|
2301
|
|
|
PDLIM1 interacting kinase 1 like |
CLIK1L, STK35L2 |
|
|
2302
|
|
|
Claudin 19 |
HOMG5 |
Astigmatism, Coloboma of macula, Congenital exomphalos, Fundus coloboma, Hypertension, Hypomagnesemia, Hypomagnesemia renal, with ocular involvement, Hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement, Kidney disease, Medullary nephrocalcinosis, Meier blumberg imahorn syndrome, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus, Retinal coloboma, Rod-cone dystrophy, StrabismusView all (3 more) |
|
2303
|
|
|
Cilia and flagella associated protein 57 |
SPGF95, VWS2, WDR65 |
|
|
2304
|
|
|
Catenin alpha 1 |
CAP102, MDBS2, MDPT2 |
Macular dystrophy, patterned, Hereditary cancer syndrome, Colorectal neoplasms, Colorectal cancer, Drusen, Gastric cancer, Gastrointestinal stromal tumor, Hereditary nonpolyposis colorectal cancer, Leukemia, Myelodysplastic syndrome, Myeloid leukemia, Patterned dystrophy of retinal pigment epithelium |
|
2305
|
|
|
Steroid receptor associated and regulated protein |
C1orf64, ERRF |
|
|
2306
|
|
|
Catenin alpha 2 |
CAP-R, CAPR, CDCBM9, CT114, CTNR |
Agyria, Alzheimer disease, Breast carcinoma, Cerebellar hypoplasia, Cortical dysplasia with other brain malformations, Developmental delay, Gastric cancer, Hypoplasia of corpus callosum, Leukemia, Lissencephaly, Mental retardation, Narcolepsy, Pachygyria, Schizophrenia, Spastic quadriplegia, Stomach neoplasmsView all (1 more) |
|
2307
|
|
|
Ring finger protein 187 |
RACO-1, RACO1 |
|
|
2308
|
|
|
Pyrin and HIN domain family member 1 |
IFIX |
|
|
2309
|
|
|
Cystinosin, lysosomal cystine transporter |
CTNS-LSB, PQLC4, SLC66A4 |
Cerebral atrophy, Cystinosis, Dwarfism, Dysphagia, Erosion of cornea, Exocrine pancreatic insufficiency, Fanconi syndrome, Frontal bossing, Hypohidrosis, Hypophosphatemic rickets, Hypopigmentation disorder, Impaired cognition, Juvenile nephropathic cystinosis, Kidney disease, Nephrolithiasis, Nephropathic cystinosis, Ocular cystinosis, Phosphate diabetes, Hypothyroidism, Rachitic rosary, Renal insufficiency, Renal tubular disorder, Retinal diseases, Retinitis pigmentosa, Rickets, Testicular hypogonadismView all (11 more) |
|
2310
|
|
|
APCDD1L divergent transcript |
APCDD1L-AS1 |
|
