|
111
|
|
|
Tandem C2 domains, nuclear |
C14orf47, C2CD1, MTAC2D1, TAC2N, Tac2-N |
|
|
112
|
|
|
Transmembrane protein 266 |
C15orf27, HVRP1, HsHVRP1, hTMEM266 |
|
|
113
|
|
|
Transmembrane protein 219 |
IGFBP-3R, IGFBP3R |
|
|
114
|
|
|
Transmembrane protein 132E |
DFNB99 |
|
|
115
|
|
|
Tetratricopeptide repeat domain 39C |
C18orf17, HsT2697 |
|
|
116
|
|
|
Transcription elongation factor A N-terminal and central domain containing 2 |
C1orf83 |
|
|
117
|
|
|
Transmembrane protein 125 |
- |
|
|
118
|
|
|
TBC1 domain family member 20 |
C20orf140, WARBM4 |
Cataract, Central visual impairment, Cerebellar atrophy, Cerebral cortical atrophy, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Dwarfism, Fundus coloboma, Glaucoma, High palate, Hydronephrosis, Hypoplasia of corpus callosum, Mental retardation, Macrotia, Micro syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Microstomia, Nervous system diseases, Optic atrophy, Pachygyria, Penis agenesis, Ptosis, Retinal coloboma, Scoliosis, Spastic quadriplegia, Warburg micro syndromeView all (15 more) |
|
119
|
|
|
Transport and golgi organization 2 homolog |
C22orf25, MECRCN |
Anemia, Brain atrophy, Cardiovascular diseases, Cerebellar atrophy, Cerebral atrophy, Developmental delay, Developmental regression, Dysarthria, Exotropia, Hearing loss, Hypoglycemia, Hypothyroidism, Intermittent lactic acidemia, Ketonuria, Mental retardation, Oropharyngeal dysphagia, Ventricular fibrillationView all (2 more) |
|
120
|
|
|
Transmembrane protein 18 |
lncND |
|
