Incidental Mutation 'R4863:Fuca2'
ID 374672
Institutional Source Beutler Lab
Gene Symbol Fuca2
Ensembl Gene ENSMUSG00000019810
Gene Name fucosidase, alpha-L- 2, plasma
MMRRC Submission 042473-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.179) question?
Stock # R4863 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 13499540-13519035 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 13505907 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 188 (D188V)
Ref Sequence ENSEMBL: ENSMUSP00000113499 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000060212] [ENSMUST00000120549] [ENSMUST00000121465] [ENSMUST00000130865]
AlphaFold Q99KR8
Predicted Effect probably damaging
Transcript: ENSMUST00000060212
AA Change: D188V

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000055519
Gene: ENSMUSG00000019810
AA Change: D188V

low complexity region 6 17 N/A INTRINSIC
Alpha_L_fucos 27 407 1.53e-235 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000120549
SMART Domains Protein: ENSMUSP00000114021
Gene: ENSMUSG00000019810

Alpha_L_fucos 1 95 1.15e-6 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000121465
AA Change: D188V

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000113499
Gene: ENSMUSG00000019810
AA Change: D188V

low complexity region 6 17 N/A INTRINSIC
Alpha_L_fucos 27 407 1.53e-235 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000130865
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150048
Predicted Effect noncoding transcript
Transcript: ENSMUST00000166466
Meta Mutation Damage Score 0.9192 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 99% (105/106)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a plasma alpha-L-fucosidase, which represents 10-20% of the total cellular fucosidase activity. The protein is a member of the glycosyl hydrolase 29 family, and catalyzes the hydrolysis of the alpha-1,6-linked fucose joined to the reducing-end N-acetylglucosamine of the carbohydrate moieties of glycoproteins. This enzyme is essential for Helicobacter pylori adhesion to human gastric cancer cells. [provided by RefSeq, Aug 2010]
PHENOTYPE: No notable phenotype was detected in a high-throughput screen of homozygous mutant mice. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 98 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930578I06Rik C T 14: 63,973,209 (GRCm38) R190H probably benign Het
Abcc12 T A 8: 86,538,376 (GRCm38) I647F probably damaging Het
Acnat2 C A 4: 49,380,172 (GRCm38) W384L probably damaging Het
Acvr1 A G 2: 58,477,711 (GRCm38) L146P possibly damaging Het
Ankrd16 T A 2: 11,784,316 (GRCm38) M238K probably benign Het
Clmn A T 12: 104,797,094 (GRCm38) I91N probably damaging Het
Cog8 A T 8: 107,050,174 (GRCm38) L523H probably damaging Het
Cpxm2 T A 7: 132,059,747 (GRCm38) K437M probably benign Het
Dhx57 A T 17: 80,253,111 (GRCm38) V999E probably damaging Het
Dnpep T C 1: 75,309,230 (GRCm38) probably benign Het
Dok3 G A 13: 55,523,457 (GRCm38) R434W probably damaging Het
Dpysl5 C T 5: 30,784,343 (GRCm38) H275Y probably benign Het
Ednra A T 8: 77,667,383 (GRCm38) N361K probably damaging Het
Ei24 A T 9: 36,784,565 (GRCm38) S210R probably damaging Het
Erich3 T A 3: 154,764,804 (GRCm38) V158E unknown Het
Fam193a T A 5: 34,466,205 (GRCm38) V1379E possibly damaging Het
Fasn A G 11: 120,808,828 (GRCm38) V2304A probably damaging Het
