Entrez Id: |
25980 |
Gene Symbol: |
AAR2 |
AAR2
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
51412 |
Gene Symbol: |
ACTL6B |
ACTL6B
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination.
|
31134736 |
2019 |
Entrez Id: |
9179 |
Gene Symbol: |
AP4M1 |
AP4M1
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
8289 |
Gene Symbol: |
ARID1A |
ARID1A
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
|
22426309 |
2012 |
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
|
26350204 |
2015 |
Entrez Id: |
673 |
Gene Symbol: |
BRAF |
BRAF
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome.
|
16439621 |
2006 |
Entrez Id: |
673 |
Gene Symbol: |
BRAF |
BRAF
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.
|
16474404 |
2006 |
Entrez Id: |
55636 |
Gene Symbol: |
CHD7 |
CHD7
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
91949 |
Gene Symbol: |
COG7 |
COG7
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
91949 |
Gene Symbol: |
COG7 |
COG7
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
1654 |
Gene Symbol: |
DDX3X |
DDX3X
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
56171 |
Gene Symbol: |
DNAH7 |
DNAH7
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
1859 |
Gene Symbol: |
DYRK1A |
DYRK1A
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
2290 |
Gene Symbol: |
FOXG1 |
FOXG1
|
Hypoplasia of corpus callosum
|
0.120 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
2917 |
Gene Symbol: |
GRM7 |
GRM7
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
8924 |
Gene Symbol: |
HERC2 |
HERC2
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
547 |
Gene Symbol: |
KIF1A |
KIF1A
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome.
|
26486474 |
2016 |
Entrez Id: |
3799 |
Gene Symbol: |
KIF5B |
KIF5B
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
4297 |
Gene Symbol: |
KMT2A |
KMT2A
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
10916 |
Gene Symbol: |
MAGED2 |
MAGED2
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
81857 |
Gene Symbol: |
MED25 |
MED25
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
81857 |
Gene Symbol: |
MED25 |
MED25
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
2475 |
Gene Symbol: |
MTOR |
MTOR
|
Hypoplasia of corpus callosum
|
0.100 |
CausalMutation |
CLINVAR |
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
|
27159400 |
2016 |
Entrez Id: |
4784 |
Gene Symbol: |
NFIX |
NFIX
|
Hypoplasia of corpus callosum
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|