BRCA2
protein-coding gene in the species Homo sapiens
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BRCA2
Summary
BRCA2 is a gene[1].
Key Facts
- BRCA2's instance of is recorded as gene[2].
- BRCA2 is a type of protein-coding gene[3].
- BRCA2's Commons category is recorded as BRCA2[4].
- BRCA2's HomoloGene ID is recorded as 41[5].
- BRCA2's genomic start is recorded as 32889611[6].
- BRCA2's genomic start is recorded as 32315086[7].
- BRCA2's genomic end is recorded as 32973805[8].
- BRCA2's genomic end is recorded as 32400268[9].
- BRCA2's ortholog is recorded as Brca2[10].
- BRCA2's ortholog is recorded as Brca2[11].
- BRCA2's encodes is recorded as BRCA2 DNA repair associated[12].
- BRCA2's found in taxon is recorded as Homo sapiens[13].
- BRCA2's chromosome is recorded as human chromosome 13[14].
- BRCA2's genetic association is recorded as BRCA2 hereditary breast and ovarian cancer syndrome[15].
- BRCA2's genetic association is recorded as Fanconi anemia complementation group D1[16].
- BRCA2's genetic association is recorded as breast carcinoma[17].
- BRCA2's genetic association is recorded as prostate carcinoma[18].
- BRCA2's genetic association is recorded as cerebellar medulloblastoma[19].
- BRCA2's genetic association is recorded as urogenital neoplasm[20].
- BRCA2's genetic association is recorded as ovarian neoplasm[21].
- BRCA2's genetic association is recorded as hereditary breast ovarian cancer[22].
- BRCA2's strand orientation is recorded as forward strand[23].
- BRCA2's exact match is recorded as http://identifiers.org/ncbigene/675[24].
- BRCA2's cytogenetic location is recorded as 13q13.1[25].
- BRCA2's expressed in is recorded as testicle[26].