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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fgf10tm1Ska
targeted mutation 1, Shigeaki Kato
MGI:1859647
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fgf10tm1Ska/Fgf10tm1Ska involves: C57BL/6 * CBA MGI:2175884
ht2
Fgf10tm1Ska/Fgf10+ involves: C57BL/6 * CBA MGI:3775805
ht3
Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck involves: C57BL/6 * CBA MGI:3629789
cn4
Fgf10tm1Ska/Fgf10tm1Sms
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Twist2tm1(cre)Dor/Twist2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA MGI:3851799
cn5
Fgf10tm1Ska/Fgf10tm1Ska
Fgf8tm1Moon/Fgf8tm1Moon
Mesp1tm2(cre)Ysa/Mesp1+
involves: C57BL/6NCrlj * CBA/JNCrlj MGI:5661383
cn6
Fgf10tm1Ska/Fgf10+
Fgf8tm1Moon/Fgf8tm1Moon
Mesp1tm2(cre)Ysa/Mesp1+
involves: C57BL/6NCrlj * CBA/JNCrlj MGI:5661384
cx7
Fgf3tm1Sng/Fgf3tm1Sng
Fgf10tm1Ska/Fgf10tm1Ska
involves: 129P2/OlaHsd * C57BL/6 * CBA MGI:3027998


Genotype
MGI:2175884
hm1
Allelic
Composition
Fgf10tm1Ska/Fgf10tm1Ska
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Submandibular gland abnormalities in Fgf10tm1Ska/Fgf10tm1Ska and Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn mice at E12.5

mortality/aging
• die shortly after birth

limbs/digits/tail
• limb bud formation is initiated, but outgrowth and muscularization of the limbs fail to occur
• at E10.5 limb bud formation is initiated but severely retarded
• the ectoderm covering the limb buds is not thickened and resembles the ectoderm of the interlimb region
• muscularization of the limbs fails to occur
• limb agenesis (J:114183)
• forelimb components of the digits, ulna, radius, humerus and the posterior scapula are missing (J:51966)
• lack hindlimb components and have a rudimentary iliac bone (J:51966)

respiratory system
• exhibit no evidence for the development of pulmonary circulation
• few present submucosal glands are located in the proximal position above the first cartilage ring of the trachea
• no submucosal glands are located distally between the tracheal rings
• the trachea forms but the lungs do not develop
• lung bud formation is absent at E11.5
• lung agenesis (J:114183)

vision/eye

endocrine/exocrine glands
• proximal region of colon displays shortened crypts
• missing submandibular gland, with fibroblastic cells instead of glandular cells occupying the corresponding portion (J:114183)
• the submandibular salivary gland is entirely absent at E13.5 (J:119849)
• the submandibular salivary gland is severely hypoplastic at E12.5
• salivary gland agenesis
• at P0, basophilic chief cells are found towards the base of the gastric gland
• at P0, a marked decrease in insulin-expressing cells is observed
• at E10, a poorly formed Rathke's pouch contains numerous apoptotic (TUNEL+) cells, unlike in wild-type embryos where only a few apoptotic cells are seen at the base of the diverticulum
• Rathke's pouch is missing at E13.5
• anterior pituitary agenesis
• the posterior infundibular recess is still present at E13.5
• by E15.5, development of the posterior pituitary is arrested
• none of the three lobes are seen at E15.5
• at P0, the thymus is smaller than normal; however, the medulla-cortex distinction is observed
• thyroid gland agenesis
• the epithelial bud of mammary gland 4 penetrates the mammary fat pad but branching is reduced or does not occur
• branching defect is due to the thin fat pad as dissected glands grafted into wild-type mammary fat pads are competent to invade and branch into the wild-type stroma
• mammary placode 4, but not placodes 1, 2, 3 and 5, is induced and maintained at E13.5 in homozygotes (J:73434)
• all placodes (1, 2, 3, 5) except 4 are absent along the mammary line (J:109476)
• few present submucosal glands are located in the proximal position above the first cartilage ring of the trachea
• no submucosal glands are located distally between the tracheal rings
• at P0
• at P0, pancreatic cells are partly replaced by fibroblastic cells

