Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6901 to 6910 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6901
Lysine rich nucleolar protein 1
101F10.1, C16orf88, FAM191A, TSG118
Insomnia

6902
Kinetochore localized astrin (SPAG5) binding protein
C15orf23, HSD11, ROCHIS, SKAP, TRAF4AF1
Androgenetic alopecia, Squamous cell carcinoma, Combined immunodeficiency with faciooculoskeletal anomalies, Combined immunodeficiency with facio-oculo-skeletal anomalies, Roifman syndrome, Secondary malignant neoplasm

6903
Kinetochore associated 1
ROD
Parkinson disease

6904
KPRP N-terminal and LCE C-terminal like protein
C1orf68, LEP7, XP32
Psoriasis

6905
Karyopherin subunit alpha 1
IPOA5, NPI-1, RCH2, SRP1
Parkinson disease, Schizophrenia

6906
Karyopherin subunit alpha 2
IPOA1, PTAC58, QIP2, RCH1, SRP1-alpha, SRP1alpha
Alzheimer disease, Insomnia, Lung disease, Peripheral arterial disease, Prostate cancer, Respiratory system disease, Hypertension, Diabetes mellitus type 2

6907
Karyopherin subunit alpha 3
IPOA4, SPG88, SRP1, SRP1gamma, SRP4, hSRP1
Eczema, Spastic paraplegia, Obstructive pulmonary disease, Inflammatory skin disease, Major depressive disorder, Obesity, Parkinson disease, Psoriasis, Schizophrenia, Diabetes mellitus type 2, Depression

6908
Karyopherin subunit alpha 4
IPOA3, QIP1, SRP3
Bipolar disorder, Cardiovascular disease, Lewy body disease, Myeloproliferative disorder, Prostate cancer, Smooth surface dental caries

6909
Karyopherin subunit alpha 7
IPOA8, OZEMA17
Alzheimer disease, Ankylosing spondylitis, Asthma, Lymphocytic leukemia, Crohn disease, Epilepsy, Inflammatory bowel disease, Intellectual disability, Oocyte maturation defect, Partial corpus callosum agenesis, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

6910
Karyopherin subunit beta 1
IMB1, IPO1, IPOB, Impnb, NTF97
Ankylosing spondylitis, Epithelial ovarian carcinoma, Multiple sclerosis, Myopathy