Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Fam169b ENSRNOG00000022822

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Description

family with sequence similarity 169, member B [Source:RGD Symbol;Acc:1585883]

Gene Synonyms

LOC680906

Location

Primary_assembly 1: 131,288,799-131,370,145 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 170 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000040147.7	Fam169b-201	2529	449aa	ENSRNOP00000046443.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LYW9	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,
ENSRNOT00000166343.1	Fam169b-203	3807	337aa	ENSRNOP00000098708.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000119682.2	Fam169b-202	2645	335aa	ENSRNOP00000095632.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ALU9	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,

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Paralogues

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