|
121
|
|
|
G protein signaling modulator 1 |
AGS3 |
|
|
122
|
|
|
Golgi associated, gamma adaptin ear containing, ARF binding protein 1 |
- |
|
|
123
|
|
|
GTPase activating protein and VPS9 domains 1 |
GAPEX5, GAPex-5, RAP6 |
|
|
124
|
|
|
Glycyl-tRNA synthetase 1 |
CMT2D, DSMAV, GARS, GlyRS, HMN5, HMN5A, HMND5, SMAD1, SMAJI |
|
|
125
|
|
|
Phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase |
AIRS, GARS, GARTF, PAIS, PGFT, PRGS |
|
|
126
|
|
|
Growth arrest specific 1 |
- |
Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Arrhinencephaly, Asthma, Choanal atresia, Congenital coloboma of iris, Congenital hypoplasia of penis, Cyclocephaly, Duodenal atresia, Dwarfism, Fused incisors, Hemangioma, Holoprosencephaly, Hypothyroidism, Lobar holoprosencephaly, Mental retardation, Microcephaly, Microform holoprosencephaly, Midline interhemispheric variant of holoprosencephaly, Panhypopituitarism, Renal agenesis, Scoliosis, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Strabismus, Tetralogy of fallotView all (12 more) |
|
127
|
|
|
Growth arrest specific 2 |
DFNB125, GAS-2 |
|
|
128
|
|
|
Growth arrest specific 6 |
AXLLG, AXSF |
|
|
129
|
|
|
GATA binding protein 1 |
CNSHA9, ERYF1, GATA-1, GF-1, GF1, HAEADA, NF-E1, NFE1, XLANP, XLTDA, XLTT |
Aase-smith syndrome, Abetalipoproteinemia, Alzheimer disease, Anemia, Atlantoaxial abnormality, Atrioventricular septal defect, Basophilic leukemia, Beta-thalassemia-thrombocytopenia syndrome, x-linked, Blackfan-diamond anemia, Brachycephaly, Congenital epicanthus, Congenital erythropoietic porphyria, Congenital thrombocytopenia, Cryptorchidism, Deficiency of uroporphyrinogen iii synthase, Down syndrome, Dwarfism, Dyserythropoietic anemia with abnormal platelets and neutropenia, x-linked, Dyserythropoietic anemia with thrombocytopenia, Ectropion, Elliptocytosis, Erosion of cornea, Hearing loss, Hirschsprung disease, Hydrops fetalis, Hypertrichosis, Hypochromic anemia, Hypothyroidism, Immunologic deficiency syndromes, Imperforate anus, Keratoconjunctivitis, Leukemia, Leukemia, megakaryoblastic, of down syndrome, Macroglossia, Macrothrombocytopenia, Megakaryoblastic leukemia in down syndrome, Megakaryocytic leukemia, Mental retardation, Microtia, Migraine, Myelodysplastic syndrome, Myeloproliferative disorder, Neutropenia, Osteopenia, Spade-like hand, Thrombocytopenia, with or without dyserythropoietic anemia, Thrombocytopenia with congenital dyserythropoietic anemia, Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis, Transient myeloproliferative disorder of down syndrome, Transient myeloproliferative syndrome, Trisomy 21View all (36 more) |
|
130
|
|
|
GATA binding protein 2 |
DCML, IMD21, MONOMAC, NFE1B |
Cardiovascular abnormalities, Cartilage diseases, Chondromalacia, Congenital neutropenia, Deafness-lymphedema-leukemia syndrome, Emberger syndrome, Hearing loss, Immunologic deficiency syndromes, Leukemia, Lymphopenia, Migraine, Milroy disease, Gata2 deficiency, Myelodysplasia, Myelodysplastic syndrome, Myeloid leukemia, Myelomonocytic leukemia, Myeloproliferative disorder, Neutropenia, Otitis media, Pancytopenia, Respiratory failure, Speech disorders, ThrombophiliaView all (9 more) |
