Phenotype: abnormal esophagus morphology

Definition
any structural anomaly of the part of the digestive canal through which food passes from the pharynx to the stomach
Synonyms
abnormal oesophagus morphology,  esophageal dysplasia,  oesophagus dysplasia,  esophagus dysplasia,  oesophageal dysplasia
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with abnormal esophagus morphology

Total number of significant genotype-phenotype associations: 5

Gene / Allele Zygosity Sex Life Stage Phenotype Parameter Phenotyping
Center
P Value
Itch
Itchtm1b(EUCOMM)Hmgu
HOM Early adult abnormal esophagus morphology Esophagus
Gross Pathology and Tissue Collection
MRC Harwell
IMPC
0.00
Mgat4d
Mgat4dtm1b(KOMP)Wtsi
HOM Early adult abnormal esophagus morphology Esophagus
Gross Pathology and Tissue Collection
BCM
IMPC
0.00
Mmp15
Mmp15tm1b(KOMP)Wtsi
HOM Early adult abnormal esophagus morphology Esophagus
Gross Pathology and Tissue Collection
BCM
IMPC
0.00
Mogs
Mogstm1(KOMP)Vlcg
HET Early adult abnormal esophagus morphology Esophagus
Gross Pathology and Tissue Collection
BCM
IMPC
0.00
Snrnp27
Snrnp27tm1b(EUCOMM)Wtsi
HET Early adult abnormal esophagus morphology Esophagus
Gross Pathology and Tissue Collection
BCM
IMPC
0.00

Download data as:   TSV   XLS

 The way we measure

 Phenotype associations stats

100.00% of tested genes with null mutations on a B6N genetic background have a phenotype association to abnormal esophagus morphology (5/5)

100.00% females (1/1) 100.00% males (4/4)

The IMPC Newsletter

Get highlights of the most important data releases, news and events, delivered straight to your email inbox

Subscribe to newsletter