Gene Gene information from NCBI Gene database.
Entrez ID 11234
Gene name HPS5 biogenesis of lysosomal organelles complex 2 subunit 2
Gene symbol HPS5
Synonyms (NCBI Gene)
AIBP63BLOC2S2
Chromosome 11
Chromosome location 11p15.1
Summary 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.
22
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.
364
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25189619, 31611645
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
GO:0005769 Component Early endosome NAS 23247405
GO:0005829 Component Cytosol IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607521 17022 ENSG00000110756
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
234
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hermansky-Pudlak syndrome Likely pathogenic; Pathogenic rs1253458479, rs886041723, rs2494158241, rs767560852, rs761811248, rs766602179, rs779921624, rs755827664 RCV002282953
RCV000851767
RCV003230859
RCV005240830
RCV003988164
RCV000852025
RCV000851734
RCV000852157
Hermansky-Pudlak syndrome 5 Likely pathogenic; Pathogenic rs778500897, rs746844529, rs577034676, rs1253458479, rs281865103, rs886041723, rs2494158241, rs1209723048, rs1262983210, rs2494478049, rs281865104, rs281865105, rs397507169, rs281865101, rs753928208
View all (12 more)
RCV001823686
RCV002503556
RCV002264887
RCV005042782
RCV000003302
RCV000495769
RCV005047475
RCV005047690
RCV005047708
RCV005047717
RCV000021029
RCV000021030
RCV000021031
RCV000021033
RCV000495763
RCV000494753
RCV000495038
RCV000495011
RCV000495374
RCV000495399
RCV000495126
RCV000495446
RCV000495420
RCV000496925
RCV000503910
RCV005047021
RCV002245658
HPS5-related disorder Likely pathogenic; Pathogenic rs758338350, rs2494418926, rs761811248 RCV003391366
RCV003393146
RCV004753735
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Abnormal bleeding Likely benign rs149229493 RCV001270595
Cervical cancer Conflicting classifications of pathogenicity rs149677540 RCV005892955
Cholangiocarcinoma Benign rs11024609, rs7128146 RCV005922061
RCV005888530
Colorectal cancer Conflicting classifications of pathogenicity rs149677540 RCV005892956
Associations from Text MiningDisease associations identified through Pubtator
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