Gene: Hnrnpk ENSRNOG00000019113

Description

heterogeneous nuclear ribonucleoprotein K [Source:RGD Symbol;Acc:71058]

Gene Synonyms

Csbp, Hnrpk

Location

Primary_assembly 17: 6,268,385-6,280,565 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 3 transcripts (splice variants), 292 orthologues, 15 paralogues and is associated with 15 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025980.9	Hnrnpk-202	3012	464aa	ENSRNOP00000025980.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F8WG62 Q5D059	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,
ENSRNOT00000107930.2	Hnrnpk-203	4301	394aa	ENSRNOP00000080312.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQ15	-
ENSRNOT00000025916.7	Hnrnpk-201	2908	440aa	ENSRNOP00000025915.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QEP8	APPRIS ALT1: 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 is conserved in at least 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 ALT1,