Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Comparative Genomics
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Gene: PLEKHM2 ENSGALG00000003439

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Description

pleckstrin homology and RUN domain containing M2 [Source:NCBI gene;Acc:419457]

Location

Chromosome 21: 4,207,169-4,227,450 forward strand.

GRCg6a:CM000113.5

About this gene

This gene has 2 transcripts (splice variants), 295 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
PLEKHM2-201	ENSGALT00000097971.1	4206	1011aa	ENSGALP00000070708.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q2U982	<p>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.</p><p>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.</p>APPRIS ALT2,
PLEKHM2-202	ENSGALT00000005447.4	3375	1040aa	ENSGALP00000005437.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1NQI4	<p>APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant.</p><p>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.</p>APPRIS P5,

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Summary

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Gene-based displays