Incidental Mutation 'R1883:F13a1'
ID 209298
Institutional Source Beutler Lab
Gene Symbol F13a1
Ensembl Gene ENSMUSG00000039109
Gene Name coagulation factor XIII, A1 subunit
Synonyms Factor XIIIA, 1200014I03Rik
MMRRC Submission 039904-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1883 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 37051152-37234220 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to C at 37172981 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Glycine at position 133 (A133G)
Ref Sequence ENSEMBL: ENSMUSP00000128316 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037491] [ENSMUST00000164727]
AlphaFold Q8BH61
Predicted Effect probably benign
Transcript: ENSMUST00000037491
AA Change: A133G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000048667
Gene: ENSMUSG00000039109
AA Change: A133G

DomainStartEndE-ValueType
Pfam:Transglut_N 47 165 9e-34 PFAM
TGc 307 400 2.01e-45 SMART
Pfam:Transglut_C 519 623 2e-26 PFAM
Pfam:Transglut_C 631 728 1.3e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000164727
AA Change: A133G

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000128316
Gene: ENSMUSG00000039109
AA Change: A133G

DomainStartEndE-ValueType
Pfam:Transglut_N 46 167 3e-38 PFAM
TGc 307 400 2.01e-45 SMART
Pfam:Transglut_C 519 623 2.2e-23 PFAM
Pfam:Transglut_C 631 728 1.1e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224446
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224783
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225168
Coding Region Coverage
  • 1x: 97.3%
  • 3x: 96.8%
  • 10x: 95.4%
  • 20x: 93.0%
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes subunit A of the coagulation factor XIII that catalyzes the final step of the blood coagulation pathway. The encoded protein associates with subunit B to form a heterotetrameric proenzyme that undergoes thrombin-mediated proteolysis to generate active factor XIIIa. The transglutaminase activity of factor XIIIa is required for the calcium-dependent crosslinking of fibrin, leading to the formation of a clot. Mice lacking the encoded protein display impaired reproduction and reduced survival due to bleeding episodes, hematothorax, hematoperitoneum and subcutaneous hemorrhage. Additionally, mice lacking the encoded protein exhibit impaired wound healing and inadequate healing of myocardial infarction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygous mutant mice exhibit bleeding symptoms, increased lethality, and impaired fertility. [provided by MGI curators]
Allele List at MGI

All alleles(2) : Targeted, knock-out(2)

