COA1 (cytochrome c oxidase assembly factor 1) - Rat Genome Database

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Gene: COA1 (cytochrome c oxidase assembly factor 1) Homo sapiens
Analyze
Symbol: COA1
Name: cytochrome c oxidase assembly factor 1
RGD ID: 1601863
HGNC Page HGNC:21868
Description: Involved in mitochondrial cytochrome c oxidase assembly and mitochondrial respiratory chain complex I assembly. Located in cytosol and mitochondrial inner membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C7orf44; cytochrome c oxidase assembly factor 1 homolog; cytochrome c oxidase assembly protein 1 homolog; cytochrome oxidase assembly 1; cytochrome oxidase assembly protein 1 homolog; FLJ10803; hypothetical protein LOC55744; mitochondrial translation regulation assembly intermediate of cytochrome c oxidase protein of 15 kDa; MITRAC15; uncharacterized protein C7orf44
RGD Orthologs
Mouse
Chinchilla
Bonobo
Dog
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: COA1P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38743,608,457 - 43,729,523 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl743,608,456 - 43,729,717 (-)EnsemblGRCh38hg38GRCh38
GRCh37743,648,056 - 43,769,122 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36743,645,384 - 43,735,608 (-)NCBINCBI36Build 36hg18NCBI36
Celera743,668,728 - 43,758,937 (-)NCBICelera
Cytogenetic Map7p13NCBI
HuRef743,555,867 - 43,654,123 (-)NCBIHuRef
CHM1_1743,674,041 - 43,773,062 (-)NCBICHM1_1
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2743,710,264 - 43,808,634 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
COA1Humanpleomorphic xanthoastrocytoma  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Pleomorphic xanthoastrocytomaClinVarPMID:28299358

1 to 20 of 35 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
COA1Human5-aza-2'-deoxycytidine affects expressionEXP 6480464Decitabine affects the expression of COA1 mRNACTDPMID:23300844
COA1Humanafimoxifene multiple interactionsEXP 6480464afimoxifene inhibits the reaction [Estrogens results in decreased expression of COA1 mRNA]CTDPMID:21233418
COA1Humanantirheumatic drug increases expressionEXP 6480464Antirheumatic Agents results in increased expression of COA1 mRNACTDPMID:24449571
COA1Humanarsane affects methylationEXP 6480464Arsenic affects the methylation of COA1 geneCTDPMID:25304211
COA1Humanarsenic atom affects methylationEXP 6480464Arsenic affects the methylation of COA1 geneCTDPMID:25304211
COA1Humanarsenite(3-) multiple interactionsEXP 6480464arsenite promotes the reaction [G3BP1 protein binds to COA1 mRNA]CTDPMID:32406909
COA1Humanbenzo[a]pyrene affects methylationEXP 6480464Benzo(a)pyrene affects the methylation of COA1 5' UTRCTDPMID:27901495
COA1Humanbicalutamide increases expressionEXP 6480464bicalutamide results in increased expression of COA1 mRNACTDPMID:16631469
COA1Humanbisphenol A decreases expressionEXP 6480464bisphenol A results in decreased expression of COA1 mRNACTDPMID:29275510
COA1Humanbisphenol A decreases methylationEXP 6480464bisphenol A results in decreased methylation of COA1 geneCTDPMID:31601247
COA1Humanbisphenol A increases expressionEXP 6480464bisphenol A results in increased expression of COA1 mRNACTDPMID:33670352
COA1Humancarbamazepine affects expressionEXP 6480464Carbamazepine affects the expression of COA1 mRNACTDPMID:25979313
COA1Humancisplatin affects expressionEXP 6480464Cisplatin affects the expression of COA1 mRNACTDPMID:23300844
COA1Humancobalt dichloride increases expressionEXP 6480464cobaltous chloride results in increased expression of COA1 mRNACTDPMID:19376846
COA1Humancoumestrol increases expressionEXP 6480464Coumestrol results in increased expression of COA1 mRNACTDPMID:19167446
COA1HumanDibutyl phosphate affects expressionEXP 6480464di-n-butylphosphoric acid affects the expression of COA1 mRNACTDPMID:37042841
COA1Humandorsomorphin multiple interactionsEXP 6480464[NOG protein co-treated with mercuric bromide co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...CTDPMID:27188386
COA1Humanformaldehyde decreases expressionEXP 6480464Formaldehyde results in decreased expression of COA1 mRNACTDPMID:20655997
COA1Humanformaldehyde increases expressionEXP 6480464Formaldehyde results in increased expression of COA1 mRNACTDPMID:23649840
COA1Humanhexamethylene diisocyanate increases methylationEXP 64804641 and 6-hexamethylene diisocyanate results in increased methylation of COA1 geneCTDPMID:25445006

