Human (GRCh37.p13)
Description

nucleic acid binding protein 1 [Source:HGNC Symbol;Acc:26232]

Gene Synonyms

DKFZp667M1322, FLJ13624, FLJ22833, MGC111163, OBFC2A, SOSS-B2, SSB2, hSSB2

Location

Chromosome 2: 192,542,794-192,561,385 forward strand.

GRCh37:CM000664.1

About this gene

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

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000410026.2NABP1-00411521124aaENSP00000387243.1
 
Protein coding
CCDS58745Q96AH0 NM_001254736.1GENCODE basic
ENST00000425611.2NABP1-0011878204aaENSP00000403683.2
 
Protein coding
CCDS33352Q96AH0 NM_001031716.2GENCODE basic
ENST00000435931.1NABP1-007915168aaENSP00000397041.1
 
Protein coding
--CDS 5' incomplete
ENST00000409510.1NABP1-010843124aaENSP00000386605.1
 
Protein coding
CCDS58745Q96AH0 -GENCODE basic
ENST00000307849.3NABP1-0023002134aaENSP00000307968.3
 
Nonsense mediated decay
F8WAF5 Q96AH0 --
ENST00000451500.1NABP1-0062015134aaENSP00000390901.1
 
Nonsense mediated decay
F8WAF5 Q96AH0 --
ENST00000307834.5NABP1-003191454aaENSP00000310819.5
 
Nonsense mediated decay
F8WAF5 --
ENST00000462712.1NABP1-008961No protein-
 
Retained intron
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ENST00000491331.1NABP1-005855No protein-
 
Retained intron
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ENST00000462824.1NABP1-009567No protein-
 
Retained intron
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