COX8C (cytochrome c oxidase subunit 8C) - Rat Genome Database

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Gene: COX8C (cytochrome c oxidase subunit 8C) Homo sapiens
Analyze
Symbol: COX8C
Name: cytochrome c oxidase subunit 8C
RGD ID: 1344927
HGNC Page HGNC:24382
Description: Predicted to be involved in mitochondrial electron transport, cytochrome c to oxygen. Located in mitochondrion.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: COX VIII-3; COX8-3; cytochrome c oxidase polypeptide 8; cytochrome c oxidase polypeptide VIII; cytochrome c oxidase subunit 8-3; cytochrome c oxidase subunit 8C, mitochondrial; cytochrome c oxidase subunit VIII; cytochrome c oxidase subunit VIIIC; MGC119774; MGC119775
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Related Pseudogenes: COX8CP1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381493,347,182 - 93,348,356 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1493,347,182 - 93,348,356 (+)EnsemblGRCh38hg38GRCh38
GRCh371493,813,528 - 93,814,702 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361492,883,290 - 92,884,453 (+)NCBINCBI36Build 36hg18NCBI36
Build 341492,883,289 - 92,884,453NCBI
Celera1473,867,551 - 73,868,714 (+)NCBICelera
Cytogenetic Map14q32.12NCBI
HuRef1473,993,564 - 73,994,727 (+)NCBIHuRef
CHM1_11493,751,557 - 93,752,720 (+)NCBICHM1_1
T2T-CHM13v2.01487,579,055 - 87,580,228 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. A third isoform of cytochrome c oxidase subunit VIII is present in mammals. Huttemann M, etal., Gene 2003 Jul 17;312:95-102.
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:12762575   PMID:15489334   PMID:20877624   PMID:21873635   PMID:22419111  