cardiovascular system
• no pulmonary arteries are seen in E17.5 embryos
• orientation of the pulmonary trunk is frequently abnormal in hearts, running transversely, orthogonal to the direction in control hearts
• no pulmonary veins are seen in E17.5 hearts
• abnormally positioned atrial appendages
• the direction of the cardiac apex is frequently abnormal, pointing either to the left in 14%, to the right in 62%, or positioned medially in 20% of mutants, however show normal rightward looping
• 4% show an extreme anterior rightward positioned ventricular apex such that the normally dorsal ventricular surface is apparent in a ventral view
• 62% exhibit a rightward-pointing cardiac apex with situs solitus
• exhibit no evidence for the development of pulmonary circulation

adipose tissue
• development of white adipose tissue is markedly impaired, with significantly reduced cell numbers compared to control tissue
• cell proliferation is reduced in white adipose tissue
• very low lipid accumulation in white adipose tissue is observed
• white adipose tissue forming the mammary fat pad is very thin

skeleton
• tooth dysgenesis
• smaller teeth
• stem cell loop is missing at E19.5
• the posterior scapula (comprising about 1/3 of the entire scapula) is missing

digestive/alimentary system
• at E10.5, gastrointestinal tract tube shows greater diameter reduction than seen in wild-type, at about one third of the length from the proximal end of hindgut
• epithelium of gastrointestinal tract is absent at a position in proximal region of colon and a position in distal region
• proliferation is reduced in colon at E10.5 relative to wild-type or heterozygous embryos while apoptosis is increased
• proximal region of colon displays shortened crypts
• development of the cecum is altered, such that a cecal bud forms but is much smaller at E12.5 and the epithelial layer does not invade the mesenchymal layer (J:87411)
• at E13.5, ceca show mesenchymal buds that fail to continue development and thus show no progressive elongation of the structure (J:87411)
• formation of cecum is arrested at E11.5 (J:115048)
• 100% show cecal atresia with absence of epithelial and muscular layers
• at E12.5 there is interruption of the colonic mesenchyme
• at E14.5 the colon is very short compared to wild-type (20% of normal length)
• at E18.5 colon is almost absent; a small pouch adjacent to the cecum represents the residual colon
• at E18.5 colon is almost absent; a small pouch adjacent to the cecum represents the residual colon
• at E14.5 the colon is very short compared to wild-type (20% of normal length)
• absence of rectum in the pelvis
• missing submandibular gland, with fibroblastic cells instead of glandular cells occupying the corresponding portion (J:114183)
• the submandibular salivary gland is entirely absent at E13.5 (J:119849)
• the submandibular salivary gland is severely hypoplastic at E12.5
• salivary gland agenesis
• at P0, basophilic chief cells are found towards the base of the gastric gland
• at P0, smooth muscle layers are absent from the stomach submucosal region
• at P0

renal/urinary system
• development of the ureteric bud is impaired in E14.5 metanephroi
• at E19.5, the medulla contains fewer renal tubules, loops of Henle, and collecting ducts with more stromal cells
• at E19.5, the kidney inner medulla is significantly smaller, with an enlarged renal calyx
• outer medullary dysplasia is already seen at E14.5
• enlarged renal calyx at E19.5
• at E16.5, urethra formation is abnormal
• the urethral groove and its proximal connection to the urogenital sinus do not form properly
• perineal hypospadias

embryo
• in E11.5-11.75 embryos, cells of the stratum germinativum are cuboidal rather than cylindrical and formation of the periderm is impaired
• formation of the periderm is impaired
• at E10.5 limb bud formation is initiated but severely retarded
• the ectoderm covering the limb buds is not thickened and resembles the ectoderm of the interlimb region

integument
• at E19.5, numerous apoptotic (TUNEL+) cells are detected in the hair bulbs and sheath cells, unlike in wild-type hair follicles
• the epithelial bud of mammary gland 4 penetrates the mammary fat pad but branching is reduced or does not occur
• branching defect is due to the thin fat pad as dissected glands grafted into wild-type mammary fat pads are competent to invade and branch into the wild-type stroma
• mammary placode 4, but not placodes 1, 2, 3 and 5, is induced and maintained at E13.5 in homozygotes (J:73434)
• all placodes (1, 2, 3, 5) except 4 are absent along the mammary line (J:109476)
• elongation of hair shafts is rarely observed at P0
• dysgenesis of hair follicles
• growth of hair bulbs appears disrupted at P0

