VPS45 (vacuolar protein sorting 45 homolog)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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11311 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Vacuolar protein sorting 45 homolog |
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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VPS45 |
SynonymsGene synonyms aliases
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H1, H1VPS45, SCN5, VPS45A, VPS45B, VPS54A, VSP45, VSP45A |
ChromosomeChromosome number
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1 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1q21.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuol |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs782269909 |
G>A |
Pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
rs879255237 |
C>A |
Pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
rs1131691903 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant, non coding transcript 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
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UniProt ID |
Q9NRW7 |
Protein name |
Vacuolar protein sorting-associated protein 45 (h-VPS45) (hlVps45) |
Protein function |
May play a role in vesicle-mediated protein trafficking from the Golgi stack through the trans-Golgi network. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00995 |
Sec1 |
23 → 546 |
Sec1 family |
Family |
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Sequence |
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Sequence length |
570 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Anemia |
Anemia |
rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505 |
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Congenital neutropenia |
Congenital neutropenia |
rs118203968, rs118203969, rs118203970, rs118203971, rs267606834, rs28936381, rs137854447, rs137854448, rs137854450, rs28931611, rs137854451, rs200478425, rs587777730, rs606231474, rs606231475, rs606231473, rs775224457, rs769441127, rs148559256, rs797044567, rs796065343, rs797045009, rs878855315, rs1555710005, rs879253750, rs879253882, rs1555354200, rs1555354198, rs1555354750, rs890101650, rs759302795, rs57246956, rs138156467, rs1194477276, rs1570588220, rs757401069, rs745582203, rs1191239079, rs1597905369, rs1599294750, rs1594996301, rs1595004126, rs1595004676, rs756667927, rs34019455 |
23599270 |
Congenital neutropenia, myelofibrosis, nephromegaly syndrome |
Congenital neutropenia, myelofibrosis, nephromegaly syndrome, Congenital neutropenia-myelofibrosis-nephromegaly syndrome |
rs879255237, rs782269909 |
23599270 |
Myelofibrosis |
Familial myelofibrosis |
rs77375493, rs587776885, rs1555760738, rs146249964, rs755257605 |
23599270 |
Neutropenia |
Neutropenia, NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE |
rs879253882 |
23738510, 23599270 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
30626913 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Leukopenia |
Leukopenia |
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Mental depression |
Major Depressive Disorder |
rs587778876, rs587778877 |
30626913 |
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