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

Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene.

Psychiatric genetics - 1 Jan 1995

Cichon S, Nöthen M M, Catalano M, Di Bella D, Maier W, Lichtermann D, Minges J, Albus M, Borrmann M, Franzek E

Abstract excerpt

We report two novel polymorphisms and a rare deletion variant in the human dopaine D4 receptor gene. The two polymorphisms are characterized by single base pair substitutions, namely a G-->C transversion changing codon 11 from GGG (encoding Gly) to CGG (encoding Arg) and a C-->T transition in position -11 upstream from the start codon. The Arg11 variant occurs at a frequency of about 1% and the C-->T transition...

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

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

Share to DNA Primers

Share to Gene Frequency

Share to Genetic Variation

Share to Molecular Sequence Data

Source

Identifiers

PMID: 8746407
DOI: 10.1097/00041444-199505030-00001

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

Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene.PMID 8746407Read ↗

Insertion/deletion variant (-141C Ins/Del) in the 5' regulatory region of the dopamine D2 receptor gene: lack of association with schizophrenia and bipolar affective disorder. Short communication.Semantic proximity Read ↗

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.Semantic proximity Read ↗

Distribution of a novel mutation in the first exon of the human dopamine D4 receptor gene in psychotic patients.Semantic proximity Read ↗

Association study of a null mutation in the dopamine D4 receptor gene in Italian patients with obsessive-compulsive disorder, bipolar mood disorder and schizophrenia.Semantic proximity Read ↗

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).Semantic proximity Read ↗

A hypervariable segment in the human dopamine receptor D4 (DRD4) gene.Semantic proximity Read ↗

A novel A/G SNP in the -615th position of the dopamine D4 receptor promoter region as a source of misgenotyping of the -616 C/G SNP.Semantic proximity Read ↗

Linkage analysis and molecular haplotyping of the dopamine D4 receptor gene promoter region.Semantic proximity Read ↗

Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4).Semantic proximity Read ↗

Validation of a tentative microsatellite marker for the dopamine D4 receptor gene by capillary gel electrophoresis.Semantic proximity Read ↗

Deletion polymorphism in the coding region of the human NESP55 alternative transcript of GNAS1.Semantic proximity Read ↗

Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.Semantic proximity Read ↗

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