Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
29886
Gene name Gene Name - the full gene name approved by the HGNC.
Sorting nexin 8
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SNX8
Synonyms (NCBI Gene) Gene synonyms aliases
Mvp1
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p22.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT048293 hsa-miR-107 CLASH 23622248
MIRT038133 hsa-miR-423-5p CLASH 23622248
MIRT719946 hsa-miR-4714-5p HITS-CLIP 19536157
MIRT719945 hsa-miR-514a-5p HITS-CLIP 19536157
MIRT719944 hsa-miR-3664-5p HITS-CLIP 19536157
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 17474147, 32296183
GO:0005768 Component Endosome IEA
GO:0005829 Component Cytosol IEA
GO:0006886 Process Intracellular protein transport IBA
GO:0006886 Process Intracellular protein transport IMP 19782049
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614905 14972 ENSG00000106266
Protein
UniProt ID Q9Y5X2
Protein name Sorting nexin-8
Protein function May be involved in several stages of intracellular trafficking. May play a role in intracellular protein transport from early endosomes to the trans-Golgi network.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00787 PX 96 178 PX domain Domain
Sequence
MTGRAMDPLPAAAVGAAAEAEADEEADPPASDLPTPQAIEPQAIVQQVPAPSRMQMPQGN
PLLLSHTLQELLARDTVQVELIPEKKGLFLKHVEYEVSSQRFKSSVYRRYNDFVVFQEML
LHKFPYRMVPALPPKRMLGADREFIEARRRALKRFVNLVARHPLFSEDVVLKLFLSFS
GS
DVQNKLKESAQCVGDEFLNCKLATRAKDFLPADIQAQFAISRELIRNIYNSFHKLRDRAE
RIASRAIDNAADLLIFGKELSAIGSDTTPLPSWAALNSSTWGSLKQALKGLSVEFALLAD
KAAQQGKQEENDVVEKLNLFLDLLQSYKDLCERHEKGVLHKHQRALHKYSLMKRQMMSAT
AQNREPESVEQLESRIVEQENAIQTMELRNYFSLYCLHQETQLIHVYLPLTSHILRAFVN
SQIQGHKEMSKVWNDLRPKLSCLFAGPHSTLTPPCSPPEDGLCPH
Sequence length 465
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 34524084
Head and Neck Neoplasms Associate 29884837
Neuralgia Associate 29884837