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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hfm1Gt(OST347241)Lex
gene trap OST347241, Lexicon Genetics
MGI:4288793
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hfm1Gt(OST347241)Lex/Hfm1Gt(OST347241)Lex involves: 129S5/SvEvBrd * C57BL/6 * SJL MGI:5506633


Genotype
MGI:5506633
hm1
Allelic
Composition
Hfm1Gt(OST347241)Lex/Hfm1Gt(OST347241)Lex
Genetic
Background
involves: 129S5/SvEvBrd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hfm1Gt(OST347241)Lex mutation (0 available); any Hfm1 mutation (85 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• decreased number of ovarian follicles
• reduced size at 45 days of age but increased number of stromal cells
• normal number of seminiferous tubules but diameter of tubules is 30-50% of normal
• reduced testis size
• testicular hypoplasia but hyperplasia of interstitial cells
• few chiasmata found
• prophase I checkpoint is not triggered
• fail to form stable divalents in normal numbers
• chromosomes often fail to form a metaphase plate
• autosomal pairing is normal but defects in synapsis
• double strand breaks form normally but repair may be delayed or inefficient as inferred from persistent RAD51 foci
• blocked
• normal X-Y pairing but defects in synapsis
• block at diakinesis of meiosis I
• apoptosis is common in spermatocytes at that point

endocrine/exocrine glands
• decreased number of ovarian follicles
• reduced size at 45 days of age but increased number of stromal cells
• normal number of seminiferous tubules but diameter of tubules is 30-50% of normal
• reduced testis size
• testicular hypoplasia but hyperplasia of interstitial cells

cellular
• few chiasmata found
• prophase I checkpoint is not triggered
• fail to form stable divalents in normal numbers
• normal X-Y pairing but defects in synapsis
• block at diakinesis of meiosis I
• apoptosis is common in spermatocytes at that point
• chromosomes often fail to form a metaphase plate
• autosomal pairing is normal but defects in synapsis
• double strand breaks form normally but repair may be delayed or inefficient as inferred from persistent RAD51 foci
• blocked





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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
11/12/2024
MGI 6.24
The Jackson Laboratory