(Q22010244)

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MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development

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MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development (English)

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1 reference

GOA release 2020-03-11

Brunella Franco

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B Franco

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B

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Franco

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7 February 2023

Eugenio Montini

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E Montini

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E

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Montini

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7 February 2023

author name string

G Buchner

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G

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Buchner

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7 February 2023

G Andolfi

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G

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Andolfi

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7 February 2023

N Quaderi

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N

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Quaderi

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7 February 2023

S Cainarca

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S

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Cainarca

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7 February 2023

S Messali

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S

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Messali

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7 February 2023

M T Bassi

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M T

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Bassi

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7 February 2023

A Ballabio

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A

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Ballabio

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7 February 2023

G Meroni

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G

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Meroni

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7 February 2023

language of work or name

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publication date

August 1999

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Human Molecular Genetics

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8

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1397-407

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8

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Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature

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7 January 2021

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A gene for FG syndrome maps in the Xq12-q21.31 region

1 reference

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7 January 2021

based on heuristic

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Mouse ret finger protein (rfp) proto-oncogene is expressed at specific stages of mouse spermatogenesis

1 reference

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7 January 2021

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Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse

1 reference

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7 January 2021

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Localization of the novel serine/threonine protein phosphatase 6 gene (PPP6C) to human chromosome Xq22.3

1 reference

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7 January 2021

based on heuristic

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A Complete YAC Contig and Cosmid Interval Map Covering the Entirety of Human Xq21.33 to Xq22.3 from DXS3 to DXS287

1 reference

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7 January 2021

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Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22

1 reference

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7 January 2021

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X-linked megalocornea: close linkage to DXS87 and DXS94.

1 reference

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7 January 2021

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Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

1 reference

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7 January 2021

based on heuristic

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Mouse chromosome X

1 reference

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7 January 2021

based on heuristic

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Localization of the gene (or genes) for a syndrome with X-linked mental retardation, ataxia, weakness, hearing impairment, loss of vision and a fatal course in early childhood.

1 reference

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7 January 2021

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Characterisation of a novel cysteine/histidine-rich metal binding domain from Xenopus nuclear factor XNF7

1 reference

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7 January 2021

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The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR

1 reference

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A novel macromolecular structure is a target of the promyelocyte-retinoic acid receptor oncoprotein

1 reference

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7 January 2021

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Retinoic acid regulates aberrant nuclear localization of PML-RAR alpha in acute promyelocytic leukemia cells

1 reference

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7 January 2021

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Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes

1 reference

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7 January 2021

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A novel zinc finger coiled-coil domain in a family of nuclear proteins

1 reference

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7 January 2021

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Coiled coils: new structures and new functions

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7 January 2021

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Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

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The RING finger domain: a recent example of a sequence-structure family

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

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7 January 2021

based on heuristic

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Chromosomal deletion complexes in mice by radiation of embryonic stem cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

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Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

A candidate gene for familial Mediterranean fever

1 reference

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7 January 2021

based on heuristic

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Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a RING protein that can interact in vivo with the BRCA1 gene product

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

In vivo and in vitro characterization of the B1 and B2 zinc-binding domains from the acute promyelocytic leukemia protooncoprotein PML

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene spans the pseudoautosomal boundary in mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

The Opitz syndrome gene product, MID1, associates with microtubules

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of DFN2 to Xq22.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of a non-specific X-linked mental retardation gene, MRX23, to Xq23-q24.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

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Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution

1 reference

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based on heuristic

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The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome

1 reference

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based on heuristic

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The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

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based on heuristic

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Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

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Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

1 reference

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based on heuristic

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RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

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https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

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A unique bipartite cysteine-histidine motif defines a subfamily of potential zinc-finger proteins

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

7 January 2021

based on heuristic

inferred from DOI database lookup

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Predicting coiled coils from protein sequences

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

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based on heuristic

inferred from DOI database lookup

Finely tuned regulation of cytoplasmic retention of Xenopus nuclear factor 7 by phosphorylation of individual threonine residues

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1397

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based on heuristic

inferred from DOI database lookup

Developmentally regulated expression of a human "finger"-containing gene encoded by the 5' half of the ret transforming gene

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1093/HMG/8.8.1397

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release_gqg2tf6ij5a7hlwxizjec5y5ta

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