Microcephalin

Microcephalin (MCPH1) is a gene that is expressed during fetal brain development. Certain mutations in MCPH1, when homozygous, cause primary microcephaly—a severely diminished brain. Hence, it has been assumed that variants have a role in brain development. However, in normal individuals no effect on mental ability or behavior has yet been demonstrated in either this or another similarly studied microcephaly gene, ASPM. However, an association has been established between normal variation in brain structure, as measured with MRI (i.e., primarily cortical surface area and total brain volume) but only in females, and common genetic variants within both the MCPH1 gene and another similarly studied microcephaly gene, CDK5RAP2.

MCPH1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMCPH1, BRIT1, MCT, microcephalin 1
External IDsOMIM: 607117 MGI: 2443308 HomoloGene: 32586 GeneCards: MCPH1
Orthologs
SpeciesHumanMouse
Entrez

79648

244329

Ensembl

ENSG00000147316
ENSG00000285262

ENSMUSG00000039842

UniProt

Q8NEM0

Q7TT79

RefSeq (mRNA)

NM_173189

RefSeq (protein)

NP_775281

Location (UCSC)Chr 8: 6.41 – 6.65 MbChr 8: 18.65 – 18.85 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse
Microcephalin protein
Microcephalin.png
Identifiers
SymbolMicrocephalin
PfamPF12258
InterProIPR022047
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
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