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genyn codio-protien yn y rhywogaeth Homo sapiens

MPDZ

MPDZ
All data from the card 12
PDB
Human UniProt search: PDBe RCSB
Cyfenwau
MPDZ, HYC2, MUPP1, multiple PDZ domain crumbs cell polarity complex component
Dynodwyr allanol
OMIM: 603785 HomoloGene: 2841 GeneCards: MPDZ
Gweithrediad moleciwlaidd
• protein C-terminus binding• GO:0001948, GO:0016582 protein binding
Prosesau biolegol
• cell adhesion• GO:0022415 viral process
Species
Bod dynol
Entrez
8777
Ensembl
ENSG00000107186
UniProt
O75970
RefSeq (mRNA)
NM_001261406NM_001261407NM_003829NM_001330637
RefSeq (protein)
NP_001248335NP_001248336NP_001317566NP_003820NP_001362342NP_001362345NP_001362346NP_001362347NP_001362348NP_001362349NP_001362350NP_001362351NP_001362352NP_001362353NP_001362354NP_001362355NP_001362356NP_001365707
Lleoliad (UCSC)
n/a

Protein sy'n cael ei godio yn y corff dynol gan y genyn MPDZ yw MPDZ a elwir hefyd yn Multiple PDZ domain protein a Multiple PDZ domain crumbs cell polarity complex component (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 9, band 9p23.

Cyfystyron

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn MPDZ.

  • HYC2
  • MUPP1

Llyfryddiaeth

  • "Genetic variability in the NMDA-dependent AMPA trafficking cascade is associated with alcohol dependence. ". Addict Biol. 2012. PMID 21762291.
  • "Structure-based identification of CaMKIIα-interacting MUPP1 PDZ domains and rational design of peptide ligands to target such interaction in human fertilization. ". Amino Acids. 2016. PMID 26984442.
  • "Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population. ". Ophthalmic Genet. 2015. PMID 25675348.
  • "The multi-PDZ domain protein-1 (MUPP-1) expression regulates cellular levels of the PALS-1/PATJ polarity complex. ". Exp Cell Res. 2013. PMID 23880463.
  • "Mutation in MPDZ causes severe congenital hydrocephalus.". J Med Genet. 2013. PMID 23240096.

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Text from Wikipedia, CC BY-SA 4.0 · Source article