Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11621 to 11630 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11621
Schwannomin interacting protein 1
SCHIP-1
B-cell acute lymphoblastic leukemia, Asthma, Color vision deficiency, Neurodevelopmental disorder, Congenital heart disease, Conotruncal cardiac defect, Non-specific syndromic intellectual disability, Biliary cholangitis, Scoliosis, Systemic lupus erythematosus

11622
SLP adaptor and CSK interacting membrane protein
C17orf87, UNQ5783
Alzheimer disease, Head and neck cancer

11623
Scinderin
-
Scoliosis, Small cell lung carcinoma

11624
Sodium channel and clathrin linker 1
CAP-1A, CAP1A
Astigmatism, Bardet-biedl syndrome, Obstructive pulmonary disease, Ciliopathy, Color vision deficiency, Cone-rod dystrophy, Global developmental delay, Hyperopia, Nystagmus, Optic atrophy, Orofaciodigital syndrome, Retinitis pigmentosa, Senior-loken syndrome

11625
Selenocysteine lyase
SCL, hSCL
Psoriasis

11626
Scm polycomb group protein homolog 1
Scml3
Atrial fibrillation, Atrial flutter, Cardioembolic stroke

11627
Scm polycomb group protein like 2
-
Medulloblastoma

11628
Scm polycomb group protein like 4
dJ47M23.1
Alzheimer disease, Color vision deficiency, Coronary artery disease, Disorder of ear, Schizophrenia, Scoliosis

11629
Sodium voltage-gated channel alpha subunit 10
FEPS2, Nav1.8, PN3, SNS
Atrial fibrillation, Atrial flutter, Atrioventricular block, Autism, Brugada syndrome, Cardiac arrhythmia, Congenital insensitivity to pain, Episodic pain syndrome, Long qt syndrome, Sick sinus syndrome, Hyperalgesia, Migraine, Orofacial cleft, Paroxysmal extreme pain disorder, Erythromelalgia
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11630
Sodium voltage-gated channel alpha subunit 11
FEPS3, HSAN7, NAV1.9, NaN, PN5, SCN12A, SNS-2
Hereditary sensory and autonomic neuropathy, Charcot-marie-tooth disease, Congenital insensitivity to pain, Congenital pain insensitivity, Dominantly inherited sensory neuropathy, Episodic pain syndrome, Motor neuron disease, Hyperalgesia, Migraine, Osteoarthritis, Paroxysmal extreme pain disorder, Erythromelalgia, Sensory neuropathy