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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Kiss1rtm1Coll
targeted mutation 1, William H Colledge
MGI:3530566
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Kiss1rtm1Coll/Kiss1rtm1Coll involves: 129S6/SvEvTac MGI:3530658


Genotype
MGI:3530658
hm1
Allelic
Composition
Kiss1rtm1Coll/Kiss1rtm1Coll
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kiss1rtm1Coll mutation (0 available); any Kiss1r mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• no sperm are detected in the lumen of seminiferous tubules or the epididymis
• very few haploid spermatids are detected, although primary spermatocytes are present
• spermatogenesis is initiated but ceases prior to the meiotic-division stage
• in mutant adrenal glands, the prepubescent zone X, which normally regresses at puberty, is still present in the innermost region of the cortex

reproductive system
• no sperm are detected in the lumen of seminiferous tubules or the epididymis
• very few haploid spermatids are detected, although primary spermatocytes are present
• mutant ovaries exhibit primary and secondary follicles and occasionally an early antral follicle but no large graafian follicles
• mutant uterine horns are thread-like
• mutant females show small vaginal openings
• spermatogenesis is initiated but ceases prior to the meiotic-division stage
• both adult male and female mutants display hypogonadotropic hypogonadism
• mutant ovaries are significantly smaller than wild-type
• mean ovary weight is reduced to 17.5% of wild-type
• mutant testes are significantly smaller than wild-type
• mean testis weight is reduced to 28% of wild-type
• adult homozygotes are viable but demonstrate pubertal delay
• sexual infantilism can be corrected by the administration of exogenous gonadotropin-releasing hormone
• mutant females fail to ovulate
• however, ovulation can be induced after sequential injection of the gonadotropins pregnant mares serum and human chorionic gonadotropin
• vaginal smears consist of non-keratinized epithelia and mucus strands similar to those seen in immature females
• mutant females fail to become pregnant after appropriate mating exposure

endocrine/exocrine glands
• in mutant adrenal glands, the prepubescent zone X, which normally regresses at puberty, is still present in the innermost region of the cortex
• mutant female show reduced mammary-duct formation
• no postpubertal maturation of branched epithelial ducts is observed
• mutant ovaries exhibit primary and secondary follicles and occasionally an early antral follicle but no large graafian follicles
• mutant ovaries are significantly smaller than wild-type
• mean ovary weight is reduced to 17.5% of wild-type
• mutant testes are significantly smaller than wild-type
• mean testis weight is reduced to 28% of wild-type

homeostasis/metabolism
• mutant males show significantly lower blood testosterone concentrations than wild-type controls
• testosterone concentrations in male mutants mice are similar to those observed in wild-type females
• female mutants display 17beta-estradiol concentrations that are similar to those in wild-type females at nonestrus stages and to base-line serum estradiol concentrations in wild-type males
• adult mutant mice exhibit low circulating gonadotropin concentrations relative to wild-type controls
• however, mutant gonads remain sensitive to exogenous gonadotropins while pituitary gonadotropes remain responsive to stimulation by gonadotropin-releasing hormone
• moreover, mutant hypothalamic extracts show normal gonadotropin-releasing hormone concentrations despite observed hypogonadotropism
• in response to kisspeptins, homozygous mutants do not exhibit a rise in plasma follicle stimulating hormone levels as occurs in wild-type controls (J:96108)
• both adult male and female mutants show a significant reduction in serum follicle-stimulating hormone levels relative to wild-type controls (J:96442)
• in response to kisspeptins (a ligand for Gpr54), homozygous mutants do not exhibit a rise in plasma luteinizing hormone levels as occurs in wild-type controls (J:96108)
• both adult male and female mutants show a moderate reduction in serum luteinizing hormone levels relative to wild-type controls (J:96442)

behavior/neurological
• no sexual mounting behavior is observed among mutant males

nervous system
N
• gonadotropin-releasing hormone neurons appear normal and exhibit correct projection into the median eminence (J:96108)
• no gross morphologic abnormalities are detected in the central nervous system (J:96442)

renal/urinary system

integument
• mutant female show reduced mammary-duct formation
• no postpubertal maturation of branched epithelial ducts is observed

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
hypogonadotropic hypogonadism 8 with or without anosmia DOID:0090074 OMIM:614837
J:96442





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory