Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

cDNA sequence of five mouse guanine deaminase (Gda) alleles and mapping to mouse chromosome 19.

Genome - 1 Apr 2002

Giese Raymond D, Snyder Floyd F

Abstract excerpt

Guanine deaminase catalyses the conversion of guanine to xanthine and ammonia, thereby irreversibly removing the guanine base from the pool of guanine-containing metabolites. We have identified five alleles at the mouse guanine deaminase locus by cDNA sequencing. These alleles were defined by single-nucleotide polymorphisms at a total of 19 positions. For each allele the representative strains are as follows:...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acid Substitution
Share to Chromosomes
Share to Codon

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA, Complementary

Share to Mice, Inbred C3H

Share to Mice, Inbred DBA

Share to Mice, Inbred Strains

Share to Sequence Alignment

Source

Identifiers

PMID: 11962625
DOI: 10.1139/g01-157

Genes

CAST

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

cDNA sequence of five mouse guanine deaminase (Gda) alleles and mapping to mouse chromosome 19.PMID 11962625Read ↗

A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci.Semantic proximity Read ↗

The human guanidinoacetate methyltransferase (GAMT) gene maps to a syntenic region on 19p13.3, homologous to band C of mouse chromosome 10, but GAMT is not mutated in jittery mice.Semantic proximity Read ↗

Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration.Semantic proximity Read ↗

Targeted disruption of the inosine 5'-monophosphate dehydrogenase type I gene in mice.Semantic proximity Read ↗

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.Semantic proximity Read ↗

The mouse ortholog of NEIL3 is a functional DNA glycosylase in vitro and in vivo.Semantic proximity Read ↗

The high growth (hg) locus maps to a deletion in mouse chromosome 10.Semantic proximity Read ↗

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)Semantic proximity Read ↗

Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19.Semantic proximity Read ↗

Scraggly, a new hair loss mutation on mouse chromosome 19.Semantic proximity Read ↗

Assignment of mouse Gfra1, the homologue of a new human HSCR candidate gene, to the telomeric region of mouse chromosome 19.Semantic proximity Read ↗

Mouse globin gene nomenclature.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.