1 to 20 of 35 rows

Biological Process

  

Cellular Component
1 to 11 of 11 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
COA1Humancytosol located_inIDA 150520179 HPAGO_REF:0000052
COA1Humanmembrane located_inIEAUniProtKB-KW:KW-0472150520179 UniProtGO_REF:0000043
COA1Humanmitochondrial inner membrane is_active_inIBAPANTHER:PTN005334306 and UniProtKB:Q9GZY4150520179 GO_CentralGO_REF:0000033
COA1Humanmitochondrial inner membrane located_inNAS 150520179 PMID:32320651ComplexPortalPMID:32320651
COA1Humanmitochondrial inner membrane located_inTAS 150520179 ReactomeReactome:R-HSA-163217 more ...
COA1Humanmitochondrial inner membrane located_inIDA 150520179 PMID:23260140UniProtPMID:23260140
COA1Humanmitochondrial inner membrane located_inIEAUniProtKB-KW:KW-0999150520179 UniProtGO_REF:0000043
COA1Humanmitochondrial inner membrane located_inIEAUniProtKB-SubCell:SL-0168150520179 UniProtGO_REF:0000044
COA1Humanmitochondrion located_inHTP 150520179 PMID:34800366FlyBasePMID:34800366
COA1Humanmitochondrion located_inIEAUniProtKB-KW:KW-0496150520179 UniProtGO_REF:0000043
COA1Humanmitochondrion located_inIDA 150520179 HPAGO_REF:0000052
1 to 11 of 11 rows

Molecular Function

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
COA1Humanprotein binding enablesIPIUniProtKB:O95298 more ...150520179 PMID:32320651UniProtPMID:32320651

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
COA1HumanPleomorphic xanthoastrocytoma  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Pleomorphic xanthoastrocytomaClinVarPMID:28299358

#
Reference Title
Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
PMID:12477932   PMID:14702039   PMID:15342556   PMID:16344560   PMID:17207965   PMID:21145461   PMID:21504906   PMID:21873635   PMID:22356826   PMID:23260140   PMID:24145035   PMID:25437307  
PMID:26186194   PMID:26655997   PMID:28514442   PMID:28561026   PMID:31152661   PMID:31721420   PMID:32320651   PMID:32877691   PMID:33961781   PMID:34081057   PMID:34800366   PMID:37827155  



COA1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38743,608,457 - 43,729,523 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl743,608,456 - 43,729,717 (-)EnsemblGRCh38hg38GRCh38
GRCh37743,648,056 - 43,769,122 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36743,645,384 - 43,735,608 (-)NCBINCBI36Build 36hg18NCBI36
Celera743,668,728 - 43,758,937 (-)NCBICelera
Cytogenetic Map7p13NCBI
HuRef743,555,867 - 43,654,123 (-)NCBIHuRef
CHM1_1743,674,041 - 43,773,062 (-)NCBICHM1_1
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2743,710,264 - 43,808,634 (-)NCBI
Traj19
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391454,437,843 - 54,437,903 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1454,437,843 - 54,437,903 (+)EnsemblGRCm39 Ensembl
GRCm381454,200,386 - 54,200,446 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1454,200,386 - 54,200,446 (+)EnsemblGRCm38mm10GRCm38
MGSCv371454,820,061 - 54,820,121 (+)NCBIGRCm37MGSCv37mm9NCBIm37
Cytogenetic Map14C2NCBI
cM Map1427.69NCBI
LOC102011844
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955460182,778 - 285,053 (+)NCBIChiLan1.0ChiLan1.0
LOC100977063
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2644,720,534 - 44,841,599 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1793,045,265 - 93,166,341 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0740,521,542 - 40,642,646 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1740,567,277 - 40,687,964 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl740,645,777 - 40,657,169 (+)Ensemblpanpan1.1panPan2
COA1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1186,505,108 - 6,577,031 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl186,505,204 - 6,577,006 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha186,350,546 - 6,449,563 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0186,547,629 - 6,647,093 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl186,548,102 - 6,620,892 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1186,535,422 - 6,635,169 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0186,503,381 - 6,577,130 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0186,616,346 - 6,690,020 (+)NCBIUU_Cfam_GSD_1.0
COA1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11851,220,759 - 51,310,989 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
COA1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12114,850,596 - 14,943,473 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2114,851,464 - 14,945,129 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660627,543,624 - 7,637,702 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
LOC101707497
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462477515,990,359 - 15,996,269 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in COA1
29 total Variants

