Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
1051 to 1060 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1051
Solute carrier family 25 member 11
OGC, PGL6, PPGL6, SLC20A4
Adrenal gland pheochromocytoma, Aniridia, Capillary hemangioma of retina, Congestive heart failure, Cranial nerve compression, Episodic paroxysmal anxiety, Extra-adrenal pheochromocytoma, Glomerulonephritis, Glomerulosclerosis, Hearing loss, Hereditary pheochromocytoma-paraganglioma, Hypercalcemia, Hypertension, Hypertensive retinopathy, Panic disorder
View all (7 more)

1052
SPARC like 1
MAST 9, MAST9, PIG33, SC1
Endometrioma, Endometriosis, Epilepsy

1053
Speckle type BTB/POZ protein
BTBD32, NEDMACE, NEDMIDF, NSDVS1, NSDVS2, TEF2
Ductal carcinoma, Endometrial cancer, Endometrial neoplasms, Endometrial carcinoma, Malignant uterine corpus neoplasm, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer

1054
Sushi repeat containing protein X-linked
DRS, ETX1, HEL-S-83p, SRPX1
Common variable immunodeficiency, Liver carcinoma

1055
Solute carrier family 10 member 7
C4orf13, P7, SSASKS
Acquired kyphoscoliosis, Amelogenesis imperfecta, Cholestasis, Congenital kyphoscoliosis, Dwarfism, High palate, Hip contracture, Osteochondrodysplasia, Scoliosis, Skeletal dysplasia, Thoracic hypoplasia

1056
Solute carrier family 7 member 6 opposite strand
EPM12, Iwr1
Schizophrenia

1057
Syntaxin 7
-
Infantile spasms, Malformation of cortical development, Neuronal heterotopia, Pachygyria

1058
Src like adaptor 2
C20orf156, MARS, SLAP-2, SLAP2
Charcot-marie-tooth disease, Pulmonary alveolar proteinosis, Spastic paraplegia

1059
SLIT and NTRK like family member 6
DFNMYP
Deafness and myopia, Hearing impairment, Hearing loss, High myopia-sensorineural deafness syndrome, Mental retardation, Myopia, Non-syndromic sensorineural deafness

1060
SH3GL interacting endocytic adaptor 1
-
Mental depression