(Q28201600)

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Identification and localization of two mouse phosphomannomutase genes, Pmm1 and Pmm2

scientific article (publication date: 30 May 2001)

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Identification and localization of two mouse phosphomannomutase genes, Pmm1 and Pmm2 (English)

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L Heykants

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1

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E Schollen

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2

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S Grünewald

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3

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G Matthijs

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4

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English

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publication date

30 May 2001

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Gene

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270

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1-2

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53-9

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cites work

Comparative mapping of 9 human chromosome 22q loci in the laboratory mouse

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Rules and guidelines for nomenclature of mouse genes. International Committee on Standardized Genetic Nomenclature for Mice.

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Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16

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PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13

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Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

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Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)

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Comparison of PMM1 with the phosphomannomutases expressed in rat liver and in human cells

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Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes

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Mapping of PRM1 to human chromosome 16 and tight linkage of Prm-1 and Prm-2 on mouse chromosome 16.

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https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900481-4

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7 January 2021

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Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene

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DOI

10.1016/S0378-1119(01)00481-4

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PubMed publication ID

11404002

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(Q28201600)

Identification and localization of two mouse phosphomannomutase genes, Pmm1 and Pmm2

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