All Phenotypes Rcn1<tm1b(EUCOMM)Hmgu> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Rcn1^{tm1b(EUCOMM)Hmgu}
targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
MGI:5613634

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Rcn1^{tm1b(EUCOMM)Hmgu}/Rcn1^{tm1b(EUCOMM)Hmgu}	C57BL/6N-Rcn1^{tm1b(EUCOMM)Hmgu}/Ieg	MGI:6263349

Allelic Composition	Rcn1^{tm1b(EUCOMM)Hmgu}/Rcn1^{tm1b(EUCOMM)Hmgu}
Genetic Background	C57BL/6N-Rcn1^{tm1b(EUCOMM)Hmgu}/Ieg
Cell Lines	HEPD0667_5_E04

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rcn1^{tm1b(EUCOMM)Hmgu} mutation (1 available); any Rcn1 mutation (27 available)

Data Sources

IMPC Data for Rcn1

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

IMPC - HMGU

homeostasis/metabolism

decreased blood urea nitrogen level ( J:211773 )

IMPC - HMGU

increased circulating alkaline phosphatase level ( J:211773 )

IMPC - HMGU

limbs/digits/tail

short tibia ( J:211773 )

IMPC - HMGU

skeleton

short tibia ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

cataract ( J:211773 )

IMPC - HMGU

persistence of hyaloid vascular system ( J:211773 )

IMPC - HMGU

abnormal retina morphology ( J:211773 )

IMPC - HMGU

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

IMPC - HMGU

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)
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