Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
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Chromosome:
Gene type:
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
3161 to 3170 of 193650 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3161
Chromosome 17 open reading frame 114
-

Curated: N/A

Unreviewed: N/A

3162
Chromosome 17 open reading frame 50
-

Curated: N/A

Unreviewed: N/A

3163
Chromosome 17 open reading frame 58
-

Curated: Alzheimer disease, Insomnia, Lung disease, Prostate cancer, Respiratory system disease, Hypertension, Diabetes mellitus type 2

Unreviewed: Diabetes Mellitus

3164
Chromosome 17 open reading frame 67
-

Curated: Androgenetic alopecia, Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Orofacial cleft, Osteoarthritis, Psoriasis, Retinal detachment, Sclerosing cholangitis, Sleep apnea, Amyotrophic lateral sclerosis, Ulcerative colitis

Unreviewed: Alzheimer disease, Androgen-Insensitivity Syndrome, Ankylosing Spondylitis, Cholangitis, Crohn Disease, Hemolytic Uremic Syndrome, Inflammatory Bowel Disease, Nephrotic Syndrome

3165
Chromosome 17 open reading frame 75
NJMU-R1, SRI2

Curated: N/A

Unreviewed: Orofaciodigital syndrome, Retinoblastoma

3166
Chromosome 17 open reading frame 78
-

Curated: N/A

Unreviewed: N/A

3167
Chromosome 17 open reading frame 99
IL-40, UNQ464

Curated: Diabetes mellitus type 1, Diabetes mellitus type 2

Unreviewed: B-Cell Lymphoma, Uterine disease

3168
Chromosome 18 putative open reading frame 15
HsT3231

Curated: N/A

Unreviewed: N/A

3169
Chromosome 18 open reading frame 32
GPIBD25

Curated: Glycosylphosphatidylinositol biosynthesis defect

Unreviewed: Alzheimer disease

3170
C18orf32 pseudogene 1
-

Curated: N/A

Unreviewed: N/A