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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: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: C1orf172 ENSG00000175707

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Description

chromosome 1 open reading frame 172 [Source:HGNC Symbol;Acc:26624]

Gene Synonyms

FLJ34633, RP11-344H11.3

Location

Chromosome 1: 27,276,053-27,286,897 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 1 transcript (splice variant) and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000320567.5	C1orf172-001	1793	398aa	ENSP00000319179.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS293	Q8NAX2	NM_152365.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, 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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