Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: plekhh1 ENSDARG00000053835

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Description

pleckstrin homology domain containing, family H (with MyTH4 domain) member 1 [Source:NCBI gene (formerly Entrezgene);Acc:565914]

Location

Chromosome 17: 37,932,433-38,023,273 forward strand.

GRCz11:CM002901.2

About this gene

This gene has 2 transcripts (splice variants), 196 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000075941.5	plekhh1-201	6240	1432aa	ENSDARP00000070420.4	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, 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,
ENSDART00000185349.1	plekhh1-202	4748	1404aa	ENSDARP00000155032.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-

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Summary

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