Incidental Mutation 'R1752:Fstl4'
ID 193639
Institutional Source Beutler Lab
Gene Symbol Fstl4
Ensembl Gene ENSMUSG00000036264
Gene Name follistatin-like 4
Synonyms SPIG1, B230374F23Rik
MMRRC Submission 039784-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.151) question?
Stock # R1752 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 52655461-53079365 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 53077622 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 793 (V793A)
Ref Sequence ENSEMBL: ENSMUSP00000042007 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036796]
AlphaFold Q5STE3
Predicted Effect probably benign
Transcript: ENSMUST00000036796
AA Change: V793A

PolyPhen 2 Score 0.094 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000042007
Gene: ENSMUSG00000036264
AA Change: V793A

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
KAZAL 87 132 4.7e-13 SMART
Blast:IG_like 215 241 6e-7 BLAST
IGc2 260 327 1.9e-6 SMART
IGc2 352 419 1e-14 SMART
Coding Region Coverage
  • 1x: 97.4%
  • 3x: 96.8%
  • 10x: 95.2%
  • 20x: 92.3%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous null mice were born at expected Mendelian ratio and healthy, fertile, apparently normal with normal retinal laminar structure. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 90 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 T C 10: 79,842,468 (GRCm39) V1134A probably benign Het
Accsl C T 2: 93,688,375 (GRCm39) G420S probably damaging Het
Adam29 A G 8: 56,325,309 (GRCm39) S382P probably damaging Het
Apob T C 12: 8,038,766 (GRCm39) L393P probably benign Het
Arhgef19 T G 4: 140,978,354 (GRCm39) S616A probably benign Het
Atp11a C T 8: 12,863,094 (GRCm39) T91I probably damaging Het
Ccdc88b C T 19: 6,830,690 (GRCm39) V751I probably benign Het
Ccni T C 5: 93,350,315 (GRCm39) probably benign Het
Cd2 G A 3: 101,183,511 (GRCm39) A266V probably benign Het
Cd33 T C 7: 43,181,722 (GRCm39) D146G probably benign Het
Cdh16 A G 8: 105,346,505 (GRCm39) probably null Het
Chd1 T C 17: 15,963,494 (GRCm39) probably null Het
Chd5 A T 4: 152,459,590 (GRCm39) I1109F probably damaging Het
Cir1 T C 2: 73,140,882 (GRCm39) E29G probably damaging Het
Clec5a T C 6: 40,559,187 (GRCm39) T66A probably damaging Het
Cpa2 A G 6: 30,552,023 (GRCm39) D250G probably damaging Het
Crybg2 T A 4: 133,800,961 (GRCm39) L707H probably damaging Het
Csmd3 T C 15: 47,523,669 (GRCm39) T2646A probably benign Het
Cul7 G A 17: 46,964,093 (GRCm39) R390Q probably benign Het
Cyp2c69 T A 19: 39,869,597 (GRCm39) I141F probably damaging Het
Dapk2 C G 9: 66,127,925 (GRCm39) R68G probably damaging Het
Dclk2 C T 3: 86,713,434 (GRCm39) V470I possibly damaging Het
Dixdc1 A G 9: 50,593,850 (GRCm39) V530A probably benign Het
Dock7 A G 4: 98,854,681 (GRCm39) F1528L probably damaging Het
Edn1 T A 13: 42,457,075 (GRCm39) V36E possibly damaging Het
Eng T C 2: 32,563,404 (GRCm39) V319A probably benign Het
Epb41l2 A G 10: 25,336,690 (GRCm39) K229E probably damaging Het
Fam184a T C 10: 53,550,666 (GRCm39) N698S probably benign Het
Fndc7 T C 3: 108,776,646 (GRCm39) N465S probably benign Het
Gm9797 A T 10: 11,485,287 (GRCm39) noncoding transcript Het
Hsd17b4 T C 18: 50,303,834 (GRCm39) S436P probably benign Het
Itsn2 T G 12: 4,761,950 (GRCm39) probably null Het
Kank3 T C 17: 34,038,791 (GRCm39) V570A probably damaging Het
Kif13a A T 13: 46,951,885 (GRCm39) F733Y probably damaging Het
Kif16b G T 2: 142,532,586 (GRCm39) D1184E probably benign Het
Kif20a A G 18: 34,764,634 (GRCm39) D727G possibly damaging Het
Kif20b T A 19: 34,915,736 (GRCm39) S504R probably benign Het
Lrrc37 T C 11: 103,505,381 (GRCm39) T2196A possibly damaging Het
