Incidental Mutation 'R7702:Flg'
ID 594044
Institutional Source Beutler Lab
Gene Symbol Flg
Ensembl Gene ENSMUSG00000102439
Gene Name filaggrin
Synonyms profilaggrin, ft, fillagrin
MMRRC Submission 045763-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.371) question?
Stock # R7702 (G1)
Quality Score 225.009
Status Not validated
Chromosome 3
Chromosomal Location 93180853-93200996 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 93200089 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 195 (H195L)
Ref Sequence ENSEMBL: ENSMUSP00000142294 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050758] [ENSMUST00000179250] [ENSMUST00000180293]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000050758
AA Change: H195L
SMART Domains Protein: ENSMUSP00000142294
Gene: ENSMUSG00000102439
AA Change: H195L

DomainStartEndE-ValueType
low complexity region 6 26 N/A INTRINSIC
low complexity region 35 98 N/A INTRINSIC
low complexity region 154 207 N/A INTRINSIC
low complexity region 235 276 N/A INTRINSIC
low complexity region 285 315 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000179250
SMART Domains Protein: ENSMUSP00000141513
Gene: ENSMUSG00000102439

DomainStartEndE-ValueType
low complexity region 9 62 N/A INTRINSIC
low complexity region 90 105 N/A INTRINSIC
low complexity region 109 138 N/A INTRINSIC
low complexity region 140 203 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000180293
SMART Domains Protein: ENSMUSP00000141844
Gene: ENSMUSG00000102439

DomainStartEndE-ValueType
low complexity region 10 63 N/A INTRINSIC
low complexity region 91 106 N/A INTRINSIC
low complexity region 112 132 N/A INTRINSIC
low complexity region 141 204 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
Validation Efficiency 100% (61/61)
MGI Phenotype PHENOTYPE: Mutations in this gene produce abnormalities in the skin of the ear, tail and dorsal trunk. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 A G 11: 110,167,278 (GRCm39) probably null Het
AU040320 T A 4: 126,708,166 (GRCm39) S261T probably benign Het
Banp T A 8: 122,705,326 (GRCm39) C65* probably null Het
Bloc1s5 T C 13: 38,787,850 (GRCm39) D178G probably benign Het
Cacna1c A G 6: 118,575,727 (GRCm39) F1941L Het
Ccdc121rt3 T C 5: 112,503,063 (GRCm39) K214E probably benign Het
Cd48 A G 1: 171,523,348 (GRCm39) I64V probably damaging Het
Cela3a A G 4: 137,135,501 (GRCm39) S21P probably benign Het
Cidec A G 6: 113,411,415 (GRCm39) Y12H possibly damaging Het
Col12a1 C G 9: 79,588,803 (GRCm39) R1104T probably damaging Het
Ctsf T G 19: 4,906,567 (GRCm39) F165V probably damaging Het
Cux2 T C 5: 122,006,648 (GRCm39) D874G possibly damaging Het
Dbnl C T 11: 5,748,048 (GRCm39) L298F probably benign Het
Dnah1 C A 14: 31,032,866 (GRCm39) V390F probably benign Het
Dnah17 T C 11: 118,012,304 (GRCm39) D486G possibly damaging Het
Dnah17 T C 11: 117,916,466 (GRCm39) I4236V probably benign Het
Dpp6 T A 5: 27,857,274 (GRCm39) D406E probably benign Het