Genomics

Comparative Map Data
COX8C
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381493,347,182 - 93,348,356 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1493,347,182 - 93,348,356 (+)EnsemblGRCh38hg38GRCh38
GRCh371493,813,528 - 93,814,702 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361492,883,290 - 92,884,453 (+)NCBINCBI36Build 36hg18NCBI36
Build 341492,883,289 - 92,884,453NCBI
Celera1473,867,551 - 73,868,714 (+)NCBICelera
Cytogenetic Map14q32.12NCBI
HuRef1473,993,564 - 73,994,727 (+)NCBIHuRef
CHM1_11493,751,557 - 93,752,720 (+)NCBICHM1_1
T2T-CHM13v2.01487,579,055 - 87,580,228 (+)NCBIT2T-CHM13v2.0
Cox8c
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3912102,865,565 - 102,866,793 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl12102,865,575 - 102,866,785 (+)EnsemblGRCm39 Ensembl
GRCm3812102,899,306 - 102,900,534 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl12102,899,316 - 102,900,526 (+)EnsemblGRCm38mm10GRCm38
MGSCv3712104,137,516 - 104,138,744 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3612103,300,356 - 103,301,584 (+)NCBIMGSCv36mm8
Celera12104,116,515 - 104,117,743 (+)NCBICelera
Cytogenetic Map12ENCBI
cM Map1252.55NCBI
Cox8c
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr86127,793,379 - 127,794,702 (+)NCBIGRCr8
mRatBN7.26122,028,566 - 122,029,889 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl6122,028,566 - 122,029,889 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx6122,166,956 - 122,168,278 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.06122,462,221 - 122,463,543 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.06121,798,339 - 121,799,672 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.06126,766,967 - 126,768,290 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl6126,766,967 - 126,768,290 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06135,972,917 - 135,974,240 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46127,161,354 - 127,162,677 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.16127,165,100 - 127,166,424 (+)NCBI
Celera6119,515,028 - 119,516,351 (+)NCBICelera
Cytogenetic Map6q32NCBI
LOC102005637
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495543815,480,509 - 15,481,812 (+)NCBIChiLan1.0ChiLan1.0
LOC100984553
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21594,493,815 - 94,571,864 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11493,707,703 - 93,772,906 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01473,979,629 - 73,984,116 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11493,316,013 - 93,317,217 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1493,316,013 - 93,317,217 (+)Ensemblpanpan1.1panPan2
LOC100856429
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11825,401,351 - 25,402,874 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1825,051,304 - 25,052,818 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01825,928,113 - 25,929,627 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.11825,496,165 - 25,497,679 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01825,140,874 - 25,142,388 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01825,753,536 - 25,755,050 (-)NCBIUU_Cfam_GSD_1.0
LOC100157935
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.17114,727,841 - 114,729,102 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.27121,313,089 - 121,314,323 (+)NCBISscrofa10.2Sscrofa10.2susScr3
COX8C
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12471,098,014 - 71,099,417 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2471,098,346 - 71,099,180 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605358,339,240 - 58,350,907 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in COX8C
4 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q32.11-32.13(chr14:90255156-95274696)x1 copy number loss See cases [RCV000051551] Chr14:90255156..95274696 [GRCh38]
Chr14:90721500..95741033 [GRCh37]
Chr14:89791253..94810786 [NCBI36]
Chr14:14q32.11-32.13		 pathogenic
GRCh38/hg38 14q31.2-32.33(chr14:83912345-106855405)x3 copy number gain See cases [RCV000052294] Chr14:83912345..106855405 [GRCh38]
Chr14:84378689..107263620 [GRCh37]
Chr14:83448442..106334665 [NCBI36]
Chr14:14q31.2-32.33		 pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] Chr14:72787506..99596719 [GRCh38]
Chr14:73254214..100063056 [GRCh37]
Chr14:72323967..99132809 [NCBI36]
Chr14:14q24.2-32.2		 pathogenic
GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3 copy number gain See cases [RCV000052295] Chr14:86094030..106832642 [GRCh38]
Chr14:86560374..107240869 [GRCh37]
Chr14:85630127..106311914 [NCBI36]
Chr14:14q31.3-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3 copy number gain See cases [RCV000052296] Chr14:91455861..106832642 [GRCh38]
Chr14:91922205..107240869 [GRCh37]
Chr14:90991958..106311914 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
NM_182971.2(COX8C):c.55C>T (p.Leu19=) single nucleotide variant Malignant melanoma [RCV000070660] Chr14:93347323 [GRCh38]
Chr14:93813669 [GRCh37]
Chr14:92883422 [NCBI36]
Chr14:14q32.12		 not provided
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:92540983-104863658)x3 copy number gain See cases [RCV000135896] Chr14:92540983..104863658 [GRCh38]
Chr14:93007328..105329995 [GRCh37]
Chr14:92077081..104401040 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3 copy number gain See cases [RCV000138230] Chr14:77222795..106879298 [GRCh38]
Chr14:77689138..107287505 [GRCh37]
Chr14:76758891..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q32.12(chr14:93813573-93814549)x3 copy number gain See cases [RCV000447280] Chr14:93813573..93814549 [GRCh37]
Chr14:14q32.12		 likely benign
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q32.12(chr14:93710666-93935402)x1 copy number loss See cases [RCV000511610] Chr14:93710666..93935402 [GRCh37]
Chr14:14q32.12		 likely benign
GRCh37/hg19 14q32.12-32.13(chr14:93498930-96059698)x3 copy number gain See cases [RCV000511246] Chr14:93498930..96059698 [GRCh37]
Chr14:14q32.12-32.13		 uncertain significance
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33		 pathogenic
GRCh37/hg19 14q31.2-32.2(chr14:84783137-96908198)x1 copy number loss not provided [RCV000683625] Chr14:84783137..96908198 [GRCh37]
Chr14:14q31.2-32.2		 pathogenic
GRCh37/hg19 14q31.2-32.2(chr14:84783523-96907490)x1 copy number loss Deletion syndrome [RCV001004048] Chr14:84783523..96907490 [GRCh37]
Chr14:14q31.2-32.2		 pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q31.3-32.13(chr14:88401076-94725706)x1 copy number loss not provided [RCV003312295] Chr14:88401076..94725706 [GRCh37]
Chr14:14q31.3-32.13		 pathogenic
GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3 copy number gain not provided [RCV000848687] Chr14:91969028..107285437 [GRCh37]
Chr14:14q32.12-32.33		 pathogenic
GRCh37/hg19 14q31.1-32.2(chr14:81593708-97059276)x3 copy number gain not provided [RCV002472541] Chr14:81593708..97059276 [GRCh37]
Chr14:14q31.1-32.2		 likely pathogenic
NC_000014.8:g.(?_93687728)_(95560403_?)del deletion DICER1-related tumor predisposition [RCV002044285] Chr14:93687728..95560403 [GRCh37]
Chr14:14q32.12-32.13		 likely pathogenic
GRCh37/hg19 14q31.3-32.13(chr14:88345625-94773741) copy number loss not specified [RCV002053117] Chr14:88345625..94773741 [GRCh37]
Chr14:14q31.3-32.13		 pathogenic
NC_000014.8:g.(?_90429459)_(97347545_?)dup duplication not provided [RCV003109490] Chr14:90429459..97347545 [GRCh37]
Chr14:14q32.11-32.2		 uncertain significance
NC_000014.8:g.(?_90429459)_(94856914_?)dup duplication Achondrogenesis, type IA [RCV003113413] Chr14:90429459..94856914 [GRCh37]
Chr14:14q32.11-32.13		 uncertain significance
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
GRCh37/hg19 14q31.2-32.33(chr14:84537502-107285437)x3 copy number gain not provided [RCV002472581] Chr14:84537502..107285437 [GRCh37]
Chr14:14q31.2-32.33		 pathogenic
NM_182971.3(COX8C):c.158C>T (p.Thr53Met) single nucleotide variant not specified [RCV004207780] Chr14:93348059 [GRCh38]
Chr14:93814405 [GRCh37]
Chr14:14q32.12		 uncertain significance
NM_182971.3(COX8C):c.28G>T (p.Ala10Ser) single nucleotide variant not specified [RCV004143500] Chr14:93347296 [GRCh38]
Chr14:93813642 [GRCh37]
Chr14:14q32.12		 uncertain significance
NM_182971.3(COX8C):c.202C>A (p.Gln68Lys) single nucleotide variant not specified [RCV004121463] Chr14:93348103 [GRCh38]
Chr14:93814449 [GRCh37]
Chr14:14q32.12		 uncertain significance
GRCh37/hg19 14q31.3-32.33(chr14:88580184-107285437)x3 copy number gain not provided [RCV003485051] Chr14:88580184..107285437 [GRCh37]
Chr14:14q31.3-32.33		 pathogenic
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
NM_182971.3(COX8C):c.14G>A (p.Arg5His) single nucleotide variant not specified [RCV004372291] Chr14:93347282 [GRCh38]
Chr14:93813628 [GRCh37]
Chr14:14q32.12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:95
Count of miRNA genes:70
Interacting mature miRNAs:76
Transcripts:ENST00000342144
Prediction methods:Microtar, Miranda, Targetscan
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.

