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: Fam98b ENSRNOG00000005366

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Description

family with sequence similarity 98, member B [Source:RGD Symbol;Acc:1564603]

Gene Synonyms

AABR07053472.1, LOC499866, RGD1564603

Location

Primary_assembly 3: 124,588,827-124,618,275 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 211 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000034950.8	Fam98b-201	1879	434aa	ENSRNOP00000038007.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AE02	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,

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Summary

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