Phenotypes associated with this allele

• Allele Symbol: Ctsh^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5616353
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ctsh^tm1b(KOMP)Wtsi/Ctsh^tm1b(KOMP)Wtsi	C57BL/6N-Ctsh^tm1b(KOMP)Wtsi/Bay	MGI:6288409

Genotype
MGI:6288409

hm1

• Allelic Composition: Ctsh^{tm1b(KOMP)Wtsi}/Ctsh^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Ctsh^{tm1b(KOMP)Wtsi}/Bay
• Cell Lines: EPD0082_4_H04

Data Sources

IMPC Data for Ctsh

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

skeleton

increased bone mineral content ( J:211773 )

IMPC - BCM

increased bone mineral density ( J:211773 )

♀

IMPC - BCM

vision/eye

abnormal eye anterior chamber depth ( J:211773 )

IMPC - BCM

abnormal retina inner nuclear layer morphology ( J:211773 )

IMPC - BCM

abnormal retina outer nuclear layer morphology ( J:211773 )

IMPC - BCM

decreased total retina thickness ( J:211773 )

IMPC - BCM