Incidental Mutation 'R7456:Slc35f3'
ID 578136
Institutional Source Beutler Lab
Gene Symbol Slc35f3
Ensembl Gene ENSMUSG00000057060
Gene Name solute carrier family 35, member F3
Synonyms B230375D17Rik
MMRRC Submission 045530-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.160) question?
Stock # R7456 (G1)
Quality Score 217.468
Status Not validated
Chromosome 8
Chromosomal Location 126865734-127122717 bp(+) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC to CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC at 127115779 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104390 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108759]
AlphaFold Q1LZI2
Predicted Effect unknown
Transcript: ENSMUST00000108759
SMART Domains Protein: ENSMUSP00000104390
Gene: ENSMUSG00000057060

DomainStartEndE-ValueType
low complexity region 25 49 N/A INTRINSIC
Pfam:EamA 67 223 3.2e-7 PFAM
Pfam:SLC35F 145 374 3.2e-6 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 75 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acer2 A G 4: 86,792,748 (GRCm39) D8G possibly damaging Het
Angpt4 T C 2: 151,780,987 (GRCm39) Y412H probably damaging Het
Ankef1 A G 2: 136,387,734 (GRCm39) D217G probably benign Het
Ano2 A T 6: 125,940,508 (GRCm39) I544F probably benign Het
App G A 16: 84,970,448 (GRCm39) Het
Arhgef26 A G 3: 62,247,476 (GRCm39) T187A probably benign Het
Axin1 T A 17: 26,362,139 (GRCm39) V161E probably damaging Het
Bbs7 A T 3: 36,648,527 (GRCm39) V407D probably damaging Het
C1qtnf3 A T 15: 10,972,137 (GRCm39) E141V probably benign Het
C2 A G 17: 35,083,558 (GRCm39) I469T probably damaging Het
Cc2d1a A G 8: 84,866,868 (GRCm39) probably null Het
Cd226 A T 18: 89,224,747 (GRCm39) I10F probably damaging Het
Cep295nl T C 11: 118,224,376 (GRCm39) K156R possibly damaging Het
Cfap20dc A T 14: 8,442,933 (GRCm38) L612* probably null Het
Cfap44 A G 16: 44,252,305 (GRCm39) T805A probably benign Het
Chd9 G T 8: 91,659,153 (GRCm39) E38* probably null Het
Cldnd2 C T 7: 43,091,109 (GRCm39) L14F not run Het
Cyp11b2 T C 15: 74,725,379 (GRCm39) T247A probably benign Het
Dennd11 T G 6: 40,383,774 (GRCm39) M423L probably benign Het
Dsc1 T C 18: 20,219,879 (GRCm39) S764G probably benign Het
Dsg3 A T 18: 20,664,420 (GRCm39) T473S probably benign Het
Fam193a A T 5: 34,578,132 (GRCm39) I209F possibly damaging Het
Foxs1 T C 2: 152,775,045 (GRCm39) K3E probably benign Het
Gabrr3 C T 16: 59,227,853 (GRCm39) Q37* probably null Het
Gcm2 A T 13: 41,256,751 (GRCm39) W333R probably benign Het
Gcn1 C T 5: 115,743,005 (GRCm39) Q1559* probably null Het
Gfm2 A T 13: 97,282,211 (GRCm39) K69* probably null Het
Gm14295 T G 2: 176,500,943 (GRCm39) C144W possibly damaging Het
Gm32742 G A 9: 51,071,270 (GRCm39) T5I probably damaging Het
Gm5093 T C 17: 46,750,679 (GRCm39) D116G probably damaging Het
Gsn A T 2: 35,172,718 (GRCm39) K3N possibly damaging Het
