Human (GRCh37.p13)
Description

non imprinted in Prader-Willi/Angelman syndrome 2 [Source:HGNC Symbol;Acc:17044]

Location

Chromosome 15: 23,004,684-23,034,427 reverse strand.

GRCh37:CM000677.1

About this gene

This gene has 10 transcripts (splice variants), 5 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000337451.3NIPA2-0013233360aaENSP00000337618.3
 
Protein coding
CCDS10010H0YMQ7 Q8N8Q9 NM_030922.6GENCODE basic
ENST00000398014.2NIPA2-2013130360aaENSP00000381096.2
 
Protein coding
CCDS10010H0YMQ7 Q8N8Q9 NM_001008860.2GENCODE basic
ENST00000398013.3NIPA2-0032280360aaENSP00000381095.3
 
Protein coding
CCDS10010H0YMQ7 Q8N8Q9 NM_001008892.2GENCODE basic
ENST00000359727.4NIPA2-0021531341aaENSP00000352762.4
 
Protein coding
CCDS32174Q8N8Q9 NM_001184888.1GENCODE basic
ENST00000539711.2NIPA2-0041412341aaENSP00000437746.2
 
Protein coding
CCDS32174Q8N8Q9 NM_001008894.2GENCODE basic
ENST00000560039.1NIPA2-00955459aaENSP00000453700.1
 
Protein coding
H0YMQ7 -CDS 3' incomplete
ENST00000559571.1NIPA2-007673No protein-
 
Processed transcript
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ENST00000560205.1NIPA2-006589No protein-
 
Processed transcript
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ENST00000561072.1NIPA2-008574No protein-
 
Processed transcript
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ENST00000560762.1NIPA2-005534No protein-
 
Processed transcript
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