Varaico: Literature-Extracted Genetic Variants

Gene:CEP152
Variant:p.K667R

CEP152

180 papers

RefSeq Summary

This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in mult...

Pfam Domains

PLK4_bind_CEP152aa 1–59UCSCCEP152, PLK4 binding region
CC_CEP63-bind_CEP152aa 1263–1313UCSCCEP152, CEP63 binding coiled coil
CC_CEP63-bind_CEP152aa 1263–1313UCSCCEP152, CEP63 binding coiled coil

Gene Aliases

HGNC Name

centrosomal protein 152

HGNC Alias Symbols

KIAA0912; SCKL5; MCPH9

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
4 papers
NM_001194998.2
p.K667R
c.2000A>G
Surrounding Variants
1 paper
NM_001194998.2
p.E669V
c.2006A>T
1 paper
NM_001194998.2
p.Q650H
c.1950A>T
1 paper
NM_001194998.2
p.E637delFs
c.1910delT
1 paper
NM_001194998.2
p.Q633*
c.1897C>T
1 paper
NM_001194998.2
p.Q629delFs
c.1887delT
1 paper
NM_001194998.2
p.D620Y
c.1858G>T
1 paper
NM_001194998.2
p.C674F
c.2021G>T
16 papers
NM_001194998.2
p.Y678*
c.2034T>G
15 papers
NM_001194998.2
p.Y678*
c.2034T>A
1 paper
NM_001194998.2
p.Y678_Q679del1
c.2034_2036delTGA
1 paper
NM_001194998.2
p.Q680H
c.2040G>C
1 paper
NM_001194998.2
p.H681Y
c.2041C>T
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