Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
399694
Gene name Gene Name - the full gene name approved by the HGNC.
SHC adaptor protein 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SHC4
Synonyms (NCBI Gene) Gene synonyms aliases
RaLP, SHCD
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q21.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017379 hsa-miR-335-5p Microarray 18185580
MIRT504427 hsa-miR-543 PAR-CLIP 20371350
MIRT504425 hsa-miR-6499-3p PAR-CLIP 20371350
MIRT504426 hsa-miR-3143 PAR-CLIP 20371350
MIRT504424 hsa-miR-455-3p PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 24658140, 24728074, 31980649
GO:0005886 Component Plasma membrane IBA 21873635
GO:0006915 Process Apoptotic process IEA
GO:0007169 Process Transmembrane receptor protein tyrosine kinase signaling pathway IBA 21873635
GO:0008284 Process Positive regulation of cell population proliferation IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617372 16743 ENSG00000185634
Protein
UniProt ID Q6S5L8
Protein name SHC-transforming protein 4 (Rai-like protein) (RaLP) (SHC-transforming protein D) (hShcD) (Src homology 2 domain-containing-transforming protein C4) (SH2 domain protein C4)
Protein function Activates both Ras-dependent and Ras-independent migratory pathways in melanomas. Contributes to the early phases of agrin-induced tyrosine phosphorylation of CHRNB1.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00640 PID 192 348 Phosphotyrosine interaction domain (PTB/PID) Domain
PF00017 SH2 526 597 SH2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Only expressed in melanomas. Weakly expressed in normal melanocytes and benign nevi. Highly expressed at the transition from radial growth phase to vertical growth phase and metastatic melanomas, when tumor cells acquire migratory comp
Sequence
MRERGQDSLAGLVLYVGLFGHPGMLHRAKYSRFRNESITSLDEGSSGGSVGNKGSPQPPH
PALAPHLPTEDATLPSQESPTPLCTLIPRMASMKLANPATLLSLKNFCLGTKEVPRLKLQ
ESRDPGSSGPSSPETSLSRSGTAPPPQQDLVGHRATALTPDSCPLPGPGEPTLRSRQDRH
FLQHLLGMGMNYCVRYMGCVEVLQSMRSLDFGMRTQVTREAISRLCEAVPGANGAIKKRK
PPVKFLSTVLGKSNLQFSGMNIKLTISTCSLTLMNLDNQQIIANHHMQSISFASGGDPDT
TDYVAYVAKDPVNQRACHILECHNGMAQDVISTIGQAFELRFKQYLKN
PSLNTSCESEEV
HIDSHAEEREDHEYYNEIPGKQPPVGGVSDMRIKVQATEQMAYCPIQCEKLCYLPGNSKC
SSVYENCLEQSRAIGNVHPRGVQSQRDTSLLKHTCRVDLFDDPCYINTQALQSTPGSAGN
QRSAQPLGSPWHCGKAPETVQPGATAQPASSHSLPHIKQQLWSEECYHGKLSRKAAESLL
VKDGDFLVRESATSPGQYVLSGLQGGQAKHLLLVDPEGKVRTKDHVFDNVGHLIRYH
MDN
SLPIISSGSEVSLKQPVRKDNNPALLHSNK
Sequence length 630
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  EGFR tyrosine kinase inhibitor resistance
Endocrine resistance
ErbB signaling pathway
Ras signaling pathway
Chemokine signaling pathway
Phospholipase D signaling pathway
Focal adhesion
Natural killer cell mediated cytotoxicity
Neurotrophin signaling pathway
Insulin signaling pathway
Estrogen signaling pathway
Prolactin signaling pathway
Relaxin signaling pathway
Growth hormone synthesis, secretion and action
Alcoholism
Bacterial invasion of epithelial cells
MicroRNAs in cancer
Glioma
Chronic myeloid leukemia
Breast cancer
Hepatocellular carcinoma
Gastric cancer
 
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Mental Depression Mental Depression GWAS
Schizophrenia Schizophrenia GWAS
Eating Disorders Eating Disorders GWAS
Associations from Text Mining
Disease Name Relationship Type References
Bipolar Disorder Associate 30503783
Heart Defects Congenital Associate 31819021
Mesothelioma Malignant Associate 26139392
Neoplasms Associate 36683494
Obesity Associate 36714595
Stomach Neoplasms Associate 33316777
Uveal melanoma Associate 36683494