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

Rat galactose-1-phosphate uridyltransferase coding sequence, transcription start site and genomic organization.

DNA sequence : the journal of DNA sequencing and mapping - 1 Jan 1993

Heidenreich R A, Mallee J, Segal S

Abstract excerpt

Galactosemia is an inborn error of metabolism in humans due to deficient activity of the enzyme galactose-1-phosphate uridyl-transferase (GALT). Using a 1.3 kb Bam HI restriction fragment of the human GALT cDNA as a probe, three cDNAs, 786 bp, 265 bp and 1.4 kb were isolated from a rat liver cDNA library. The total rat GALT coding sequence obtained from these three clones was 1051 nt. Repeat cDNA library...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Base Sequence
Share to Cloning, Molecular

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

Share to Genetic Variation

Share to Molecular Sequence Data

Share to Restriction Mapping

Source

Identifiers

PMID: 8400361
DOI: 10.3109/10425179309020829

Genes

GALT

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

Rat galactose-1-phosphate uridyltransferase coding sequence, transcription start site and genomic organization.PMID 8400361Read ↗

The human galactose-1-phosphate uridyltransferase gene.Semantic proximity Read ↗

Functional analysis of the mouse galactose-1-phosphate uridyl transferase (GALT)promoter.Semantic proximity Read ↗

Molecular basis of galactosemia: mutations and polymorphisms in the gene encoding human galactose-1-phosphate uridylyltransferase.Semantic proximity Read ↗

Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene.Semantic proximity Read ↗

Mutation database for the galactose-1-phosphate uridyltransferase (GALT) gene.Semantic proximity Read ↗

Genetic and functional studies reveal a novel noncoding variant in GALT associated with a false positive newborn screening result for galactosemia.Semantic proximity Read ↗

The molecular biology of galactosemia.Semantic proximity Read ↗

Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. Online.Semantic proximity Read ↗

A yeast expression system for human galactose-1-phosphate uridylyltransferase.Semantic proximity Read ↗

A Family of Human β3-GalactosyltransferasesSemantic proximity Read ↗

Molecular characterization of two galactosemia mutations and one polymorphism: implications for structure-function analysis of human galactose-1-phosphate uridyltransferase.Semantic proximity Read ↗

Simultaneous occurrence of various mutations and polymorphisms in cis and in trans of the galactose-1-phosphate uridyltransferase gene in a Turkish family with classical galactosemia.Semantic proximity Read ↗

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