Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: Fam81b ENSRNOG00000026845

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Description

family with sequence similarity 81, member B [Source:RGD Symbol;Acc:1561830]

Gene Synonyms

LOC309925, RGD1561830

Location

Primary_assembly 2: 7,502,278-7,644,862 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 3 transcripts (splice variants), 157 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000158493.1	Fam81b-203	2450	426aa	ENSRNOP00000108478.1	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, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000144991.1	Fam81b-202	2504	409aa	ENSRNOP00000111366.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000036547.8	Fam81b-201	1403	419aa	ENSRNOP00000032467.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M276	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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