Entrez Id: |
9024 |
Gene Symbol: |
BRSK2 |
BRSK2
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.
|
30879638 |
2019 |
Entrez Id: |
9024 |
Gene Symbol: |
BRSK2 |
BRSK2
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.
|
30879638 |
2019 |
Entrez Id: |
7701 |
Gene Symbol: |
ZNF142 |
ZNF142
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
|
31036918 |
2019 |
Entrez Id: |
8216 |
Gene Symbol: |
LZTR1 |
LZTR1
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants.
|
29469822 |
2018 |
Entrez Id: |
26960 |
Gene Symbol: |
NBEA |
NBEA
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
NBEA: Developmental disease gene with early generalized epilepsy phenotypes.
|
30269351 |
2018 |
Entrez Id: |
815 |
Gene Symbol: |
CAMK2A |
CAMK2A
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
|
29100089 |
2017 |
Entrez Id: |
8942 |
Gene Symbol: |
KYNU |
KYNU
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
|
28792876 |
2017 |
Entrez Id: |
816 |
Gene Symbol: |
CAMK2B |
CAMK2B
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
|
29100089 |
2017 |
Entrez Id: |
816 |
Gene Symbol: |
CAMK2B |
CAMK2B
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
|
29100089 |
2017 |
Entrez Id: |
815 |
Gene Symbol: |
CAMK2A |
CAMK2A
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
|
29100089 |
2017 |
Entrez Id: |
54084 |
Gene Symbol: |
TSPEAR |
TSPEAR
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.
|
27736875 |
2016 |
Entrez Id: |
2257 |
Gene Symbol: |
FGF12 |
FGF12
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.
|
27872899 |
2016 |
TSPEAR-AS1
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.
|
27736875 |
2016 |
Entrez Id: |
2475 |
Gene Symbol: |
MTOR |
MTOR
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.
|
27159400 |
2016 |
Entrez Id: |
23096 |
Gene Symbol: |
IQSEC2 |
IQSEC2
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
A novel splicing mutation in the IQSEC2 gene that modulates the phenotype severity in a family with intellectual disability.
|
26733290 |
2016 |
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
|
26350204 |
2015 |
Entrez Id: |
7994 |
Gene Symbol: |
KAT6A |
KAT6A
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.
|
25728777 |
2015 |
Entrez Id: |
27245 |
Gene Symbol: |
AHDC1 |
AHDC1
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
|
24791903 |
2014 |
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
|
22426309 |
2012 |
Entrez Id: |
80208 |
Gene Symbol: |
SPG11 |
SPG11
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
|
19194956 |
2009 |
Entrez Id: |
64324 |
Gene Symbol: |
NSD1 |
NSD1
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
79876 |
Gene Symbol: |
UBA5 |
UBA5
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
23126 |
Gene Symbol: |
POGZ |
POGZ
|
Delayed speech and language development
|
0.100 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
6942 |
Gene Symbol: |
TCF20 |
TCF20
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
6016 |
Gene Symbol: |
RIT1 |
RIT1
|
Delayed speech and language development
|
0.100 |
CausalMutation |
CLINVAR |
|
|
|