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Allele : Trappc10<b2b2613Clo> trafficking protein particle complex 10; Bench to Bassinet Program (B2B/CVDC), mutation 2613 Cecilia Lo

Primary Identifier  MGI:5615094 Allele Type  Chemically induced (ENU)
Gene  Trappc10 Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiovascular phenotypes: Atrioventricular septal defect (AVSD), muscular ventricular septal defect (mVSD), and ventricular myocardial non-compaction

Noncardiovascular phenotype: Micrognathia, cleft palate, micropthalmia, and hypoplastic thymus.

Fyler Codes
The Fyler code developed by The Boston Children's Heart Foundation in Boston Children's Hospital provides a hierarchical clinical diagnosis of congenital cardiovascular defects and other disorders. These codes are used to delineate pathology in the mutant mouse models that parallel human disease and can be cross referenced to the International Pediatric and Congenital Cardiac Code (IPCCC) (http://www.ipccc.net/).

Fyler Codes Code Description
1100 Atrioventricular canal (endocardial cushion defect)
1300 Ventricular septal defect
1320 Ventricular septal defect, muscular
1802 Excessive myocardial trabeculation or noncompaction
4163 Micrognathia
4609 Velocardiofacial syndrome
4876 Cleft palate
4877 Microphthalmia

molecularNote  This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. The molecular lesion is a T to C substitution at coding nucleotide 2329 in exon 15 of the cDNA (c.2329T>C, NM_001081055). This changes the tyrosine residue to histidine at position 777 of the encoded protein (p.Y777H).
  • mutations:
  • Undefined
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

4 Publication categories