Phenotypes associated with this allele

• Allele Symbol: Cxcl17^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5582438
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cxcl17^tm1b(EUCOMM)Wtsi/Cxcl17^tm1b(EUCOMM)Wtsi	C57BL/6N-Cxcl17^tm1b(EUCOMM)Wtsi/Ucd	MGI:5700855

Genotype
MGI:5700855

hm1

• Allelic Composition: Cxcl17^{tm1b(EUCOMM)Wtsi}/Cxcl17^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Cxcl17^{tm1b(EUCOMM)Wtsi}/Ucd
• Cell Lines: EPD0802_1_A03

Data Sources

IMPC Data for Cxcl17

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

hematopoietic system

increased mean platelet volume ( J:211773 )

♀

IMPC - UCD

homeostasis/metabolism

increased circulating alanine transaminase level ( J:211773 )

♀

IMPC - UCD

integument

abnormal coat/hair pigmentation ( J:211773 )

♂

IMPC - UCD

abnormal skin morphology ( J:211773 )

♂

IMPC - UCD

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

♂

IMPC - UCD

renal/urinary system

abnormal kidney morphology ( J:211773 )

♂

IMPC - UCD

reproductive system

abnormal uterus morphology ( J:211773 )

♀

IMPC - UCD

enlarged uterus ( J:211773 )

♀

IMPC - UCD