COX7B gene homepage

General information
Gene symbol COX7B
Gene name cytochrome c oxidase subunit VIIb
Chromosome X
Chromosomal band q21.1
Imprinted Unknown
Genomic reference NG_033027.1
Transcript reference NM_001866.2
Associated with diseases ID, Aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 14
Unique public DNA variants reported 12
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 2291
Entrez Gene 1349
PubMed articles COX7B
OMIM - Gene 300885
OMIM - Diseases Aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies

Active transcripts




NCBI ID     

NCBI Protein ID     

00005568 X cytochrome c oxidase subunit VIIb NM_001866.2 NP_001857.1 14

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