Other mutations in this stock
Total: 89 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ano9 T C 7: 140,682,244 (GRCm39) E677G probably benign Het
Auh G A 13: 52,989,532 (GRCm39) P308L probably benign Het
Bhmt1b T C 18: 87,774,669 (GRCm39) L64P probably damaging Het
Brs3 T C X: 56,092,449 (GRCm39) I311T probably benign Het
Capn9 A G 8: 125,338,297 (GRCm39) K552R probably benign Het
Catsperg1 C T 7: 28,881,661 (GRCm39) probably null Het
Cdc16 A G 8: 13,825,738 (GRCm39) N449D probably damaging Het
Cdyl2 A T 8: 117,321,902 (GRCm39) N208K probably damaging Het
Cnot4 C T 6: 35,055,092 (GRCm39) V66I probably damaging Het
Cntn4 A G 6: 106,656,353 (GRCm39) T885A probably benign Het
Col20a1 C T 2: 180,634,703 (GRCm39) T131I possibly damaging Het
Crybg2 C A 4: 133,801,594 (GRCm39) S918* probably null Het
Dact2 A T 17: 14,418,085 (GRCm39) S207T possibly damaging Het
Dbnl G A 11: 5,749,247 (GRCm39) G356E probably benign Het
Ddx18 C A 1: 121,495,645 (GRCm39) probably benign Het
Dis3 A T 14: 99,328,905 (GRCm39) H282Q probably benign Het
Dnah3 T C 7: 119,677,142 (GRCm39) D453G probably benign Het
Dst T C 1: 34,228,389 (GRCm39) V1994A possibly damaging Het
Dusp8 C T 7: 141,638,085 (GRCm39) probably null Het
Eipr1 A T 12: 28,816,850 (GRCm39) H69L possibly damaging Het
Eml1 A G 12: 108,429,911 (GRCm39) R65G probably damaging Het
Epha7 C T 4: 28,950,362 (GRCm39) H722Y possibly damaging Het
Epyc A T 10: 97,511,695 (GRCm39) K229N possibly damaging Het
Extl1 A G 4: 134,091,917 (GRCm39) I312T probably benign Het
Fam185a G T 5: 21,630,242 (GRCm39) C26F possibly damaging Het
Fam186b T C 15: 99,176,679 (GRCm39) N737S probably damaging Het
Fam78b A G 1: 166,829,171 (GRCm39) I13V probably benign Het
Fat1 A T 8: 45,504,184 (GRCm39) Q4559L probably benign Het
Fnip1 T C 11: 54,406,373 (GRCm39) S1157P probably damaging Het
Foxj3 A C 4: 119,467,226 (GRCm39) M190L probably benign Het
Heatr3 T C 8: 88,871,221 (GRCm39) Y192H possibly damaging Het
Hexd T A 11: 121,098,524 (GRCm39) S3T probably benign Het
Klf3 C T 5: 64,980,224 (GRCm39) P5S probably damaging Het
Klf9 C T 19: 23,142,101 (GRCm39) S187L probably damaging Het
Krt9 T C 11: 100,079,523 (GRCm39) H623R unknown Het
Krtap2-4 G C 11: 99,505,505 (GRCm39) probably benign Het
Lmtk3 T C 7: 45,436,273 (GRCm39) Y84H probably damaging Het
Mroh3 G T 1: 136,134,731 (GRCm39) A166D probably damaging Het
Musk C A 4: 58,373,189 (GRCm39) P697T probably benign Het
Nek9 A G 12: 85,379,330 (GRCm39) L192P probably damaging Het
Nipbl A C 15: 8,356,616 (GRCm39) F1590C probably damaging Het
Nrk G T X: 137,907,922 (GRCm39) V1455F probably damaging Het
Nsun3 T C 16: 62,555,656 (GRCm39) D290G probably damaging Het
Obscn T C 11: 58,969,029 (GRCm39) T222A probably damaging Het
Or2a12 T C 6: 42,904,764 (GRCm39) S200P probably damaging Het
Or51f1d T C 7: 102,701,189 (GRCm39) I228T probably benign Het
Or6b9 T C 7: 106,555,981 (GRCm39) H54R probably benign Het
Osbpl11 T G 16: 33,034,723 (GRCm39) H237Q probably benign Het
Pde10a A T 17: 9,197,776 (GRCm39) T671S possibly damaging Het
Pkd2 A T 5: 104,631,094 (GRCm39) N506I probably damaging Het
Ppp3cb A G 14: 20,573,913 (GRCm39) V274A possibly damaging Het
Prex1 T C 2: 166,425,192 (GRCm39) D938G probably benign Het
Ptch1 G A 13: 63,659,841 (GRCm39) Q1134* probably null Het
Rasgrf2 A G 13: 92,117,149 (GRCm39) V820A probably benign Het
Rimbp2 C T 5: 128,880,998 (GRCm39) V137M possibly damaging Het
Rpa1 A G 11: 75,209,309 (GRCm39) V137A probably benign Het
Rps6ka1 A C 4: 133,591,354 (GRCm39) I299S probably damaging Het
Scn3b A C 9: 40,190,669 (GRCm39) probably null Het
Sdha A T 13: 74,481,255 (GRCm39) I317N probably damaging Het
Serpina1d T A 12: 103,732,037 (GRCm39) D274V possibly damaging Het
Sik3 C G 9: 46,132,387 (GRCm39) H1276Q probably benign Het
Snx14 T A 9: 88,284,314 (GRCm39) E451D probably benign Het
Spmip4 T C 6: 50,551,433 (GRCm39) T339A probably benign Het
Swt1 T A 1: 151,299,284 (GRCm39) K8* probably null Het
Tas1r3 G T 4: 155,946,610 (GRCm39) P332T probably damaging Het
Tas2r126 A T 6: 42,411,961 (GRCm39) T165S probably benign Het
Tecpr1 A G 5: 144,143,347 (GRCm39) V676A probably benign Het
Tg A G 15: 66,543,158 (GRCm39) E24G probably damaging Het
Tlr7 C T X: 166,089,468 (GRCm39) G673S probably benign Het
Tnxb T A 17: 34,908,539 (GRCm39) D1520E probably benign Het
Trabd A G 15: 88,966,184 (GRCm39) E47G probably damaging Het
Trim29 T A 9: 43,222,702 (GRCm39) I177N probably damaging Het
Ubxn2a A T 12: 4,944,563 (GRCm39) L53* probably null Het
Ulk2 A G 11: 61,721,438 (GRCm39) L208P probably damaging Het