1 to 10 of 53 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7p14.1-12.3(chr7:39814159-45749735)x1 copy number loss See cases [RCV000053132] Chr7:39814159..45749735 [GRCh38]
Chr7:39853758..45789334 [GRCh37]
Chr7:39820283..45755859 [NCBI36]
Chr7:7p14.1-12.3
pathogenic
GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3 copy number gain See cases [RCV000053532] Chr7:33328312..62377476 [GRCh38]
Chr7:33367924..61831899 [GRCh37]
Chr7:33334449..61469334 [NCBI36]
Chr7:7p14.3-q11.21
pathogenic
GRCh38/hg38 7p14.1-11.2(chr7:40534157-56107122)x1 copy number loss See cases [RCV000136092] Chr7:40534157..56107122 [GRCh38]
Chr7:40573756..56174815 [GRCh37]
Chr7:40540281..56142309 [NCBI36]
Chr7:7p14.1-11.2
pathogenic
GRCh38/hg38 7p14.1-12.1(chr7:40020598-50543500)x1 copy number loss See cases [RCV000136904] Chr7:40020598..50543500 [GRCh38]
Chr7:40060197..50611198 [GRCh37]
Chr7:40026722..50578692 [NCBI36]
Chr7:7p14.1-12.1
pathogenic
GRCh38/hg38 7p14.1-13(chr7:39063400-45363096)x1 copy number loss See cases [RCV000137305] Chr7:39063400..45363096 [GRCh38]
Chr7:39103000..45402695 [GRCh37]
Chr7:39069525..45369220 [NCBI36]
Chr7:7p14.1-13
pathogenic
GRCh38/hg38 7p14.1-13(chr7:38177999-45304100)x1 copy number loss See cases [RCV000142297] Chr7:38177999..45304100 [GRCh38]
Chr7:38217601..45343699 [GRCh37]
Chr7:38184126..45310224 [NCBI36]
Chr7:7p14.1-13
pathogenic
NM_004760.2(STK17A):c.838T>A (p.Leu280Ile) single nucleotide variant Malignant melanoma [RCV000061649] Chr7:43623806 [GRCh38]
Chr7:43663405 [GRCh37]
Chr7:43629930 [NCBI36]
Chr7:7p13
not provided
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7p14.1-12.3(chr7:37303478-48660738)x1 copy number loss See cases [RCV000137139] Chr7:37303478..48660738 [GRCh38]
Chr7:37343082..48700334 [GRCh37]
Chr7:37309607..48670880 [NCBI36]
Chr7:7p14.1-12.3
pathogenic
1 to 10 of 53 rows

Predicted Target Of
Summary Value
Count of predictions:5215
Count of miRNA genes:1327
Interacting mature miRNAs:1760
Transcripts:ENST00000223336, ENST00000310564, ENST00000395879, ENST00000395880, ENST00000415076, ENST00000415798, ENST00000418140, ENST00000420441, ENST00000431651, ENST00000438444, ENST00000446330, ENST00000446564, ENST00000448704, ENST00000451651, ENST00000457939, ENST00000459713, ENST00000470156, ENST00000478504, ENST00000488813, ENST00000490251
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1558711BP56_HBlood pressure QTL 56 (human)2.240.000002Blood pressuresystolic73634937162349371Human
597385627GWAS1481701_Hhigh density lipoprotein cholesterol measurement QTL GWAS1481701 (human)0.000005high density lipoprotein cholesterol measurementblood high density lipoprotein cholesterol level (CMO:0000052)74363692143636922Human
407215475GWAS864451_Hmean corpuscular hemoglobin concentration QTL GWAS864451 (human)5e-12mean corpuscular hemoglobin concentrationmean corpuscular hemoglobin concentration (CMO:0000291)74361447143614472Human
597520279GWAS1616353_Hpatellar tendinitis QTL GWAS1616353 (human)2e-11patellar tendinitis74364204043642041Human
1559132SAPOB3_HSerum apolipoprotein B level QTL 3 (human)20.4Apolipoprotein levelapolipoprotein B73289107458891074Human
597384599GWAS1480673_Herythrocyte count QTL GWAS1480673 (human)7e-08erythrocyte countred blood cell count (CMO:0000025)74361628643616287Human
2302781MAMTS16_HMammary tumor susceptibility QTL 16 (human)0.033Mammary tumor susceptibility73634937162349371Human
2289453BW297_HBody weight QTL 297 (human)3.83Body weightbody mass index72334946449349464Human

GDB:4585463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,680,260 - 43,680,358UniSTSGRCh37
Build 36743,646,785 - 43,646,883RGDNCBI36
Celera743,670,129 - 43,670,227RGD
Cytogenetic Map7p13UniSTS
HuRef743,565,353 - 43,565,451UniSTS
CRA_TCAGchr7v2743,719,766 - 43,719,864UniSTS
D7S2799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,678,878 - 43,679,079UniSTSGRCh37
Build 36743,645,403 - 43,645,604RGDNCBI36
Celera743,668,747 - 43,668,948RGD
Cytogenetic Map7p13UniSTS
HuRef743,563,971 - 43,564,172UniSTS
CRA_TCAGchr7v2743,718,384 - 43,718,585UniSTS
Whitehead-YAC Contig Map7 UniSTS
A001X28  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,678,911 - 43,679,023UniSTSGRCh37
Build 36743,645,436 - 43,645,548RGDNCBI36
Celera743,668,780 - 43,668,892RGD
Cytogenetic Map7p13UniSTS
HuRef743,564,004 - 43,564,116UniSTS
CRA_TCAGchr7v2743,718,417 - 43,718,529UniSTS
GeneMap99-GB4 RH Map7209.52UniSTS
RH16240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,704,094 - 43,704,218UniSTSGRCh37