muscle
N
• all untreated mutant mice develop fully formed, well-muscularized diaphragms despite lung agenesis
• muscularization of the limbs fails to occur
• a portion of mutant embryos exposed to a combination of nitrofen, bisdiamine, and SB-210661 teratogens on E8 develop posterolateral left-sided diaphragmatic hernias, indicating that lung tissue is not required for the induction of diaphragmatic defects

cellular
• at E19.5, numerous apoptotic (TUNEL+) cells are detected in the hair bulbs and sheath cells, unlike in wild-type hair follicles

craniofacial
• tooth dysgenesis
• smaller teeth
• stem cell loop is missing at E19.5

hearing/vestibular/ear
• inner ear dysgenesis
• at E10.5, a smaller otic capsule is observed
• however, the endolymphatic duct is formed

hematopoietic system
• at P0, the thymus is smaller than normal; however, the medulla-cortex distinction is observed

immune system
• at P0, the thymus is smaller than normal; however, the medulla-cortex distinction is observed

nervous system
• at E10, a poorly formed Rathke's pouch contains numerous apoptotic (TUNEL+) cells, unlike in wild-type embryos where only a few apoptotic cells are seen at the base of the diverticulum
• Rathke's pouch is missing at E13.5
• anterior pituitary agenesis
• the posterior infundibular recess is still present at E13.5
• by E15.5, development of the posterior pituitary is arrested
• none of the three lobes are seen at E15.5

growth/size/body
• smaller teeth
• tooth dysgenesis
• stem cell loop is missing at E19.5

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
intestinal atresia DOID:10486 J:92361




Genotype
MGI:3775805
ht2
Allelic
Composition
Fgf10tm1Ska/Fgf10+
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Hypoplastic submandibular glands are seen in Fgfr2tm1.1Dsn/Fgfr2+ and Fgf10tm1Ska/Fgf10+ mice

endocrine/exocrine glands
• at E13.5, glands show fewer ducts and terminal buds
• submandibular salivary gland branching hypoplasia at E13.5

digestive/alimentary system
• at E13.5, glands show fewer ducts and terminal buds
• submandibular salivary gland branching hypoplasia at E13.5

growth/size/body

respiratory system
• decrease in forced expiratory volume in 75 ms (FEV75), forced vital capacity (FVC) and FEV75/FVC quota
• however, lung morphology and histopathology appear normal and lung/body weight ratio is normal




Genotype
MGI:3629789
ht3
Allelic
Composition
Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10Tg(Myl3-lacZ)24Buck mutation (0 available); any Fgf10 mutation (33 available)
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• colon displays defined but shortened crypt
• placode 3 is not detected at E11.5 and E12.5

homeostasis/metabolism
• in mutants gelatinase activity in the lung mesenchyme is decreased

respiratory system
• at E12.5, embryos have lungs with decreased branching
• at E12.5 mice have slightly smaller lungs than wild-type
• at birth, elastin deposition around the bronchi is reduced compared to wild-type

digestive/alimentary system
• mice exhibit epithelial hypocellularity along the proximal-distal axis of the colon
• colon displays defined but shortened crypt
• at E18.5, the colon is 56% of wild-type length
• mid region exhibits enlarged lumen with rudimentary crypts and meconium accumulation in lumen

embryo
• mutants fail to generate a stratum intermedium at E11.5
• cells of the stratum germinativum are still cuboidal at E11, not cylindrical

