761
|
|
|
Patatin like domain 6, lysophospholipase |
BNHS, LNMS, NTE, NTEMND, OMCS, SPG39, iPLA2delta, sws |
Amyotrophic lateral sclerosis, Ataxia-hypogonadism-choroidal dystrophy syndrome, Spastic paraplegia, Boucher-neuhauser syndrome, Cerebellar ataxia, Cerebellar ataxia and hypogonadotropic hypogonadism, Cerebellar ataxia-hypogonadism, Cerebellar atrophy, Chorioretinal dystrophy, spinocerebellar ataxia, hypogonadotropic hypogonadism syndrome, Desbuquois syndrome, Dysarthria, Female infertility, Hypogonadotropic hypogonadism, Kallmann syndrome, Motor neuron disease, Mucolipidosis, Nervous system disease, Non-neoplastic peripheral nervous system disease, Optic atrophy, Pelvic inflammatory disease, Peripheral nervous system disease, Peripheral neuropathy, Polyneuropathy, Retinitis pigmentosa, Rod-cone dystrophy, Spastic ataxia, Hereditary spastic paraplegia, Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, Uterine inflammatory diseaseView all (14 more) |
762
|
|
|
Patatin like domain 7, lysophospholipase |
C9orf111, NTE-R1, NTEL1 |
|
763
|
|
|
Patatin like domain 8, phospholipase A2 |
IPLA2-2, IPLA2G, MMLA, PNPLA-gamma, iPLA2gamma |
|
764
|
|
|
Pyridoxamine 5'-phosphate oxidase |
HEL-S-302, PDXPO |
|
765
|
|
|
Polyribonucleotide nucleotidyltransferase 1 |
COXPD13, DFNB70, OLD35, PNPASE, SCA25, old-35 |
Amyotrophic lateral sclerosis, Androgenetic alopecia, Autoimmune thyroid disease, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Hepatocellular carcinoma, Obstructive pulmonary disease, Combined oxidative phosphorylation deficiency, Deafness, Disorder of visual system, Diverticular disease, Eye disease, Eyelid disease, Glaucoma, Global developmental delay, Hearing impairment, Hearing loss, Hypertension, Hypothyroidism, Leigh syndrome, Neurodevelopmental disorder, Neuropathy, Open angle glaucoma, Optic neuritis, Pelvic organ prolapse, Schizophrenia, Nonsyndromic hearing loss, Spinocerebellar ataxia, Uterine prolapse, Visual impairmentView all (15 more) |
766
|
|
|
POC1 centriolar protein A |
PIX2, SOFT, WDR51A |
|
767
|
|
|
POC1 centriolar protein B |
CORD20, PIX1, TUWD12, WDR51B |
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Cholecystolithiasis, Ciliopathy, Cone-rod dystrophy, Gallstones, Heart failure, Insomnia, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Peptic ulcer disease, Retinitis pigmentosa, Schizophrenia, Substance abuse, Diabetes mellitus type 2View all (2 more) |
768
|
|
|
POC1B-GALNT4 readthrough |
GALNT4, GalNAc-T4 |
|
769
|
|
|
POC5 centriolar protein |
C5orf37 |
Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Cancer, Coronary artery disease, Diabetes mellitus, Heart failure, Metabolic syndrome, Migraine, Obesity, Optic atrophy, Retinitis pigmentosa, Scoliosis, Stroke, Diabetes mellitus type 2 |
770
|
|
|
Podocan like 1 |
SLRR5B |
|
