Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
Log in to save this view

Save This View

Selected (0) TSV CSV PDF
This Page (10) TSV CSV PDF
All Matching (193650) TSV CSV PDF
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
193241 to 193250 of 193650 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

193241
Zinc finger protein 584
-

Curated: Attention deficit hyperactivity disorder

Unreviewed: Breast neoplasm

193242
ZNF584 divergent transcript
-

Curated: N/A

Unreviewed: N/A

193243
Zinc finger protein 585A
Zfp27

Curated: N/A

Unreviewed: N/A

193244
Zinc finger protein 585B
SZFP41, Zfp27

Curated: Alzheimer disease, Obesity

Unreviewed: Leukemia

193245
Zinc finger protein 586
-

Curated: N/A

Unreviewed: Esophageal neoplasm

193246
Zinc finger protein 587
ZF6

Curated: N/A

Unreviewed: N/A

193247
Zinc finger protein 587B
-

Curated: N/A

Unreviewed: Alzheimer disease, Colorectal neoplasm, Down Syndrome, Megakaryocytic Leukemia

193248
Zinc finger protein 587 pseudogene 1
-

Curated: N/A

Unreviewed: N/A

193249
Zinc finger protein 589
SZF1

Curated: Neurodevelopmental disorder, Non-specific syndromic intellectual disability

Unreviewed: Autism, Mental retardation

193250
Zinc finger protein 592
CAMOS, SCAR5

Curated: Anorexia nervosa, Autism, Bipolar disorder, Camos syndrome, Color vision deficiency, Bipolar depression, Dilated cardiomyopathy, Galloway-mowat syndrome, Heart failure, Hirschsprung disease, Hypertrophic cardiomyopathy, Mitral valve prolapse, Osteoarthritis, Sarcoidosis, Schizophrenia, Spinocerebellar ataxia

Unreviewed: Bipolar Disorder, Brain atrophy, Breast Cancer, Breast Carcinoma, CAMOS Syndrome, Cerebellar ataxia, Cerebral Atrophy, Congenital Cerebellar Ataxia, Dysarthria, Galloway-Mowat Syndrome, Intellectual developmental disorder, Manic Disorder, Mental retardation, Microcephaly, Motor delay, Nephrotic Syndrome, Optic Atrophy, Renal Insufficiency, Skin abnormalities, Spinocerebellar Ataxia