Markers in Region
UniSTS:484220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371493,813,562 - 93,814,564UniSTSGRCh37
Celera1473,867,576 - 73,868,578UniSTS
HuRef1473,993,589 - 73,994,591UniSTS


Expression

RNA-SEQ Expression

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
renal system
reproductive system
respiratory system
sensory system
805 1808 2169 1947 3889 1226 1606 5 360 756 256 1300 5067 4423 44 3386 639 1535 1119 113

Sequence


Ensembl Acc Id: ENST00000342144   ⟹   ENSP00000340568
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1493,347,182 - 93,348,356 (+)Ensembl
RefSeq Acc Id: NM_182971   ⟹   NP_892016
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381493,347,182 - 93,348,356 (+)NCBI
GRCh371493,813,537 - 93,814,700 (+)RGD
Build 361492,883,290 - 92,884,453 (+)NCBI Archive
Celera1473,867,551 - 73,868,714 (+)RGD
HuRef1473,993,564 - 73,994,727 (+)ENTREZGENE
CHM1_11493,751,557 - 93,752,720 (+)NCBI
T2T-CHM13v2.01487,579,055 - 87,580,228 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_892016 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI01126 (Get FASTA)   NCBI Sequence Viewer  
  AAI01127 (Get FASTA)   NCBI Sequence Viewer  
  AAO26193 (Get FASTA)   NCBI Sequence Viewer  
  EAW81530 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000340568
  ENSP00000340568.2
  ENSP00000480706.1
GenBank Protein Q7Z4L0 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_892016   ⟸   NM_182971
- UniProtKB: Q495K7 (UniProtKB/Swiss-Prot),   Q7Z4L0 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000340568   ⟸   ENST00000342144

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7Z4L0-F1-model_v2 AlphaFold Q7Z4L0 1-72 view protein structure

Promoters
RGD ID:7228469
Promoter ID:EPDNEW_H19980
Type:initiation region
Name:COX8C_2
Description:cytochrome c oxidase subunit 8C
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19979  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381493,347,183 - 93,347,243EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24382 AgrOrtholog
COSMIC COX8C COSMIC
Ensembl Genes ENSG00000187581 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000277018 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000342144 ENTREZGENE
  ENST00000342144.3 UniProtKB/Swiss-Prot
  ENST00000620478.2 UniProtKB/Swiss-Prot
Gene3D-CATH 4.10.81.10 UniProtKB/Swiss-Prot
GTEx ENSG00000187581 GTEx
  ENSG00000277018 GTEx
HGNC ID HGNC:24382 ENTREZGENE
Human Proteome Map COX8C Human Proteome Map
InterPro Cyt_c_oxidase_su8 UniProtKB/Swiss-Prot
  Cyt_c_oxidase_su8_sf UniProtKB/Swiss-Prot
KEGG Report hsa:341947 UniProtKB/Swiss-Prot
NCBI Gene 341947 ENTREZGENE
OMIM 616855 OMIM
PANTHER CYTOCHROME C OXIDASE SUBUNIT 8C, MITOCHONDRIAL UniProtKB/Swiss-Prot
  PTHR16717 UniProtKB/Swiss-Prot
Pfam COX8 UniProtKB/Swiss-Prot
PharmGKB PA134909890 PharmGKB
Superfamily-SCOP SSF81431 UniProtKB/Swiss-Prot
UniProt COX8C_HUMAN UniProtKB/Swiss-Prot
  Q495K7 ENTREZGENE
  Q7Z4L0 ENTREZGENE
UniProt Secondary Q495K7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-16 COX8C  cytochrome c oxidase subunit 8C    cytochrome c oxidase subunit VIIIC  Symbol and/or name change 5135510 APPROVED
2011-07-27 COX8C  cytochrome c oxidase subunit VIIIC  COX8C  cytochrome c oxidase subunit 8C  Symbol and/or name change 5135510 APPROVED