Ltbp3 C A 19: 5,795,685 (GRCm39) H180Q probably benign Het
Luzp2 T C 7: 54,914,088 (GRCm39) S306P possibly damaging Het
Macf1 T C 4: 123,377,465 (GRCm39) I1490V possibly damaging Het
Manba T A 3: 135,212,706 (GRCm39) W72R probably damaging Het
Mast1 A G 8: 85,651,965 (GRCm39) V339A probably benign Het
Mnx1 A G 5: 29,682,727 (GRCm39) S183P unknown Het
Muc5b T G 7: 141,421,488 (GRCm39) L4326R possibly damaging Het
Myb T C 10: 21,032,336 (GRCm39) D15G possibly damaging Het
Ncapg2 A T 12: 116,390,338 (GRCm39) D429V probably damaging Het
Neurod6 A G 6: 55,656,511 (GRCm39) V42A probably benign Het
Nfxl1 A T 5: 72,698,218 (GRCm39) C276S probably damaging Het
Nptx2 C A 5: 144,492,171 (GRCm39) T316N probably damaging Het
Nrp2 T A 1: 62,777,600 (GRCm39) F135Y probably damaging Het
Nxpe3 A T 16: 55,686,837 (GRCm39) F57Y probably benign Het
Or4c109 C A 2: 88,817,659 (GRCm39) A296S possibly damaging Het
Or51ag1 T A 7: 103,155,765 (GRCm39) R129S probably benign Het
Osbpl11 T C 16: 33,025,205 (GRCm39) Y144H probably damaging Het
Pax5 T C 4: 44,609,729 (GRCm39) Y233C probably damaging Het
Pck1 A G 2: 172,998,906 (GRCm39) N388S probably benign Het
Plcd3 T A 11: 102,971,085 (GRCm39) Q157L probably benign Het
Pnma2 A C 14: 67,153,785 (GRCm39) M70L probably benign Het
Pogk T C 1: 166,235,997 (GRCm39) K35E probably damaging Het
Ptprb T A 10: 116,176,895 (GRCm39) V1227E probably benign Het
Pygm T A 19: 6,441,064 (GRCm39) V450E probably damaging Het
Rb1 T A 14: 73,525,064 (GRCm39) I190F probably damaging Het
Setd2 T A 9: 110,423,673 (GRCm39) Y2243N probably damaging Het
Slc11a2 A T 15: 100,303,687 (GRCm39) L182Q probably damaging Het
Slc45a3 T C 1: 131,905,259 (GRCm39) L94P probably damaging Het
Slc9a4 T C 1: 40,668,421 (GRCm39) F688S probably benign Het
Slit3 A T 11: 35,455,480 (GRCm39) I196F probably damaging Het
Sprn G A 7: 139,733,408 (GRCm39) probably benign Het
Spsb2 A G 6: 124,787,292 (GRCm39) D242G probably benign Het
Srpk2 A G 5: 23,733,017 (GRCm39) I111T probably damaging Het
St8sia4 T A 1: 95,519,537 (GRCm39) Y317F probably benign Het
Stat5a T A 11: 100,774,884 (GRCm39) *798K probably null Het
Sult1c2 C T 17: 54,271,777 (GRCm39) V137M possibly damaging Het
Synj1 T C 16: 90,735,361 (GRCm39) T1531A probably benign Het
Tasor T A 14: 27,193,885 (GRCm39) Y1028* probably null Het
Tax1bp1 A G 6: 52,698,398 (GRCm39) T37A probably damaging Het
Tet1 T A 10: 62,648,768 (GRCm39) D1888V probably damaging Het
Tln1 T C 4: 43,536,311 (GRCm39) T1994A probably damaging Het
Tmco3 A C 8: 13,341,741 (GRCm39) D5A probably benign Het
Tnk1 T A 11: 69,747,532 (GRCm39) N74I possibly damaging Het
Ttc16 A T 2: 32,662,162 (GRCm39) S120T probably damaging Het
Ttn T A 2: 76,774,448 (GRCm39) T2153S probably damaging Het
Ttn A G 2: 76,594,606 (GRCm39) V20480A probably damaging Het
Usp4 T C 9: 108,251,441 (GRCm39) Y539H probably damaging Het
Zar1 A C 5: 72,734,715 (GRCm39) V168G probably damaging Het
Zcchc9 T C 13: 91,953,899 (GRCm39) K119E possibly damaging Het
Zfp251 T C 15: 76,737,863 (GRCm39) N410S possibly damaging Het
Zfp605 A T 5: 110,271,639 (GRCm39) D10V probably damaging Het
Zyg11a A T 4: 108,062,479 (GRCm39) N107K possibly damaging Het
Other mutations in Fstl4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00093:Fstl4 APN 11 53,077,102 (GRCm39) missense probably benign 0.01
IGL00885:Fstl4 APN 11 53,039,809 (GRCm39) missense possibly damaging 0.90
IGL00915:Fstl4 APN 11 53,067,825 (GRCm39) missense probably benign
IGL00933:Fstl4 APN 11 53,077,588 (GRCm39) missense possibly damaging 0.80
IGL01022:Fstl4 APN 11 53,077,568 (GRCm39) missense probably benign 0.18
IGL01121:Fstl4 APN 11 52,705,464 (GRCm39) missense probably benign 0.00
