Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
1391 to 1400 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1391
Solute carrier family 7 member 9
BAT1, CSNU3
Cystinuria, Drachtman weinblatt sitarz syndrome, Kidney disease, Kidney failure, Nephritis, Nephrolithiasis, Renal insufficiency

1392
-
DHS6S1, MCDR1, PBCRA
North carolina macular dystrophy

1393
TBC1 domain family member 8
AD3, GRAMD8, HBLP1, TBC1D8A, VRP
Impaired cognition, Osteoporosis

1394
Chromogranin B
SCG1
Schizophrenia

1395
Cell division cycle 37, HSP90 cochaperone
P50CDC37
Ankylosing spondylitis, Crohn disease, Hypercholesterolemia, Inflammatory bowel disease, Multiple sclerosis

1396
Interleukin 1 receptor accessory protein like 1
IL-1-RAPL-1, IL-1RAPL-1, IL1R8, IL1RAPL, IL1RAPL-1, MRX10, MRX21, MRX34, OPHN4, TIGIRR-2
Atkin-flaitz syndrome, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Bronchopulmonary dysplasia, Cardiovascular diseases, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Macrocephaly, Malocclusion, Meckel diverticulum, Melanoma, Mental retardation, x-linked
View all (7 more)

1397
CAMP-dependent protein kinase inhibitor gamma
PKI-gamma
Adenosine deaminase deficiency, Ankylosing spondylitis, Cholangitis, Crohn disease, Psoriasis, Severe combined immunodeficiency disease, Ulcerative colitis

1398
DNA meiotic recombinase 1
DMC1H, LIM15, dJ199H16.1
Ovarian failure

1399
Glomulin, FKBP associated protein
FAP, FAP48, FAP68, FKBPAP, GLML, GVM, VMGLOM
Blue rubber bleb nevus, Venous malformation, Glomuvenous malformation

1400
Coronin 1A
CLABP, CLIPINA, HCORO1, IMD8, TACO, p57
Anaplastic carcinoma, Carcinoma, Developmental delay, Immunodeficiency, Immunologic deficiency syndromes, Lymphopenia, Omenn syndrome, Severe combined immunodeficiency disease