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GENE INFORMATION

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Gene name

PHLDA2 (HGNC Symbol)

Synonyms

BWR1C, HLDA2, IPL, TSSC3

Description

pleckstrin homology-like domain, family A, member 2 (HGNC Symbol)

Entrez gene summary

This gene is located in a cluster of imprinted genes on chromosome 11p15.5, which is considered to be an important tumor suppressor gene region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene has been shown to be imprinted, with preferential expression from the maternal allele in placenta and liver. [provided by RefSeq, Oct 2010]

Chromosome

11 (Chromosome progress)

Cytoband

p15.4

Chromosome location (bp)

2949503 - 2950685

Ensembl

ENSG00000181649 (version 69.37)

Entrez gene

7262

UniProt

Q53GA4

neXtProt

NX_Q53GA4

Antibodypedia

PHLDA2 antibodies
 

PROTEIN VIEW

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PHLDA2-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

PHLDA2-001 ENSP00000319231
ENST00000314222
Q53GA4
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