Incidental Mutation 'R8127:Fut10'
ID 651984
Institutional Source Beutler Lab
Gene Symbol Fut10
Ensembl Gene ENSMUSG00000046152
Gene Name fucosyltransferase 10
Synonyms
MMRRC Submission 067556-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.074) question?
Stock # R8127 (G1)
Quality Score 57.0073
Status Validated
Chromosome 8
Chromosomal Location 31677359-31751766 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) G to A at 31684999 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124437 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066173] [ENSMUST00000110527] [ENSMUST00000161502] [ENSMUST00000161788]
AlphaFold Q5F2L2
Predicted Effect probably benign
Transcript: ENSMUST00000066173
SMART Domains Protein: ENSMUSP00000069816
Gene: ENSMUSG00000046152

DomainStartEndE-ValueType
transmembrane domain 9 31 N/A INTRINSIC
Pfam:Glyco_tran_10_N 79 184 5e-13 PFAM
Pfam:Glyco_transf_10 209 410 7.9e-38 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000110527
SMART Domains Protein: ENSMUSP00000106156
Gene: ENSMUSG00000046152

DomainStartEndE-ValueType
Pfam:Glyco_transf_10 7 134 3e-9 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000161502
SMART Domains Protein: ENSMUSP00000125265
Gene: ENSMUSG00000046152

DomainStartEndE-ValueType
Pfam:Glyco_transf_10 7 412 4.1e-92 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000161788
SMART Domains Protein: ENSMUSP00000124437
Gene: ENSMUSG00000046152

