Gene Gene information from NCBI Gene database.
Entrez ID 8440
Gene name NCK adaptor protein 2
Gene symbol NCK2
Synonyms (NCBI Gene)
GRB4NCKbeta
Chromosome 2
Chromosome location 2q12.2
Summary This gene encodes a member of the NCK family of adaptor proteins. The protein contains three SH3 domains and one SH2 domain. The protein has no known catalytic function but has been shown to bind and recruit various proteins involved in the regulation of
miRNA miRNA information provided by mirtarbase database.
129
miRTarBase ID miRNA Experiments Reference
MIRT021929 hsa-miR-128-3p Microarray 17612493
MIRT036831 hsa-miR-877-3p CLASH 23622248
MIRT297070 hsa-miR-1277-5p HITS-CLIP 21572407
MIRT707144 hsa-miR-648 HITS-CLIP 21572407
MIRT297079 hsa-miR-5692b HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
50
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0001771 Process Immunological synapse formation IEA
GO:0001784 Function Phosphotyrosine residue binding IPI 20624904
GO:0005515 Function Protein binding IPI 10026169, 10574708, 12074588, 12110186, 12606549, 15350535, 15721255, 15764601, 16189514, 16273093, 16337946, 16752908, 17617578, 18086875, 18539162, 19807924, 21516116, 22074159, 23455922, 24338975, 24728074, 24902122, 25416956, 25814554, 25910212, 26871637, 28514442, 29892012, 315
GO:0005737 Component Cytoplasm IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604930 7665 ENSG00000071051
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O43639
Protein name Cytoplasmic protein NCK2 (Growth factor receptor-bound protein 4) (NCK adaptor protein 2) (Nck-2) (SH2/SH3 adaptor protein NCK-beta)
Protein function Adapter protein which associates with tyrosine-phosphorylated growth factor receptors or their cellular substrates. Maintains low levels of EIF2S1 phosphorylation by promoting its dephosphorylation by PP1. Plays a role in ELK1-dependent transcri
PDB 1U5S , 1WX6 , 1Z3K , 2B86 , 2CIA , 2FRW , 2FRY , 2JXB , 4E6R
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00018 SH3_1 8 53 SH3 domain Domain
PF14604 SH3_9 118 166 Variant SH3 domain Domain
PF00018 SH3_1 201 249 SH3 domain Domain
PF00017 SH2 285 359 SH2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous.
Sequence
MTEEVIVIAKWDYTAQQDQELDIKKNERLWLLDDSKTWWRVRNAANRTGYVPSNYVERKN
SLKKGSLVKNLKDTLGLGKTRRKTSARDASPTPSTDAEYPANGSGADRIYDLNIPAFVKF
AYVAEREDELSLVKGSRVTVMEKCSDGWWRGSYNGQIGWFPSNYVL
EEVDEAAAESPSFL
SLRKGASLSNGQGSRVLHVVQTLYPFSSVTEEELNFEKGETMEVIEKPENDPEWWKCKNA
RGQVGLVPK
NYVVVLSDGPALHPAHAPQISYTGPSSSGRFAGREWYYGNVTRHQAECALN
ERGVEGDFLIRDSESSPSDFSVSLKASGKNKHFKVQLVDNVYCIGQRRFHTMDELVEHY
K
KAPIFTSEHGEKLYLVRALQ
Sequence length 380
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  ErbB signaling pathway
Axon guidance
T cell receptor signaling pathway
Pathogenic Escherichia coli infection
  Downstream signal transduction
Nephrin family interactions
Ephrin signaling
VEGFA-VEGFR2 Pathway
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
10
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ALZHEIMER'S DISEASE NEUROPATHOLOGIC CHANGE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ALZHEIMERS DISEASE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CEREBRAL AMYLOID ANGIOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 40528303
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Celiac Disease Associate 27836013
★☆☆☆☆
Found in Text Mining only
Hypoxia Associate 29218693
★☆☆☆☆
Found in Text Mining only
Low Tension Glaucoma Associate 23349798
★☆☆☆☆
Found in Text Mining only
Melanoma Associate 15900300
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 29218693
★☆☆☆☆
Found in Text Mining only
Ovarian Neoplasms Associate 29218693
★☆☆☆☆
Found in Text Mining only
Personality Disorders Associate 29218693
★☆☆☆☆
Found in Text Mining only