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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Tmem98tm1b(EUCOMM)Wtsi
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:6355415
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
 		Tmem98tm1b(EUCOMM)Wtsi/Tmem98Rwhs involves: BALB/cAnN * C3H/HeN * C57BL/6N MGI:6358125
ht2
 		Tmem98em1Jkn/Tmem98tm1b(EUCOMM)Wtsi involves: C57BL/6J * C57BL/6N MGI:6358123


Genotype
MGI:6358125
ht1
Allelic
Composition		 Tmem98tm1b(EUCOMM)Wtsi/Tmem98Rwhs
Genetic
Background		 involves: BALB/cAnN * C3H/HeN * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tmem98Rwhs mutation (2 available); any Tmem98 mutation (25 available)
Tmem98tm1b(EUCOMM)Wtsi mutation (0 available); any Tmem98 mutation (25 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
mortality/aging
mortality/aging ( J:277123 )
N
• viable




Genotype
MGI:6358123
ht2
Allelic
Composition		 Tmem98em1Jkn/Tmem98tm1b(EUCOMM)Wtsi
Genetic
Background		 involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tmem98em1Jkn mutation (0 available); any Tmem98 mutation (25 available)
Tmem98tm1b(EUCOMM)Wtsi mutation (0 available); any Tmem98 mutation (25 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
mortality/aging
mortality/aging ( J:277123 )
N
• viable

vision/eye
vision/eye phenotype ( J:277123 )
N
• normal retinal pigmentation, except three faint retinal white spots in 1 of 17 mice at age 1 year




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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory