Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Fam167a ENSRNOG00000011316

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Description

family with sequence similarity 167, member A [Source:RGD Symbol;Acc:1561302]

Gene Synonyms

LOC498533, RGD1561302

Location

Primary_assembly 15: 41,861,227-41,891,418 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 1 transcript (splice variant), 211 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000015055.6	Fam167a-201	4244	215aa	ENSRNOP00000015055.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K6G2 D3ZQX1	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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