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1261
|
|
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Patatin like domain 6, lysophospholipase |
BNHS, LNMS, NTE, NTEMND, OMCS, SPG39, iPLA2delta, sws |
Accessory nipple, Alopecia, Anterior horn cell disease, Spinocerebellar ataxia, Ataxia-hypogonadism-choroidal dystrophy syndrome, Atrophy of the spinal cord, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Cerebellar ataxia-hypogonadism syndrome, Cerebellar atrophy, Charcot-marie-tooth disease, Chorioretinal dystrophy, Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism, Congenital coloboma of iris, Congenital epicanthus, Congenital hepatic fibrosis, Congenital hypoplasia of penis, Cryptorchidism, Dementia, Diabetes mellitus, Distal amyotrophy, Dwarfism, Dysarthria, Gordon holmes syndrome, Gynecomastia, Hearing loss, Hemiplegia/hemiparesis, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Lateral sclerosis, Laurence-moon syndrome, Limb muscle atrophy, Mental retardation, Motor neuron disease, Nervous system diseases, Nervous system disorder, Nystagmus, Obesity, Oliver-mcfarlane syndrome, Optic atrophy, Penis agenesis, Peripheral axonal neuropathy, Polydactyly, Polyneuropathy, Renal insufficiency, Retinal dystrophy, Retinitis pigmentosa, Sick building syndrome, Somatotropin deficiency, Spastic paraplegia, Speech disorders, Strabismus, Syndactyly of fingers, Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, Hereditary spastic paraplegia, x-linkedView all (42 more) |
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1262
|
|
|
Urotensin 2 |
PRO1068, U-II, UCN2, UII |
|
|
1263
|
|
|
Ectodysplasin A receptor |
DL, ECTD10A, ECTD10B, ED1R, ED3, ED5, EDA-A1R, EDA1R, EDA3, HRM1 |
Alopecia, Alopecia, male pattern, Alpers syndrome, Androgenetic alopecia, Anhidrosis, Anodontia, Ectodermal dysplasia, Eczema, Frontal bossing, Hypodontia, Hypohidrosis, Hypohidrotic ectodermal dysplasia, Hypohidrotic ectodermal dysplasia, x-linked, Hypoplasia of teeth, Hypotrichosis, Microdontia, Mitochondrial dna depletion syndrome, Nail diseases, Nail dysplasiaView all (4 more) |
|
1264
|
|
|
Poly(A) polymerase alpha |
PAP, PAP-alpha |
|
|
1265
|
|
|
Transcription elongation regulator 1 |
CA150, TAF2S, Urn1 |
|
|
1266
|
|
|
MAGE family member D2 |
11B6, BARTS5, BCG-1, BCG1, HCA10, MAGE-D2 |
|
|
1267
|
|
|
Euchromatic histone lysine methyltransferase 2 |
BAT8, C6orf30, G9A, GAT8, KMT1C, NG36 |
Development disorder, Diabetes mellitus, Leukemia, Lung neoplasms, Lung cancer, Lupus erythematosus, Membranous glomerulonephritis, Multiple sclerosis, Myeloid leukemia, Oral ulcer, Ovarian epithelial carcinoma, Rheumatoid arthritis, Schizophrenia, Subfertility, Takayasu arteritis, Vesicular stomatitisView all (1 more) |
|
1268
|
|
|
RNA binding protein with serine rich domain 1 |
E5.1 |
|
|
1269
|
|
|
Fas activated serine/threonine kinase |
FAST |
|
|
1270
|
|
|
SUB1 regulator of transcription |
P15, PC4, p14 |
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