The domain within your query sequence starts at position 224 and ends at position 597; the E-value for the Microcephalin domain shown below is 1.2e-143.
ESFASGSHSSFGDSCGDQERKLGRSANEMTTVTCPSSPVLRASSFYGSASPNHLRQPRPQ KAPDSPSKESINCQKDATGAVADSERKQAAGVSQGVPDEKLCLSPTMSIIEEHQVRLGPK NSSAKRKRAADLGSSPKGKLKKRYKRKSALAIQLFKSDQSPPSTIRLIPGTPDVEASSYE DYFSPDNLKERNSERLPPEAQQLASPSLFHCRGLSKWERRNMLEMCDFTCIGEKHRSISS ISDLISKSASSLEKPVKEEVNTASTCLLLVETSANDSPGLCSQPGPQLRDDTGPEGSSHP DTLSSSAHHITPLKGNSTETRDPGDGKGSPKEGSTPPASASPEDEVHICNLSLGEDCNVE KSVEEKENIATGYS
Microcephalin |
![]() |
---|
PFAM accession number: | PF12258 |
---|---|
Interpro abstract (IPR029504): | Microcephalin is implicated in chromosome condensation and DNA damage induced cellular responses [ (PUBMED:15199523) (PUBMED:15220350) ]. It may play a role in neurogenesis and regulation of the size of the cerebral cortex in animals. It is a protein, which if expressed homozygously, causes the organism to have the condition microcephaly - a drastically reduced brain mass and volume [ (PUBMED:12046007) ]. Microcephalin is predicted to contain three BRCA1 C-terminal domains, the first of which is the probable microcephaly mutation site. |
GO process: | cerebral cortex development (GO:0021987) |
This is a PFAM domain. For full annotation and more information, please see the PFAM entry Microcephalin