HPS6 (HPS6 biogenesis of lysosomal organelles complex 2 subunit 3)

2012-03-01  

Identity

HGNC
LOCATION
10q24.32
LOCUSID
ALIAS
BLOC2S3
FUSION GENES

Other Information

Locus ID:

NCBI: 79803
MIM: 607522
HGNC: 18817
Ensembl: ENSG00000166189

Variants:

dbSNP: 79803
ClinVar: 79803
TCGA: ENSG00000166189
COSMIC: HPS6

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000166189ENST00000299238Q86YV9

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
380919592024Novel Variants of HPS6 Cause Suspected Ocular Albinism: A Report of 2 Cases and the Profile of HPS6 Variants.0
380919592024Novel Variants of HPS6 Cause Suspected Ocular Albinism: A Report of 2 Cases and the Profile of HPS6 Variants.0
338784812021Hermansky-Pudlak syndrome: Five Chinese patients with novel variants in HPS1 and HPS6.2
338784812021Hermansky-Pudlak syndrome: Five Chinese patients with novel variants in HPS1 and HPS6.2
303690442018Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant.5
303690442018Severe bleeding with subclinical oculocutaneous albinism in a patient with a novel HPS6 missense variant.5
279175942017A novel two-nucleotide deletion in HPS6 affects mepacrine uptake and platelet dense granule secretion in a family with Hermansky-Pudlak syndrome.5
279175942017A novel two-nucleotide deletion in HPS6 affects mepacrine uptake and platelet dense granule secretion in a family with Hermansky-Pudlak syndrome.5
268233952016The ophthalmic presentation of Hermansky-Pudlak syndrome 6.3
272258482016Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism.5
276419502016Identification of a novel mutation in HPS6 in a patient with hemophilia B and oculocutaneous albinism.7
268233952016The ophthalmic presentation of Hermansky-Pudlak syndrome 6.3
272258482016Novel HPS6 mutations identified by whole-exome sequencing in two Japanese sisters with suspected ocular albinism.5
276419502016Identification of a novel mutation in HPS6 in a patient with hemophilia B and oculocutaneous albinism.7
251896192014HPS6 interacts with dynactin p150Glued to mediate retrograde trafficking and maturation of lysosomes.16

Citation

Dessen P

HPS6 (HPS6 biogenesis of lysosomal organelles complex 2 subunit 3)

Atlas Genet Cytogenet Oncol Haematol. 2012-03-01

Online version: http://atlasgeneticsoncology.org/gene/52631/hps6