About   Help   FAQ
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




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
11/19/2024
MGI 6.24 		The Jackson Laboratory