Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Plekhb2 ENSRNOG00000014162

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Description

pleckstrin homology domain containing B2 [Source:RGD Symbol;Acc:1310954]

Gene Synonyms

LOC301337

Location

Primary_assembly 9: 44,534,539-44,578,119 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 4 transcripts (splice variants), 200 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000100581.2	Plekhb2-203	3515	324aa	ENSRNOP00000095041.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AN59	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,
ENSRNOT00000019419.7	Plekhb2-201	3210	208aa	ENSRNOP00000019419.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A263	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,
ENSRNOT00000097171.2	Plekhb2-202	3118	186aa	ENSRNOP00000086810.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A2Z3	-
ENSRNOT00000106381.2	Plekhb2-204	857	283aa	ENSRNOP00000096100.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AND6	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,

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Summary

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