The C12orf65 gene homepage

General information
Gene symbol C12orf65
Gene name chromosome 12 open reading frame 65
Chromosome 12
Chromosomal band q24.31
Imprinted Unknown
Genomic reference NG_027517.1
Transcript reference NM_152269.4
Associated with diseases COXPD-7, SPG-55
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 18
Unique public DNA variants reported 11
Individuals with public variants 31
Hidden variants 2
Date created May 03, 2013
Date last updated February 08, 2021
Version C12orf65:210208

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 26784
Entrez Gene 91574
PubMed articles C12orf65
OMIM - Gene 613541
OMIM - Diseases COXPD-7 (combined oxidative phosphorylation deficiency, type 7 (COXPD-7))
SPG-55 (paraplegia, spastic, autosomal recessive, type 55 (SPG-55))
Orphanet C12orf65


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00004004 12 transcript variant 1 NM_152269.4 NP_689482.1 18


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