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: Foxk2 ENSRNOG00000036663

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Description

forkhead box K2 [Source:RGD Symbol;Acc:1305408]

Gene Synonyms

LOC303753

Location

Primary_assembly 10: 107,040,933-107,195,823 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 5 transcripts (splice variants), 268 orthologues, 34 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000054916.5	Foxk2-201	4514	835aa	ENSRNOP00000051799.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B2RYN1	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,
ENSRNOT00000099287.2	Foxk2-204	4981	650aa	ENSRNOP00000087268.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A5H3	-
ENSRNOT00000054919.5	Foxk2-202	4359	400aa	ENSRNOP00000051802.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HLP0 D3ZY28	-
ENSRNOT00000150007.1	Foxk2-205	2120	607aa	ENSRNOP00000098790.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000095855.2	Foxk2-203	2080	628aa	ENSRNOP00000086990.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A2D9	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,

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Orthologues

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