IGL01656:Fstl4 APN 11 52,891,201 (GRCm39) missense probably damaging 1.00
IGL01805:Fstl4 APN 11 53,077,184 (GRCm39) missense probably damaging 1.00
IGL01997:Fstl4 APN 11 53,053,881 (GRCm39) nonsense probably null
IGL02386:Fstl4 APN 11 52,664,698 (GRCm39) missense probably benign 0.21
IGL02536:Fstl4 APN 11 53,024,851 (GRCm39) splice site probably benign
IGL02807:Fstl4 APN 11 53,077,501 (GRCm39) missense probably benign 0.03
IGL03037:Fstl4 APN 11 53,059,050 (GRCm39) missense possibly damaging 0.83
R0462:Fstl4 UTSW 11 53,077,229 (GRCm39) missense probably benign 0.09
R1190:Fstl4 UTSW 11 52,959,373 (GRCm39) missense probably benign
R1300:Fstl4 UTSW 11 52,959,454 (GRCm39) missense probably benign
R1626:Fstl4 UTSW 11 52,891,117 (GRCm39) nonsense probably null
R1695:Fstl4 UTSW 11 53,056,705 (GRCm39) splice site probably null
R1699:Fstl4 UTSW 11 53,059,005 (GRCm39) missense possibly damaging 0.81
R1727:Fstl4 UTSW 11 52,959,478 (GRCm39) missense probably damaging 1.00
R1866:Fstl4 UTSW 11 53,077,225 (GRCm39) missense probably benign 0.00
R4689:Fstl4 UTSW 11 52,959,477 (GRCm39) nonsense probably null
R5126:Fstl4 UTSW 11 53,077,388 (GRCm39) missense possibly damaging 0.71
R5129:Fstl4 UTSW 11 53,077,266 (GRCm39) missense probably damaging 1.00
R5499:Fstl4 UTSW 11 52,959,374 (GRCm39) missense probably benign 0.01
R5578:Fstl4 UTSW 11 53,056,608 (GRCm39) missense probably damaging 1.00
R5715:Fstl4 UTSW 11 52,891,243 (GRCm39) missense possibly damaging 0.53
R6125:Fstl4 UTSW 11 53,077,130 (GRCm39) missense probably benign
R6177:Fstl4 UTSW 11 53,059,031 (GRCm39) missense probably benign 0.00
R6236:Fstl4 UTSW 11 53,077,162 (GRCm39) missense probably benign 0.00
R6311:Fstl4 UTSW 11 53,067,804 (GRCm39) missense probably damaging 1.00
R6611:Fstl4 UTSW 11 53,077,552 (GRCm39) missense probably benign 0.01
R6886:Fstl4 UTSW 11 53,077,277 (GRCm39) missense probably damaging 1.00
R7404:Fstl4 UTSW 11 53,024,898 (GRCm39) missense probably benign 0.03
R7423:Fstl4 UTSW 11 52,959,382 (GRCm39) missense possibly damaging 0.54
R7586:Fstl4 UTSW 11 52,963,256 (GRCm39) missense probably benign 0.00
R7756:Fstl4 UTSW 11 53,059,123 (GRCm39) missense possibly damaging 0.69
R7758:Fstl4 UTSW 11 53,059,123 (GRCm39) missense possibly damaging 0.69
R7775:Fstl4 UTSW 11 53,067,798 (GRCm39) nonsense probably null
R7953:Fstl4 UTSW 11 52,891,050 (GRCm39) missense probably benign 0.01
R8026:Fstl4 UTSW 11 52,959,496 (GRCm39) missense probably damaging 0.99
R8043:Fstl4 UTSW 11 52,891,050 (GRCm39) missense probably benign 0.01
R8375:Fstl4 UTSW 11 53,053,502 (GRCm39) missense possibly damaging 0.63
R8866:Fstl4 UTSW 11 52,963,233 (GRCm39) missense possibly damaging 0.54
R9103:Fstl4 UTSW 11 52,664,696 (GRCm39) missense probably benign 0.21
R9182:Fstl4 UTSW 11 53,024,905 (GRCm39) missense probably damaging 0.98
R9297:Fstl4 UTSW 11 53,024,973 (GRCm39) missense possibly damaging 0.50
R9390:Fstl4 UTSW 11 52,891,102 (GRCm39) missense probably benign
R9396:Fstl4 UTSW 11 52,664,778 (GRCm39) missense probably benign
R9447:Fstl4 UTSW 11 53,077,166 (GRCm39) missense probably damaging 1.00
R9506:Fstl4 UTSW 11 53,024,950 (GRCm39) missense probably benign 0.18
R9518:Fstl4 UTSW 11 53,056,647 (GRCm39) missense possibly damaging 0.71
R9523:Fstl4 UTSW 11 53,075,466 (GRCm39) missense probably benign 0.04
R9586:Fstl4 UTSW 11 53,077,729 (GRCm39) missense probably benign 0.02
R9594:Fstl4 UTSW 11 52,664,694 (GRCm39) missense probably benign
X0013:Fstl4 UTSW 11 53,053,446 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CACAGAAGGTAGTCAGTACAACGCC -3'
(R):5'- ACGGAGATGACTTTCCTGCACAC -3'

Sequencing Primer
(F):5'- GTAGTCAGTACAACGCCTATGC -3'
(R):5'- TGGCttgtttttttgtttgttttttg -3'
Posted On 2014-05-23