MKS1
protein-coding gene in the species Homo sapiens
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MKS1
Summary
MKS1 is a gene[1].
Key Facts
- MKS1's instance of is recorded as gene[2].
- MKS1 is a type of protein-coding gene[3].
- MKS1's HomoloGene ID is recorded as 9833[4].
- MKS1's genomic start is recorded as 56282803[5].
- MKS1's genomic start is recorded as 58205441[6].
- MKS1's genomic end is recorded as 58219605[7].
- MKS1's genomic end is recorded as 56296966[8].
- MKS1's ortholog is recorded as Mks1[9].
- MKS1's ortholog is recorded as Mks1[10].
- MKS1's ortholog is recorded as mks1[11].
- MKS1's encodes is recorded as MKS transition zone complex subunit 1[12].
- MKS1's encodes is recorded as Meckel syndrome type 1 protein[13].
- MKS1's found in taxon is recorded as Homo sapiens[14].
- MKS1's chromosome is recorded as human chromosome 17[15].
- MKS1's genetic association is recorded as Meckel syndrome 1[16].
- MKS1's genetic association is recorded as Bardet-Biedl syndrome 13[17].
- MKS1's genetic association is recorded as Joubert syndrome 28[18].
- MKS1's genetic association is recorded as Joubert syndrome[19].
- MKS1's strand orientation is recorded as reverse strand[20].
- MKS1's exact match is recorded as http://identifiers.org/ncbigene/54903[21].
- MKS1's cytogenetic location is recorded as 17q22[22].
- MKS1's expressed in is recorded as right uterine tube[23].
- MKS1's expressed in is recorded as olfactory zone of nasal mucosa[24].
- MKS1's expressed in is recorded as left ovary[25].
- MKS1's expressed in is recorded as right ovary[26].