Fcgbp A C 7: 28,086,344 (GRCm38) D402A probably benign Het
Fkbp14 T C 6: 54,585,945 (GRCm38) probably benign Het
Fnip1 G A 11: 54,515,556 (GRCm38) V1160I possibly damaging Het
Fsd2 T C 7: 81,552,964 (GRCm38) K289R probably null Het
Gfpt2 T C 11: 49,810,970 (GRCm38) V116A probably benign Het
Gm10770 T A 2: 150,178,896 (GRCm38) K234* probably null Het
Gm9887 A G 12: 69,371,989 (GRCm38) probably benign Het
Gtf3c2 A G 5: 31,159,233 (GRCm38) probably benign Het
H2-M10.3 T C 17: 36,366,636 (GRCm38) D250G probably damaging Het
Hapln4 G A 8: 70,084,492 (GRCm38) V26M possibly damaging Het
Hook3 G A 8: 26,038,029 (GRCm38) A611V probably damaging Het
Hr T C 14: 70,571,972 (GRCm38) L1141P probably damaging Het
Ifngr1 T C 10: 19,609,416 (GRCm38) S388P probably damaging Het
Itga3 T A 11: 95,061,967 (GRCm38) Q326L probably damaging Het
Itgb3 T A 11: 104,665,520 (GRCm38) I729N probably damaging Het
Kcnab2 A G 4: 152,401,946 (GRCm38) S132P probably damaging Het
Lama3 T C 18: 12,498,678 (GRCm38) probably benign Het
Lama3 C T 18: 12,539,793 (GRCm38) A2481V probably damaging Het
Lce1e A T 3: 92,707,871 (GRCm38) C56* probably null Het
Lmcd1 T C 6: 112,287,871 (GRCm38) probably benign Het
Lrrc14 T A 15: 76,713,362 (GRCm38) probably null Het
Lypd8l A T 11: 58,612,512 (GRCm38) probably null Het
Map4k5 G A 12: 69,818,438 (GRCm38) P591L probably benign Het
Mapk13 C A 17: 28,776,310 (GRCm38) D168E probably damaging Het
Marf1 A C 16: 14,132,665 (GRCm38) H952Q possibly damaging Het
Megf6 T C 4: 154,254,281 (GRCm38) probably null Het
Mical3 T C 6: 121,033,787 (GRCm38) I411M probably damaging Het
Myo5a A T 9: 75,217,507 (GRCm38) K1781N probably damaging Het
N4bp2 T C 5: 65,808,130 (GRCm38) V1174A probably benign Het
Ncdn A T 4: 126,750,423 (GRCm38) L202Q probably damaging Het
Ncor1 T A 11: 62,392,638 (GRCm38) M408L possibly damaging Het
Nf1 T C 11: 79,409,409 (GRCm38) L249P probably damaging Het
Nlrp9b T A 7: 20,049,596 (GRCm38) probably null Het
Nxpe3 A T 16: 55,849,633 (GRCm38) Y370N probably damaging Het
P2rx2 T A 5: 110,341,568 (GRCm38) T167S probably benign Het
Pcdhb19 G T 18: 37,499,108 (GRCm38) R652L probably benign Het
Pcdhga12 T C 18: 37,768,281 (GRCm38) L722P probably benign Het
Pde6a A T 18: 61,245,592 (GRCm38) I329F probably damaging Het
Pdpr T A 8: 111,101,951 (GRCm38) S29T probably benign Het
Pfkfb3 T C 2: 11,486,312 (GRCm38) D173G probably benign Het
Plcd4 A G 1: 74,565,802 (GRCm38) probably null Het
Polr1g T A 7: 19,357,759 (GRCm38) Q141L probably damaging Het
Pou2f2 A G 7: 25,097,108 (GRCm38) probably benign Het
Ppp1r14c TGGCGGCGGCGGCGGCGG TGGCGGCGGCGGCGG 10: 3,366,702 (GRCm38) probably benign Het
Ppp1r42 T C 1: 10,003,386 (GRCm38) probably benign Het
Ptpre C T 7: 135,669,132 (GRCm38) H346Y probably benign Het
Ptpro T A 6: 137,443,594 (GRCm38) V1007D probably damaging Het
Rab12 A T 17: 66,498,108 (GRCm38) Y142N probably damaging Het
Rai14 A C 15: 10,572,470 (GRCm38) M857R probably damaging Het
Ranbp2 A G 10: 58,492,421 (GRCm38) K2753R probably damaging Het
Rasa4 A T 5: 136,103,911 (GRCm38) K6* probably null Het
Rasgef1a A G 6: 118,089,139 (GRCm38) M438V probably benign Het
Recql T G 6: 142,359,006 (GRCm38) probably benign Het
Rftn2 A G 1: 55,172,039 (GRCm38) V425A probably benign Het
Ror1 A G 4: 100,409,804 (GRCm38) Y234C probably damaging Het
Sap30l T A 11: 57,806,054 (GRCm38) L70Q probably damaging Het
