NCKIPSD
close
Please copy/paste those URLs into your code to get same results in machine-readable formats:
|
Homo sapiens |
|
NCKIPSD is differentially expressed in 223 experiments: 113 organism parts: bone marrow, amygdala, ... (111 more);, 157 disease states: normal, Emery-Dreifuss muscular dystrophy, ... (155 more);, 76 cell types 250 cell lines 26 compound treatments and 59 other conditions. |
| Synonyms |
ORF1, DIP1, SPIN90, AF3P21, WISH, WASLBP |
| Orthologs |
ENSCING00000002255
(Ciona intestinalis)
Nckipsd
(Rattus norvegicus)
ENSCING00000016244
(Ciona intestinalis)
NCKIPSD
(Gallus gallus)
Nckipsd
(Mus musculus)
NCKIPSD
(Bos taurus)
NCKIPSD
(Danio rerio)
CG2258
(Drosophila melanogaster)
nckipsd
(Xenopus laevis)
NCKIPSD
(Canis familiaris)
(Compare orthologs)
|
| Gene Ontology ID |
GO:0008180, GO:0008092, GO:0007010, GO:0007165, GO:0005515, GO:0005634, GO:0005882, GO:0006607, GO:0017124 |
| Gene Ontology Term |
cytoskeleton organization, protein binding, SH3 domain binding, NLS-bearing substrate import into nucleus, nucleus, signalosome, cytoskeletal protein binding, intermediate filament, signal transduction |
| InterPro ID |
IPR001452, IPR011511, IPR018556 |
| InterPro Term |
SH3_domain, SH3_2, DUF2013 |
| Ensembl Family |
ENSFM00250000006300 |
| Ensembl Family Description |
NCK INTERACTING WITH SH3 DOMAIN 54 KDA VACA INTERACTING KDA INTERACTING 90 KDA SH3 INTERACTING WITH NCK SH3 ADAPTER SPIN90 WASP INTERACTING SH3 DOMAIN WISH WISKOTT ALDRICH SYNDROME |
| Description |
NCK interacting protein with SH3 domain [Source:HGNC Symbol;Acc:15486] |
| EMBL-Bank ID |
AC141002, AC121252, AY453794, AF178432, AF303581, BC026280, AB069981, AB069982, AJ242655, AK294151, BC016052 |
| Ensembl Protein ID |
ENSP00000342621, ENSP00000409675, ENSP00000416144, ENSP00000416904, ENSP00000408588, ENSP00000396683, ENSP00000389059, ENSP00000406442, ENSP00000294129 |
| HGNC Symbol |
NCKIPSD |
| RefSeq ID |
NP_057537, NM_016453, NM_184231, NP_909119 |
| UniProt Accession |
Q9NZQ3, C9JC20, C9JMQ4, C9JSC3, F8WCR8 |
| UniGene ID |
Hs.655006 |
| Ensembl Gene ID |
ENSG00000213672 |
| Entrez Gene ID |
51517 |
| Ensembl Transcript ID |
ENST00000426678, ENST00000416649, ENST00000454134, ENST00000453349, ENST00000341520, ENST00000415281, ENST00000439518, ENST00000294129, ENST00000470006, ENST00000413374 |
| Design Element |
Hs.102929.1.S1_3p_at, ENST00000454134, ENST00000294129, ENST00000341520, ENST00000470006, ENST00000453349, ENST00000413374, ENST00000415281, g7705265_3p_at, 56174_at, ENST00000439518, ENST00000426678, 218697_at, ENST00000416649, 233165_at, 60710_at |
| Search EB-eye |
ENSG00000213672
|
 Show more
properties
|
|
