Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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79083 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Melanophilin |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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MLPH |
SynonymsGene synonyms aliases
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SLAC2-A |
ChromosomeChromosome number
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2 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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2q37.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the exophilin subfamily of Rab effector proteins. The protein forms a ternary complex with the small Ras-related GTPase Rab27A in its GTP-bound form and the motor protein myosin Va. A similar protein complex in mouse function |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs119473031 |
C>A,T |
Pathogenic |
Non coding transcript variant, coding sequence variant, missense variant, synonymous variant, genic upstream transcript variant |
rs140470472 |
C>T |
Pathogenic |
Non coding transcript variant, coding sequence variant, genic upstream transcript variant, stop gained |
rs786205551 |
G>A |
Likely-pathogenic |
Coding sequence variant, non coding transcript variant, missense variant, genic upstream transcript variant |
rs786205641 |
C>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant, non coding transcript variant, intron variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
Q9BV36 |
Protein name |
Melanophilin (Exophilin-3) (Slp homolog lacking C2 domains a) (SlaC2-a) (Synaptotagmin-like protein 2a) |
Protein function |
Rab effector protein involved in melanosome transport. Serves as link between melanosome-bound RAB27A and the motor protein MYO5A. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF02318 |
FYVE_2 |
8 → 125 |
FYVE-type zinc finger |
Family |
PF04698 |
Rab_eff_C |
452 → 513 |
Rab effector MyRIP/melanophilin C-terminus |
Family |
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Sequence |
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Sequence length |
600 |
Interactions |
View interactions |
Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Griscelli syndrome |
GRISCELLI SYNDROME, TYPE 3, Griscelli syndrome type 3 |
rs119473031, rs28938176, rs1595695268, rs104894498, rs104894499, rs1595700039, rs104894500, rs764371254, rs786205551, rs786205641, rs767481076, rs753966933, rs200956636, rs1555394745, rs770601673, rs769021352, rs756071120, rs140470472, rs766575263 |
12897212 |
Piebaldism |
Piebaldism |
rs121913679, rs794726672, rs794726673, rs121913680, rs794726674, rs794726675, rs121913684, rs121913687, rs28933371, rs387907217, rs1560419312, rs1560418178 |
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Prostate cancer |
Malignant neoplasm of prostate, Prostate carcinoma |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
21743057, 21743057, 29892016 |
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