Unc80 G A 1: 66,564,929 (GRCm39) C872Y possibly damaging Het
Vac14 A G 8: 111,438,319 (GRCm39) H644R probably damaging Het
Vmn1r20 C A 6: 57,409,306 (GRCm39) H211N probably benign Het
Vmn1r31 C T 6: 58,449,029 (GRCm39) V279I probably damaging Het
Vmn2r18 G T 5: 151,499,190 (GRCm39) Q425K probably benign Het
Vmn2r60 T C 7: 41,786,094 (GRCm39) V299A probably damaging Het
Vps54 A T 11: 21,262,967 (GRCm39) T685S possibly damaging Het
Vwa5b1 A G 4: 138,302,700 (GRCm39) W932R probably damaging Het
Wdr53 A T 16: 32,075,316 (GRCm39) I174F possibly damaging Het
Zfp157 A G 5: 138,443,102 (GRCm39) D31G probably damaging Het
Zfp60 T C 7: 27,449,435 (GRCm39) L701P probably benign Het
Zfp609 A T 9: 65,702,040 (GRCm39) M204K probably benign Het
Zfp831 A G 2: 174,545,870 (GRCm39) H1325R possibly damaging Het
Zfp995 A T 17: 22,099,622 (GRCm39) I204N probably benign Het
Zp2 C T 7: 119,732,624 (GRCm39) D641N probably benign Het
Other mutations in F13a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01304:F13a1 APN 13 37,172,852 (GRCm39) missense probably benign 0.11
IGL01444:F13a1 APN 13 37,102,551 (GRCm39) missense probably null 1.00
IGL02188:F13a1 APN 13 37,090,035 (GRCm39) splice site probably benign
IGL02591:F13a1 APN 13 37,082,031 (GRCm39) missense probably damaging 1.00
IGL02660:F13a1 APN 13 37,127,868 (GRCm39) missense possibly damaging 0.92
IGL03244:F13a1 APN 13 37,172,870 (GRCm39) missense possibly damaging 0.82
IGL03401:F13a1 APN 13 37,082,054 (GRCm39) missense probably benign 0.00
F6893:F13a1 UTSW 13 37,155,999 (GRCm39) missense probably damaging 1.00
R0082:F13a1 UTSW 13 37,172,927 (GRCm39) missense probably damaging 0.99
R0657:F13a1 UTSW 13 37,152,079 (GRCm39) missense probably damaging 0.96
R1225:F13a1 UTSW 13 37,209,825 (GRCm39) missense probably benign
R1430:F13a1 UTSW 13 37,082,105 (GRCm39) missense probably damaging 1.00
R1608:F13a1 UTSW 13 37,052,785 (GRCm39) missense probably damaging 1.00
R2115:F13a1 UTSW 13 37,172,831 (GRCm39) missense probably damaging 1.00
R2121:F13a1 UTSW 13 37,209,653 (GRCm39) missense probably benign 0.01
R2122:F13a1 UTSW 13 37,209,653 (GRCm39) missense probably benign 0.01
R2125:F13a1 UTSW 13 37,076,815 (GRCm39) missense probably benign 0.15
R2392:F13a1 UTSW 13 37,127,971 (GRCm39) missense possibly damaging 0.65
R3618:F13a1 UTSW 13 37,127,967 (GRCm39) missense probably damaging 1.00
R3625:F13a1 UTSW 13 37,082,067 (GRCm39) missense probably benign 0.31
R3772:F13a1 UTSW 13 37,082,108 (GRCm39) missense probably benign
R3838:F13a1 UTSW 13 37,231,398 (GRCm39) missense probably damaging 1.00
R3857:F13a1 UTSW 13 37,209,668 (GRCm39) missense probably benign 0.32
R3937:F13a1 UTSW 13 37,100,875 (GRCm39) missense probably damaging 1.00
R4934:F13a1 UTSW 13 37,061,736 (GRCm39) missense probably benign 0.00
R4974:F13a1 UTSW 13 37,100,837 (GRCm39) critical splice donor site probably null
R5033:F13a1 UTSW 13 37,172,830 (GRCm39) missense probably damaging 1.00
R5194:F13a1 UTSW 13 37,156,037 (GRCm39) missense probably damaging 1.00
R5740:F13a1 UTSW 13 37,082,178 (GRCm39) missense probably benign 0.02
R5753:F13a1 UTSW 13 37,082,082 (GRCm39) nonsense probably null
R6188:F13a1 UTSW 13 37,209,752 (GRCm39) missense probably benign 0.12
R7048:F13a1 UTSW 13 37,082,117 (GRCm39) missense probably benign 0.02
R7197:F13a1 UTSW 13 37,100,860 (GRCm39) missense probably damaging 1.00
R7816:F13a1 UTSW 13 37,209,745 (GRCm39) missense probably benign 0.00
R7843:F13a1 UTSW 13 37,209,745 (GRCm39) missense probably benign 0.00
R7902:F13a1 UTSW 13 37,172,913 (GRCm39) missense probably damaging 1.00
R8124:F13a1 UTSW 13 37,209,779 (GRCm39) missense probably damaging 1.00
R8443:F13a1 UTSW 13 37,209,692 (GRCm39) missense probably damaging 1.00
R8856:F13a1 UTSW 13 37,100,859 (GRCm39) missense probably damaging 1.00
R8864:F13a1 UTSW 13 37,061,753 (GRCm39) missense probably damaging 1.00
R9026:F13a1 UTSW 13 37,102,506 (GRCm39) missense probably null 1.00
R9092:F13a1 UTSW 13 37,089,993 (GRCm39) missense probably benign 0.17
R9268:F13a1 UTSW 13 37,076,910 (GRCm39) missense probably benign 0.00
R9274:F13a1 UTSW 13 37,052,761 (GRCm39) missense probably damaging 1.00
R9497:F13a1 UTSW 13 37,082,118 (GRCm39) missense probably benign 0.05
R9645:F13a1 UTSW 13 37,082,154 (GRCm39) missense probably benign
Z1088:F13a1 UTSW 13 37,172,986 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- TACCTTCACACCAAGGGTTG -3'
(R):5'- CAGCTACTATCACATCCCTTGG -3'

Sequencing Primer
(F):5'- TACCTTCACACCAAGGGTTGAAGAG -3'
(R):5'- TATCACATCCCTTGGCAGTGGAG -3'
Posted On 2014-06-30