Incidental Mutation 'IGL00590:Fndc1'
ID 5780
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Fndc1
Ensembl Gene ENSMUSG00000071984
Gene Name fibronectin type III domain containing 1
Synonyms 1110027O12Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # IGL00590
Quality Score
Status
Chromosome 17
Chromosomal Location 7957401-8046134 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 7983933 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 1331 (T1331I)
Ref Sequence ENSEMBL: ENSMUSP00000095036 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097425]
AlphaFold A0A6I8MWX0
Predicted Effect noncoding transcript
Transcript: ENSMUST00000097424
Predicted Effect unknown
Transcript: ENSMUST00000097425
AA Change: T1331I
SMART Domains Protein: ENSMUSP00000095036
Gene: ENSMUSG00000071984
AA Change: T1331I

DomainStartEndE-ValueType
Blast:FN3 1 50 6e-25 BLAST
FN3 54 137 7.82e-4 SMART
FN3 156 240 1.48e-4 SMART
FN3 256 340 3.67e-9 SMART
low complexity region 377 388 N/A INTRINSIC
low complexity region 579 601 N/A INTRINSIC
low complexity region 646 676 N/A INTRINSIC
low complexity region 766 777 N/A INTRINSIC
low complexity region 868 884 N/A INTRINSIC
low complexity region 1021 1027 N/A INTRINSIC
low complexity region 1036 1050 N/A INTRINSIC
low complexity region 1076 1090 N/A INTRINSIC
Blast:FN3 1227 1276 2e-18 BLAST
low complexity region 1277 1354 N/A INTRINSIC
low complexity region 1395 1403 N/A INTRINSIC
low complexity region 1407 1423 N/A INTRINSIC
FN3 1494 1577 4.32e-6 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000114579
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 T G 7: 120,023,038 (GRCm39) F58C probably damaging Het
Adgrf5 G T 17: 43,764,038 (GRCm39) G1320V probably damaging Het
Akap13 A G 7: 75,260,417 (GRCm39) K211E probably benign Het
Akap8l T C 17: 32,552,071 (GRCm39) D402G possibly damaging Het
Akna T C 4: 63,290,115 (GRCm39) I1198V probably benign Het
Apaf1 T A 10: 90,859,650 (GRCm39) I832F probably damaging Het
Cbl A C 9: 44,112,495 (GRCm39) L67V probably damaging Het
Chl1 T C 6: 103,670,022 (GRCm39) Y471H probably benign Het
Cystm1 T A 18: 36,499,728 (GRCm39) Y48N unknown Het
Dennd5b T C 6: 148,969,806 (GRCm39) T216A probably benign Het
Dpep2 A T 8: 106,715,453 (GRCm39) M356K probably damaging Het
Dtymk A G 1: 93,722,446 (GRCm39) probably null Het
Fam91a1 A G 15: 58,287,565 (GRCm39) D4G possibly damaging Het
Fbxl20 A G 11: 97,983,955 (GRCm39) L306P probably damaging Het
Fchsd1 C T 18: 38,098,946 (GRCm39) probably benign Het
Gpatch8 T C 11: 102,371,375 (GRCm39) D721G unknown Het
Gsg1 A T 6: 135,221,348 (GRCm39) I17N possibly damaging Het
Heyl A G 4: 123,140,423 (GRCm39) *327W probably null Het
Kif13b G T 14: 65,016,911 (GRCm39) R1359L probably damaging Het
Map3k14 C T 11: 103,128,380 (GRCm39) G414S probably damaging Het
Meis2 C T 2: 115,699,274 (GRCm39) A330T probably damaging Het
Mrpl9 T C 3: 94,351,003 (GRCm39) L61P probably damaging Het
Mrps6 A G 16: 91,896,548 (GRCm39) N38D probably benign Het
Muc4 C T 16: 32,575,465 (GRCm39) T1407I probably benign Het
