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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
srn
siren
MGI:1857054
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
srn/srn involves: BUA/Hn * SM/J MGI:4412006


Genotype
MGI:4412006
hm1
Allelic
Composition
srn/srn
Genetic
Background
involves: BUA/Hn * SM/J
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phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

digestive/alimentary system
• underdeveloped or blind

embryo
• apodal, monopodal or dipodal
• more males than females are affected

limbs/digits/tail
• apodal, monopodal or dipodal
• more males than females are affected
• femurs are usually medially fused because the ischium is missing or vestigial
• some affected mice have no hindlimbs although most show degrees of sirenomelia
• some mice have twisted, kinked, or otherwise abnormal tails

renal/urinary system
• occasionally both kidneys are missing
• usually one kidney is missing

skeleton
• femurs are usually medially fused because the ischium is missing or vestigial
• ischium is missing or vestigial

craniofacial
• many mice of this genotype also have a small mouth

endocrine/exocrine glands
• in some but not all of this genotype

growth/size/body
• many mice of this genotype also have a small mouth





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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last database update
10/22/2024
MGI 6.24
The Jackson Laboratory