Scn4a T C 11: 106,320,002 (GRCm38) R1730G probably damaging Het
Serinc5 T G 13: 92,690,980 (GRCm38) I268R probably damaging Het
Sin3b G A 8: 72,744,948 (GRCm38) V432I possibly damaging Het
Slc30a6 T C 17: 74,412,654 (GRCm38) M203T possibly damaging Het
Soat1 T C 1: 156,432,328 (GRCm38) N481S probably damaging Het
Sos2 G A 12: 69,640,154 (GRCm38) T206I probably benign Het
Sp100 G T 1: 85,705,003 (GRCm38) A132S probably benign Het
Sp140l1 C T 1: 85,088,800 (GRCm38) probably benign Het
Spata31d1c T A 13: 65,035,790 (GRCm38) L382* probably null Het
Stard9 T A 2: 120,700,860 (GRCm38) W2533R probably benign Het
Tas2r126 A G 6: 42,435,390 (GRCm38) T286A probably benign Het
Tedc2 T A 17: 24,217,936 (GRCm38) K275M probably damaging Het
Ten1 A T 11: 116,218,231 (GRCm38) K242N probably benign Het
Thoc2l A T 5: 104,517,750 (GRCm38) D46V possibly damaging Het
Tial1 C T 7: 128,455,028 (GRCm38) V1I probably damaging Het
Tle2 G A 10: 81,588,891 (GRCm38) R649H possibly damaging Het
Tmem178 A G 17: 80,944,945 (GRCm38) D86G probably benign Het
Trim29 T A 9: 43,329,575 (GRCm38) D528E possibly damaging Het
Vmn2r61 A T 7: 42,300,708 (GRCm38) T851S probably benign Het
Vmn2r72 T A 7: 85,750,598 (GRCm38) Q414H possibly damaging Het
Yars1 A T 4: 129,189,882 (GRCm38) probably benign Het
Yipf4 A G 17: 74,494,092 (GRCm38) Q135R probably damaging Het
Zfp341 G A 2: 154,645,866 (GRCm38) probably benign Het
Zfp426 T C 9: 20,470,038 (GRCm38) Y536C probably damaging Het
Zp2 T G 7: 120,135,772 (GRCm38) Y430S probably damaging Het
Other mutations in Fuca2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00562:Fuca2 APN 10 13,505,907 (GRCm38) missense probably damaging 0.99
IGL00563:Fuca2 APN 10 13,505,907 (GRCm38) missense probably damaging 0.99
IGL02935:Fuca2 APN 10 13,507,319 (GRCm38) missense probably null 0.00
IGL02953:Fuca2 APN 10 13,507,429 (GRCm38) splice site probably benign
R0366:Fuca2 UTSW 10 13,505,763 (GRCm38) missense probably benign
R0543:Fuca2 UTSW 10 13,503,126 (GRCm38) missense probably damaging 1.00
R0731:Fuca2 UTSW 10 13,506,027 (GRCm38) missense probably benign 0.08
R1573:Fuca2 UTSW 10 13,505,843 (GRCm38) missense possibly damaging 0.90
R1879:Fuca2 UTSW 10 13,507,256 (GRCm38) missense possibly damaging 0.64
R2026:Fuca2 UTSW 10 13,512,647 (GRCm38) missense probably damaging 0.97
R2030:Fuca2 UTSW 10 13,506,774 (GRCm38) missense probably damaging 0.99
R2142:Fuca2 UTSW 10 13,505,865 (GRCm38) missense probably damaging 1.00
R2883:Fuca2 UTSW 10 13,505,951 (GRCm38) missense probably benign 0.01
R4462:Fuca2 UTSW 10 13,503,235 (GRCm38) missense probably damaging 1.00
R5466:Fuca2 UTSW 10 13,512,697 (GRCm38) nonsense probably null
R5640:Fuca2 UTSW 10 13,507,430 (GRCm38) splice site probably null
R6199:Fuca2 UTSW 10 13,506,039 (GRCm38) missense probably damaging 0.96
R7136:Fuca2 UTSW 10 13,505,921 (GRCm38) missense probably benign 0.27
R7555:Fuca2 UTSW 10 13,507,430 (GRCm38) splice site probably null
R8111:Fuca2 UTSW 10 13,514,801 (GRCm38) missense probably benign 0.02
R8266:Fuca2 UTSW 10 13,512,889 (GRCm38) intron probably benign
R9177:Fuca2 UTSW 10 13,514,819 (GRCm38) nonsense probably null
R9268:Fuca2 UTSW 10 13,514,819 (GRCm38) nonsense probably null
R9340:Fuca2 UTSW 10 13,506,774 (GRCm38) missense probably damaging 0.99
R9630:Fuca2 UTSW 10 13,503,076 (GRCm38) missense probably benign 0.01
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2016-03-17