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

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Gene: PLEKHH1 ENSBTAG00000018297

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Description

pleckstrin homology, MyTH4 and FERM domain containing H1 [Source:VGNC Symbol;Acc:VGNC:33020]

Location

Primary_assembly 10: 79,408,161-79,464,977 forward strand.

ARS-UCD1.3:CM008177.2

About this gene

This gene has 2 transcripts (splice variants), 191 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000024351.7	PLEKHH1-201	5280	1359aa	ENSBTAP00000024351.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BF01	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,
ENSBTAT00000112200.1	PLEKHH1-202	4886	1261aa	ENSBTAP00000079180.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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