NIPA2

GENE INFORMATION

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Gene name

NIPA2

Synonyms

Description

non imprinted in Prader-Willi/Angelman syndrome 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]

Chromosome

15 (Chromosome progress)

Cytoband

q11.2

Chromosome location (bp)

23004684 - 23034427

Ensembl

ENSG00000140157 (version 73.37)

Entrez gene

81614

UniProt

Q8N8Q9 (UniProt - Evidence at transcript level)

neXtProt

NX_Q8N8Q9

Antibodypedia

NIPA2 antibodies
 

PROTEIN VIEW

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NIPA2-001
 
NIPA2-002
 
NIPA2-003
 
NIPA2-004
 
NIPA2-009
 
NIPA2-201
 
 
 
 
 

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)

NIPA2-001 ENSP00000337618
ENST00000337451
Q8N8Q9
Show all »
Show » Show » 360 39.2 No 9
NIPA2-002 ENSP00000352762
ENST00000359727
Q8N8Q9
Show all »
Show » Show » 341 37 No 8
NIPA2-003 ENSP00000381095
ENST00000398013
Q8N8Q9
Show all »
Show » Show » 360 39.2 No 9
NIPA2-004 ENSP00000437746
ENST00000539711
Q8N8Q9
Show all »
Show » Show » 341 37 No 8
NIPA2-009 ENSP00000453700
ENST00000560039
H0YMQ7
Show all »
Show » Show » 59 6.5 No 1
NIPA2-201 ENSP00000381096
ENST00000398014
Q8N8Q9
Show all »
Show » Show » 360 39.2 No 9