Gene Gene information from NCBI Gene database.
Entrez ID 254122
Gene name Sorting nexin 32
Gene symbol SNX32
Synonyms (NCBI Gene)
SNX6B
Chromosome 11
Chromosome location 11q13.1
miRNA miRNA information provided by mirtarbase database.
28
miRTarBase ID miRNA Experiments Reference
MIRT018071 hsa-miR-335-5p Microarray 18185580
MIRT1378095 hsa-miR-3132 CLIP-seq
MIRT1378096 hsa-miR-4326 CLIP-seq
MIRT1378097 hsa-miR-4451 CLIP-seq
MIRT1378098 hsa-miR-4687-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21516116, 25416956, 28514442, 32296183, 33961781, 37158588, 39073202
GO:0005768 Component Endosome IBA
GO:0005769 Component Early endosome IDA 37158588
GO:0005770 Component Late endosome IDA 39073202
GO:0005802 Component Trans-Golgi network IDA 37158588
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621073 26423 ENSG00000172803
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86XE0
Protein name Sorting nexin-32 (Sorting nexin-6B)
Protein function May be involved in several stages of intracellular trafficking.
PDB 6E8R
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00787 PX 50 164 PX domain Domain
PF09325 Vps5 182 342 Vps5 C terminal like Domain
PF09325 Vps5 324 392 Vps5 C terminal like Domain
Sequence
Sequence length 403
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Endocytosis  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
BASAL CELL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST NEOPLASMS CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alzheimer Disease Alzheimer disease Pubtator 32413284 Stimulate
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Alzheimer disease Pubtator 34937778 Associate
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma CTD_human_DG 29915430
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 29316957 Associate
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant neoplasm of breast Breast Cancer CTD_human_DG 29915430
★☆☆☆☆
Found in Text Mining only
Mammary Carcinoma, Human Marfan Syndrome CTD_human_DG 29915430
★☆☆☆☆
Found in Text Mining only
Mammary Neoplasms Mammary Neoplasms CTD_human_DG 29915430
★☆☆☆☆
Found in Text Mining only
Mammary Neoplasms, Human Mammary Neoplasms CTD_human_DG 29915430
★☆☆☆☆
Found in Text Mining only