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
11811 to 11820 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11811
Serpin family D member 1
D22S673, HC2, HCF2, HCII, HLS2, LS2, THPH10
Carotid artery thrombosis, Deep vein thrombosis, Heparin cofactor 2 deficiency, Thrombophilia, Venous thromboembolism

11812
Serpin family E member 1
PAI, PAI-1, PAI1, PLANH1
Alzheimer disease, Amyloidosis, Asthma, Atherosclerosis, Autism, Behcet disease, Cholelithiasis, Ischemic heart disease, Colitis, Congenital plasminogen activator inhibitor deficiency type 1, Congestive heart failure, Coronary artery disease, Experimental diabetes, Diabetic angiopathies, Diabetic neuropathy
View all (33 more)

11813
Serpin family E member 2
GDN, GDNPF, PI-7, PI7, PN-1, PN1, PNI
Alzheimer disease

11814
Serpin family F member 1
EPC-1, OI12, OI6, PEDF, PIG35
Alzheimer disease, Bone fragility with contractures, arterial rupture, and deafness, Adenoid cystic carcinoma, Corneal neovascularization, Corneal ulcer, Desbuquois syndrome, Diabetes mellitus type 2, Diabetic angiopathies, Diabetic peripheral angiopathy, Diabetic retinopathy, Endometriosis, Obesity, Osteogenesis imperfecta, Osteoporosis, Osteoporosis-pseudoglioma syndrome
View all (7 more)

11815
Serpin family F member 2
A2AP, AAP, ALPHA-2-PI, API, PLI, alpha2AP
Alpha-2-plasmin inhibitor deficiency, Alzheimer disease, Congenital plasmin inhibitor deficiency, Congenital alpha-2-antiplasmin deficiency, Gout, Hodgkin lymphoma, Hypogonadism, Scoliosis, Diabetes mellitus type 2

11816
Serpin family G member 1
C1IN, C1INH, C1NH, HAE1, HAE2
Angioedema, C1 esterase inhibitor deficiency, Central nervous system cancer, Ischemic stroke, Complement component deficiency, Glioblastoma, Glioma, Hereditary angioedema, Hereditary c1 esterase inhibitor deficiency, Insomnia, Liver cirrhosis, Lung neoplasms, Lupus nephritis, Macular degeneration, Neurotic disorder
View all (4 more)

11817
Serpin family H member 1
AsTP3, CBP1, CBP2, HSP47, OI10, PIG14, PPROM, RA-A47, SERPINH2, gp46
Bone fragility with contractures, arterial rupture, and deafness, Colorectal cancer, Coronary artery disease, Desbuquois syndrome, Endometrial neoplasms, Heart disease, Liver cirrhosis, Myocardial infarction, Myocardial ischemia, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

11818
Serpin family I member 1
HNS-S1, HNS-S2, PI12, neuroserpin
Cavernous malformations of cns, Congenital neurologic anomalies, Diabetic retinopathy, Hypertension, Metabolic syndrome, Progressive myoclonic epilepsy, Schizophrenia, Diabetes mellitus type 2

11819
SERTA domain containing 1
SEI1, TRIP-Br1, TRIPBR1
Colonic neoplasms, Mood disorder

11820
SERTA domain containing 2
Sei-2, TRIP-Br2, TRIPBR2
Astrocytoma, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Glioblastoma, Glioma, Hemorrhoid