Glossary entry

Russian term or phrase:

каталожный номер в базе генов человека OMIM № 191117

English translation:

#191117 in the OMIM catalog of human genes (and genetic disorders)

Added to glossary by Frank Szmulowicz, Ph. D.
Feb 27, 2020 12:15
4 yrs ago
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Russian term

каталожный номер в базе генов человека OMIM № 191117

Russian to English Medical Genetics
Одним из наиболее хорошо изученных генов-супрессоров является ген TP53 (каталожный номер в базе генов человека OMIM № 191117), регулирующий процессы контроля клеточного цикла, апоптоза, репарации ДНК и ангиогенеза.
Change log

Feb 29, 2020 12:28: Frank Szmulowicz, Ph. D. Created KOG entry

Discussion

Frank Szmulowicz, Ph. D. Feb 27, 2020:
@Igor: Yes, unless the text is addressed to a wider audience.
Igor Andreev Feb 27, 2020:
ИМХО, в статье можно обойтись и просто OMIM 191170 или OMIM#191170

The p53 tumor suppressor protein, encoded by the TP53 gene (OMIM 191170), lies at the center of an elaborated circuit controlling cell proliferation and interconnecting with many cellular functions.
https://www.nature.com/articles/cgt201063.pdf?origin=ppub

Это в русскоязычной приходится изощряться, чтобы было понятно, что такое OMIM

Proposed translations

15 mins
Selected

#191117 in the OMIM catalog of human genes (and genetic disorders)

Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. As of 28 June 2019, approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes; the rest represented genes, many of which were related to known phenotypes
https://en.wikipedia.org/wiki/Online_Mendelian_Inheritance_i...

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The tumor suppressor gene TP53 (OMIM no. 191117) encodes a transcription factor which is activated in response to several forms of cellular stress and exerts
https://go.gale.com/ps/anonymous?id=GALE|A189043985&sid=goog...
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4 KudoZ points awarded for this answer.
12 mins

OMIM reference number

https://www.google.ru/search?newwindow=1&biw=1067&bih=750&tb...

Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. As of 28 June 2019, approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes; the rest represented genes, many of which were related to known phenotypes.[1]
https://en.wikipedia.org/wiki/Online_Mendelian_Inheritance_i...
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