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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FAM69C ENSG00000187773

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Description

family with sequence similarity 69, member C [Source:HGNC Symbol;Acc:31729]

Gene Synonyms

C18orf51

Location

Chromosome 18: 72,102,963-72,125,179 reverse strand.

GRCh37:CM000680.1

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000343998.6	FAM69C-001	2013	419aa	ENSP00000344331.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS42445	Q0P6D2	NM_001044369.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000400291.2	FAM69C-002	1329	120aa	ENSP00000383148.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q0P6D2	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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