Phenotypes associated with this allele

• Allele Symbol: Tmem30b^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5692820
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Tmem30b^tm1b(EUCOMM)Wtsi/Tmem30b^tm1b(EUCOMM)Wtsi	C57BL/6N-Tmem30b^tm1b(EUCOMM)Wtsi/Ucd	MGI:5706113

Genotype
MGI:5706113

hm1

• Allelic Composition: Tmem30b^{tm1b(EUCOMM)Wtsi}/Tmem30b^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Tmem30b^{tm1b(EUCOMM)Wtsi}/Ucd
• Cell Lines: EPD0921_3_B08

Data Sources

IMPC Data for Tmem30b

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - UCD

integument

abnormal coat/hair pigmentation ( J:211773 )

IMPC - UCD

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

IMPC - UCD

renal/urinary system

abnormal urinary bladder morphology ( J:211773 )

♂

IMPC - UCD

vision/eye

abnormal eye morphology ( J:211773 )

♀

IMPC - UCD