Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12701 to 12710 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12701
SPRY domain containing 3
-
Oligodendroglioma, Diabetes mellitus type 1, Diabetes mellitus type 2

12702
SPRY domain containing 4
-
Gout

12703
SPRY domain containing 7
C13orf1, CLLD6
Hypertension

12704
SplA/ryanodine receptor domain and SOCS box containing 1
SSB-1, SSB1
Aneurysm, Aortic aneurysm, Asthma, Eczema, Dental caries, Respiratory system disease, Hypertension, Venous thromboembolism

12705
SplA/ryanodine receptor domain and SOCS box containing 2
GRCC9, SSB2
Colorectal cancer, Corneal astigmatism, Hyperopia

12706
SplA/ryanodine receptor domain and SOCS box containing 3
C16orf31, SSB3
Ocular hypertension

12707
SplA/ryanodine receptor domain and SOCS box containing 4
SSB-4, SSB4
Astrocytoma, Central nervous system cancer, Gastric cancer, Glioma, Schizophrenia, Stroke

12708
Spectrin alpha, erythrocytic 1
EL2, HPP, HS3, SPH3, SPTA
Anemia, Hemolytic anemia, Hereditary elliptocytosis, Spherocytosis

12709
Spectrin alpha, non-erythrocytic 1
DEE5, DEVEP, EIEE5, HMN11, HMND11, NEAS, SPG91, SPTA2
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Degenerative disorder, Developmental and epileptic encephalopathy, Developmental delay with or without epilepsy, Developmental disability, Distal spinal muscular atrophy, Partial epilepsy, Rolandic epilepsy, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Jeune thoracic dystrophy, Neurodegenerative disorder, Neurodevelopmental disorder, Neuromuscular disease, Distal hereditary motor neuropathy
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12710
Spectrin beta, erythrocytic
EL3, HS2, HSPTB1, SPH2
Anemia, Hemolytic anemia, Neonatal anemia, Perinatal hemolytic anemia, Chagas cardiomyopathy, Chudley-mccullough syndrome, Hereditary elliptocytosis, Obesity, Spherocytosis, Diabetes mellitus type 2