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Nip7m1Anu
Chemically induced Allele Detail
Summary
Symbol: Nip7m1Anu
Name: NIP7, nucleolar pre-rRNA processing protein; mutation 1, Australian National University
MGI ID: MGI:5563445
Synonyms: ENU23:015:NIP7
Gene: Nip7  Location: Chr8:107783509-107787563 bp, + strand  Genetic Position: Chr8, 53.57 cM, cytoband D2
Alliance: Nip7m1Anu page
Mutation
origin
Strain of Origin:  C57BL/6NCrlAnu
Project Collection: APF ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a A to G point mutation at position 192 on cDNA (ENSMUST00000034392) in exon 2 and results in the amino acid substitution of Tyrosine to Cysteine at position 45. (J:104190)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Nip7 Mutation:  19 strains or lines available
References
Original:  J:104190 The Australian Phenomics Facility at The Australian National University, Heritable mouse mutants from the ENU mutagenesis program at the Australian Phenomics Facility at The Australian National University. MGI Direct Data Submission. 2006-2014;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory