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: Fam181a ENSRNOG00000048412

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Description

family with sequence similarity 181, member A [Source:RGD Symbol;Acc:6504274]

Gene Synonyms

LOC100909401, LOC299265, RGD1309028

Location

Primary_assembly 6: 128,232,240-128,236,625 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 2 transcripts (splice variants), 98 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000071976.3	Fam181a-201	2078	362aa	ENSRNOP00000067135.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RC29	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,
ENSRNOT00000075399.4	Fam181a-202	1401	292aa	ENSRNOP00000067372.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCP7	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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