188701
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Transmembrane protein 212 |
- |
Curated: Central nervous system cancer, Glioblastoma, Glioma, Hypertension, Diabetes mellitus type 2
Unreviewed: N/A
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188702
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TMEM212 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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188703
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|
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TMEM212 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
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188704
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|
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Transmembrane protein 213 |
- |
Curated: Hearing loss, Keratoconus
Unreviewed: Renal Carcinoma, Renal cell carcinoma, Squamous cell carcinoma
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188705
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Transmembrane protein 214 |
- |
Curated: Anxiety disorder, Autism
Unreviewed: N/A
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188706
|
|
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Transmembrane protein 215 |
- |
Curated: Alzheimer disease
Unreviewed: Colorectal neoplasm, Neoplasms
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188707
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Transmembrane protein 216 |
HSPC244, RP98 |
Curated: Arima syndrome, Ciliopathy, Congenital brain malformation, Congenital hypoplasia of part of brain, Congenital neurologic anomalies, Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Lissencephaly, Macrogyria, Meckel-gruber syndrome, Microgyria, Orofaciodigital syndrome, Retinitis pigmentosa
Unreviewed: Anencephaly, Arima Syndrome, Asplenia, Autism, Brachydactyly, Cataract, Cerebellar vermis agenesis, Ciliopathies, Clinodactyly, Coloboma of optic disc, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Epicanthus, Congenital heart defects, Congenital Hepatic Fibrosis, Congenital Meningocele, Cryptorchidism, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Disorder Of Eye, Dolichocephaly, Double Ureter, Dwarfism, Dysmorphic Features, Esotropia, Fibrosis Of Pancreas, Foot Polydactyly, Frontal bossing, Fundus Coloboma, Hearing Loss, High palate, Hirschsprung Disease, Hydrocephalus, Hypothalamic Hamartomas, Joubert Syndrome, Joubert Syndrome With Oculorenal Defect, Kidney Disease, Lobar Holoprosencephaly, Macrocephaly, Male Pseudohermaphroditism, Malformation of cortical development, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Multiple Congenital Anomalies, Nephronophthisis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Osteofibrous Dysplasia, Pancreatic Cyst, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Postaxial hand polydactyly, Ptosis, Radial Polydactyly, Renal agenesis, Renal cyst, Renal Insufficiency, Retinal coloboma, Retinal Dystrophy, Rhyns syndrome, Sclerocornea, Scoliosis, Situs Inversus, Sleep Apnea, Strabismus, Syndactyly, Syndromic microphthalmia, Talipes, True Hermaphroditism, Urethral atresia
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188708
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Transmembrane protein 217 |
C6orf128, dJ355M6.2 |
Curated: Bipolar disorder, Basal cell carcinoma, Pulmonary arterial hypertension
Unreviewed: Diabetic Retinopathy, Pigmentary Disorder, Reticulate, With Systemic Manifestations
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188709
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|
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Transmembrane protein 217B |
- |
Curated: N/A
Unreviewed: N/A
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188710
|
|
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Transmembrane protein 218 |
JBTS39 |
Curated: Ciliopathy, Congenital brain malformation, Congenital hypoplasia of part of brain, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Lissencephaly, Lung cancer, Macrogyria, Meckel-gruber syndrome, Microgyria
Unreviewed: Ischemic stroke
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