AP3M1

AP3M1
Identifiers
Aliases AP3M1
External IDs MGI: 1929212 HomoloGene: 22693 GeneCards: AP3M1
RNA expression pattern


More reference expression data
Orthologs
Species Human Mouse
Entrez

26985

55946

Ensembl

ENSG00000185009

ENSMUSG00000021824

UniProt

Q9Y2T2

Q9JKC8

RefSeq (mRNA)

NM_012095
NM_207012
NM_001320263
NM_001320264
NM_001320265

NM_018829

RefSeq (protein)

NP_036227.1
NP_996895.1
NP_001307192.1
NP_001307193.1

NP_061299.3

Location (UCSC) Chr 10: 74.12 – 74.15 Mb Chr 14: 21.03 – 21.05 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

AP-3 complex subunit mu-1 is a protein that in humans is encoded by the AP3M1 gene.[3][4]

The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane and may be directly involved in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternatively spliced transcript variants encoding the same protein have been observed.[4]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. Dell'Angelica EC, Shotelersuk V, Aguilar RC, Gahl WA, Bonifacino JS (Mar 1999). "Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor". Mol Cell. 3 (1): 11–21. doi:10.1016/S1097-2765(00)80170-7. PMID 10024875.
  4. 1 2 "Entrez Gene: AP3M1 adaptor-related protein complex 3, mu 1 subunit".

Further reading


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