Build 36743,670,619 - 43,670,743RGDNCBI36
Celera743,693,955 - 43,694,079RGD
Cytogenetic Map7p13UniSTS
HuRef743,589,175 - 43,589,299UniSTS
CRA_TCAGchr7v2743,743,602 - 43,743,726UniSTS
GeneMap99-GB4 RH Map7201.34UniSTS
NCBI RH Map7652.7UniSTS
RH26508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,704,012 - 43,704,183UniSTSGRCh37
Build 36743,670,537 - 43,670,708RGDNCBI36
Celera743,693,873 - 43,694,044RGD
Cytogenetic Map7p13UniSTS
HuRef743,589,093 - 43,589,264UniSTS
CRA_TCAGchr7v2743,743,520 - 43,743,691UniSTS
RH91776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,678,953 - 43,679,079UniSTSGRCh37
Build 36743,645,478 - 43,645,604RGDNCBI36
Celera743,668,822 - 43,668,948RGD
Cytogenetic Map7p13UniSTS
HuRef743,564,046 - 43,564,172UniSTS
CRA_TCAGchr7v2743,718,459 - 43,718,585UniSTS
GeneMap99-GB4 RH Map7208.36UniSTS
G17155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,726,217 - 43,726,429UniSTSGRCh37
Build 36743,692,742 - 43,692,954RGDNCBI36
Celera743,716,072 - 43,716,284RGD
Cytogenetic Map7p13UniSTS
HuRef743,611,268 - 43,611,480UniSTS
CRA_TCAGchr7v2743,765,719 - 43,765,931UniSTS
D7S743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,733,759 - 43,733,924UniSTSGRCh37
Build 36743,700,284 - 43,700,449RGDNCBI36
Celera743,723,614 - 43,723,779RGD
Cytogenetic Map7p13UniSTS
HuRef743,618,377 - 43,618,542UniSTS
CRA_TCAGchr7v2743,773,259 - 43,773,424UniSTS
G17198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,707,262 - 43,707,402UniSTSGRCh37
Build 36743,673,787 - 43,673,927RGDNCBI36
Celera743,697,123 - 43,697,263RGD
Cytogenetic Map7p13UniSTS
HuRef743,592,343 - 43,592,483UniSTS
CRA_TCAGchr7v2743,746,770 - 43,746,910UniSTS
STS-T51004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,690,102 - 43,690,236UniSTSGRCh37
Build 36743,656,627 - 43,656,761RGDNCBI36
Celera743,679,963 - 43,680,097RGD
Cytogenetic Map7p13UniSTS
HuRef743,575,187 - 43,575,321UniSTS
CRA_TCAGchr7v2743,729,608 - 43,729,742UniSTS
GeneMap99-GB4 RH Map7223.06UniSTS
NCBI RH Map7654.4UniSTS
D7S1397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,687,502 - 43,687,608UniSTSGRCh37
Build 36743,654,027 - 43,654,133RGDNCBI36
Celera743,677,363 - 43,677,469RGD
Cytogenetic Map7p13UniSTS
HuRef743,572,587 - 43,572,693UniSTS
CRA_TCAGchr7v2743,727,008 - 43,727,114UniSTS
WI-11641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37743,685,913 - 43,686,037UniSTSGRCh37
Build 36743,652,438 - 43,652,562RGDNCBI36
Celera743,675,774 - 43,675,898RGD
Cytogenetic Map7p13UniSTS
HuRef743,570,998 - 43,571,122UniSTS
CRA_TCAGchr7v2743,725,419 - 43,725,543UniSTS
GeneMap99-GB4 RH Map7201.96UniSTS
Whitehead-RH Map7150.9UniSTS
NCBI RH Map7652.6UniSTS




adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1


1 to 30 of 183 rows
RefSeq Transcripts NM_001321197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001350928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371307 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371316 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001371318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_135582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 183 rows

Ensembl Acc Id: ENST00000223336   ⟹   ENSP00000223336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,639,257 - 43,729,523 (-)Ensembl
Ensembl Acc Id: ENST00000310564   ⟹   ENSP00000312100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,639,257 - 43,729,489 (-)Ensembl
Ensembl Acc Id: ENST00000395879   ⟹   ENSP00000379218
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,639,257 - 43,650,296 (-)Ensembl
Ensembl Acc Id: ENST00000415076   ⟹   ENSP00000400759
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,608,456 - 43,729,513 (-)Ensembl
Ensembl Acc Id: ENST00000415798   ⟹   ENSP00000405582
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,640,573 - 43,729,523 (-)Ensembl
Ensembl Acc Id: ENST00000418140   ⟹   ENSP00000410365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,646,472 - 43,729,483 (-)Ensembl
Ensembl Acc Id: ENST00000420441   ⟹   ENSP00000398886
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,648,188 - 43,729,510 (-)Ensembl
Ensembl Acc Id: ENST00000431651   ⟹   ENSP00000417046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,645,251 - 43,729,505 (-)Ensembl
Ensembl Acc Id: ENST00000438444   ⟹   ENSP00000395586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,631,152 - 43,729,717 (-)Ensembl
Ensembl Acc Id: ENST00000446330   ⟹   ENSP00000416406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,608,819 - 43,729,513 (-)Ensembl
Ensembl Acc Id: ENST00000446564   ⟹   ENSP00000413777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,609,233 - 43,729,483 (-)Ensembl
Ensembl Acc Id: ENST00000448704   ⟹   ENSP00000400271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,647,228 - 43,729,501 (-)Ensembl
Ensembl Acc Id: ENST00000451651   ⟹   ENSP00000411540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,646,297 - 43,729,474 (-)Ensembl
Ensembl Acc Id: ENST00000457939   ⟹   ENSP00000387433
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,647,351 - 43,729,497 (-)Ensembl
Ensembl Acc Id: ENST00000459713
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,647,216 - 43,648,754 (-)Ensembl
Ensembl Acc Id: ENST00000470156
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,647,275 - 43,729,483 (-)Ensembl
Ensembl Acc Id: ENST00000478504
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,657,222 - 43,729,499 (-)Ensembl
Ensembl Acc Id: ENST00000488813
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,639,257 - 43,642,164 (-)Ensembl
Ensembl Acc Id: ENST00000490251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl743,638,799 - 43,646,425 (-)Ensembl
RefSeq Acc Id: NM_001321197   ⟹   NP_001308126
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
CHM1_1743,682,136 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321198   ⟹   NP_001308127
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
CHM1_1743,682,136 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321199   ⟹   NP_001308128
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
CHM1_1743,682,136 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321200   ⟹   NP_001308129
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
CHM1_1743,682,136 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321201   ⟹   NP_001308130
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
CHM1_1743,682,136 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321202   ⟹   NP_001308131
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,646,472 - 43,729,523 (-)NCBI
CHM1_1743,689,361 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,804,543 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321203   ⟹   NP_001308132
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,646,472 - 43,729,523 (-)NCBI
CHM1_1743,689,361 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,804,543 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321204   ⟹   NP_001308133
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,646,472 - 43,729,523 (-)NCBI
CHM1_1743,689,361 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,804,543 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321205   ⟹   NP_001308134
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,646,472 - 43,729,523 (-)NCBI
CHM1_1743,689,361 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,804,543 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350924   ⟹   NP_001337853
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350925   ⟹   NP_001337854
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350926   ⟹   NP_001337855
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350927   ⟹   NP_001337856
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001350928   ⟹   NP_001337857
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371307   ⟹   NP_001358236
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371308   ⟹   NP_001358237
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371309   ⟹   NP_001358238
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371310   ⟹   NP_001358239
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371311   ⟹   NP_001358240
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371312   ⟹   NP_001358241
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371313   ⟹   NP_001358242
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371314   ⟹   NP_001358243
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371315   ⟹   NP_001358244
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371316   ⟹   NP_001358245
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371317   ⟹   NP_001358246
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001371318   ⟹   NP_001358247
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NM_018224   ⟹   NP_060694
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
GRCh37743,648,052 - 43,769,140 (-)NCBI
Build 36743,645,384 - 43,735,608 (-)NCBI Archive
Celera743,668,728 - 43,758,937 (-)RGD
HuRef743,555,867 - 43,654,123 (-)NCBI
CHM1_1743,682,136 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
CRA_TCAGchr7v2743,710,264 - 43,808,634 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135580
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
CHM1_1743,651,349 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135581
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
CHM1_1743,651,349 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135582
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
CHM1_1743,651,349 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_135583
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
CHM1_1743,651,349 - 43,773,062 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146940
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146941
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146942
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146943
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146944
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_146945
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163914
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163915
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163916
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163917
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163918
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163919
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,729,523 (-)NCBI
T2T-CHM13v2.0743,797,316 - 43,887,637 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047420603   ⟹   XP_047276559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,665,722 (-)NCBI
RefSeq Acc Id: XM_047420604   ⟹   XP_047276560
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,665,722 (-)NCBI
RefSeq Acc Id: XM_047420605   ⟹   XP_047276561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,639,257 - 43,665,722 (-)NCBI
RefSeq Acc Id: XM_054358632   ⟹   XP_054214607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,797,316 - 43,823,800 (-)NCBI
RefSeq Acc Id: XM_054358633   ⟹   XP_054214608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,797,316 - 43,823,800 (-)NCBI
