|
1881
|
|
|
Small nucleolar RNA host gene 11 |
C20orf198, LINC00101, NCRNA00101 |
|
|
1882
|
|
|
Collagen type IV alpha 3 chain |
ATS2, ATS3, ATS3A, ATS3B, BFH2 |
Alport syndrome, Alport syndrome, x-linked, Azotemia, Benign hematuria, Cataract, Corneal erosion, Exudative macular degeneration, Genetic steroid-resistant nephrotic syndrome, Geographic atrophy, Glomerulonephritis, Hearing loss, Hematuria, Hereditary nephritis, Hypertension, Hypertensive nephropathy, Kidney disease, Lenticonus, Leukemia, Age-related macular degeneration, Myopia, Nephritis, Nephrocalcinosis, Nephrotic syndrome, Renal glomerular disease, Renal insufficiency, Thin basement membrane diseaseView all (11 more) |
|
1883
|
|
|
Collagen type IV alpha 4 chain |
ATS2, BFH, BFH1, CA44 |
Alport syndrome, Alport syndrome, x-linked, Alzheimer disease, Benign hematuria, Cataract, Corneal erosion, Hematuria, Hypertension, Hypertensive nephropathy, Kidney disease, Lenticonus, Myopia, Nephritis, Nephrotic syndrome, Renal glomerular disease, Renal insufficiency, Thin basement membrane diseaseView all (2 more) |
|
1884
|
|
|
Zinc finger protein 831 |
C20orf174 |
Ankylosing spondylitis, Cardiovascular diseases, Cholangitis, Coronary artery disease, Coronary heart disease, Crohn disease, Hypertension, Inflammatory bowel disease, Melanoma, Psoriasis, Ulcerative colitis |
|
1885
|
|
|
TBC1 domain family member 20 |
C20orf140, WARBM4 |
Cataract, Central visual impairment, Cerebellar atrophy, Cerebral cortical atrophy, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Dwarfism, Fundus coloboma, Glaucoma, High palate, Hydronephrosis, Hypoplasia of corpus callosum, Mental retardation, Macrotia, Micro syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Microstomia, Nervous system diseases, Optic atrophy, Pachygyria, Penis agenesis, Ptosis, Retinal coloboma, Scoliosis, Spastic quadriplegia, Warburg micro syndromeView all (15 more) |
|
1886
|
|
|
Prokineticin receptor 2 |
GPR73L1, GPR73b, GPRg2, HH3, KAL3, PKR2, dJ680N4.3 |
Agenesis of corpus callosum, Anxiety disorder, Autism, Bipolar disorder, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital hypoplasia of penis, Congenital pectus excavatum, Congenital sensorineural hearing loss, Cryptorchidism, Developmental delay, Diabetes insipidus, Dwarfism, Dysarthria, Dyssomnia, Erectile dysfunction, Esophageal atresia, Female hypogonadism syndrome, Gynecomastia, Hearing loss, Hemiplegia/hemiparesis, Hypoglycemia, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypohidrosis, Hypopituitarism, Hypothyroidism, Ichthyosis, Kallmann syndrome, Mental depression, Mental retardation, Mirror movements, Mood disorder, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Pituitary stalk interruption syndrome, Ptosis, Renal agenesis, Renal aplasia, Secondary physiologic amenorrhea, Septo-optic dysplasia, Skeletal dysplasia, Sleep disorders, Strabismus, Testicular hypogonadismView all (39 more) |
|
1887
|
|
|
Collagen type IV alpha 5 chain |
ASLN, ATS, ATS1, CA54 |
Alport syndrome, Alport syndrome, x-linked, Benign hematuria, Corneal erosion, Diffuse leiomyomatosis, Focal segmental glomerulosclerosis, Glomerulosclerosis, Hearing loss, Hematuria, Hypertension, Hypoparathyroidism, Ichthyosis, Kidney disease, Leiomyoma, Leiomyosarcoma, Lenticonus, Myopia, Nephritis, Nephrotic syndrome, Renal glomerular disease, Renal insufficiency, Renal tubular disorder, Sensorineural hearing loss, Thoracic aortic aneurysm and aortic dissectionView all (9 more) |
|
1888
|
|
|
Collagen type IV alpha 6 chain |
CXDELq22.3, DELXq22.3, DFNX6 |
|
|
1889
|
|
|
MIR1-1 host gene |
C20orf166, MIR133A2HG |
|
|
1890
|
|
|
BPI fold containing family A member 3 |
C20orf71, SPLUNC3 |
|
