1091
|
|
|
Transmembrane protein 223 |
Mrx15 |
Curated: N/A
Unreviewed: Breast neoplasm
|
1092
|
|
|
Transmembrane protein 225 |
PMP22CD, PPP1R154, SPATA47 |
Curated: N/A
Unreviewed: Neoplasms
|
1093
|
|
|
Transmembrane protein 225B |
GS1-259H13.2 |
Curated: N/A
Unreviewed: N/A
|
1094
|
|
|
Transmembrane protein 229A |
- |
Curated: Atrial fibrillation, Atrial flutter, Coronary thrombosis, Major depressive disorder
Unreviewed: Squamous cell carcinoma
|
1095
|
|
|
Transmembrane protein 229B |
C14orf83 |
Curated: Bipolar disorder, Major depressive disorder, Obesity, Oligodendroglioma, Parkinson disease, Schizophrenia, Vascular dementia
Unreviewed: Crohn disease, Kidney Disease, Kidney Failure
|
1096
|
|
|
TMEM229B pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1097
|
|
|
Transmembrane protein 230 |
C20orf30, HSPC274, dJ1116H23.2.1 |
Curated: Parkinson disease, Hereditary parkinson disease
Unreviewed: Autoimmune disease, Lewy Body Disease, Neurodegenerative Disorders, Rheumatoid arthritis, Senile Plaques
|
1098
|
|
|
TMEM230 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1099
|
|
|
TMEM230 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1100
|
|
|
Transmembrane protein 231 |
ALYE870, JBTS20, MKS11, PRO1886 |
Curated: Arima syndrome, Congenital anomalies of the kidney and urinary tract, Ciliopathy, Congenital cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Gastrointestinal stromal tumor, Joubert syndrome, Meckel-gruber syndrome, Orofaciodigital syndrome
Unreviewed: Anencephaly, Arima Syndrome, Asplenia, Asthma, Autism, Cataract, Cerebellar vermis agenesis, Ciliopathies, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Congenital Pectus Excavatum, Coronary Heart Disease, Coronary Syndrome, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Diastrophic Dysplasia, Double Ureter, Dysmorphic Features, Exotropia, Eyelid myoclonias, Fibrosis Of Pancreas, Foot Polydactyly, Fundus Coloboma, Hirschsprung Disease, Hydrocephalus, Joubert Syndrome, Joubert Syndrome With Oculorenal Defect, Keratosis Follicularis, Kidney Disease, Lobar Holoprosencephaly, Male Pseudohermaphroditism, Malformation of cortical development, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, MOHR-TRANEBJAERG SYNDROME, Multicystic renal dysplasia, Nystagmus, Occipital Encephalocele, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Pancreatic Cyst, Polycystic kidney disease, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Postaxial hand polydactyly, Ptosis, Renal cyst, Renal Insufficiency, Retinal coloboma, Retinal Dystrophy, Sclerocornea, Scoliosis, Situs Inversus, Strabismus, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
|