DomainStartEndE-ValueType
Pfam:Glyco_transf_10 7 411 1.3e-92 PFAM
low complexity region 418 429 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.6%
  • 10x: 98.9%
  • 20x: 97.0%
Validation Efficiency 100% (45/45)
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik T C 5: 144,980,249 (GRCm39) M66T possibly damaging Het
Acvr1 A T 2: 58,367,638 (GRCm39) N174K probably benign Het
Ago1 A T 4: 126,348,214 (GRCm39) C342S possibly damaging Het
Anapc1 A G 2: 128,474,547 (GRCm39) S1423P probably damaging Het
Antxr2 A T 5: 98,127,876 (GRCm39) C218* probably null Het
Arsa A G 15: 89,359,067 (GRCm39) Y200H probably damaging Het
Atad3a C T 4: 155,838,396 (GRCm39) R207Q probably damaging Het
Carmil3 A G 14: 55,735,701 (GRCm39) D551G probably damaging Het
Cdk9 A G 2: 32,598,009 (GRCm39) I349T probably benign Het
Cmya5 A T 13: 93,231,122 (GRCm39) V1322E probably damaging Het
Col4a3 T A 1: 82,627,481 (GRCm39) I95K unknown Het
Dab2ip T C 2: 35,534,138 (GRCm39) probably benign Het
Dnaaf6rt T C 1: 31,262,201 (GRCm39) F61S probably benign Het
Dok7 A G 5: 35,244,345 (GRCm39) S530G probably benign Het
Dst C T 1: 34,217,310 (GRCm39) T1250M probably damaging Het
Dzank1 A C 2: 144,330,736 (GRCm39) W439G probably damaging Het
Evx1 T A 6: 52,290,902 (GRCm39) S25T possibly damaging Het
Gatad1 T C 5: 3,693,540 (GRCm39) R210G probably benign Het
Hyal5 C A 6: 24,891,487 (GRCm39) R434S probably benign Het
Lrrc43 C T 5: 123,630,334 (GRCm39) P66S probably damaging Het
Mib1 T A 18: 10,741,031 (GRCm39) I93N probably damaging Het
Mug2 G A 6: 122,052,567 (GRCm39) E1038K probably benign Het
Nsd2 T A 5: 34,042,834 (GRCm39) C1033S probably damaging Het
Or6k4 C T 1: 173,965,155 (GRCm39) P282S probably damaging Het
Or8d4 T A 9: 40,038,360 (GRCm39) H299L probably benign Het
Otogl A T 10: 107,731,613 (GRCm39) F176Y probably damaging Het
Polr3b A G 10: 84,515,653 (GRCm39) K609E probably benign Het
Prdm15 T C 16: 97,638,910 (GRCm39) N50S probably benign Het
Rlf G T 4: 121,005,093 (GRCm39) Q1406K possibly damaging Het
Rusc2 T C 4: 43,423,747 (GRCm39) V1023A possibly damaging Het
Scn11a C T 9: 119,633,578 (GRCm39) G385D probably damaging Het
Slc44a1 T C 4: 53,528,714 (GRCm39) S155P probably benign Het
Spam1 T A 6: 24,796,970 (GRCm39) V307D possibly damaging Het
Srgap1 A C 10: 121,691,271 (GRCm39) M321R probably null Het
Stam A G 2: 14,122,284 (GRCm39) I128V probably damaging Het
Sytl2 A G 7: 90,024,798 (GRCm39) D262G possibly damaging Het
Taf2 G A 15: 54,923,384 (GRCm39) R298C probably damaging Het
Tcl1b5 A T 12: 105,146,262 (GRCm39) T112S probably benign Het
Trim33 T C 3: 103,239,043 (GRCm39) S674P possibly damaging Het
Trip12 T C 1: 84,716,463 (GRCm39) N1602S probably damaging Het
Vmn1r44 T C 6: 89,870,845 (GRCm39) I197T probably benign Het
Wdtc1 C T 4: 133,029,693 (GRCm39) probably null Het
Zfp583 G T 7: 6,326,821 (GRCm39) probably null Het
Zfyve16 T A 13: 92,642,185 (GRCm39) I1213F probably damaging Het
Other mutations in Fut10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00336:Fut10 APN 8 31,685,319 (GRCm39) critical splice donor site probably null
IGL00566:Fut10 APN 8 31,725,712 (GRCm39) missense probably damaging 1.00
IGL00858:Fut10 APN 8 31,725,733 (GRCm39) missense probably damaging 0.97
IGL00861:Fut10 APN 8 31,725,733 (GRCm39) missense probably damaging 0.97
IGL00862:Fut10 APN 8 31,725,733 (GRCm39) missense probably damaging 0.97
IGL01916:Fut10 APN 8 31,725,734 (GRCm39) missense probably benign 0.01
IGL02030:Fut10 APN 8 31,726,006 (GRCm39) nonsense probably null
IGL02318:Fut10 APN 8 31,726,286 (GRCm39) missense probably damaging 1.00
IGL02354:Fut10 APN 8 31,691,398 (GRCm39) missense probably damaging 0.99
IGL02361:Fut10 APN 8 31,691,398 (GRCm39) missense probably damaging 0.99
IGL02932:Fut10 APN 8 31,749,965 (GRCm39) missense probably damaging 1.00
IGL03345:Fut10 APN 8 31,750,069 (GRCm39) missense probably damaging 1.00
R0234:Fut10 UTSW 8 31,726,225 (GRCm39) missense probably damaging 1.00
R0234:Fut10 UTSW 8 31,726,225 (GRCm39) missense probably damaging 1.00
R1728:Fut10 UTSW 8 31,691,418 (GRCm39) missense probably benign 0.00
R1729:Fut10 UTSW 8 31,691,418 (GRCm39) missense probably benign 0.00
R1845:Fut10 UTSW 8 31,726,328 (GRCm39) missense probably damaging 1.00
R2173:Fut10 UTSW 8 31,726,159 (GRCm39) missense probably damaging 1.00
R2518:Fut10 UTSW 8 31,726,495 (GRCm39) missense probably benign 0.19
R3692:Fut10 UTSW 8 31,726,048 (GRCm39) missense possibly damaging 0.94
R4449:Fut10 UTSW 8 31,726,285 (GRCm39) missense probably damaging 1.00
R5015:Fut10 UTSW 8 31,726,148 (GRCm39) missense probably damaging 0.96
R5942:Fut10 UTSW 8 31,691,485 (GRCm39) missense possibly damaging 0.62
R6497:Fut10 UTSW 8 31,726,278 (GRCm39) missense probably damaging 0.99
R7566:Fut10 UTSW 8 31,749,950 (GRCm39) missense probably benign 0.00
R7645:Fut10 UTSW 8 31,726,232 (GRCm39) missense possibly damaging 0.92
R8241:Fut10 UTSW 8 31,750,034 (GRCm39) nonsense probably null
R8899:Fut10 UTSW 8 31,726,514 (GRCm39) missense possibly damaging 0.46
R9314:Fut10 UTSW 8 31,691,504 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TTGAGACTTGGGAGTTGATGAAAC -3'
(R):5'- CAGAGACAGCTTCACATGGAG -3'

Sequencing Primer
(F):5'- TTGATGAAACTGTGGCCCC -3'
(R):5'- AGCTTCACATGGAGGAACC -3'
Posted On 2020-09-18