RefSeq Acc Id: XM_054358634   ⟹   XP_054214609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,797,316 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_007060076
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060077
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060078
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060079
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060080
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060081
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060082
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060083
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060084
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060085
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060086
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060087
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060088
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060089
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060090
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060091
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060092
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060093
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060094
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,651,773 (-)NCBI
RefSeq Acc Id: XR_007060095
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060096
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060097
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060098
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060099
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060100
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060101
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060102
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060103
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060104
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060105
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060106
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060107
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060108
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060109
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060110
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060111
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060112
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,729,523 (-)NCBI
RefSeq Acc Id: XR_007060113
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060114
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,665,722 (-)NCBI
RefSeq Acc Id: XR_007060115
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,608,457 - 43,651,829 (-)NCBI
RefSeq Acc Id: XR_008487664
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487665
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487666
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487667
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,781,935 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487668
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487669
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487670
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487671
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487672
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487673
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487674
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487675
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487676
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487677
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487678
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487679
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487680
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_008487681
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487682
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487683
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,809,836 (-)NCBI
RefSeq Acc Id: XR_008487684
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487685
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487686
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487687
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487688
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_008487689
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487690
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_008487691
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487692
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487693
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_008487694
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487695
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487696
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487697
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487698
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487699
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_008487700
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487701
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,887,637 (-)NCBI
RefSeq Acc Id: XR_008487702
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,823,800 (-)NCBI
RefSeq Acc Id: XR_008487703
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0743,766,512 - 43,809,892 (-)NCBI
1 to 30 of 60 rows
Protein RefSeqs NP_001308126 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308127 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308128 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308129 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308130 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308131 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308132 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308133 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308134 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337853 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337854 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337855 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337856 (Get FASTA)   NCBI Sequence Viewer  
  NP_001337857 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358236 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358237 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358238 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358239 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358240 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358241 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358242 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358243 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358244 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358245 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358246 (Get FASTA)   NCBI Sequence Viewer  
  NP_001358247 (Get FASTA)   NCBI Sequence Viewer  
  NP_060694 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276559 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276560 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276561 (Get FASTA)   NCBI Sequence Viewer  
1 to 30 of 60 rows
1 to 5 of 47 rows
1 to 5 of 47 rows
RefSeq Acc Id: NP_060694   ⟸   NM_018224
- Peptide Label: isoform a
- UniProtKB: Q9HAB7 (UniProtKB/Swiss-Prot),   A8KAH8 (UniProtKB/Swiss-Prot),   A6NJU8 (UniProtKB/Swiss-Prot),   Q9NVD2 (UniProtKB/Swiss-Prot),   Q9GZY4 (UniProtKB/Swiss-Prot),   B3KUH1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308130   ⟸   NM_001321201
- Peptide Label: isoform b
- UniProtKB: B3KUH1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308127   ⟸   NM_001321198
- Peptide Label: isoform a
- UniProtKB: Q9HAB7 (UniProtKB/Swiss-Prot),   A8KAH8 (UniProtKB/Swiss-Prot),   A6NJU8 (UniProtKB/Swiss-Prot),   Q9NVD2 (UniProtKB/Swiss-Prot),   Q9GZY4 (UniProtKB/Swiss-Prot),   B3KUH1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308126   ⟸   NM_001321197
- Peptide Label: isoform a
- UniProtKB: Q9HAB7 (UniProtKB/Swiss-Prot),   A8KAH8 (UniProtKB/Swiss-Prot),   A6NJU8 (UniProtKB/Swiss-Prot),   Q9NVD2 (UniProtKB/Swiss-Prot),   Q9GZY4 (UniProtKB/Swiss-Prot),   B3KUH1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308129   ⟸   NM_001321200
- Peptide Label: isoform a
- UniProtKB: Q9HAB7 (UniProtKB/Swiss-Prot),   A8KAH8 (UniProtKB/Swiss-Prot),   A6NJU8 (UniProtKB/Swiss-Prot),   Q9NVD2 (UniProtKB/Swiss-Prot),   Q9GZY4 (UniProtKB/Swiss-Prot),   B3KUH1 (UniProtKB/TrEMBL)
- Sequence:

