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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Phl1101/H
101/H
MGI:3664205
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		Phl1101/H/Phl1101/H involves: 101/H * MAI/Pas MGI:3664211
hm2
 		Phl1101/H/Phl1101/H involves: 101/H * MBT/Pas MGI:3664214
ht3
 		Phl1101/H/Phl1MAI/Pas involves: 101/H * MAI/Pas MGI:3664212
ht4
 		Phl1101/H/Phl1MBT/Pas involves: 101/H * MBT/Pas MGI:3664213
cx5
 		Phl1101/H/Phl1101/H
Phl2101/H/? 		involves: 101/H * MAI/Pas * MBT/Pas MGI:3664219
cx6
 		Phl1101/H/?
Phl2101/H/? 		involves: 101/H * MAI/Pas * MBT/Pas MGI:3664220


Genotype
MGI:3664211
hm1
Allelic
Composition		 Phl1101/H/Phl1101/H
Genetic
Background		 involves: 101/H * MAI/Pas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold

nervous system
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
autosomal recessive nonsyndromic deafness 38 DOID:0110496 OMIM:608219
 J:111682




Genotype
MGI:3664214
hm2
Allelic
Composition		 Phl1101/H/Phl1101/H
Genetic
Background		 involves: 101/H * MBT/Pas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold

nervous system
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
autosomal recessive nonsyndromic deafness 38 DOID:0110496 OMIM:608219
 J:111682




Genotype
MGI:3664212
ht3
Allelic
Composition		 Phl1101/H/Phl1MAI/Pas
Genetic
Background		 involves: 101/H * MAI/Pas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold

nervous system
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold




Genotype
MGI:3664213
ht4
Allelic
Composition		 Phl1101/H/Phl1MBT/Pas
Genetic
Background		 involves: 101/H * MBT/Pas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold

nervous system
increased cochlear nerve compound action potential ( J:111682 )
• increased compound action potential at 24 kHz threshold




Genotype
MGI:3664219
cx5
Allelic
Composition		 Phl1101/H/Phl1101/H
Phl2101/H/?
Genetic
Background		 involves: 101/H * MAI/Pas * MBT/Pas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
decreased cochlear nerve compound action potential ( J:111682 )
• decreased compound action potential thresholds
• may indicate heterozygote advantage

nervous system
decreased cochlear nerve compound action potential ( J:111682 )
• decreased compound action potential thresholds
• may indicate heterozygote advantage




Genotype
MGI:3664220
cx6
Allelic
Composition		 Phl1101/H/?
Phl2101/H/?
Genetic
Background		 involves: 101/H * MAI/Pas * MBT/Pas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
decreased cochlear nerve compound action potential ( J:111682 )
• decreased compound action potential thresholds
• may indicate heterozygote advantage

nervous system
decreased cochlear nerve compound action potential ( J:111682 )
• decreased compound action potential thresholds
• may indicate heterozygote advantage




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)
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory