Entrez Id: |
56776 |
Gene Symbol: |
FMN2 |
FMN2
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
1968 |
Gene Symbol: |
EIF2S3 |
EIF2S3
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
7994 |
Gene Symbol: |
KAT6A |
KAT6A
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.
|
25728777 |
2015 |
Entrez Id: |
171023 |
Gene Symbol: |
ASXL1 |
ASXL1
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
SMARCAL1
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
9373 |
Gene Symbol: |
PLAA |
PLAA
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
57479 |
Gene Symbol: |
PRR12 |
PRR12
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
84947 |
Gene Symbol: |
SERAC1 |
SERAC1
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
9927 |
Gene Symbol: |
MFN2 |
MFN2
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
1859 |
Gene Symbol: |
DYRK1A |
DYRK1A
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies.
|
25944381 |
2015 |
Entrez Id: |
7274 |
Gene Symbol: |
TTPA |
TTPA
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
5190 |
Gene Symbol: |
PEX6 |
PEX6
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
79813 |
Gene Symbol: |
EHMT1 |
EHMT1
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
118426 |
Gene Symbol: |
BORCS5 |
BORCS5
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
11113 |
Gene Symbol: |
CIT |
CIT
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
259266 |
Gene Symbol: |
ASPM |
ASPM
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
ASPM is a major determinant of cerebral cortical size.
|
12355089 |
2002 |
Entrez Id: |
11128 |
Gene Symbol: |
POLR3A |
POLR3A
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
3832 |
Gene Symbol: |
KIF11 |
KIF11
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature.
|
25115524 |
2014 |
Entrez Id: |
9757 |
Gene Symbol: |
KMT2B |
KMT2B
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
9343 |
Gene Symbol: |
EFTUD2 |
EFTUD2
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
57038 |
Gene Symbol: |
RARS2 |
RARS2
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
79644 |
Gene Symbol: |
SRD5A3 |
SRD5A3
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
81857 |
Gene Symbol: |
MED25 |
MED25
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
57728 |
Gene Symbol: |
WDR19 |
WDR19
|
Microcephaly (physical finding)
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
51010 |
Gene Symbol: |
EXOSC3 |
EXOSC3
|
Microcephaly (physical finding)
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|