Nup107 A G 10: 117,599,708 (GRCm39) Y604H probably damaging Het
Pgm2l1 T C 7: 99,904,826 (GRCm39) probably null Het
Pisd T C 5: 32,895,756 (GRCm39) I441V probably benign Het
Rb1cc1 T C 1: 6,308,520 (GRCm39) F52S probably damaging Het
Rnft1 T A 11: 86,386,740 (GRCm39) W383R probably damaging Het
Tas2r104 A T 6: 131,662,530 (GRCm39) W60R probably damaging Het
Tlr11 A G 14: 50,598,373 (GRCm39) T120A probably benign Het
Tmem150b T G 7: 4,726,896 (GRCm39) I71L probably benign Het
Zfp296 A G 7: 19,311,760 (GRCm39) D89G possibly damaging Het
Other mutations in Fndc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00513:Fndc1 APN 17 7,984,086 (GRCm39) missense unknown
IGL00765:Fndc1 APN 17 7,991,525 (GRCm39) missense unknown
IGL00904:Fndc1 APN 17 7,975,195 (GRCm39) missense probably benign 0.35
IGL01153:Fndc1 APN 17 7,998,874 (GRCm39) critical splice donor site probably null
IGL01557:Fndc1 APN 17 7,975,221 (GRCm39) missense probably damaging 0.99
IGL02493:Fndc1 APN 17 7,994,377 (GRCm39) missense unknown
IGL02501:Fndc1 APN 17 7,984,230 (GRCm39) missense unknown
IGL02503:Fndc1 APN 17 7,990,348 (GRCm39) missense unknown
IGL02887:Fndc1 APN 17 7,992,470 (GRCm39) missense unknown
IGL03348:Fndc1 APN 17 7,991,479 (GRCm39) missense unknown
pinnacle UTSW 17 7,992,154 (GRCm39) missense unknown
spire UTSW 17 7,990,312 (GRCm39) missense unknown
IGL02988:Fndc1 UTSW 17 7,972,355 (GRCm39) missense possibly damaging 0.95
PIT4466001:Fndc1 UTSW 17 7,969,206 (GRCm39) missense probably damaging 1.00
R0336:Fndc1 UTSW 17 7,983,939 (GRCm39) missense unknown
R0403:Fndc1 UTSW 17 7,994,420 (GRCm39) splice site probably null
R0403:Fndc1 UTSW 17 7,972,555 (GRCm39) missense probably damaging 1.00
R0538:Fndc1 UTSW 17 8,003,173 (GRCm39) splice site probably benign
R0646:Fndc1 UTSW 17 7,960,505 (GRCm39) missense possibly damaging 0.92
R1140:Fndc1 UTSW 17 7,994,258 (GRCm39) missense unknown
R1523:Fndc1 UTSW 17 7,992,041 (GRCm39) missense unknown
R1609:Fndc1 UTSW 17 7,991,598 (GRCm39) missense unknown
R1632:Fndc1 UTSW 17 7,992,032 (GRCm39) missense unknown
R1888:Fndc1 UTSW 17 7,990,621 (GRCm39) missense unknown
R1888:Fndc1 UTSW 17 7,990,621 (GRCm39) missense unknown
R2004:Fndc1 UTSW 17 8,023,761 (GRCm39) missense probably damaging 1.00
R2007:Fndc1 UTSW 17 7,997,580 (GRCm39) unclassified probably benign
R2128:Fndc1 UTSW 17 7,997,497 (GRCm39) unclassified probably benign
R2187:Fndc1 UTSW 17 7,960,604 (GRCm39) missense probably damaging 1.00
R2251:Fndc1 UTSW 17 7,972,439 (GRCm39) missense probably damaging 1.00
R2322:Fndc1 UTSW 17 8,007,847 (GRCm39) missense probably damaging 0.98
R2425:Fndc1 UTSW 17 8,023,850 (GRCm39) missense probably damaging 1.00
R2921:Fndc1 UTSW 17 8,023,707 (GRCm39) missense probably damaging 0.98
R2985:Fndc1 UTSW 17 7,975,155 (GRCm39) missense possibly damaging 0.93
R3436:Fndc1 UTSW 17 7,969,189 (GRCm39) missense probably damaging 0.99
R3499:Fndc1 UTSW 17 7,972,416 (GRCm39) missense possibly damaging 0.70
R3508:Fndc1 UTSW 17 7,983,940 (GRCm39) nonsense probably null
