Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
12631 to 12640 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

12631
Sperm associated antigen 8
BS-84, CILD28, CT142, HSD-1, SMP1, SPAG3, hSMP-1
Colorectal cancer, Familial focal epilepsy with variable foci

12632
Sperm associated antigen 9
CT89, HLC-6, HLC4, HLC6, JIP-4, JIP4, JLP, PHET, PIG6
Liver cirrhosis, Myocardial infarction, Schizophrenia

12633
Sperm adhesion molecule 1
HEL-S-96n, HYA1, HYAL1, HYAL3, HYAL5, PH-20, PH20, SPAG15
Atrial fibrillation, Atrial flutter

12634
SPANX family member N1
CT11.6
Chromosome xq28 duplication syndrome

12635
SPANX family member N3
CT11.8, SPANX-N3
Uterine fibroid

12636
SPANX family member N4
CT11.9
Chondromalacia, Conotruncal cardiac defect, Major depressive disorder, Mood disorder, Prostate cancer

12637
Secreted protein acidic and cysteine rich
BM-40, OI17, ON, ONT
Bone fragility with contractures, arterial rupture, and deafness, Carcinogenesis, Cervical disc degenerative disorder, Persistent hepatitis, Colonic neoplasms, Colorectal neoplasms, Desbuquois syndrome, Hepatitis, Hyperalgesia, Intervertebral disc disease, Kidney disease, Myeloid leukemia, Liver cirrhosis, Multiple myeloma, Myocardial ischemia
View all (7 more)

12638
SPARC like 1
MAST 9, MAST9, PIG33, SC1
Congenital stromal corneal dystrophy, Corneal dystrophy, Endometriosis, Epilepsy, Esophageal adenocarcinoma, Gout

12639
Spartin
SPG20, TAHCCP1
Spastic paraplegia, Cerebellar ataxia, Dysarthria, Eye disease, Global developmental delay, Hereditary spastic paraplegia, Strabismus, Troyer syndrome

12640
Spastin
ADPSP, FSP2, SPG4
Atypical femoral fracture, Spastic paraplegia, Cerebral palsy, Littles disease, Neurodevelopmental disorder, Spastic ataxia, Spastic paraplegia, x-linked, Hereditary spastic paraplegia, Hypertension