RET
protein-coding gene in the species Homo sapiens
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RET
Summary
RET is a gene[1].
Key Facts
- RET's instance of is recorded as gene[2].
- RET is a type of protein-coding gene[3].
- RET's HomoloGene ID is recorded as 7517[4].
- RET's genomic start is recorded as 43572475[5].
- RET's genomic start is recorded as 43077064[6].
- RET's genomic end is recorded as 43130351[7].
- RET's genomic end is recorded as 43625799[8].
- RET's ortholog is recorded as Ret[9].
- RET's ortholog is recorded as Ret[10].
- RET's ortholog is recorded as ret[11].
- RET's encodes is recorded as ret proto-oncogene[12].
- RET's encodes is recorded as Ret proto-oncogene (Multiple endocrine neoplasia and medullary thyroid carcinoma 1, Hirschsprung disease), isoform CRA_d[13].
- RET's encodes is recorded as Proto-oncogene tyrosine-protein kinase receptor Ret[14].
- RET's found in taxon is recorded as Homo sapiens[15].
- RET's chromosome is recorded as human chromosome 10[16].
- RET's genetic association is recorded as colorectal cancer[17].
- RET's genetic association is recorded as familial medullary thyroid carcinoma[18].
- RET's genetic association is recorded as multiple endocrine neoplasia type 2B[19].
- RET's genetic association is recorded as phaeochromocytoma[20].
- RET's genetic association is recorded as multiple endocrine neoplasia type 2A[21].
- RET's genetic association is recorded as hereditary pheochromocytoma-paraganglioma[22].
- RET's genetic association is recorded as adrenal gland pheochromocytoma[23].
- RET's genetic association is recorded as thyroid medullary carcinoma[24].
- RET's strand orientation is recorded as forward strand[25].
- RET's exact match is recorded as http://identifiers.org/ncbigene/5979[26].