|
2601
|
|
|
DEAD-box helicase 6 |
HLR2, IDDILF, P54, RCK, Rck/p54 |
|
|
2602
|
|
|
Serine palmitoyltransferase small subunit B |
ADMP, C3orf57, SSSPTB |
|
|
2603
|
|
|
Dmx like 1 |
- |
|
|
2604
|
|
|
Xin actin binding repeat containing 1 |
CMYA1, Xin |
|
|
2605
|
|
|
Ring finger protein 168 |
RIDL, hRNF168 |
Arthritis, Bronchitis, Conjunctival telangiectasis, Demyelinating neuropathy, Developmental delay, Dwarfism, Enlarged lymph nodes, Immunologic deficiency syndromes, Lung diseases, Microcephaly, Mood swings, Nocturnal enuresis, Otitis media, Postnatal asphyxia, Pulmonary fibrosis, Respiratory failure, Riddle syndrome, Sinusitis, Specific learning disorderView all (4 more) |
|
2606
|
|
|
TLE family member 5, transcriptional modulator |
AES, AES-1, AES-2, ESP1, GRG, GRG5, Grg-5 |
|
|
2607
|
|
|
DEAD-box helicase 10 |
Dbp4, HRH-J8 |
|
|
2608
|
|
|
DEAD/H-box helicase 11 |
CHL1, CHLR1, KRG2, WABS |
Clinodactyly, Coloboma of optic disc, Congenital epicanthus, Cutis marmorata, Developmental delay, High palate, Macrostomia, Mental retardation, Microcephaly, Syndactyly of the toes, Ventricular septal defect, Warsaw breakage syndrome |
|
2609
|
|
|
Prickle planar cell polarity protein 2 |
EPM5 |
|
|
2610
|
|
|
Bardet-Biedl syndrome 12 |
C4orf24 |
Bardet-biedl syndrome, Ciliopathies, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Disorder of eye, Dwarfism, Hypertension, Hypogonadism, Impaired cognition, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Myopia, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, Polydactyly, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (10 more) |
