Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11234
Gene name Gene Name - the full gene name approved by the HGNC.
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HPS5
Synonyms (NCBI Gene) Gene synonyms aliases
AIBP63, BLOC2S2
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p15.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 6 protein and may interact with the cytoplasmic domain of i
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs61884288 G>A Benign, pathogenic, likely-benign Coding sequence variant, missense variant, non coding transcript variant
rs113304476 T>C Pathogenic Intron variant
rs200449378 T>A,C Pathogenic Intron variant
rs281865101 ->G Pathogenic Non coding transcript variant, coding sequence variant, frameshift variant
rs281865102 A>C Pathogenic Non coding transcript variant, coding sequence variant, intron variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT030698 hsa-miR-21-5p Microarray 18591254
MIRT1054261 hsa-miR-1183 CLIP-seq
MIRT1054262 hsa-miR-1197 CLIP-seq
MIRT1054263 hsa-miR-1207-5p CLIP-seq
MIRT1054264 hsa-miR-1227 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25189619
GO:0005829 Component Cytosol IDA
GO:0006996 Process Organelle organization IEA
GO:0007596 Process Blood coagulation IEA
GO:0031084 Component BLOC-2 complex IPI 15030569
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607521 17022 ENSG00000110756
Protein
UniProt ID Q9UPZ3
Protein name BLOC-2 complex member HPS5 (Alpha-integrin-binding protein 63) (Hermansky-Pudlak syndrome 5 protein) (Ruby-eye protein 2 homolog) (Ru2)
Protein function May regulate the synthesis and function of lysosomes and of highly specialized organelles, such as melanosomes and platelet dense granules. Regulates intracellular vesicular trafficking in fibroblasts. May be involved in the regulation of genera
Family and domains
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Isoform 1:Highly expressed in lungs and testis. Isoform 2:Highly expressed in placenta, kidney, testis ovary, lung and thymus. {ECO:0000269|PubMed:15296495}.
Sequence
MAFVPVIPESYSHVLAEFESLDPLLSALRLDSSRLKCTSIAVSRKWLALGSSGGGLHLIQ
KEGWKHRLFLSHREGAISQVACCLHDDDYVAVATSQGLVVVWELNQERRGKPEQMYVSSE
HKGRRVTALCWDTAILRVFVGDHAGKVSAIKLNTSKQAKAAAAFVMFPVQTITTVDSCVV
QLDYLDGRLLISSLTRSFLCDTEREKFWKIGNKERDGEYGACFFPGRCSGGQQPLIYCAR
PGSRMWEVNFDGEVISTHQFKKLLSLPPLPVITLRSEPQYDHTAGSSQSLSFPKLLHLSE
HCVLTWTERGIYIFIPQNVQVLLWSEVKDIQDVAVCRNELFCLHLNGKVSHLSLISVERC
VERLLRRGLWNLAARTCCLFQNSVIASRARKTLTADKLEHLKSQLDHGTYNDLISQLEEL
ILKFEPLDSACSSRRSSISSHESFSILDSGIYRIISSRRGSQSDEDSCSLHSQTLSEDER
FKEFTSQQEEDLPDQCCGSHGNEDNVSHAPVMFETDKNETFLPFGIPLPFRSPSPLVSLQ
AVKESVSSFVRKTTEKIGTLHTSPDLKVRPELRGDEQSCEEDVSSDTCPKEEDTEEEKEV
TSPPPEEDRFQELKVATAEAMTKLQDPLVLFESESLRMVLQEWLSHLEKTFAMKDFSGVS
DTDNSSMKLNQDVLLVNESKKGILDEDNEKEKRDSLGNEESVDKTACECVRSPRESLDDL
FQICSPCAIASGLRNDLAELTTLCLELNVLNSKIKSTSGHVDHTLQQYSPEILACQFLKK
YFFLLNLKRAKESIKLSYSNSPSVWDTFIEGLKEMASSNPVYMEMEKGDLPTRLKLLDDE
VPFDSPLLVVYATRLYEKFGESALRSLIKFFPSILPSDIIQLCHHHPAEFLAYLDSLVKS
RPEDQRSSFLESLLQPESLRLDWLLLAVSLDAPPSTSTMDDEGYPRPHSHLLSWGYSQLI
LHLIKLPADFITKEKMTDICRSCGFWPGYLILCLELERRREAFTNIVYLNDMSLMEGDNG
WIPETVEEWKLLLHLIQSKSTRPAPQESLNGSLSDGPSPINVENVALLLAKAMGPDRAWS
LLQECGLALELSEKFTRTCDILRIAEKRQRALIQSMLEKCDRFLWSQQA
Sequence length 1129
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Albinism Albinism rs28940876, rs387906560, rs62635045, rs140365820, rs141949212, rs1384042381, rs62635042
Hermansky-pudlak syndrome Hermanski-Pudlak Syndrome, HERMANSKY-PUDLAK SYNDROME 5 rs281865116, rs281865113, rs281865103, rs104893945, rs119471021, rs281865100, rs281865097, rs119471022, rs119471023, rs119471024, rs119471025, rs201227603, rs281865093, rs397507168, rs281865095
View all (101 more)
31064749, 26785811, 28296950, 12548288, 15296495, 28640947
Ocular albinism Albinism, Ocular rs137852296, rs137852297, rs62635018, rs62645741, rs281865178, rs281865183, rs281865184, rs672601353, rs1057518841, rs1057518763, rs1057518787
Unknown
Disease term Disease name Evidence References Source
Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis Hermansky-Pudlak syndrome without pulmonary fibrosis GenCC
Lewy Body Disease Lewy Body Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Albinism Associate 35488210
Blood Coagulation Disorders Associate 33259846
Blood Platelet Disorders Associate 38007062
Hermanski Pudlak Syndrome Associate 15030569, 15296495, 18947387, 25054620, 34608437, 38007062