About   Help   FAQ
Marveld2tm1Sats
Targeted Allele Detail
Summary
Symbol: Marveld2tm1Sats
Name: MARVEL (membrane-associating) domain containing 2; targeted mutation 1, Sachiko Tsukita
MGI ID: MGI:6156852
Synonyms: Tric-
Gene: Marveld2  Location: Chr13:100732465-100753479 bp, - strand  Genetic Position: Chr13, 53.23 cM
Alliance: Marveld2tm1Sats page
Progressive degeneration of hair cells in the organ of Corti of Marveld2tm1Sats/Marveld2tm1Sats mice

Show the 4 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:261357
Parent Cell Line:  TT2 (ES Cell)
Strain of Origin:  (C57BL/6NCrlj x CBA/JNCrlj)F1
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA loxP-flanked PGK-Neo cassette replaced exon 2. Western blot analysis confirmed the absence of protein in homozygotes. (J:261357)
Generation of the Marveld2tm1Sats allele
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Marveld2 Mutation:  30 strains or lines available
References
Original:  J:261357 Kamitani T, et al., Deletion of Tricellulin Causes Progressive Hearing Loss Associated with Degeneration of Cochlear Hair Cells. Sci Rep. 2015 Dec 18;5:18402
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory