Slc39a14^{tm1d(NCOM)Mfgc}
Targeted Allele Detail

Summary

• Symbol: Slc39a14^{tm1d(NCOM)Mfgc}
• Name: solute carrier family 39 (zinc transporter), member 14; targeted mutation 1d, Mammalian Functional Genomics Centre
• MGI ID: MGI:7257822
• Gene: Slc39a14 Location: Chr14:70540918-70588874 bp, - strand Genetic Position: Chr14, 36.32 cM
• Alliance: Slc39a14^{tm1d(NCOM)Mfgc} page
• IMPC: Slc39a14 gene page

Mutation origin

• Mutant Cell Line: M00047_C_388W_B08
• Germline Transmission: Earliest citation of germline transmission: J:322048
• Parent Cell Line: C2 (Tcp) (ES Cell)
• Strain of Origin: C57BL/6N
• Project Collection: NorCOMM

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion Vector: L1L2_MFGC3
• Mutation details: This allele was created by performing a Cre-excision IVF with TAT-Cre with Slc39a14 sperm to generate the allele. (J:322048)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Slc39a14 Mutation: 71 strains or lines available

References

• Original: J:322048 The Centre for Phenogenomics, Direct Data Submission for The Centre for Phenogenomics Alleles. MGI Direct Data Submission. 2022
• All: 1 reference(s)