H2-M2 C T 17: 37,792,552 (GRCm39) D240N possibly damaging Het
Habp2 G C 19: 56,307,957 (GRCm39) G482R probably damaging Het
Hnrnpm A T 17: 33,865,622 (GRCm39) Y680N possibly damaging Het
Hrc T A 7: 44,986,320 (GRCm39) D490E possibly damaging Het
Impg2 A G 16: 56,080,276 (GRCm39) I693M probably benign Het
Itga7 A G 10: 128,777,805 (GRCm39) Y262C probably damaging Het
Kif1c A G 11: 70,619,424 (GRCm39) T1020A probably benign Het
Kif23 T C 9: 61,844,402 (GRCm39) I139V probably benign Het
Klk1b5 A G 7: 43,500,255 (GRCm39) E281G probably benign Het
Kpna4 A G 3: 69,000,181 (GRCm39) V275A probably damaging Het
Lamb2 C A 9: 108,362,979 (GRCm39) D787E possibly damaging Het
Ldlrad3 A C 2: 101,785,270 (GRCm39) V235G probably damaging Het
Maneal A G 4: 124,750,767 (GRCm39) S330P probably damaging Het
Maz G A 7: 126,625,489 (GRCm39) Q35* probably null Het
Mthfd1l C T 10: 4,039,998 (GRCm39) T803M probably damaging Het
Muc5ac A G 7: 141,346,904 (GRCm39) Q325R probably benign Het
Myo3a C A 2: 22,412,255 (GRCm39) A758E probably benign Het
Ndufb7 A G 8: 84,293,482 (GRCm39) D12G probably benign Het
Nsun2 T A 13: 69,781,725 (GRCm39) C677S probably damaging Het
Obscn A G 11: 58,899,384 (GRCm39) F6471S probably benign Het
Or4c106 A T 2: 88,682,563 (GRCm39) I90F probably damaging Het
Or51k1 A G 7: 103,661,045 (GRCm39) V288A possibly damaging Het
Or7g32 T C 9: 19,408,844 (GRCm39) S267P probably damaging Het
Otof T C 5: 30,552,005 (GRCm39) D313G probably damaging Het
Paqr5 T C 9: 61,880,072 (GRCm39) D74G probably benign Het
Pigq A G 17: 26,153,580 (GRCm39) V365A unknown Het
Podn A T 4: 107,875,002 (GRCm39) N588K probably benign Het
Polr3b G A 10: 84,458,355 (GRCm39) G9R probably benign Het
Proser1 A G 3: 53,385,939 (GRCm39) H607R probably damaging Het
Ryr2 C T 13: 11,767,168 (GRCm39) V1241I probably benign Het
Sar1b G A 11: 51,682,181 (GRCm39) A170T probably benign Het
Slc22a17 T C 14: 55,149,716 (GRCm39) T191A probably benign Het
Slco6d1 A T 1: 98,349,082 (GRCm39) D51V possibly damaging Het
Snx16 G A 3: 10,500,541 (GRCm39) R143* probably null Het
Sytl2 T A 7: 89,998,055 (GRCm39) L19Q probably damaging Het
Tmcc3 A G 10: 94,418,174 (GRCm39) E345G possibly damaging Het
Ttn C T 2: 76,555,998 (GRCm39) A30336T probably damaging Het
Vmn1r44 A G 6: 89,870,401 (GRCm39) D49G probably benign Het
Vps35l C T 7: 118,403,340 (GRCm39) P628S probably benign Het
Vps41 T A 13: 19,048,204 (GRCm39) D801E probably benign Het
Wif1 G A 10: 120,932,554 (GRCm39) E311K probably benign Het
Zfp513 G T 5: 31,357,759 (GRCm39) R207S possibly damaging Het
Zfp52 C A 17: 21,781,615 (GRCm39) H488N probably damaging Het
Zfp738 A G 13: 67,817,619 (GRCm39) Y791H probably damaging Het
Other mutations in Slc35f3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00687:Slc35f3 APN 8 127,108,903 (GRCm39) missense probably benign 0.02
IGL00956:Slc35f3 APN 8 127,108,963 (GRCm39) missense probably damaging 1.00
