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Former Names C57BL/6J-Kcne1nmf190/J (Changed: 15-DEC-04 ) C57BL/6J-nmf190/J (Changed: 15-DEC-04 ) NMF190 (Changed: 15-DEC-04 ) Type Chemically Induced Mutation; Coisogenic; Mutant Strain; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse H2 Haplotype b Generation N2F2+N1p (26-SEP-04) Appearance
black
Related Genotype: a/aImportant Note
The C57BL/6J background strain is homozygous for the age related hearing loss mutation Cdh23ahl, which on this background causes progressive hearing loss with onset after 10 months of age.Description
View strain phenotype and additional information on the Neuroscience Mutagenesis Facility web page for Kcne12J entry.
| Control | ||
|---|---|---|
| Untyped from the colony | ||
| Considerations for Choosing Controls | ||
Strains carrying Cdh23ahl allele
001137 129P1/ReJ 000690 129P3/J 000691 129X1/SvJ 000646 A/J 000647 A/WySnJ 003070 ALR/LtJ 003072 ALS/LtJ 004502 B6;AKR-Lxl2/GrsrJ 001026 BALB/cByJ 000653 BUB/BnJ 005494 C3.129S1(B6)-Grm1rcw/J 000664 C57BL/6J 004764 C57BL/6J-Cdh23v-8J/J 003129 C57BL/6J-Epha4rb-2J/GrsrJ 004703 C57BL/6J-Kcnq2Nmf134/J 004811 C57BL/6J-nmf110/J 004812 C57BL/6J-nmf111/J 004747 C57BL/6J-nmf118/J 004656 C57BL/6J-nmf88/J 004391 C57BL/6J-Chr 13A/J/NaJ 004385 C57BL/6J-Chr 7A/J/NaJ 000662 C57BLKS/J 000667 C57BR/cdJ 000668 C57L/J 000669 C58/J 000657 CE/J 000670 DBA/1J 001140 DBA/1LacJ 000671 DBA/2J 007048 DBA/2J-Gpnmb+/SjJ 002106 KK/HlJ 000675 LG/J 000676 LP/J 000677 MA/MyJ 001976 NOD/ShiLtJ 002050 NOR/LtJ 000679 P/J 002747 SENCARB/PtJ 002335 SKH2/J 003392 STOCK Crb1rd8/J View Strains carrying Cdh23ahl (40 strains)
Strains carrying other alleles of Cdh23
002756 B6.CAST-Cdh23Ahl+/Kjn 002432 B6J x B6.C-H2-Kbm1/ByJ-Cdh23v-J/J 002552 C57BL/6J-Cdh23v-2J/J 004764 C57BL/6J-Cdh23v-8J/J 004819 C57BL/6J-Cdh23v-9J/J 005016 CByJ;B6-Cdh23v-10J/J 000275 V/LeJ View Strains carrying other alleles of Cdh23 (7 strains)
Strains carrying other alleles of Kcne1
003009 129-Kcne1tm1Sfh/J View Strains carrying other alleles of Kcne1 (1 strain)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Kcne12J/Kcne12J
C57BL/6J-Kcne12J/J
- behavior/neurological phenotype
- head bobbing (MGI Ref ID J:82238)
- discernable by weaning age
- head tilt (MGI Ref ID J:82238)
- discernable by weaning age
- hearing/vestibular/ear phenotype
- abnormal brainstem auditory evoked potential (MGI Ref ID J:82238)
- deafness (MGI Ref ID J:82238)
- one mutant was subject to testing by ABR and found to be deaf
- head bobbing (MGI Ref ID J:82238)
- discernable by weaning age
- head tilt (MGI Ref ID J:82238)
- discernable by weaning age
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Cdh23ahl related
Kcne12J relatedNeurobiology Research
Vestibular and Hearing Defects
Age related hearing loss
Sensorineural Research
Vestibular and Hearing Defects
Age related hearing loss
Cell Biology Research
Channel and Transporter Defects
potassium
Neurobiology Research
Channel and Transporter Defects
potassium
Neuroscience Mutagenesis Facility Strain
Vestibular and Hearing Defects
| Allele Symbol | Kcne12J | ||
|---|---|---|---|
| Allele Name | 2 Jackson | ||
| Allele Type | Chemically induced (ENU) | ||
| Common Name(s) | Kcne1nmf190; NMF190; neuroscience mutagenesis facility, 190; | ||
| Strain of Origin | C57BL/6J | ||
| Gene Symbol and Name | Kcne1, potassium voltage-gated channel, Isk-related subfamily, member 1 | ||
| Chromosome | 16 | ||
| Gene Common Name(s) | FLJ18426; FLJ38123; FLJ94103; ISK; JLNS; JLNS2; LQT2/5; LQT5; MGC33114; MinK; m; neuroscience mutagenesis facility, 190; nmf190; | ||
| Molecular Note | This phenotypic mutant was identified in an ENU mutagenesis screen. Complemetation tests demonstrated that this mutation is an allele of Kcne1. | ||
| Allele Symbol | Cdh23ahl | ||
| Allele Name | age related hearing loss 1 | ||
| Allele Type | QTL | ||
| Common Name(s) | Cdh23753A; mdfw; | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Genotyping resources and troubleshooting
Kcne12J relatedJAX Neuroscience Mutagenesis Facility URL: http://www.jax.org/nmf. 2003. Heritable mouse mutants from JAX NMF ENU Mutagenesis Program MGI Direct Data Submission :. [MGI Ref ID J:82238]
Currently there no information available for this strain. This may be due to the supply level of this strain.
| Pricing for USA, Canada and Mexico shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Standard Supply | Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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| Important Note | |
| The C57BL/6J background strain is homozygous for the age related hearing loss mutation Cdh23ahl, which on this background causes progressive hearing loss with onset after 10 months of age. | |
| Control | ||
|---|---|---|
| Untyped from the colony | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
Purchasing Information
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Contact Information
Orders & Technical Support
Tel: 1-800-422-6423 or 1-207-288-5845
Fax: 1-207-288-6150
Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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