Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Fam169a ENSRNOG00000016505

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Description

family with sequence similarity 169, member A [Source:RGD Symbol;Acc:1590893]

Gene Synonyms

LOC310013

Location

Primary_assembly 2: 30,119,381-30,175,962 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000109459.2	Fam169a-202	5032	666aa	ENSRNOP00000078762.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G2A6	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,
ENSRNOT00000022120.8	Fam169a-201	4852	606aa	ENSRNOP00000022120.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZKX8	-

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Summary

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