Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: PLEKHB1 ENSBTAG00000009830

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Description

pleckstrin homology domain containing B1 [Source:VGNC Symbol;Acc:VGNC:33009]

Location

Primary_assembly 15: 53,117,212-53,136,353 forward strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 5 transcripts (splice variants), 198 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000012961.7	PLEKHB1-201	2136	319aa	ENSBTAP00000012961.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MY34	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 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,
ENSBTAT00000104840.1	PLEKHB1-204	2189	266aa	ENSBTAP00000102109.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TU36	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,
ENSBTAT00000065185.2	PLEKHB1-203	2115	243aa	ENSBTAP00000054461.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MY34	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,
ENSBTAT00000065711.4	PLEKHB1-202	2031	284aa	ENSBTAP00000055083.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MZT0	-
ENSBTAT00000079735.3	PLEKHB1-205	1669	138aa	ENSBTAP00000058439.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LNA2	-

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Summary

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