Dsp C T 13: 38,359,183 (GRCm39) A318V possibly damaging Het
Duox1 T C 2: 122,160,120 (GRCm39) L745P possibly damaging Het
Ell C A 8: 70,992,364 (GRCm39) A3E possibly damaging Het
Fer1l5 T A 1: 36,459,775 (GRCm39) L1832* probably null Het
Filip1 G T 9: 79,727,931 (GRCm39) N229K probably benign Het
Fndc7 G T 3: 108,770,129 (GRCm39) P685H probably damaging Het
Ggt1 A G 10: 75,412,116 (GRCm39) N120S probably benign Het
Gm4952 A T 19: 12,604,428 (GRCm39) H280L probably benign Het
Golim4 A T 3: 75,794,091 (GRCm39) D551E probably damaging Het
H3c13 C A 3: 96,176,309 (GRCm39) Y100* probably null Het
Hmbs A C 9: 44,248,147 (GRCm39) probably null Het
Ino80 T C 2: 119,273,054 (GRCm39) D474G probably benign Het
Ipo4 A C 14: 55,869,787 (GRCm39) H343Q probably damaging Het
Jade2 C T 11: 51,707,744 (GRCm39) R823H probably damaging Het
Jakmip1 C T 5: 37,274,841 (GRCm39) T453I probably damaging Het
Klk6 T C 7: 43,478,689 (GRCm39) S199P probably damaging Het
Ltn1 A T 16: 87,223,166 (GRCm39) Y105N probably damaging Het
Map3k19 G T 1: 127,756,827 (GRCm39) T394N probably damaging Het
Megf6 G A 4: 154,354,927 (GRCm39) D1445N probably benign Het
Mmp21 A G 7: 133,280,791 (GRCm39) Y60H probably damaging Het
Mylk4 C T 13: 32,904,585 (GRCm39) probably null Het
Nckipsd A T 9: 108,691,216 (GRCm39) R38* probably null Het
Nob1 G A 8: 108,139,737 (GRCm39) R341* probably null Het
Or11g25 A G 14: 50,723,751 (GRCm39) T279A possibly damaging Het
Or1e19 T A 11: 73,324,175 (GRCm39) probably benign Het
Or5ac22 A G 16: 59,134,997 (GRCm39) Y258H probably damaging Het
Pcdh1 A G 18: 38,336,569 (GRCm39) L22P unknown Het
Pebp4 T A 14: 70,297,056 (GRCm39) N198K probably benign Het
Pkp4 T C 2: 59,138,757 (GRCm39) S336P probably damaging Het
Prr5l T A 2: 101,547,442 (GRCm39) D361V probably benign Het
Ralgapa1 C G 12: 55,756,340 (GRCm39) V1086L probably damaging Het
Ralgapa1 T A 12: 55,756,341 (GRCm39) Q1085H probably damaging Het
Ryr2 T C 13: 11,705,219 (GRCm39) N2849S probably damaging Het
Slc6a18 A T 13: 73,820,915 (GRCm39) L223H probably damaging Het
Sqstm1 T G 11: 50,096,932 (GRCm39) probably null Het
Syne1 T C 10: 5,195,835 (GRCm39) E3945G probably damaging Het
Syne2 A G 12: 76,037,161 (GRCm39) Y3780C probably benign Het
Tecpr1 A G 5: 144,140,236 (GRCm39) Y840H probably damaging Het
Tmem183a T C 1: 134,288,539 (GRCm39) Q108R probably benign Het
Tmtc1 A T 6: 148,345,415 (GRCm39) C95S probably benign Het
Trappc8 C T 18: 20,958,119 (GRCm39) V1250I probably damaging Het
Tshz1 A G 18: 84,032,461 (GRCm39) V649A probably damaging Het
Ttll3 CAAAGTAA CAAAGTAAAGTAA 6: 113,376,118 (GRCm39) probably null Het
Vmn1r123 A C 7: 20,896,302 (GRCm39) T65P probably damaging Het
Vmn2r63 A T 7: 42,577,553 (GRCm39) H328Q possibly damaging Het
Zeb1 T C 18: 5,766,802 (GRCm39) S438P probably damaging Het
Other mutations in Flg
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01080:Flg APN 3 93,186,906 (GRCm39) missense probably benign 0.41
