Gene Symbol | Ranbp1 |
Entrez Gene ID | 19385 |
Full Name | RAN binding protein 1 |
Synonyms | Htf9a |
General protein information |
|
Gene Type | protein-coding |
Organism | Mus musculus(house mouse) |
Genome |
ORF » Species Summary » Mus musculus » Ranbp1 cDNA ORF clone
Gene Symbol | Ranbp1 |
Entrez Gene ID | 19385 |
Full Name | RAN binding protein 1 |
Synonyms | Htf9a |
General protein information |
|
Gene Type | protein-coding |
Organism | Mus musculus(house mouse) |
Genome |
mRNA | Protein | Name |
---|---|---|
NM_011239.2 | NP_035369.2 | ran-specific GTPase-activating protein |
Mus musculus (house mouse) | Ranbp1 | NP_035369.2 |
Rattus norvegicus (Norway rat) | Ranbp1 | NP_001101794.1 |
Saccharomyces cerevisiae (baker's yeast) | YRB1 | NP_010285.1 |
Oryza sativa (rice) | Os05g0350600 | NP_001055275.1 |
Homo sapiens (human) | RANBP1 | NP_001265569.1 |
Pan troglodytes (chimpanzee) | RANBP1 | XP_514990.3 |
Neurospora crassa | NCU00443 | XP_956707.1 |
Arabidopsis thaliana (thale cress) | SIRANBP | NP_172194.1 |
Danio rerio (zebrafish) | ranbp1 | NP_997931.1 |
Kluyveromyces lactis | KLLA0E17227g | XP_454726.1 |
Schizosaccharomyces pombe (fission yeast) | sbp1 | NP_595122.1 |
Arabidopsis thaliana (thale cress) | RANBP1 | NP_200667.2 |
Xenopus tropicalis (tropical clawed frog) | ranbp1 | NP_989020.1 |
Canis lupus familiaris (dog) | RANBP1 | XP_005636631.1 |
Magnaporthe oryzae (rice blast fungus) | MGG_05203 | XP_003712748.1 |
RANBP1 | XP_001113683.2 | |
Bos taurus (cattle) | RANBP1 | NP_001029758.1 |
Gallus gallus (chicken) | RANBP1 | NP_001006183.1 |
Eremothecium gossypii | AGOS_AER002W | NP_984862.2 |
Arabidopsis thaliana (thale cress) | AT2G30060 | NP_180567.1 |
Oryza sativa (rice) | Os03g0292800 | NP_001049806.1 |
Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Paronett EM, Meechan DW, Karpinski BA, LaMantia AS, Maynard TM
Cerebral cortex (New York, N.Y. : 1991)25(10)3977-93(2015 Oct)
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.
Karpinski BA, Maynard TM, Fralish MS, Nuwayhid S, Zohn IE, Moody SA, LaMantia AS
Disease models & mechanisms7(2)245-57(2014 Feb)
Activation of Ran GTPase by a Legionella effector promotes microtubule polymerization, pathogen vacuole motility and infection.
Rothmeier E, Pfaffinger G, Hoffmann C, Harrison CF, Grabmayr H, Repnik U, Hannemann M, W?lke S, Bausch A, Griffiths G, M?ller-Taubenberger A, Itzen A, Hilbi H
PLoS pathogens9(9)e1003598(2013 Sep)
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.
Maynard TM, Gopalakrishna D, Meechan DW, Paronett EM, Newbern JM, LaMantia AS
Human molecular genetics22(2)300-12(2013 Jan)
Mice lacking Ran binding protein 1 are viable and show male infertility.
Nagai M, Moriyama T, Mehmood R, Tokuhiro K, Ikawa M, Okabe M, Tanaka H, Yoneda Y
FEBS letters585(5)791-6(2011 Mar)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
Ranbp1 emerges as a microcephaly gene within the 22q11.2 deleted region that may contribute to altered cortical precursor proliferation and neurogenesis associated with broader 22q11.2 deletion.
Title: Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Data suggest Ran activation by RanBP1 in macrophages promotes Legionella phagosome formation and phagocytosis; LegG1 functions as bacterial Ran activator, localizes to phagosomes, and promotes microtubule stabilization, phagocytosis, and replication.
Title: Activation of Ran GTPase by a Legionella effector promotes microtubule polymerization, pathogen vacuole motility and infection.
The dramatic decrease in "RanBP" activity impairs germ cell viability and affects spermatogenesis decisively in RanBP1-knockout mice.
Title: Mice lacking Ran binding protein 1 are viable and show male infertility.
Downregulation of the Ran GTPase effector RanBP1 is required for nuclear reorganisation.
Title: Nuclear reformation after mitosis requires downregulation of the Ran GTPase effector RanBP1 in mammalian cells.
Tax directly binds Ran and Ran-binding protein-1, locates to centrosomes/spindle poles, and causes supernumerary centrosomes
Title: Abnormal centrosome amplification in cells through the targeting of Ran-binding protein-1 by the human T cell leukemia virus type-1 Tax oncoprotein.
The following Ranbp1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the Ranbp1 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
CloneID | OMu14976 | |
Clone ID Related Accession (Same CDS sequence) | NM_011239.2 | |
Accession Version | NM_011239.2 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 612bp) Protein sequence SNP |
|
Vector | pcDNA3.1-C-(k)DYK or customized vector | User Manual |
Clone information | Clone Map | MSDS |
Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
ORF Insert Method | CloneEZ™ Seamless cloning technology | |
Insert Structure | linear | |
Update Date | 2019-08-04 | |
Organism | Mus musculus(house mouse) | |
Product | ran-specific GTPase-activating protein | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from AK166642.1. On Jul 25, 2007 this sequence version replaced NM_011239.1. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AK166642.1, BC061140.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMN01164140, SAMN01164141 [ECO:0000348] ##Evidence-Data-END## |
1 | ATGGCGGCCG CCAAGGACAG TCACGAGGAC CATGATACTT CCACAGAGAA TGCAGATGAG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_035369.2 |
CDS | 133..744 |
Translation |
Target ORF information:
Target ORF information:
|
NM_011239.2 |
1 | ATGGCGGCCG CCAAGGACAG TCACGAGGAC CATGATACTT CCACAGAGAA TGCAGATGAG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation. |
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome. |
Activation of Ran GTPase by a Legionella effector promotes microtubule polymerization, pathogen vacuole motility and infection. |
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development. |
Mice lacking Ran binding protein 1 are viable and show male infertility. |