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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FAM222B ENSPPAG00000041467

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Description

family with sequence similarity 222 member B [Source:HGNC Symbol;Acc:HGNC:25563]

Location

Chromosome 17: 28,467,785-28,526,048 forward strand.

panpan1.1:CM003400.1

About this gene

This gene has 1 transcript (splice variant), 264 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPPAT00000060310.1	FAM222B-201	4256	562aa	ENSPPAP00000037410.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R9C666	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,

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Summary

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