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: Fam151b ENSRNOG00000024136

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Description

family with sequence similarity 151, member B [Source:RGD Symbol;Acc:1561110]

Gene Synonyms

LOC499507, RGD1561110

Location

Primary_assembly 2: 25,409,383-25,445,466 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 188 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000031909.7	Fam151b-201	921	278aa	ENSRNOP00000032254.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I4R1	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,
ENSRNOT00000114357.2	Fam151b-202	1334	258aa	ENSRNOP00000091224.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AFQ9	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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