b2b1941Clo Gene Detail

Summary

• Symbol
  b2b1941Clo
• Name
  Mutant line 1941

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:5446153
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Human Diseases

• Diseases
  2 with b2b1941Clo mouse models

Human Disease

Mouse Models

DiGeorge syndrome

IDs

DiGeorge syndrome      

DOID:11198
ICD10CM:D82.1
ICD9CM:279.11
MESH:D004062
NCI:C2989
OMIM:188400
UMLS_CUI:C0012236

View 1 model

Mouse Models

Human Disease Modeled: DiGeorge syndrome

Allelic Composition	Genetic Background	Reference	Phenotypes
b2b1941Clo/b2b1941Clo	C57BL/6J-b2b1941Clo	J:175213	View

velocardiofacial syndrome

IDs

velocardiofacial syndrome      

DOID:12583
ICD10CM:Q93.81
ICD9CM_2006:758.32
ICD9CM:758.32
MESH:D004062
OMIM:192430
UMLS_CUI:C0220704

View 1 model

Mouse Models

Human Disease Modeled: velocardiofacial syndrome

Allelic Composition	Genetic Background	Reference	Phenotypes
b2b1941Clo/b2b1941Clo	C57BL/6J-b2b1941Clo	J:175213	View

Click on a disease name to see all genes associated with that disease.

• Mutations/Alleles
  1 with disease annotations

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  13 phenotypes from 1 allele in 1 genetic background
  23 images
  3 phenotype references
  

• All Mutations and Alleles
  1
• Chemically induced (ENU)
  1
• Find Mice (IMSR)
  1 strains or lines available

References

• Summaries
  All 3

  Diseases 1

  Phenotypes 3
• Earliest
  J:222159 Li Y, et al., Global genetic analysis in mice unveils central role for cilia in congenital heart disease. Nature. 2015 May 28;521(7553):520-4
• Latest
  J:294771 Lantz B, et al., Finding the Unicorn, a New Mouse Model of Midfacial Clefting. Genes (Basel). 2020 Jan 11;11(1)