431
|
|
|
SHC adaptor protein 4 |
RaLP, SHCD |
|
432
|
|
|
SHC binding and spindle associated 1 |
PAL |
|
433
|
|
|
Src homology 2 domain containing E |
- |
|
434
|
|
|
Src homology 2 domain containing F |
- |
|
435
|
|
|
Shiftless antiviral inhibitor of ribosomal frameshifting |
C19orf66, IRAV, RyDEN, SFL |
|
436
|
|
|
Sonic hedgehog signaling molecule |
HHG1, HLP3, HPE3, MCOPCB5, SMMCI, ShhNC, TPT, TPTPS |
Anemia, Asthma, Autism, Preaxial polydactyly with upper back hypertrichosis, Byzanthine arch palate, Hepatocellular carcinoma, Obstructive pulmonary disease, Colobomatous microphthalmia, Color vision deficiency, Corneal astigmatism, Desbuquois syndrome, Skeletal system disorder, Dry eye syndrome, Eye abnormalities, Facial dysmorphism syndrome, Gout, Hemolytic anemia, Hirschsprung disease, Holoprosencephaly, Microform holoprosencephaly, Microphthalmia, Microphthalmos, Syntelencephaly, Neurodevelopmental disorder, Obesity, Secondary parkinson disease, Partial agenesis of corpus callosum, Peripheral arterial disease, Polydactyly, Schizencephaly, Semilobar holoprosencephaly, Septo-optic dysplasia, Septopreoptic holoprosencephaly, Skeletal system disease, Syndactyly, Testicular disease, Triphalangeal thumb-polysyndactyly syndrome, Urinary bladder cancerView all (23 more) |
437
|
|
|
Shisa family member 2 |
C13orf13, PRO28631, TMEM46, WGAR9166, bA398O19.2, hShisa |
|
438
|
|
|
Shisa family member 3 |
hShisa3 |
|
439
|
|
|
Shisa family member 4 |
C1orf40, TMEM58 |
|
440
|
|
|
Shisa family member 6 |
- |
Alzheimer disease, Conotruncal cardiac defect, Developmental dysplasia of the hip, Eye disease, Gastroesophageal reflux disease, Hyperopia, Insomnia, Irritable bowel syndrome, Obesity, Schizophrenia, Squamous cell carcinoma, Stroke |