Gene: Fam161b ENSRNOG00000011112

Description

FAM161 centrosomal protein B [Source:RGD Symbol;Acc:1309058]

Gene Synonyms

LOC314311, RGD1309058

Location

Primary_assembly 6: 109,722,569-109,750,036 reverse strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants), 178 orthologues, 2 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000110567.2	Fam161b-202	2088	617aa	ENSRNOP00000092000.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AGZ6	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 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,
ENSRNOT00000172365.1	Fam161b-203	2855	589aa	ENSRNOP00000110477.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000014814.8	Fam161b-201	1974	579aa	ENSRNOP00000014814.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A7T7	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

Strains

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

Gene: Fam161b ENSRNOG00000011112

Strains

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Gene: Fam161b ENSRNOG00000011112

Strains

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