Gene Gene information from NCBI Gene database.
Entrez ID 22895
Gene name Rabphilin 3A
Gene symbol RPH3A
Synonyms (NCBI Gene)
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Chromosome 12
Chromosome location 12q24.13
Summary The protein encoded by this gene is thought to be an effector for RAB3A, which is a small G protein that acts in the late stages of neurotransmitter exocytosis. The encoded protein may be involved in neurotransmitter release and synaptic vesicle traffic.
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs779991033 G>C Pathogenic Genic upstream transcript variant, missense variant, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
159
miRTarBase ID miRNA Experiments Reference
MIRT048316 hsa-miR-106a-5p CLASH 23622248
MIRT654140 hsa-miR-3177-5p HITS-CLIP 21572407
MIRT654139 hsa-miR-6867-5p HITS-CLIP 21572407
MIRT707181 hsa-miR-124-5p HITS-CLIP 21572407
MIRT654138 hsa-miR-4666a-5p HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
39
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding ISS
GO:0005515 Function Protein binding IPI 11377421, 15207266, 32296183
GO:0005544 Function Calcium-dependent phospholipid binding ISS
GO:0005546 Function Phosphatidylinositol-4,5-bisphosphate binding ISS
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612159 17056 ENSG00000089169
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y2J0
Protein name Rabphilin-3A (Exophilin-1)
Protein function Plays an essential role in docking and fusion steps of regulated exocytosis (By similarity). At the presynaptic level, RPH3A is recruited by RAB3A to the synaptic vesicle membrane in a GTP-dependent manner where it modulates synaptic vesicle tra
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02318 FYVE_2 48 161 FYVE-type zinc finger Family
PF00168 C2 407 516 C2 domain Domain
PF00168 C2 565 671 C2 domain Domain
Sequence
MTDTVFSNSSNRWMYPSDRPLQSNDKEQLQAGWSVHPGGQPDRQRKQEELTDEEKEIINR
VIARAEKMEEMEQERIGRLVDRLENMRKNVAGDGVNRCILCGEQLGMLGSACVVCEDCKK
NVCTKCGVETNNRLHSVWLCKICIEQREVWKRSGAWFFKGF
PKQVLPQPMPIKKTKPQQP
VSEPAAPEQPAPEPKHPARAPARGDSEDRRGPGQKTGPDPASAPGRGNYGPPVRRASEAR
MSSSSRDSESWDHSGGAGDSSRSPAGLRRANSVQASRPAPGSVQSPAPPQPGQPGTPGGS
RPGPGPAGRFPDQKPEVAPSDPGTTAPPREERTGGVGGYPAVGAREDRMSHPSGPYSQAS
AAAPQPAAARQPPPPEEEEEEANSYDSDEATTLGALEFSLLYDQDNSSLQCTIIKAKGLK
PMDSNGLADPYVKLHLLPGASKSNKLRTKTLRNTRNPIWNETLVYHGITDEDMQRKTLRI
SVCDEDKFGHNEFIGETRFSLKKLKPNQRKNFNICL
ERVIPMKRAGTTGSARGMALYEEE
QVERVGDIEERGKILVSLMYSTQQGGLIVGIIRCVHLAAMDANGYSDPFVKLWLKPDMGK
KAKHKTQIKKKTLNPEFNEEFFYDIKHSDLAKKSLDISVWDYDIGKSNDYIGGCQLGISA
KGERLKHWYEC
LKNKDKKIERWHQLQNENHVSSD
Sequence length 694
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
RPH3A-related condition Likely benign rs138056234 RCV004758936
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Huntington Disease Associate 17877635
Learning Disabilities Associate 29441694
Myasthenic Syndromes Congenital Associate 29441694
Nervous System Diseases Associate 29441694
Neuromuscular Junction Diseases Associate 29441694