FR4342:Flg UTSW 3 93,197,820 (GRCm39) unclassified probably benign
R0046:Flg UTSW 3 93,185,028 (GRCm39) splice site probably benign
R0046:Flg UTSW 3 93,185,028 (GRCm39) splice site probably benign
R0538:Flg UTSW 3 93,186,767 (GRCm39) missense probably damaging 1.00
R1751:Flg UTSW 3 93,187,220 (GRCm39) missense possibly damaging 0.91
R1767:Flg UTSW 3 93,187,220 (GRCm39) missense possibly damaging 0.91
R2024:Flg UTSW 3 93,186,722 (GRCm39) missense probably damaging 0.99
R2213:Flg UTSW 3 93,200,335 (GRCm39) unclassified probably benign
R2311:Flg UTSW 3 93,200,260 (GRCm39) unclassified probably benign
R2513:Flg UTSW 3 93,187,093 (GRCm39) missense possibly damaging 0.83
R3892:Flg UTSW 3 93,186,833 (GRCm39) missense probably benign 0.01
R3911:Flg UTSW 3 93,187,307 (GRCm39) missense probably benign 0.01
R4207:Flg UTSW 3 93,187,169 (GRCm39) missense probably benign 0.10
R4385:Flg UTSW 3 93,200,316 (GRCm39) unclassified probably benign
R4939:Flg UTSW 3 93,187,154 (GRCm39) missense probably benign 0.00
R5084:Flg UTSW 3 93,184,922 (GRCm39) missense probably damaging 0.99
R5540:Flg UTSW 3 93,184,923 (GRCm39) missense probably damaging 1.00
R5925:Flg UTSW 3 93,186,706 (GRCm39) missense probably damaging 0.98
R5972:Flg UTSW 3 93,186,849 (GRCm39) missense probably benign 0.00
R6130:Flg UTSW 3 93,200,023 (GRCm39) unclassified probably benign
R6144:Flg UTSW 3 93,190,515 (GRCm39) unclassified probably benign
R6184:Flg UTSW 3 93,187,357 (GRCm39) missense probably benign 0.04
R6230:Flg UTSW 3 93,186,782 (GRCm39) missense probably damaging 1.00
R6268:Flg UTSW 3 93,195,482 (GRCm39) unclassified probably benign
R6360:Flg UTSW 3 93,197,908 (GRCm39) unclassified probably benign
R6400:Flg UTSW 3 93,187,228 (GRCm39) missense probably benign 0.41
R6464:Flg UTSW 3 93,188,688 (GRCm39) unclassified probably benign
R6586:Flg UTSW 3 93,200,290 (GRCm39) unclassified probably benign
R6685:Flg UTSW 3 93,186,716 (GRCm39) missense possibly damaging 0.53
R6769:Flg UTSW 3 93,195,630 (GRCm39) unclassified probably benign
R6771:Flg UTSW 3 93,195,630 (GRCm39) unclassified probably benign
R6948:Flg UTSW 3 93,195,475 (GRCm39) unclassified probably benign
R7102:Flg UTSW 3 93,200,335 (GRCm39) missense unknown
R7186:Flg UTSW 3 93,187,252 (GRCm39) nonsense probably null
R7222:Flg UTSW 3 93,195,621 (GRCm39) missense unknown
R7248:Flg UTSW 3 93,189,041 (GRCm39) missense probably benign 0.33
R7962:Flg UTSW 3 93,193,984 (GRCm39) missense unknown
R8109:Flg UTSW 3 93,197,734 (GRCm39) missense unknown
R8308:Flg UTSW 3 93,190,586 (GRCm39) missense unknown
R8322:Flg UTSW 3 93,191,639 (GRCm39) missense unknown
R8544:Flg UTSW 3 93,195,448 (GRCm39) unclassified probably benign
R9219:Flg UTSW 3 93,198,406 (GRCm39) missense possibly damaging 0.72
Z1176:Flg UTSW 3 93,187,269 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TTCTCAGAAGGCCAGGCAGTAG -3'
(R):5'- TCCTGTTGGCAGATGAGGAC -3'

Sequencing Primer
(F):5'- TAGGAGCTCACAGGCAGTC -3'
(R):5'- ACTCCAGAATGGACTTGGCTGTC -3'
Posted On 2019-11-12