IGL01105:Slc35f3 APN 8 127,025,553 (GRCm39) missense probably damaging 1.00
IGL01710:Slc35f3 APN 8 127,115,900 (GRCm39) missense probably benign 0.00
IGL01771:Slc35f3 APN 8 127,115,951 (GRCm39) missense probably benign 0.00
IGL02254:Slc35f3 APN 8 127,115,862 (GRCm39) missense probably damaging 1.00
IGL02610:Slc35f3 APN 8 127,047,956 (GRCm39) missense probably damaging 1.00
R1666:Slc35f3 UTSW 8 127,115,960 (GRCm39) missense probably damaging 0.98
R2510:Slc35f3 UTSW 8 127,025,445 (GRCm39) start gained probably benign
R2520:Slc35f3 UTSW 8 127,121,312 (GRCm39) missense possibly damaging 0.81
R3807:Slc35f3 UTSW 8 127,115,978 (GRCm39) missense probably damaging 1.00
R4644:Slc35f3 UTSW 8 127,047,809 (GRCm39) missense possibly damaging 0.87
R4675:Slc35f3 UTSW 8 127,047,935 (GRCm39) nonsense probably null
R4976:Slc35f3 UTSW 8 127,116,020 (GRCm39) splice site probably null
R5037:Slc35f3 UTSW 8 127,116,011 (GRCm39) missense probably damaging 0.99
R5225:Slc35f3 UTSW 8 127,117,846 (GRCm39) missense probably damaging 0.98
R5259:Slc35f3 UTSW 8 127,115,872 (GRCm39) missense probably damaging 1.00
R5856:Slc35f3 UTSW 8 127,047,819 (GRCm39) missense probably benign 0.07
R5925:Slc35f3 UTSW 8 127,115,946 (GRCm39) missense probably benign 0.24
R6254:Slc35f3 UTSW 8 127,047,833 (GRCm39) missense possibly damaging 0.96
R6748:Slc35f3 UTSW 8 127,121,377 (GRCm39) nonsense probably null
R6785:Slc35f3 UTSW 8 127,121,198 (GRCm39) missense probably benign 0.02
R7002:Slc35f3 UTSW 8 127,115,773 (GRCm39) critical splice acceptor site unknown
R7291:Slc35f3 UTSW 8 127,121,297 (GRCm39) missense probably benign 0.02
R7411:Slc35f3 UTSW 8 127,115,777 (GRCm39) critical splice acceptor site probably benign
R7790:Slc35f3 UTSW 8 127,115,777 (GRCm39) critical splice acceptor site probably benign
R7852:Slc35f3 UTSW 8 127,121,219 (GRCm39) missense probably damaging 1.00
R8000:Slc35f3 UTSW 8 127,047,812 (GRCm39) missense probably benign
R8277:Slc35f3 UTSW 8 127,115,925 (GRCm39) missense possibly damaging 0.88
R8827:Slc35f3 UTSW 8 127,115,780 (GRCm39) critical splice acceptor site probably benign
R8983:Slc35f3 UTSW 8 127,115,775 (GRCm39) critical splice acceptor site probably benign
R9205:Slc35f3 UTSW 8 127,115,928 (GRCm39) missense probably damaging 0.96
R9355:Slc35f3 UTSW 8 127,108,967 (GRCm39) missense probably damaging 0.97
R9475:Slc35f3 UTSW 8 127,108,993 (GRCm39) missense probably damaging 1.00
R9492:Slc35f3 UTSW 8 127,048,026 (GRCm39) missense probably damaging 1.00
R9714:Slc35f3 UTSW 8 127,115,781 (GRCm39) critical splice acceptor site probably benign
R9729:Slc35f3 UTSW 8 127,115,777 (GRCm39) critical splice acceptor site probably benign
R9769:Slc35f3 UTSW 8 127,121,336 (GRCm39) missense probably damaging 0.99
X0067:Slc35f3 UTSW 8 127,109,062 (GRCm39) missense probably damaging 0.99
Predicted Primers
Posted On 2019-10-07