IMPAD1

GENE INFORMATION

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Gene name

IMPAD1 (HGNC Symbol)

Synonyms

FLJ20421, gPAPP, IMPA3

Description

Inositol monophosphatase domain containing 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011]

Chromosome

8

Cytoband

q12.1

Chromosome location (bp)

56957933 - 56993844

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000104331 (version 78.38)

Entrez gene

54928

UniProt

Q9NX62 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NX62

Antibodypedia

IMPAD1 antibodies
 

PROTEIN VIEW

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IMPAD1-001
 
IMPAD1-002
 
 
 
 
 

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)

IMPAD1-001 ENSP00000262644
ENST00000262644
Q9NX62
Show all »
Show » Show » 359 38.7 No 1
IMPAD1-002 ENSP00000430185
ENST00000517461
H0YBS3
Show all »
Show » Show » 82 9.3 No 0