTCTGCCTCATCCTTTTTCTTTCAGTACCTCAGG CCACTTCTAGCAAGAAGTGAACACAAAGAACAAACCAGGTAGAACATGTTGAGTAAATACTGAAATCCTGCTGCTCCGTGGCGTAGAGAGCCATAAGATTGGCATTATCTGGTATGGGGTCGAACTTG CAGAGGGTCTCTAATTCCTTCCCTTTTTCATGCCTTTTTTGCCAGATAGGAGGGCGTGACCAGACCTGGGAAGTGAGGCAGAGTAGTCAGTAGTGCTGACCCCTTTTCTTTAAAAACCTTAAGTCCCA CACACATTTCCCTGAGATGGCTTCAGACCTCACTGTCTATGTCTTCCGGTTCTGGAGTAGGGCTGTAGTGTTTAAATCTGGCGCGCTTCACATGGATTGGCTACACCGGAGAGTGGTTTGCTGTGGGC TCGCTGCAGCTCCTCCTCGCCTCTTTCCCCGGGCAGAAGGTTTTCAAATTCTACCAATCGGAGGGCGCGTTCTCTCAGCCGGGGCGCGCCACCGATTGGTTAACTGCAGCCAACCGGAGGCGGGTATT AAAGAAAAGAGCCAATCAGGAGGGCGCGGGGGTGTGCCCTGGGGGGCTTATAAGGGCGGCTTCTGGGCGCGCGCGGCACCAGTTGGACTGCGGCGGCGGCTGTTTTTCGTCCCTGCGAGGCGTTCTCC TCAACGTACATCTACCTCACGCAGCATGTCGGGCCGCGGCAAGACCGGCGGCAAGGCCCGCGCCAAGGCCAAGTCTCGCTCATCACGCGCCGGCCTCCAGTTCCCGGTGGGCCGCGTGCACCGCCTGC TGCGCAAGGGCCACTATGCCGAGCGAGTGGGCGCCGGCGCGCCAGTCTACCTGGCGGCGGTGCTCGAGTACCTCACCGCCGAGATCCTGGAGCTGGCGGGCAACGCGGCCCGCGACAACAAGAAGACG CGGATCATCCCTCGCCACCTGCAGTTGGCCATCCGCAACGACGAGGAGCTCAACAAGCTGCTGGGCGGCGTGACGATCGCCCAGGGAGGCGTCCTGCCCAATATCCAGGCCGTGTTGCTGCCCAAGAA GACCAGCGCCACCGTGGGGCCGAAGGCGCCCGCCGGCGGCAAGAAGGCCACCCAGGCCTCGCAGGAGTACTGAGGCCGCCTGCGCCGCCACGGCCGCCGCCCGGTCTTCCCTTCGCCACCACAAAGGC CCTTTTAAGGGCCACCACAGCCCTCACGGAAAGAGCTGGGCCACGACGGGCTCCCGGCCGCGCGCTCGCCCCCTCCCCAGCCTCGCCGCCGCCGCCGCCGCCTGCCCGCCCCTCCCCCGCGCGGCCCG CTCCCGCTGTGGCTCCGCCGAGGACGGCCGTTTGAAAGCCGCTCGGCCCCGGGGTCCAGCTCGTGACTGCTGGCCTGGCCGCAGACGCTGATGGGCTGCGGGGAGGACGCGGCGCCTAATGGAAGGCT GGGCCGGCCGTGCTGACGCAGGGCCGGGGAGCGCGGCGGGAAGGTGAGTGGGTGCAGAGGCCGCCGGCGGGGCCGCGCGCGTTACTCTCCAGCCCGTTGCTCCGGCCGCGACTTCAGACGGAACTCGA TTTCGGGCGGCGGCGGAGTCGGTCACATTTGTTCCGGGGCCCCTTTGCTGCCGGGTCCCGGGCCTTGCACGTCCGCGCTCCCTCCATCTCCGCTCGCAGGCCCGTGCGCGTCCGGACGAGACACTTGG CGGTGTGAGCGTCTCCCGCGGTGGCCGGTCCGGGCGGGGTGGGGGCCGCGCCCCCAGGCCCGCTCCCCTCCCGGCGGGCCCACTGGGCAAGCCAAGCACCTAGATACCAGCACTACTAGTCCATTAAC CCCCGTCTGGACTGAGCCGCCGTTGGCTTCGGAACTGGAATTTTGCAGCTAACCCATCCGAGACTAGTACTTTAGATATTGGGGAGTTTCAGATGGACTAATTTTGTTTATTAAAGGATTGGTTTTTA TATATA
hide sequence
RefSeq Acc Id:
XP_003129975 ⟸ XM_003129927
- UniProtKB:
F1SAH5 (UniProtKB/TrEMBL), A0A4X1SFQ6 (UniProtKB/TrEMBL), A0A8D1UNA2 (UniProtKB/TrEMBL), A0A8D0XE71 (UniProtKB/TrEMBL)
- Sequence:
MWAFPELPMPLLVNLIGSLLGFVATLTLIPAFRGHFIAARLCGQDLNKSNRQQIPESQGVISGAVFLIILFCFIPFPFLNCFVEEHCKAFPHHEFVALIGALLAICCMIFLGFADDVLNLRWRHKLLL PTAASLPLLMVYFTNFGNTTIVVPKPFRPILGLHLDLGILYYVYMGLLAVFCTNAINILAGINGLEAGQSLVISASIIVFNLVELEGDYRDDHVFSLYFMIPFFFTTLGLLYHNWYPSRVFVGDTFCY FAGMTFAVVGILGHFSKTMLLFFMPQVFNFLYSLPQLLHIIPCPRHRMPRLNTKTGKLEMSYSKFKTKSLSFLGTFILKVAESLRLVTVRQSENEDGAFTECNNMTLINLLLKVFGPMHERNLTLFLL LLQVVGSAVTFSIRYQLVRLFYDV
hide sequence
Ensembl Acc Id:
ENSSSCP00000016033 ⟸ ENSSSCT00000016476
Ensembl Acc Id:
ENSSSCP00000078582 ⟸ ENSSSCT00000103127