Gene Gene information from NCBI Gene database.
Entrez ID 8943
Gene name Adaptor related protein complex 3 subunit delta 1
Gene symbol AP3D1
Synonyms (NCBI Gene)
ADTDHPS10hBLVR
Chromosome 19
Chromosome location 19p13.3
Summary The protein encoded by this gene is a subunit of the AP3 adaptor-like complex, which is not clathrin-associated, but is associated with the golgi region, as well as more peripheral structures. The AP-3 complex facilitates the budding of vesicles from the
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs879255646 CA>- Pathogenic Frameshift variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
293
miRTarBase ID miRNA Experiments Reference
MIRT001386 hsa-miR-1-3p pSILAC 18668040
MIRT016660 hsa-miR-425-5p Sequencing 20371350
MIRT017505 hsa-miR-335-5p Microarray 18185580
MIRT001386 hsa-miR-1-3p Proteomics;Other 18668040
MIRT031574 hsa-miR-16-5p Sequencing 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
62
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 15598649
GO:0005737 Component Cytoplasm IEA
GO:0005765 Component Lysosomal membrane HDA 17897319
GO:0005769 Component Early endosome NAS 23247405
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607246 568 ENSG00000065000
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O14617
Protein name AP-3 complex subunit delta-1 (AP-3 complex subunit delta) (Adaptor-related protein complex 3 subunit delta-1) (Delta-adaptin)
Protein function Part of the AP-3 complex, an adaptor-related complex which is not clathrin-associated. The complex is associated with the Golgi region as well as more peripheral structures. It facilitates the budding of vesicles from the Golgi membrane and may
PDB 4AFI , 9C58 , 9C59 , 9C5B , 9C5C
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01602 Adaptin_N 32 583 Adaptin N terminal region Family
PF06375 AP3D1 661 807 Family
Tissue specificity TISSUE SPECIFICITY: Present in all adult tissues examined with the highest levels in skeletal muscle, heart, pancreas and testis. {ECO:0000269|PubMed:9151686}.
Sequence
MALKMVKGSIDRMFDKNLQDLVRGIRNHKEDEAKYISQCIDEIKQELKQDNIAVKANAVC
KLTYLQMLGYDISWAAFNIIEVMSASKFTFKRIGYLAASQSFHEGTDVIMLTTNQIRKDL
SSPSQYDTGVALTGLSCFVTPDLARDLANDIMTLMSHTKPYIRKKAVLIMYKVFLKYPES
LRPAFPRLKEKLEDPDPGVQSAAVNVICELARRNPKNYLSLAPLFFKLMTSSTNNWVLIK
IIKLFGALTPLEPRLGKKLIEPLTNLIHSTSAMSLLYECVNTVIAVLISLSSGMPNHSAS
IQLCVQKLRILIEDSDQNLKYLGLLAMSKILKTHPKSVQSHKDLILQCLDDKDESIRLRA
LDLLYGMVSKKNLMEIVKKLMTHVDKAEGTTYRDELLTKIIDICSQSNYQYITNFEWYIS
ILVELTRLEGTRHGHLIAAQMLDVAIRVKAIRKFAVSQMSALLDSAHLLASSTQRNGICE
VLYAAAWICGEFSEHLQEPHHTLEAMLRPRVTTLPGHIQAVYVQNVVKLYASILQQKEQA
GEAEGAQAVTQLMVDRLPQFVQSADLEVQERASCILQLVKHIQ
KLQAKDVPVAEEVSALF
AGELNPVAPKAQKKVPVPEGLDLDAWINEPLSDSESEDERPRAVFHEEEQRRPKHRPSEA
DEEELARRREARKQEQANNPFYIKSSPSPQKRYQDTPGVEHIPVVQIDLSVPLKVPGLPM
SDQYVKLEEERRHRQKLEKDKRRKKRKEKEKKGKRRHSSLPTESDEDIAPAQQVDIVTEE
MPENALPSDEDDKDPNDPYRALDIDLD
KPLADSEKLPIQKHRNTETSKSPEKDVPMVEKK
SKKPKKKEKKHKEKERDKEKKKEKEKKKSPKPKKKKHRKEKEERTKGKKKSKKQPPGSEE
AAGEPVQNGAPEEEQLPPESSYSLLAENSYVKMTCDIRGSLQEDSQVTVAIVLENRSSSI
LKGMELSVLDSLNARMARPQGSSVHDGVPVPFQLPPGVSNEAQYVFTIQSIVMAQKLKGT
LSFIAKNDEGATHEKLDFRLHFSCSSYLITTPCYSDAFAKLLESGDLSMSSIKVDGIRMS
FQNLLAKICFHHHFSVVERVDSCASMYSRSIQGHHVCLLVKKGENSVSVDGKCSDSTLLS
NLLEEMKATLAKC
Sequence length 1153
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Lysosome  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
80
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hermansky-Pudlak syndrome 10 Pathogenic rs879255646 RCV000239510
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Abnormal bleeding Uncertain significance rs200459002, rs772939299 RCV001270585
RCV001270523
Acute myeloid leukemia Benign; Uncertain significance; Likely benign rs734727, rs367888440, rs752064454 RCV005920263
RCV005925391
RCV005931388
Adrenocortical carcinoma, hereditary Uncertain significance rs750640235 RCV005930996
AP3D1-related disorder Conflicting classifications of pathogenicity; Likely benign; Benign; Uncertain significance rs756601658, rs367708267, rs763068481, rs25673, rs199895376, rs376574497, rs201113371, rs534880813, rs750853882, rs772395600, rs369183606, rs567035565, rs771185707, rs201880859, rs376667593
View all (26 more)
RCV003938655
RCV004756236
RCV003953799
RCV003980538
RCV004756332
RCV003416591
RCV004756325
RCV003923373
RCV003911063
RCV003923374
RCV003903479
RCV003950949
RCV003903366
RCV003911240
RCV003933643
RCV003933405
RCV003895978
RCV003933429
RCV003898455
RCV003395550
RCV003418989
RCV003948935
RCV004756540
RCV003956603
RCV003904599
RCV003899296
RCV003947088
RCV003934700
RCV003943097
RCV003906050
RCV003905928
RCV003920819
RCV003920640
RCV003950500
RCV003902837
RCV004756104
RCV003950821
RCV003958407
RCV003958348
RCV003923254
RCV003950755
RCV003903094
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Albinism Associate 26744459
Atherosclerosis Associate 24916648, 34188129
Cardiovascular Diseases Associate 34188129
Colorectal Neoplasms Associate 34188129
Diabetes Mellitus Associate 34188129
Epileptic Encephalopathy Early Infantile 3 Associate 34831286
Esophageal Squamous Cell Carcinoma Stimulate 34188129
Hermanski Pudlak Syndrome Associate 26744459, 34608437
Hypopigmentation Associate 26744459
Immunologic Deficiency Syndromes Associate 26744459