|
91
|
|
|
SIX homeobox 2 |
- |
Amyotrophic lateral sclerosis, Congenital anomalies of kidney and urinary tract, Dwarfism, Frontal bossing, Frontonasal dysplasia, Kidney disease, Lateral sclerosis, Macrocephaly, Metopic synostosis, Nephroblastoma, Posteriorly rotated ear, Ptosis, Wilms tumor |
|
92
|
|
|
Serine and arginine rich splicing factor 10 |
FUSIP1, FUSIP2, NSSR, PPP1R149, SFRS13, SFRS13A, SRp38, SRrp40, TASR, TASR1, TASR2 |
|
|
93
|
|
|
Solute carrier family 17 member 3 |
GOUT4, NPT4, UAQTL4 |
|
|
94
|
|
|
Septin 9 |
AF17q25, MSF, MSF1, NAPB, PNUTL4, SEPT9, SINT1, SeptD1 |
Blepharophimosis, Brachial plexus neuralgia, Brachial plexus neuropathy, Cardiovascular diseases, Cervicobrachial neuralgia, Congenital epicanthus, Dwarfism, Dyssomnia, Hereditary neuralgic amyotrophy, Leukemia, Microstomia, Myeloid leukemia, Myocardial infarction, Nervous system diseases, Neuralgic amyotrophy, Polyneuropathy, Ptosis, Sleep disorders, Speech disorders, Sprengel deformityView all (5 more) |
|
95
|
|
|
SHH signaling and ciliogenesis regulator SDCCAG8 |
BBS16, CCCAP, CCCAP SLSN7, HSPC085, NPHP10, NY-CO-8, SLSN7, hCCCAP |
Bardet-biedl syndrome, Bipolar disorder, Bronchiolitis, Cataract, Ciliopathies, Congenital hepatic fibrosis, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Cystic kidney disease, Developmental delay, Disorder of eye, Dwarfism, Hypertension, Hypogonadism, Impaired cognition, Kidney disease, Kidney failure, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Nephronophthisis, Nephrotic syndrome, Nystagmus, Obesity, Otitis media, Premature menopause, Renal agenesis, Renal cyst, Renal dysplasia, Renal dysplasia and retinal aplasia, Renal insufficiency, Retinal diseases, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Schizoaffective disorder, Schizophrenia, Senior-loken syndrome, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (27 more) |
|
96
|
|
|
StAR related lipid transfer domain containing 10 |
CGI-52, NY-CO-28, PCTP2, SDCCAG28 |
|
|
97
|
|
|
Snf2 related CREBBP activator protein |
DEHMBA, DOMO1, EAF1, FLHS, SWR1 |
Adenocarcinoma, Brachydactyly, Camptodactyly of fingers, Celiac disease, Short clavicles, Congenital hypoplasia of penis, Congenital posterior urethral valves, Developmental delay, Dwarfism, Dysmorphic features, Exotropia, Facial wart, Floating-harbor syndrome, Hyperopia, Hyperopic astigmatism, Macrostomia, Macrotia, Malabsorption syndrome, Mental retardation, Micrognathism, Microstomia, Multiple congenital anomalies, Multiple myeloma, Neurodevelopmental disorders, Nystagmus, Oral aversion, Oral cleft, Otitis media, Penile hypospadias, Persistent pupillary membranes, Posteriorly rotated ear, Sleep apnea, Speech disorders, Strabismus, Submucosal cleft palate, TrigonocephalyView all (21 more) |
|
98
|
|
|
Solute carrier family 26 member 1 |
CAON, CAON1, EDM4, HYSULF, SAT-1, SAT1 |
|
|
99
|
|
|
Solute carrier family 22 member 7 |
NLT, OAT2, hOAT11 |
|
|
100
|
|
|
SUB1 regulator of transcription |
P15, PC4, p14 |
|
