Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11751 to 11760 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11751
Serpin family B member 5
PI5, maspin
Breast neoplasms, Ductal carcinoma of breast, Colonic neoplasms, Colorectal neoplasms

11752
Serpin family B member 6
CAP, DFNB91, MSTP057, PI-6, PI6, PTI, SPI3
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Lymphocytic leukemia, Crohn disease, Deafness, Hearing impairment, Hearing loss, Inflammatory bowel disease, Nonsyndromic hearing loss, Usher syndrome, Vitiligo

11753
Serpin family B member 7
MEGSIN, PPKN, TP55
Asthma, Iga nephropathy, Respiratory system disease

11754
Serpin family B member 8
C18orf53, CAP2, PI-8, PI8, PSS5
Generalized anxiety disorder, Major depressive disorder, Peeling skin syndrome, Psoriasis

11755
Serpin family B member 9
CAP-3, CAP3, PI-9, PI9
Chloracne, Venous thromboembolism, Vitiligo

11756
Serpin family C member 1
AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2, THPH7
Angina pectoris, Antithrombin deficiency, Blood coagulation disorder, Brain injuries, Cerebral hemorrhage, Cerebral thrombosis, Craniocerebral trauma, Deep vein thrombosis, Disseminated intravascular coagulation, Hereditary antithrombin deficiency, Insomnia, Intracranial thrombosis, Liver failure, Nephrotic syndrome, Psychiatric disorders
View all (4 more)

11757
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

11758
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, Diabetic angiopathies, Diabetic neuropathy, Diabetic peripheral angiopathy
View all (31 more)

11759
Serpin family E member 2
GDN, GDNPF, PI-7, PI7, PN-1, PN1, PNI
Alzheimer disease

11760
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)