|
601
|
|
|
ATPase copper transporting beta |
PWD, WC1, WD, WND |
Alzheimer disease, Anaptoglobinemia, Breast neoplasm, Carcinoma, Persistent hepatitis, Colorectal neoplasm, Congenital disorder of glycosylation, Deafness, Developmental and epileptic encephalopathy, Dyslipidemias, Fatty liver, Fatty liver, alcoholic, Hepatitis, Hepatolenticular degeneration, Kidney neoplasm, Liver cirrhosis, Liver disease, Liver failure, Liver neoplasm, Major depressive disorder, Intellectual developmental disorder, Mouth neoplasm, Neuropathy, Optic neuritis, Ovarian neoplasm, Prostatic neoplasm, Sensory peripheral neuropathy, Spastic ataxia, Squamous cell carcinoma, Depression, Wilson diseaseView all (16 more) |
|
602
|
|
|
Anillin, actin binding protein |
FSGS8, Scraps, scra |
Appendicitis, Hepatocellular carcinoma, Kidney disease, Coronary artery disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Steroid-resistant nephrotic syndrome, Nephrotic syndrome, Focal segmental glomerulosclerosis , Obesity, Polycystic ovary syndrome, Prostate cancer |
|
603
|
|
|
ATPase family AAA domain containing 2B |
- |
|
|
604
|
|
|
Ankyrin repeat and IBR domain containing 1 |
- |
|
|
605
|
|
|
ATR checkpoint kinase |
FCTCS, FRP1, MEC1, SCKL, SCKL1 |
|
|
606
|
|
|
ADAMTS like 4 |
ADAMTSL-4, ECTOL2, TSRC1 |
|
|
607
|
|
|
Amyloid beta precursor protein binding family B member 1 interacting protein |
INAG1, PREL1, RARP1, RIAM |
|
|
608
|
|
|
Ankyrin repeat domain 16 |
- |
|
|
609
|
|
|
ATRX chromatin remodeler |
JMS, MRX52, RAD54, RAD54L, XH2, XNP, ZNF-HX |
Alpha thalassemia x-linked intellectual disability, Atr-x syndrome, Adenoid cystic carcinoma, Congenital neurologic anomalies , Craniofacial abnormalities, Cryptorchidism, Cushing syndrome, Developmental disability, Glioma, Global developmental delay, Growth disorder, Hemoglobin barts fetalis syndrome, Hemoglobin h disease, Intellectual developmental disorder, Intellectual developmental disorder hypotonic x-linked, Male infertility single gene azoospermia, Intellectual developmental disorder, x-linked, Myelodysplastic syndrome, Neuroblastoma, Neurodevelopmental disorders, Pancreatic neoplasm, Penile disease, Cushing's disease, Schizophrenia, X-linked alpha-thalassemia-intellectual disability syndrome, X-linked intellectual disabilityView all (11 more) |
|
610
|
|
|
ARF like GTPase 15 |
ARFRP2 |
Barrett esophagus, Cardiovascular disease, Coronary artery disease, Diabetes mellitus, Esophageal adenocarcinoma, Gout, Kidney disease, Metabolic syndrome, Migraine, Nonalcoholic fatty liver disease, Psychiatric disorders, Rheumatoid arthritis, Schizophrenia, Diabetes mellitus, type 2, Upper aerodigestive tract neoplasm |
