Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Fam222b ENSRNOG00000029570

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Description

family with sequence similarity 222, member B [Source:RGD Symbol;Acc:1566149]

Gene Synonyms

LOC497960, RGD1566149

Location

Primary_assembly 10: 63,484,652-63,550,288 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 264 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000124208.1	Fam222b-202	2729	562aa	ENSRNOP00000100302.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HH08	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,
ENSRNOT00000045107.6	Fam222b-201	3807	529aa	ENSRNOP00000049924.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZPE2	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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