integument
• placode 3 is not detected at E11.5 and E12.5




Genotype
MGI:3851799
cn4
Allelic
Composition
Fgf10tm1Ska/Fgf10tm1Sms
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Twist2tm1(cre)Dor/Twist2+
Genetic
Background
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
Fgf10tm1Sms mutation (0 available); any Fgf10 mutation (33 available)
Gt(ROSA)26Sortm1Sor mutation (7 available); any Gt(ROSA)26Sor mutation (993 available)
Twist2tm1(cre)Dor mutation (0 available); any Twist2 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
respiratory system
• E17.5 embryos often have hemorrhaging in the lung
• at E12, moderate increases in apoptosis are observed in the primary bronchi of both lungs
• cell death extended farther into the medial and accessory branches and there was a small area of ectopic death observed in the mesenchyme of either the vestigial rostral lobe or at the distal tip of the accessory lobe
• all lobes exhibit reduced branching following outgrowth of the initial branch that established the lobe
• mesenchymal protrusions without an accompanying epithelial branch are occasionally observed during embryonic development
• such protrusions are observed only in the right lung in positions that correspond to lobes
• at E17.5, mutant lobes are smaller and much flatter than control lobes
• at E12.5, the accessory lobe is reduced in size and often misshapen
• most E11.5 embryos have a reduction or absence of the nascent rostral lobe
• at E12.5, the rostral lobe is absent in the majority of mice
• at E12.5, the medial lobe is reduced in size and often misshapen
• at E17.5, mutant lobes are smaller than control lobes
• at E12.5, mutant lungs are smaller than control lungs
• at E17.5, mutant lungs are severely hypoplastic

cardiovascular system
• E17.5 embryos often have hemorrhaging in the lung




Genotype
MGI:5661383
cn5
Allelic
Composition
Fgf10tm1Ska/Fgf10tm1Ska
Fgf8tm1Moon/Fgf8tm1Moon
Mesp1tm2(cre)Ysa/Mesp1+
Genetic
Background
involves: C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
Fgf8tm1Moon mutation (1 available); any Fgf8 mutation (21 available)
Mesp1tm2(cre)Ysa mutation (3 available); any Mesp1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• absence of the left common carotid artery in some mice
• various defects are detected at E10.5, including missing third, fourth and sixth PAAs and retention of the second PAA
• incidence of defects is increased compared to mutant mice wild-type for Fgf10
• hypomorphic at E9.5
• more severe than in mutant mice wild-type for Fgf10
• smaller and misshapen at E10.5
• more frequent than in mutant mice wild-type for Fgf10
• more frequent than in mutant mice wild-type for Fgf10
• hypomorphic at E9.5
• more severe than in mutant mice wild-type for Fgf10

craniofacial
• various defects are detected at E10.5, including missing third, fourth and sixth PAAs and retention of the second PAA
• incidence of defects is increased compared to mutant mice wild-type for Fgf10

cellular
• compromised invasion of the outflow tract at E10.5

embryo
• various defects are detected at E10.5, including missing third, fourth and sixth PAAs and retention of the second PAA
• incidence of defects is increased compared to mutant mice wild-type for Fgf10
• compromised invasion of the outflow tract at E10.5




Genotype
MGI:5661384
cn6
Allelic
Composition
Fgf10tm1Ska/Fgf10+
Fgf8tm1Moon/Fgf8tm1Moon
Mesp1tm2(cre)Ysa/Mesp1+
Genetic
Background
involves: C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
Fgf8tm1Moon mutation (1 available); any Fgf8 mutation (21 available)
Mesp1tm2(cre)Ysa mutation (3 available); any Mesp1 mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• absence of the left common carotid artery in some mice
• various defects are detected at E10.5, including missing third, fourth and sixth PAAs and retention of the second PAA
• incidence of defects is increased compared to mutant mice wild-type for Fgf10
• hypomorphic at E9.5
• more severe than in mutant mice wild-type for Fgf10
• more frequent than in mutant mice wild-type for Fgf10
• more frequent than in mutant mice wild-type for Fgf10
• hypomorphic at E9.5
• more severe than in mutant mice wild-type for Fgf10

craniofacial
• various defects are detected at E10.5, including missing third, fourth and sixth PAAs and retention of the second PAA
• incidence of defects is increased compared to mutant mice wild-type for Fgf10

embryo
• various defects are detected at E10.5, including missing third, fourth and sixth PAAs and retention of the second PAA
• incidence of defects is increased compared to mutant mice wild-type for Fgf10




Genotype
MGI:3027998
cx7
Allelic
Composition
Fgf3tm1Sng/Fgf3tm1Sng
Fgf10tm1Ska/Fgf10tm1Ska
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf10tm1Ska mutation (1 available); any Fgf10 mutation (33 available)
Fgf3tm1Sng mutation (1 available); any Fgf3 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no double homozygous embryos found after E10

hearing/vestibular/ear
• severe loss of otic tissue by E8-E10
• reduced size of otic vesicles and more ventrally located by E9-E10
• extent of effect on otic vesicle was variable

nervous system





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