Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: Fam149a ENSRNOG00000021693

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Description

family with sequence similarity 149, member A [Source:RGD Symbol;Acc:1586153]

Gene Synonyms

LOC361153

Location

Primary_assembly 16: 53,587,841-53,647,072 forward strand.

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants), 143 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000171229.1	Fam149a-202	5209	800aa	ENSRNOP00000108183.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000034448.7	Fam149a-201	5552	790aa	ENSRNOP00000029147.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LUX5	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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