Gene: Fam187b ENSRNOG00000021060

Description

family with sequence similarity 187, member B [Source:RGD Symbol;Acc:1597448]

Gene Synonyms

LOC689038, LOC689048, Tmem162

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 99 orthologues, 1 paralogue and is associated with 3 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000168667.1	Fam187b-202	1300	423aa	ENSRNOP00000102666.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000099997.2	Fam187b-201	1496	366aa	ENSRNOP00000078846.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZPK2 A6JA44	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

Summary