Incidental Mutation 'R8140:Fgl1'
ID 643785
Institutional Source Beutler Lab
Gene Symbol Fgl1
Ensembl Gene ENSMUSG00000031594
Gene Name fibrinogen-like protein 1
MMRRC Submission 067568-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # R8140 (G1)
Quality Score 181.009
Status Validated
Chromosome 8
Chromosomal Location 41191434-41215156 bp(-) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 41200609 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000034003 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034003] [ENSMUST00000034003]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000034003
SMART Domains Protein: ENSMUSP00000034003
Gene: ENSMUSG00000031594

signal peptide 1 22 N/A INTRINSIC
FBG 80 307 1.4e-131 SMART
Predicted Effect probably null
Transcript: ENSMUST00000034003
SMART Domains Protein: ENSMUSP00000034003
Gene: ENSMUSG00000031594

signal peptide 1 22 N/A INTRINSIC
FBG 80 307 1.4e-131 SMART
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.6%
  • 10x: 98.6%
  • 20x: 93.9%
Validation Efficiency 97% (64/66)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Fibrinogen-like 1 is a member of the fibrinogen family. This protein is homologous to the carboxy terminus of the fibrinogen beta- and gamma- subunits which contains the four conserved cysteines of fibrinogens and fibrinogen related proteins. However, this protein lacks the platelet-binding site, cross-linking region and a thrombin-sensitive site which are necessary for fibrin clot formation. This protein may play a role in the development of hepatocellular carcinomas. Four alternatively spliced transcript variants encoding the same protein exist for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased body weight, decreased circulating cholesterol and free fatty acid, hyperglycemia, impaired glucose tolerance, increased gluconeogenesis, increased white adipose tissue and decreased respiratory quotient. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik T A 5: 63,898,611 (GRCm38) V230E possibly damaging Het
Amotl1 G A 9: 14,572,715 (GRCm38) probably null Het
Atp7b C A 8: 22,028,560 (GRCm38) E87D probably damaging Het
Bcat2 C T 7: 45,588,351 (GRCm38) P347L probably damaging Het
Brox A T 1: 183,293,873 (GRCm38) probably null Het
Cd37 A G 7: 45,238,535 (GRCm38) I58T probably damaging Het
Cep295 A T 9: 15,341,533 (GRCm38) M333K probably benign Het
Chtop A G 3: 90,505,393 (GRCm38) probably null Het
Cpa2 A T 6: 30,544,905 (GRCm38) K54N probably benign Het
Cpa6 A G 1: 10,325,294 (GRCm38) S383P probably damaging Het
Dnah7a A T 1: 53,501,589 (GRCm38) I2542N probably benign Het
Eif5b G A 1: 38,051,276 (GRCm38) V1179I probably benign Het
Erbin T C 13: 103,920,294 (GRCm38) probably null Het
Fastkd5 A T 2: 130,615,250 (GRCm38) D473E possibly damaging Het
Fchsd1 T C 18: 37,964,342 (GRCm38) E372G probably damaging Het
Fzd8 T G 18: 9,213,797 (GRCm38) V293G probably damaging Het
Gm4787 T A 12: 81,378,151 (GRCm38) H411L probably benign Het
Gm49380 G T 9: 44,111,972 (GRCm38) D326E probably benign Het
Hcrtr1 G A 4: 130,135,290 (GRCm38) R240C probably damaging Het
Hdac5 A T 11: 102,197,355 (GRCm38) Y948N probably damaging Het
Hepacam A G 9: 37,383,871 (GRCm38) S301G probably benign Het
Htra4 A T 8: 25,030,558 (GRCm38) D362E possibly damaging Het
Ighv1-9 G A 12: 114,583,741 (GRCm38) P60L probably damaging Het
Kcnq3 A G 15: 65,995,541 (GRCm38) I751T probably damaging Het
Magi3 T C 3: 104,034,086 (GRCm38) Y851C probably damaging Het
Mefv A G 16: 3,713,635 (GRCm38) S470P probably benign Het
Mfsd2a C T 4: 122,949,298 (GRCm38) V397I probably benign Het
Mroh1 C A 15: 76,433,873 (GRCm38) H867N probably benign Het
Mthfd1l C T 10: 4,007,745 (GRCm38) R261* probably null Het
Myo3a A G 2: 22,407,346 (GRCm38) I725M probably damaging Het
Neb T C 2: 52,209,540 (GRCm38) D4766G possibly damaging Het
Nek11 G T 9: 105,392,957 (GRCm38) P22Q probably damaging Het
Olfr1179 T C 2: 88,402,113 (GRCm38) T274A possibly damaging Het
Olfr1497 A T 19: 13,795,239 (GRCm38) V124E possibly damaging Het
Olfr178 T C 16: 58,889,585 (GRCm38) T212A probably benign Het
Peg10 C G 6: 4,756,113 (GRCm38) Q230E unknown Het
Pipox T C 11: 77,883,909 (GRCm38) D116G probably benign Het
Pkd1l2 C T 8: 117,047,497 (GRCm38) R993H probably benign Het
Pkdrej A C 15: 85,818,410 (GRCm38) N1108K probably damaging Het
Polr2a C T 11: 69,746,376 (GRCm38) R291Q probably benign Het
Pomt1 T A 2: 32,244,297 (GRCm38) Y277N probably damaging Het
Rasal2 A G 1: 157,299,235 (GRCm38) S78P probably damaging Het
Rgl1 A T 1: 152,557,501 (GRCm38) L171Q probably damaging Het
Sfta2 A G 17: 35,601,774 (GRCm38) E14G unknown Het
Sh3rf3 T A 10: 59,049,355 (GRCm38) S353R possibly damaging Het
Slc37a1 A T 17: 31,322,259 (GRCm38) I242F probably damaging Het
Srfbp1 T A 18: 52,488,690 (GRCm38) D274E probably damaging Het
Syne2 T A 12: 75,912,353 (GRCm38) S685R possibly damaging Het
Tenm4 A C 7: 96,895,176 (GRCm38) D2170A probably damaging Het
Tnr A G 1: 159,863,695 (GRCm38) T472A probably damaging Het
Tspan9 T C 6: 127,965,278 (GRCm38) H203R probably damaging Het
Ttn T C 2: 76,771,651 (GRCm38) T18556A possibly damaging Het
Usp25 T A 16: 77,071,681 (GRCm38) Y323* probably null Het
Usp31 G T 7: 121,649,026 (GRCm38) R1065S possibly damaging Het
Vmn2r103 A T 17: 19,811,796 (GRCm38) T611S probably damaging Het
Wdfy4 A G 14: 33,142,360 (GRCm38) V552A Het
Zap70 G T 1: 36,771,181 (GRCm38) R124L possibly damaging Het
Zfand6 A T 7: 84,632,749 (GRCm38) S91T possibly damaging Het
Other mutations in Fgl1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01619:Fgl1 APN 8 41,196,971 (GRCm38) missense probably damaging 1.00
IGL03158:Fgl1 APN 8 41,209,773 (GRCm38) missense probably benign 0.00
IGL02796:Fgl1 UTSW 8 41,197,058 (GRCm38) missense probably benign 0.01
R0639:Fgl1 UTSW 8 41,191,624 (GRCm38) missense probably benign 0.27
R0673:Fgl1 UTSW 8 41,191,624 (GRCm38) missense probably benign 0.27
R1413:Fgl1 UTSW 8 41,191,601 (GRCm38) missense possibly damaging 0.82
R1458:Fgl1 UTSW 8 41,210,459 (GRCm38) missense possibly damaging 0.54
R1603:Fgl1 UTSW 8 41,197,018 (GRCm38) missense probably damaging 1.00
R1951:Fgl1 UTSW 8 41,197,350 (GRCm38) missense probably benign 0.02
R5686:Fgl1 UTSW 8 41,200,557 (GRCm38) nonsense probably null
R5796:Fgl1 UTSW 8 41,199,759 (GRCm38) splice site probably benign
R6052:Fgl1 UTSW 8 41,200,511 (GRCm38) missense probably damaging 1.00
R7391:Fgl1 UTSW 8 41,210,446 (GRCm38) missense probably benign 0.04
R7492:Fgl1 UTSW 8 41,191,587 (GRCm38) nonsense probably null
R8114:Fgl1 UTSW 8 41,191,583 (GRCm38) missense probably damaging 0.99
R8809:Fgl1 UTSW 8 41,197,331 (GRCm38) nonsense probably null
R8824:Fgl1 UTSW 8 41,199,711 (GRCm38) missense probably benign 0.00
R8930:Fgl1 UTSW 8 41,209,831 (GRCm38) missense probably benign 0.44
R8932:Fgl1 UTSW 8 41,209,831 (GRCm38) missense probably benign 0.44
R8983:Fgl1 UTSW 8 41,200,459 (GRCm38) missense probably benign 0.38
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2020-08-14