Entity Details

Primary name C12orf57
Entity type gene
Source Source Link

Details

PrimaryID113246
RefseqGeneNG_034262
SymbolC12orf57
Namechromosome 12 open reading frame 57
Chromosome12
Location12p13.31
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-08-22
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsC10_HUMAN

GO terms

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GOName
GO:0005737 cytoplasm
GO:0009791 post-embryonic development
GO:0014819 regulation of skeletal muscle contraction
GO:0016607 nuclear speck
GO:0021540 corpus callosum morphogenesis
GO:0021678 third ventricle development
GO:0036343 psychomotor behavior
GO:0048593 camera-type eye morphogenesis
GO:0050890 cognition

Diseases

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Disease IDSourceNameDescription
218340 OMIMTemtamy syndrome (TEMTYS)A mental retardation/multiple congenital anomaly syndrome characterized by variable craniofacial dysmorphism, ocular coloboma, seizures, and brain abnormalities, including abnormalities of the corpus callosum and thalamus. The disease is caused by variants affecting the gene represented in this entry. A variant resulting in a GUG start codon may be able to produce some protein because of a consensus Kozak sequence, although less efficiently than the wild type. This would explain the phenotypic variability observed.