201
|
|
|
C21orf91 overlapping transcript 1 |
D21S2089E, NCRNA00285 |
Curated: N/A
Unreviewed: N/A
|
202
|
|
|
Chromosome 22 open reading frame 15 |
N27C7-3 |
Curated: N/A
Unreviewed: N/A
|
203
|
|
|
Chromosome 22 open reading frame 23 |
EVG1, dJ1039K5.6 |
Curated: N/A
Unreviewed: N/A
|
204
|
|
|
Chromosome 22 open reading frame 31 |
HS747E2A, bK747E2.1 |
Curated: Cardiovascular disease, Kidney disease, Metabolic syndrome, Diabetes mellitus type 2, Uterine fibroid
Unreviewed: Cardiovascular Diseases
|
205
|
|
|
Chromosome 22 open reading frame 39 |
Pants |
Curated: Central nervous system cancer, Glioblastoma, Glioma
Unreviewed: Impaired Cognition
|
206
|
|
|
Chromosome 22 open reading frame 42 |
dJ90G24.6 |
Curated: Polycystic ovary syndrome, Selective iga deficiency disease, Diabetes mellitus type 2
Unreviewed: Azoospermia
|
207
|
|
|
Chromosome 22 open reading frame 46, pseudogene |
C22orf46 |
Curated: N/A
Unreviewed: N/A
|
208
|
|
|
C2 calcium dependent domain containing 2 |
C21orf25, C21orf258, TMEM24L |
Curated: Colorectal adenoma, Insomnia
Unreviewed: N/A
|
209
|
|
|
C2CD2 like |
DLNB23, TMEM24 |
Curated: N/A
Unreviewed: N/A
|
210
|
|
|
C2 domain containing 3 centriole elongation regulator |
OFD14 |
Curated: Aplasia of the vermis, Gastrointestinal stromal tumor, Jeune thoracic dystrophy, Orofaciodigital syndrome, Schizophrenia, orofaciodigital syndrome type 14
Unreviewed: Alzheimer disease, Aplasia of the epiglottis, Asphyxiating thoracic dystrophy, Atrial Septal Defect, Cerebellar Hypoplasia, Cerebellar vermis agenesis, Ciliopathies, Ciliopathy, Cleft palate, Coloboma of optic disc, Cryptorchidism, Dandy-Walker Syndrome, Developmental Delay, Epispadias, Fundus Coloboma, Holoprosencephaly, Hypoplasia Of Corpus Callosum, Mental retardation, Microcephaly, Mohr Syndrome, Neoplasms, Occipital Encephalocele, Osteochondrodysplasia, Osteofibrous Dysplasia, Patent ductus arteriosus, Penis Agenesis, Periventricular Nodular Heterotopia, Polydactyly, Polymicrogyria, Posteriorly Rotated Ear, Radial Polydactyly, Retinal coloboma, Retinitis, Skeletal Dysplasia, Trigonocephaly, Ventricular septal defect
|