- CT62 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; INTERACTS WITH benzo[a]pyrene; bisphenol A; cisplatin
- Fam227b [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; INTERACTS WITH 17beta-estradiol; aflatoxin B1; beta-lapachone
- him-6 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Enables 3'-5' DNA helicase activity and enzyme binding activity. Involved in several processes, including determination of adult lifespan; meiotic nuclear division; and resolution of DNA recombination intermediates. Located in chromosome and nucleus. Used to study Bloom syndrome. Human ortholog(s) of this gene implicated in Bloom syndrome. Is an ortholog of human BLM (BLM RecQ like helicase).
- PAK6-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; mosaic variegated aneuploidy syndrome 1; INTERACTS WITH cadmium dichloride; resveratrol; valproic acid
- LINC02694 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; Legius syndrome; INTERACTS WITH 2-palmitoylglycerol; aflatoxin B1; benzo[a]pyrene
- LINC00928 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; D-2-hydroxyglutaric aciduria 2; INTERACTS WITH acrylamide; benzo[a]pyrene
- Ankrd63 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; mosaic variegated aneuploidy syndrome 1; INTERACTS WITH iron dichloride; lipopolysaccharide; okadaic acid
- Lysmd2 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; developmental and epileptic encephalopathy 13; INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine; actinomycin D
- LINC02915 [Search on AGR]
Homo sapiens ASSOCIATED WITH Bloom syndrome; colorectal cancer; mosaic variegated aneuploidy syndrome 1; INTERACTS WITH 2-palmitoylglycerol; benzo[a]pyrene; cobalt dichloride
- Blm [Search on AGR]
Homo sapiens The Bloom syndrome is an autosomal recessive disorder characterized by growth deficiency, microcephaly and immunodeficiency among others. It is caused by homozygous or compound heterozygous mutation in the gene encoding DNA helicase RecQ protein on chromosome 15q26. This Bloom-associated helicase unwinds a variety of DNA substrates including Holliday junction, and is involved in several pathways contributing to the maintenance of genome stability. Identification of pathogenic Bloom variants is required for heterozygote testing in at-risk families. [provided by RefSeq, May 2020]