Incidental Mutation 'R8000:Slc35f3'
ID 616324
Institutional Source Beutler Lab
Gene Symbol Slc35f3
Ensembl Gene ENSMUSG00000057060
Gene Name solute carrier family 35, member F3
Synonyms B230375D17Rik
MMRRC Submission 046040-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.160) question?
Stock # R8000 (G1)
Quality Score 225.009
Status Not validated
Chromosome 8
Chromosomal Location 126865734-127122717 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 127047812 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 51 (T51A)
Ref Sequence ENSEMBL: ENSMUSP00000104390 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108759]
AlphaFold Q1LZI2
Predicted Effect probably benign
Transcript: ENSMUST00000108759
AA Change: T51A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000104390
Gene: ENSMUSG00000057060
AA Change: T51A

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: 99.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2 A G 3: 59,924,796 (GRCm39) K121R possibly damaging Het
Acaca A G 11: 84,283,057 (GRCm39) K2208E possibly damaging Het
Actn1 A G 12: 80,245,782 (GRCm39) F134L probably damaging Het
Akt3 A T 1: 176,877,763 (GRCm39) V335D probably damaging Het
Arhgef10 T G 8: 14,980,054 (GRCm39) I98S probably damaging Het
Celf4 T C 18: 25,637,574 (GRCm39) N209S probably benign Het
Col4a4 G A 1: 82,519,018 (GRCm39) P59L unknown Het
Dmwd C T 7: 18,814,660 (GRCm39) L437F probably damaging Het
Dock4 T A 12: 40,883,118 (GRCm39) L1642I probably benign Het
Fads2b A G 2: 85,349,070 (GRCm39) V14A probably benign Het
Fap A G 2: 62,333,142 (GRCm39) probably null Het
Fbh1 A T 2: 11,772,100 (GRCm39) Y194N probably benign Het
Fras1 A G 5: 96,910,536 (GRCm39) T3322A probably damaging Het
Frey1 A G 2: 92,215,872 (GRCm39) K69E unknown Het
Gabra4 A G 5: 71,781,304 (GRCm39) F369S probably damaging Het
Igkv9-124 T A 6: 67,919,136 (GRCm39) D92V probably damaging Het
Kcna6 C A 6: 126,715,948 (GRCm39) E314* probably null Het
Kyat1 A C 2: 30,082,065 (GRCm39) S25A probably benign Het
Lars2 G A 9: 123,265,309 (GRCm39) G455D probably damaging Het
Mertk A G 2: 128,613,418 (GRCm39) H478R probably benign Het
Mier1 A T 4: 102,988,240 (GRCm39) T83S probably damaging Het
Mmp1a C A 9: 7,476,215 (GRCm39) H437Q probably benign Het
Muc4 C G 16: 32,575,221 (GRCm39) Q1269E probably benign Het
Neb G T 2: 52,178,856 (GRCm39) A1300D probably damaging Het
Nell2 T A 15: 95,333,155 (GRCm39) L167F probably damaging Het
Or10h1 G C 17: 33,418,321 (GRCm39) A100P probably damaging Het
Or12j2 T A 7: 139,916,255 (GRCm39) M160K possibly damaging Het
Or4d10c T C 19: 12,065,358 (GRCm39) D266G probably damaging Het
Pald1 T C 10: 61,183,218 (GRCm39) T339A probably benign Het
Pex13 A C 11: 23,605,915 (GRCm39) L105W probably damaging Het
Prxl2a A C 14: 40,716,483 (GRCm39) *230G probably null Het
Ptprd A C 4: 75,984,479 (GRCm39) F556V possibly damaging Het
Rgp1 T A 4: 43,581,664 (GRCm39) C314S probably benign Het
Rnaseh2a G A 8: 85,692,678 (GRCm39) probably benign Het
Rpl7 A T 1: 16,172,949 (GRCm39) M154K probably benign Het
Samd9l A T 6: 3,373,034 (GRCm39) L1409Q probably damaging Het
Slc7a10 A G 7: 34,899,865 (GRCm39) Y76C Het
Slk G T 19: 47,597,344 (GRCm39) A51S Het
Son AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG 16: 91,457,222 (GRCm39) probably benign Het
Stk38 A T 17: 29,211,422 (GRCm39) V51E probably benign Het
Tecta A T 9: 42,278,480 (GRCm39) C1009* probably null Het
Vmn1r228 A T 17: 20,997,227 (GRCm39) M97K possibly damaging Het
Xpo4 T C 14: 57,827,403 (GRCm39) D931G probably damaging Het
Zfp503 T C 14: 22,036,227 (GRCm39) T230A possibly 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
R7456:Slc35f3 UTSW 8 127,115,779 (GRCm39) critical splice acceptor site unknown
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
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 PCR Primer
(F):5'- CAGCTGTAGTCCAGAGCATTACC -3'
(R):5'- TGTGGATTTGCACACATGTCC -3'

Sequencing Primer
(F):5'- GTAGTCCAGAGCATTACCCAGCATC -3'
(R):5'- CACATGTCCTGCGTAGTACAATGG -3'
Posted On 2020-01-23