Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FAM222B ENSBTAG00000047717

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Description

family with sequence similarity 222 member B [Source:VGNC Symbol;Acc:VGNC:28801]

Location

Primary_assembly 19: 20,173,363-20,228,801 reverse strand.

ARS-UCD1.3:CM008186.2

About this gene

This gene has 3 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
ENSBTAT00000064131.3	FAM222B-203	2892	563aa	ENSBTAP00000056561.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BFC5	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,
ENSBTAT00000089776.1	FAM222B-201	4502	530aa	ENSBTAP00000094624.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000075811.2	FAM222B-202	2884	523aa	ENSBTAP00000061818.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BFC5	-

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Summary

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