Name Modeler Protein Id AA Range Protein Structure
AF-Q9GZY4-F1-model_v2 AlphaFold Q9GZY4 1-146 view protein structure

RGD ID:6805325
Promoter ID:HG_KWN:57173
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_2Hour,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000313665
Position:
Human AssemblyChrPosition (strand)Source
Build 36743,647,756 - 43,649,282 (-)MPROMDB
RGD ID:6805326
Promoter ID:HG_KWN:57174
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000313666
Position:
Human AssemblyChrPosition (strand)Source
Build 36743,651,441 - 43,653,397 (-)MPROMDB
RGD ID:6805328
Promoter ID:HG_KWN:57175
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   K562,   Lymphoblastoid
Transcripts:ENST00000395879,   OTTHUMT00000313669
Position:
Human AssemblyChrPosition (strand)Source
Build 36743,655,001 - 43,657,097 (-)MPROMDB
RGD ID:7210463
Promoter ID:EPDNEW_H10976
Type:initiation region
Name:COA1_1
Description:cytochrome c oxidase assembly factor 1 homolog
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38743,729,483 - 43,729,543EPDNEW
RGD ID:6805329
Promoter ID:HG_KWN:57176
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000310564,   ENST00000395880,   NM_018224,   OTTHUMT00000250928,   OTTHUMT00000313662,   OTTHUMT00000313667,   OTTHUMT00000338847,   OTTHUMT00000338848,   OTTHUMT00000338850,   OTTHUMT00000338851,   OTTHUMT00000338852,   OTTHUMT00000338853,   OTTHUMT00000338854,   OTTHUMT00000338855,   UC003TII.2,   UC003TIJ.2,   UC003TIK.2,   UC003TIM.1,   UC003TIP.1,   UC010KXU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36743,735,449 - 43,735,949 (-)MPROMDB


1 to 40 of 41 rows
Database
Acc Id
Source(s)
COSMIC COA1 COSMIC
Ensembl Genes ENSG00000106603 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000223336 ENTREZGENE
  ENST00000223336.11 UniProtKB/Swiss-Prot
  ENST00000310564 ENTREZGENE
  ENST00000310564.10 UniProtKB/Swiss-Prot
  ENST00000395879.5 UniProtKB/Swiss-Prot
  ENST00000415076.6 UniProtKB/Swiss-Prot
  ENST00000418140 ENTREZGENE
  ENST00000438444 ENTREZGENE
  ENST00000438444.5 UniProtKB/Swiss-Prot
  ENST00000446330.6 UniProtKB/Swiss-Prot
  ENST00000446564 ENTREZGENE
  ENST00000446564.5 UniProtKB/Swiss-Prot
  ENST00000457939 ENTREZGENE
GTEx ENSG00000106603 GTEx
HGNC ID HGNC:21868 ENTREZGENE
Human Proteome Map COA1 Human Proteome Map
InterPro Cyt_oxidase_assembly-1 UniProtKB/Swiss-Prot
KEGG Report hsa:55744 UniProtKB/Swiss-Prot
NCBI Gene 55744 ENTREZGENE
OMIM 614769 OMIM
PANTHER CYTOCHROME C OXIDASE ASSEMBLY FACTOR 1 HOMOLOG UniProtKB/Swiss-Prot
  CYTOCHROME C OXIDASE ASSEMBLY FACTOR 1 HOMOLOG UniProtKB/Swiss-Prot
Pfam Coa1 UniProtKB/Swiss-Prot
PharmGKB PA162380473 PharmGKB
UniProt A6NJU8 ENTREZGENE
  A8KAH8 ENTREZGENE
  B3KUH1 ENTREZGENE, UniProtKB/TrEMBL
  C9J6J1_HUMAN UniProtKB/TrEMBL
  C9JA07_HUMAN UniProtKB/TrEMBL
  COA1_HUMAN UniProtKB/Swiss-Prot
  F2Z2J3 ENTREZGENE, UniProtKB/TrEMBL
  F8WBS2_HUMAN UniProtKB/TrEMBL
  Q9GZY4 ENTREZGENE
  Q9HAB7 ENTREZGENE
  Q9NVD2 ENTREZGENE
UniProt Secondary A6NJU8 UniProtKB/Swiss-Prot
  A8KAH8 UniProtKB/Swiss-Prot
  Q9HAB7 UniProtKB/Swiss-Prot
1 to 40 of 41 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2021-04-26 COA1  cytochrome c oxidase assembly factor 1  COA1  cytochrome c oxidase assembly factor 1 homolog  Symbol and/or name change 19259463 PROVISIONAL
2015-07-07 COA1  cytochrome c oxidase assembly factor 1 homolog    cytochrome c oxidase assembly factor 1 homolog (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED
2012-10-23 COA1  cytochrome c oxidase assembly factor 1 homolog (S. cerevisiae)    cytochrome C oxidase assembly factor 1 homolog (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED
2012-06-27 COA1  cytochrome C oxidase assembly factor 1 homolog (S. cerevisiae)  C7orf44  chromosome 7 open reading frame 44  Symbol and/or name change 5135510 APPROVED