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Human (GRCh37.p13)
Description

NCK interacting protein with SH3 domain [Source:HGNC Symbol;Acc:15486]

Gene Synonyms

AF3P21, DIP, DIP1, ORF1, SPIN90, VIP54, WASLBP, WISH

Location

Chromosome 3: 48,701,364-48,723,797 reverse strand.

GRCh37:CM000665.1

About this gene

This gene has 10 transcripts (splice variants) and is associated with 36 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000294129.2NCKIPSD-0012989722aaENSP00000294129.2
 
Protein coding
CCDS2776C9JC20 C9JMQ4 Q9NZQ3
NM_016453.3Ensembl CanonicalGENCODE basic
ENST00000416649.2NCKIPSD-0022925715aaENSP00000389059.2
 
Protein coding
CCDS46827Q9NZQ3 NM_184231.2GENCODE basic
ENST00000341520.4NCKIPSD-2012263722aaENSP00000342621.4
 
Protein coding
C9JC20 C9JMQ4 Q9NZQ3
-GENCODE basic
ENST00000439518.1NCKIPSD-0061214395aaENSP00000409675.1
 
Protein coding
C9JC20 C9JMQ4 C9JSC3
-CDS 3' incomplete
ENST00000426678.1NCKIPSD-011897165aaENSP00000416904.1
 
Protein coding
C9JC20 -CDS 3' incomplete
ENST00000453349.1NCKIPSD-010889203aaENSP00000408588.1
 
Protein coding
C9JC20 C9JMQ4 -CDS 3' incomplete
ENST00000415281.1NCKIPSD-008803268aaENSP00000406442.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000413374.1NCKIPSD-007725151aaENSP00000396683.1
 
Protein coding
H7C0T9 -CDS 5' incomplete
ENST00000454134.1NCKIPSD-00999858aaENSP00000416144.1
 
Nonsense mediated decay
F8WCR8 --
ENST00000470006.1NCKIPSD-005814No protein-
 
Retained intron
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