5191
|
|
|
Glucuronic acid epimerase |
HSEPI |
|
5192
|
|
|
Glycine decarboxylase |
GCE, GCE1, GCSP, HYGN1 |
|
5193
|
|
|
Gliomedin |
CLOM, COLM, CRG-L2, CRGL2, LCCS11, UNC-112, UNC-122 |
Arthrogryposis multiplex congenita, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Congenital joint contractures, Contracture of multiple joints, Fetal akinesia deformation sequence, Lethal congenital contracture syndrome, Pena-shokeir syndrome , Pericarditis, Primary aldosteronism, Urinary bladder cancerView all (1 more) |
5194
|
|
|
GLE1 RNA export mediator |
CAAHC, CAAHD, GLE1L, LCCS, LCCS1, hGLE1 |
|
5195
|
|
|
Golgi glycoprotein 1 |
CFR-1, ESL-1, MG-160, MG160 |
|
5196
|
|
|
GLI family zinc finger 1 |
GLI, PAPA8, PPD1 |
Bardet-biedl syndrome, Hepatocellular carcinoma, Ellis-van creveld syndrome, Gastrointestinal stromal tumor, Gout, Insomnia, Promyelocytic leukemia, Diffuse large b-cell lymphoma, Non-neoplastic peripheral nervous system disease, Premature ovarian failure, Peripheral nervous system disease, Peripheral neuropathy, Polydactyly, Postaxial polydactyly, Urinary bladder neoplasms |
5197
|
|
|
GLI family zinc finger 2 |
CJS, HPE9, PHS2, THP1, THP2 |
Alzheimer disease, Androgenetic alopecia, Cerebral arteriovenous malformations, Asthma, Bardet-biedl syndrome, Basal cell nevus syndrome, Bifid nose, Breast cancer, Basal cell carcinoma, Cleft face, Coloboma, Combined pituitary hormone deficiency, Congenital arteriovenous malformation, Craniosynostosis, Culler-jones syndrome, Dementia, Desbuquois syndrome, Developmental disability, Erectile dysfunction, Exostoses, Facial dysmorphism syndrome, Gastrointestinal stromal tumor, Holoprosencephaly, Intellectual developmental disorder, Promyelocytic leukemia, Male infertility single gene azoospermia, Microform holoprosencephaly, Syntelencephaly, Oligodendroglioma, Pituitary stalk interruption syndrome, , Prostate cancer, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Skin neoplasms, Diabetes mellitus type 2, White sutton syndromeView all (22 more) |
5198
|
|
|
GLI family zinc finger 3 |
ACLS, GCPS, GLI3-190, GLI3FL, PAP-A, PAPA, PAPA1, PAPB, PHS, PPDIV |
Acrocallosal syndrome, Asthma, Blepharoptosis, Tibial hemimelia, Congenital diaphragmatic hernia, Craniosynostosis, Crohn disease, Cronkhite-canada syndrome, Desbuquois syndrome, Tooth agenesis, Pilosebaceous disorder, Emphysema, Gastrointestinal stromal tumor, Glaucoma, Global developmental delay, Inflammatory bowel disease, Ovarian epithelial cancer, Migraine, Multiple sclerosis, Neural tube defect, Neural tube defects, x-linked, Ovarian cancer, Polydactyly, Postaxial polydactyly, Psychiatric disorders, Retinopathy of prematurity, Sarcoidosis, Seasonal allergic rhinitis, Squamous cell carcinoma, Stomach neoplasms, Syndactyly, Diabetes mellitus type 2, Ulcerative colitis, White sutton syndromeView all (19 more) |
5199
|
|
|
GLI family zinc finger 4 |
HKR4, ZNF928 |
|
5200
|
|
|
GLI pathogenesis related 1 |
CRISP7, GLIPR, RTVP1 |
|
