Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
2901 to 2910 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2901
Phospholipase D family member 5
PLDC
Autism

2902
Sperm associated antigen 17
CT143, PF6, SPGF55
Alopecia, Breast carcinoma, Colorectal cancer, Brain malformation, Cranioectodermal dysplasia, Non-syndromic male infertility due to sperm motility disorder

2903
Iron-sulfur cluster assembly factor IBA57
C1orf69, MMDS3, SPG74
Arthrogryposis multiplex congenita, Cerebellar atrophy, Cerebral atrophy, Developmental regression, Distal amyotrophy, Distal peripheral sensory neuropathy, Epileptic encephalopathy, High palate, Hypoplasia of corpus callosum, Impaired cognition, Leukodystrophy, Microcephaly, Multiple mitochondrial dysfunctions syndrome, Nystagmus, Optic atrophy
View all (5 more)

2904
Long intergenic non-protein coding RNA 528
C22orf37
Asthma

2905
Apolipoprotein B mRNA editing enzyme catalytic subunit 3A
A3A, ARP3, PHRBN, bK150C2.1
Arthritis, Benign neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Juvenile arthritis, Malignant neoplasm, Marfan syndrome, Neoplasms, Nonorganic psychosis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Psychosis, Still disease

2906
Cilia and flagella associated protein 221
CILD55, FAP221, PCDP1
Attention deficit hyperactivity disorder, Chronic obstructive pulmonary disease, Ciliary dyskinesia, Bronchitis, Kartagener syndrome

2907
ETS transcription factor ELK3
ERP, NET, SAP-2, SAP2
Breast cancer, Mammary neoplasms, Breast carcinoma, Heart failure, Lymphoblastic leukemia, Marfan syndrome

2908
Von Willebrand factor A domain containing 3B
SCAR22
Spinocerebellar ataxia, Cerebellar atrophy, Dysarthria, Hypoplasia of corpus callosum, Mental retardation, Nystagmus

2909
ALMS1 pseudogene 1
ALMS1L, ALMS1P
Kidney disease, Kidney failure

2910
Tet methylcytosine dioxygenase 3
BEFAHRS, hCG_40738
Autism spectrum disorder, Autism, Developmental delay, Macrocephaly, Mental retardation, Movement disorders