RTEL1
protein-coding gene in the species Homo sapiens
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RTEL1
Summary
RTEL1 is a gene[1].
Key Facts
- RTEL1's instance of is recorded as gene[2].
- RTEL1 is a type of protein-coding gene[3].
- RTEL1's HomoloGene ID is recorded as 13168[4].
- RTEL1's genomic start is recorded as 63657810[5].
- RTEL1's genomic start is recorded as 62289163[6].
- RTEL1's genomic end is recorded as 63696253[7].
- RTEL1's genomic end is recorded as 62328416[8].
- RTEL1's ortholog is recorded as Rtel1[9].
- RTEL1's ortholog is recorded as Rtel1[10].
- RTEL1's ortholog is recorded as rtel1[11].
- RTEL1's ortholog is recorded as CG4078[12].
- RTEL1's ortholog is recorded as rtel-1[13].
- RTEL1's encodes is recorded as Regulator of telomere elongation helicase 1[14].
- RTEL1's found in taxon is recorded as Homo sapiens[15].
- RTEL1's chromosome is recorded as human chromosome 20[16].
- RTEL1's genetic association is recorded as pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3[17].
- RTEL1's genetic association is recorded as Hoyeraal-Hreidarsson syndrome[18].
- RTEL1's strand orientation is recorded as forward strand[19].
- RTEL1's exact match is recorded as http://identifiers.org/ncbigene/51750[20].
- RTEL1's cytogenetic location is recorded as 20q13.33[21].
- RTEL1's expressed in is recorded as sural nerve[22].
- RTEL1's expressed in is recorded as right hemisphere of cerebellum[23].
- RTEL1's expressed in is recorded as pituitary gland[24].
- RTEL1's expressed in is recorded as gastric mucosa[25].
- RTEL1's expressed in is recorded as anterior pituitary[26].