Gene Gene information from NCBI Gene database.
Entrez ID 28966
Gene name Sorting nexin 24
Gene symbol SNX24
Synonyms (NCBI Gene)
PRO1284SBBI31
Chromosome 5
Chromosome location 5q23.2
miRNA miRNA information provided by mirtarbase database.
257
miRTarBase ID miRNA Experiments Reference
MIRT027406 hsa-miR-98-5p Microarray 19088304
MIRT437611 hsa-miR-145-5p MicroarrayqRT-PCR 22815788
MIRT437687 hsa-miR-223-3p MicroarrayqRT-PCR 22815788
MIRT437718 hsa-miR-29a-3p MicroarrayqRT-PCR 22815788
MIRT437719 hsa-miR-29b-3p MicroarrayqRT-PCR 22815788
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0008289 Function Lipid binding IEA
GO:0010314 Function Phosphatidylinositol-5-phosphate binding IEA
GO:0015031 Process Protein transport IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y343
Protein name Sorting nexin-24
Protein function May be involved in several stages of intracellular trafficking.
PDB 4AZ9 , 8TBV , 8TBW , 8U9G
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00787 PX 26 103 PX domain Domain
Sequence
MEVYIPSFRYEESDLERGYTVFKIEVLMNGRKHFVEKRYSEFHALHKKLKKCIKTPEIPS
KHVRNWVPKVLEQRRQGLETYLQAVILENEELPKLFLDFLNVR
HLPSLPKAESCGSFDET
ESEESSKLSHQPVLLFLRDPYVLPAASDFPNVVIEGVLHGIFYPHLQPR
Sequence length 169
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
DIVERTICULAR DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MIGRAINE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OCULAR HYPOTENSION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations