901
|
|
|
Transmembrane channel like 8 |
EV2, EVER2, EVIN2 |
Curated: Diabetes mellitus, Epidermodysplasia verruciformis, Diabetes mellitus type 2
Unreviewed: Actinic keratosis, Breast neoplasm, Cafe-au-lait spot, Carcinoma, Carcinoma Of The Head And Neck, Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Epidermodysplasia Verruciformis, Head and neck cancer, Head And Neck Carcinoma, Head and neck neoplasm, Immune system disease, Lupus Erythematosus, Malignant Neoplasm, Melanoma, Neoplasms, Papilloma, Renal cell carcinoma, Seborrheic dermatitis, Skin cancer, Skin carcinoma, Skin disease, Skin Lesion, Skin neoplasm, Squamous cell carcinoma, Uterine disease, Uterine neoplasm
|
902
|
|
|
Transmembrane and coiled-coil domain family 1 |
- |
Curated: Diabetes mellitus type 2
Unreviewed: Hepatocellular carcinoma
|
903
|
|
|
TMCC1 divergent transcript |
TMCC1-AS1 |
Curated: N/A
Unreviewed: N/A
|
904
|
|
|
Transmembrane and coiled-coil domain family 1 pseudogene 1 |
TMCC1P |
Curated: N/A
Unreviewed: N/A
|
905
|
|
|
Transmembrane and coiled-coil domain family 2 |
HUCEP11 |
Curated: Basal cell carcinoma, Melanoma, Dupuytren contracture, Metabolic syndrome, Diabetes mellitus type 2
Unreviewed: N/A
|
906
|
|
|
TMCC2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
907
|
|
|
Transmembrane and coiled-coil domain family 3 |
- |
Curated: Alzheimer disease, Basal cell carcinoma, Schizophrenia, Squamous cell carcinoma
Unreviewed: Hypertension, Lymphocytic Leukemia
|
908
|
|
|
Transmembrane and coiled-coil domains 1 |
CFSMR1, HP10122, PCIA3, PNAS-136, TMCC4 |
Curated: Bone disease, Cerebrofaciothoracic dysplasia, Congenital musculoskeletal anomalies, Craniofacial abnormalities, Craniofacial dysmorphism skeletal anomalies intellectual disability syndrome, Eye disease, Glaucoma, Intellectual developmental disorder, Open angle glaucoma, Oropharyngeal cancer, Tooth abnormalities
Unreviewed: Accessory Nipple, Angle Closure Glaucoma, Atrial Septal Defect, Autism, Bipolar disorder, Bone Disease, Brachycephaly, Cerebral cortical atrophy, Cerebrofaciothoracic Dysplasia, Cleft Palate And Bilateral Cleft Lip, Colorectal neoplasm, Complement component deficiency, Congenital Epicanthus, Congenital Musculoskeletal Anomalies, Congenital myopathy with fiber type disproportion, Cryptorchidism, Development Disorder, Developmental Delay, Dwarfism, Dysmorphic Features, Dysmorphism, Epilepsy, Facial dysmorphism, Hearing Loss, High palate, Hypoplasia Of Corpus Callosum, Hypoplasia of the maxilla, Hypotonia, Impaired Cognition, Macrocephaly, Macrostomia, Malignant Neoplasm, Megalencephalic Leukoencephalopathy With Subcortical Cysts, Mental retardation, Micrognathism, Motor delay, Multiple Congenital Anomalies, Odontome, Open Angle Glaucoma, Osteoporosis, Periventricular Leukomalacia, Poliosis, Postaxial hand polydactyly, Posteriorly Rotated Ear, Pulmonary Stenosis, Renal agenesis, Renal aplasia, Rib fusion, Schizophrenia, Scoliosis, Sprengel Deformity, Squamous cell carcinoma, Strabismus, Synophrys, Uranostaphyloschisis, Van maldergem syndrome
|
909
|
|
|
TMCO1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Glaucoma
|
910
|
|
|
Transmembrane and coiled-coil domains 2 |
dJ39G22.2 |
Curated: N/A
Unreviewed: N/A
|