|
101
|
|
|
Bromodomain and WD repeat domain containing 1 |
C21orf107, CILD51, DCAF19, N143, WDR9, WRD9 |
|
|
102
|
|
|
Butyrophilin subfamily 2 member A3, pseudogene |
BTN2.3, BTN2A3 |
|
|
103
|
|
|
Basonuclin zinc finger protein 2 |
BSN2, LUTO, bn2 |
Asthma, Chronic obstructive pulmonary disease, Congenital posterior urethral valves, Diabetes mellitus, Eczema, Hydronephrosis, Hypertension, Kidney disease, Melanosis, Nocturnal enuresis, Ovarian neoplasm, Ovarian cancer, Pyelonephritis, Renal dysplasia, Vesicoureteral reflux |
|
104
|
|
|
BCAS3 microtubule associated cell migration factor |
GAOB1, HEMARS, MAAB, PHAF2 |
Alzheimer disease, Cardiovascular diseases, Chronic obstructive pulmonary disease, Coronary artery disease, Crohn disease, Diabetes, Diabetes mellitus, Gout, Gouty arthritis, Kidney disease, Kidney failure, Urolithiasis |
|
105
|
|
|
BCL6 corepressor |
ANOP2, MAA2, MCOPS2 |
Cubitus valgus, Acquired kyphoscoliosis, Adenocarcinoma, Anemia, Anorexia, Aortic valve sclerosis, Atrial septal defect, Bicuspid aortic valve, Blepharophimosis, Camptodactyly of fingers, Cataract, Ciliary body coloboma, Clinodactyly, Coloboma of optic disc, Congenital ankyloblepharon, Congenital camptodactyly, Congenital cataract, Congenital coloboma of iris, Short clavicles, Congenital kyphoscoliosis, Congenital malrotation of intestine, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Diffuse alveolar hemorrhage, Disorder of eye, Disseminated intravascular coagulation, Dwarfism, Ectopia lentis, Embryonal rhabdomyosarcoma, Exotropia, Fibrinogen deficiency, Fundus coloboma, Fused incisors, Gangrene, Glaucoma, Hearing loss, Heart septal defects, Hirschsprung disease, Hydronephrosis, Hypodontia, Hypofibrinogenemia, Hypoplasia of thumb, Hypospadias, Imperforate anus, Kidney neoplasm, Kidney cancer, Leukemia, Leukopenia, Spastic diplegia, Mental retardation, Microcephaly, Microcornea, Microphthalmia, Syndromic microphthalmia, Microphthalmos, Mitral valve prolapse, Motor delay, Multiple congenital anomalies, Neck webbing, Nephroblastoma, Neutropenia, Nystagmus, Oculofaciocardiodental syndrome, Oligodontia, Oral cleft, Osteosarcoma, Otitis media, Pancytopenia, Patent ductus arteriosus, Peripheral pulmonary artery stenosis, Persistent hyperplastic primary vitreous, Posteriorly rotated ear, Promyelocytic leukemia, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Retinal coloboma, Retinal detachment, Retinoblastoma, Sarcoma, Sarcoma of kidney, Scoliosis, Spade-like hand, Speech disorders, Stomatitis, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Ventricular septal defect, Wilms tumorView all (79 more) |
|
106
|
|
|
3'(2'), 5'-bisphosphate nucleotidase 2 |
GPAPP, IMP 3, IMP-3, IMPA3, IMPAD1 |
|
|
107
|
|
|
BTG3 associated nuclear protein |
BEND1, SMAR1, SMARBP1 |
|
|
108
|
|
|
B cell scaffold protein with ankyrin repeats 1 |
BANK |
Ankylosing spondylitis, Cardiovascular diseases, Cholangitis, Crohn disease, Inflammatory bowel disease, Lymphocytic leukemia, Lupus erythematosus, Multiple sclerosis, Nonbacterial verrucal endocardiosis, Psoriasis, Systemic lupus erythematosus, Ulcerative colitis |
|
109
|
|
|
Bardet-Biedl syndrome 7 |
BBS2L1 |
Bardet-biedl syndrome, Ciliopathies, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Disorder of eye, Dwarfism, Hypertension, Hypogonadism, Mental retardation, Liver fibrosis, Multicystic renal dysplasia, Nephrotic syndrome, Nystagmus, Obesity, Polydactyly, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (7 more) |
|
110
|
|
|
Basic leucine zipper ATF-like transcription factor 3 |
JDP1, JUNDM1, SNFT |
|
