NUS1
protein-coding gene in the species Homo sapiens
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NUS1
Summary
NUS1 is a gene[1].
Key Facts
- NUS1's instance of is recorded as gene[2].
- NUS1 is a type of protein-coding gene[3].
- NUS1's HomoloGene ID is recorded as 12719[4].
- NUS1's genomic start is recorded as 117996665[5].
- NUS1's genomic start is recorded as 117675469[6].
- NUS1's genomic end is recorded as 118031803[7].
- NUS1's genomic end is recorded as 117710727[8].
- NUS1's ortholog is recorded as Nus1[9].
- NUS1's ortholog is recorded as Nus1[10].
- NUS1's ortholog is recorded as nus1[11].
- NUS1's encodes is recorded as NUS1 dehydrodolichyl diphosphate synthase subunit[12].
- NUS1's found in taxon is recorded as Homo sapiens[13].
- NUS1's chromosome is recorded as human chromosome 6[14].
- NUS1's genetic association is recorded as autosomal dominant mental retardation 55[15].
- NUS1's genetic association is recorded as congenital disorder of glycosylation type I[16].
- NUS1's strand orientation is recorded as forward strand[17].
- NUS1's exact match is recorded as http://identifiers.org/ncbigene/116150[18].
- NUS1's cytogenetic location is recorded as 6q22.1[19].
- NUS1's expressed in is recorded as endometrium[20].
- NUS1's expressed in is recorded as tibia[21].
- NUS1's expressed in is recorded as islet of Langerhans[22].
- NUS1's expressed in is recorded as skin of arm[23].
- NUS1's expressed in is recorded as cartilage tissue[24].
- NUS1's expressed in is recorded as mucosa of ileum[25].
- NUS1's expressed in is recorded as oocyte[26].