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: Fam89b ENSRNOG00000024239

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Description

family with sequence similarity 89, member B [Source:RGD Symbol;Acc:1311544]

Gene Synonyms

LOC309170, MGC112670, Mtvr2

Location

Primary_assembly 1: 212,445,102-212,446,738 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 152 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000016987.7	Fam89b-201	1190	189aa	ENSRNOP00000016987.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q566R4-1	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,
ENSRNOT00000099768.2	Fam89b-202	646	149aa	ENSRNOP00000096796.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AMJ7	-

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Summary

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