Gene: FAM90A22 ENSG00000285687

Description

family with sequence similarity 90 member A22 [Source:HGNC Symbol;Acc:HGNC:32270]

Gene Synonyms

FAM90A22P

Location

GRCh38:CM000670.2

View alleles of this gene on alternative sequences

About this gene

This gene has 1 transcript (splice variant), 1 gene allele, 105 orthologues and 21 paralogues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000648590.1	FAM90A22-202	1395	464aa	ENSP00000496925.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS94251	A8MWA6	NM_001397382.1	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,

Summary