|
| Entrez Id: |
23141 |
| Gene Symbol: |
ANKLE2 |
ANKLE2
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
29123 |
| Gene Symbol: |
ANKRD11 |
ANKRD11
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
|
|
|
|
| Entrez Id: |
29123 |
| Gene Symbol: |
ANKRD11 |
ANKRD11
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
124401 |
| Gene Symbol: |
ANKS3 |
ANKS3
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
|
|
|
|
| Entrez Id: |
84168 |
| Gene Symbol: |
ANTXR1 |
ANTXR1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
118429 |
| Gene Symbol: |
ANTXR2 |
ANTXR2
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
|
|
|
|
| Entrez Id: |
8905 |
| Gene Symbol: |
AP1S2 |
AP1S2
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
8120 |
| Gene Symbol: |
AP3B2 |
AP3B2
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
10717 |
| Gene Symbol: |
AP4B1 |
AP4B1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
23431 |
| Gene Symbol: |
AP4E1 |
AP4E1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
9179 |
| Gene Symbol: |
AP4M1 |
AP4M1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
11154 |
| Gene Symbol: |
AP4S1 |
AP4S1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
359 |
| Gene Symbol: |
AQP2 |
AQP2
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
361 |
| Gene Symbol: |
AQP4 |
AQP4
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
|
|
|
|
AQP4-AS1
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
|
|
|
|
| Entrez Id: |
8289 |
| Gene Symbol: |
ARID1A |
ARID1A
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
57492 |
| Gene Symbol: |
ARID1B |
ARID1B
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
|
26350204 |
2015 |
|
| Entrez Id: |
57492 |
| Gene Symbol: |
ARID1B |
ARID1B
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
57492 |
| Gene Symbol: |
ARID1B |
ARID1B
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
|
22426309 |
2012 |
|
| Entrez Id: |
196528 |
| Gene Symbol: |
ARID2 |
ARID2
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
196528 |
| Gene Symbol: |
ARID2 |
ARID2
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
|
|
|
|
| Entrez Id: |
84100 |
| Gene Symbol: |
ARL6 |
ARL6
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
9915 |
| Gene Symbol: |
ARNT2 |
ARNT2
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
415 |
| Gene Symbol: |
ARSL |
ARSL
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
64801 |
| Gene Symbol: |
ARV1 |
ARV1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|