R3766:Fndc1 UTSW 17 8,003,253 (GRCm39) missense probably damaging 1.00
R3813:Fndc1 UTSW 17 7,992,154 (GRCm39) missense unknown
R3814:Fndc1 UTSW 17 7,992,154 (GRCm39) missense unknown
R4031:Fndc1 UTSW 17 7,988,584 (GRCm39) nonsense probably null
R4544:Fndc1 UTSW 17 7,992,376 (GRCm39) missense unknown
R4583:Fndc1 UTSW 17 7,958,081 (GRCm39) missense probably damaging 1.00
R4619:Fndc1 UTSW 17 7,984,036 (GRCm39) missense unknown
R4700:Fndc1 UTSW 17 7,990,312 (GRCm39) missense unknown
R4743:Fndc1 UTSW 17 7,991,111 (GRCm39) nonsense probably null
R4803:Fndc1 UTSW 17 7,972,538 (GRCm39) missense probably damaging 0.98
R4862:Fndc1 UTSW 17 7,988,567 (GRCm39) missense unknown
R4876:Fndc1 UTSW 17 7,990,471 (GRCm39) missense unknown
R5057:Fndc1 UTSW 17 7,990,802 (GRCm39) nonsense probably null
R5327:Fndc1 UTSW 17 7,991,540 (GRCm39) missense unknown
R5372:Fndc1 UTSW 17 7,984,042 (GRCm39) missense unknown
R5533:Fndc1 UTSW 17 7,991,608 (GRCm39) missense unknown
R5754:Fndc1 UTSW 17 7,988,585 (GRCm39) missense unknown
R5762:Fndc1 UTSW 17 7,990,366 (GRCm39) missense unknown
R5830:Fndc1 UTSW 17 8,007,918 (GRCm39) missense possibly damaging 0.87
R5924:Fndc1 UTSW 17 7,992,442 (GRCm39) missense unknown
R6147:Fndc1 UTSW 17 7,972,594 (GRCm39) splice site probably null
R6175:Fndc1 UTSW 17 7,991,479 (GRCm39) missense unknown
R6303:Fndc1 UTSW 17 7,977,317 (GRCm39) missense probably damaging 0.98
R6377:Fndc1 UTSW 17 7,988,567 (GRCm39) missense unknown
R6704:Fndc1 UTSW 17 7,990,642 (GRCm39) missense unknown
R6857:Fndc1 UTSW 17 7,991,002 (GRCm39) missense unknown
R6865:Fndc1 UTSW 17 7,991,672 (GRCm39) missense unknown
R7069:Fndc1 UTSW 17 7,988,567 (GRCm39) missense unknown
R7153:Fndc1 UTSW 17 8,020,477 (GRCm39) missense probably damaging 1.00
R7159:Fndc1 UTSW 17 8,019,763 (GRCm39) missense probably damaging 0.97
R7359:Fndc1 UTSW 17 8,032,318 (GRCm39) splice site probably null
R7731:Fndc1 UTSW 17 7,992,271 (GRCm39) missense unknown
R7743:Fndc1 UTSW 17 7,983,969 (GRCm39) missense unknown
R7884:Fndc1 UTSW 17 7,992,029 (GRCm39) missense unknown
R8071:Fndc1 UTSW 17 7,991,362 (GRCm39) missense unknown
R8100:Fndc1 UTSW 17 7,990,685 (GRCm39) missense unknown
R8317:Fndc1 UTSW 17 8,019,720 (GRCm39) nonsense probably null
R8362:Fndc1 UTSW 17 8,001,207 (GRCm39) missense unknown
R8835:Fndc1 UTSW 17 7,958,111 (GRCm39) missense probably damaging 1.00
R8841:Fndc1 UTSW 17 7,992,181 (GRCm39) missense unknown
R8912:Fndc1 UTSW 17 8,019,778 (GRCm39) missense probably null 0.26
R9236:Fndc1 UTSW 17 7,992,460 (GRCm39) missense unknown
R9392:Fndc1 UTSW 17 7,991,957 (GRCm39) missense unknown
R9412:Fndc1 UTSW 17 7,991,198 (GRCm39) missense unknown
R9618:Fndc1 UTSW 17 7,990,313 (GRCm39) missense unknown
R9632:Fndc1 UTSW 17 7,991,622 (GRCm39) missense unknown
R9748:Fndc1 UTSW 17 7,991,929 (GRCm39) missense unknown
Z1088:Fndc1 UTSW 17 8,001,311 (GRCm39) missense probably damaging 0.96
Z1176:Fndc1 UTSW 17 8,023,709 (GRCm39) missense possibly damaging 0.90
Z1176:Fndc1 UTSW 17 7,992,425 (GRCm39) nonsense probably null
Posted On 2012-04-20