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
External references
Supporting evidence
ID History
- Gene history

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Gene: Klrb1c ENSRNOG00000007811

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Description

killer cell lectin like receptor B1C [Source:RGD Symbol;Acc:1583336]

Gene Synonyms

Klrb1f, LOC683758, NKR-P1F

Location

Primary_assembly 4: 164,045,716-164,080,760 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 3 transcripts (splice variants), 290 orthologues and 58 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000154237.1	Klrb1c-203	1897	241aa	ENSRNOP00000101137.1	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,
ENSRNOT00000153277.1	Klrb1c-202	2166	217aa	ENSRNOP00000107942.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IM28	-
ENSRNOT00000010312.6	Klrb1c-201	1742	203aa	ENSRNOP00000010312.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q63378	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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Summary

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