Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: BLNK ENSSSCG00000010504

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Description

B cell linker [Source:VGNC Symbol;Acc:VGNC:85829]

Location

Primary_assembly 14: 107,625,803-107,715,364 reverse strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000075374.1	BLNK-202	6513	463aa	ENSSSCP00000063770.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UGW7 A0A8D0W3D3	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 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,
ENSSSCT00000079366.2	BLNK-201	375	67aa	ENSSSCP00000062717.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UEH6 A0A8D0M8Y1	-

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Summary

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