Incidental Mutation 'R9396:Slc2a13'
ID 710856
Institutional Source Beutler Lab
Gene Symbol Slc2a13
Ensembl Gene ENSMUSG00000036298
Gene Name solute carrier family 2 (facilitated glucose transporter), member 13
Synonyms A630029G22Rik
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9396 (G1)
Quality Score 225.009
Status Validated
Chromosome 15
Chromosomal Location 91151899-91457464 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 91227915 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 426 (T426A)
Ref Sequence ENSEMBL: ENSMUSP00000104906 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109283]
AlphaFold Q3UHK1
Predicted Effect probably benign
Transcript: ENSMUST00000109283
AA Change: T426A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000104906
Gene: ENSMUSG00000036298
AA Change: T426A

DomainStartEndE-ValueType
low complexity region 36 54 N/A INTRINSIC
Pfam:Sugar_tr 73 412 2e-87 PFAM
Pfam:MFS_1 77 411 6.6e-23 PFAM
Pfam:Sugar_tr 487 598 8.1e-28 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 98% (56/57)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg8 T A 17: 85,000,282 (GRCm39) F281I probably damaging Het
Acad8 A G 9: 26,887,041 (GRCm39) M402T probably damaging Het
Apcdd1 C T 18: 63,055,731 (GRCm39) probably benign Het
Apol7a T C 15: 77,273,925 (GRCm39) E179G possibly damaging Het
Asmt A G X: 169,110,141 (GRCm39) T217A probably benign Het
Cadm2 T C 16: 66,544,102 (GRCm39) Y318C probably damaging Het
Cckar G A 5: 53,864,623 (GRCm39) T26M probably damaging Het
Cd300ld G A 11: 114,878,230 (GRCm39) T94I probably damaging Het
Cdk5rap2 A G 4: 70,172,903 (GRCm39) Y1390H possibly damaging Het
Cdk5rap2 C T 4: 70,182,895 (GRCm39) S1268N probably damaging Het
Csrnp3 C T 2: 65,832,841 (GRCm39) R127C probably damaging Het
Dsc2 T A 18: 20,174,773 (GRCm39) R501* probably null Het
Dusp2 C T 2: 127,179,638 (GRCm39) R294C probably damaging Het
Edrf1 A G 7: 133,261,838 (GRCm39) K878E possibly damaging Het
Evc T C 5: 37,476,434 (GRCm39) T372A possibly damaging Het
Fcgr1 T A 3: 96,194,390 (GRCm39) K166* probably null Het
Fstl4 C A 11: 52,664,778 (GRCm39) P36Q probably benign Het
Gas2l2 A T 11: 83,313,659 (GRCm39) I551N probably benign Het
Hc G T 2: 34,927,615 (GRCm39) S333* probably null Het
Ibsp A G 5: 104,458,297 (GRCm39) Y278C probably damaging Het
Ifitm10 A T 7: 141,924,704 (GRCm39) V45D probably damaging Het
Kcnc3 T C 7: 44,240,937 (GRCm39) S210P possibly damaging Het
Klhl3 T G 13: 58,161,662 (GRCm39) T531P probably damaging Het
Mapt C A 11: 104,189,555 (GRCm39) P191Q possibly damaging Het
Myh9 T C 15: 77,647,496 (GRCm39) T1840A probably benign Het
Myof A T 19: 37,923,294 (GRCm39) C1320S probably damaging Het
Myom3 G T 4: 135,513,199 (GRCm39) V626L probably benign Het
Nalf2 C T X: 98,889,097 (GRCm39) R321W probably damaging Het
Ndor1 A G 2: 25,138,921 (GRCm39) L321P probably benign Het
Nhsl1 T A 10: 18,399,749 (GRCm39) M291K probably damaging Het
Nubp2 C T 17: 25,103,476 (GRCm39) V134I probably benign Het
Nuf2 T C 1: 169,337,917 (GRCm39) I287V probably benign Het
Or1d2 T A 11: 74,256,089 (GRCm39) M198K probably benign Het
Or2n1 T A 17: 38,486,421 (GRCm39) W149R probably damaging Het
Or4k42 A G 2: 111,319,864 (GRCm39) L213P probably benign Het
Or51i2 A G 7: 103,689,720 (GRCm39) N239S probably benign Het
Or55b4 A C 7: 102,134,180 (GRCm39) V49G possibly damaging Het
Or5k3 G A 16: 58,969,302 (GRCm39) V30M probably damaging Het
Or8k28 A T 2: 86,285,845 (GRCm39) C257S probably benign Het
Pals1 G T 12: 78,871,521 (GRCm39) R367L possibly damaging Het
Pkd1l3 GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA 8: 110,350,827 (GRCm39) probably benign Het
Ppp1r12a A G 10: 108,100,571 (GRCm39) E863G probably damaging Het
Pskh1 C T 8: 106,640,091 (GRCm39) T257M possibly damaging Het
Rasgef1b T C 5: 99,377,188 (GRCm39) I334V probably benign Het
Rnf180 T A 13: 105,318,027 (GRCm39) K462* probably null Het
Sin3a A G 9: 57,008,445 (GRCm39) D455G probably benign Het
Slc15a4 A G 5: 127,694,463 (GRCm39) probably benign Het
Smarca5 T C 8: 81,463,358 (GRCm39) K70R probably benign Het
Smg1 A G 7: 117,807,303 (GRCm39) V182A unknown Het
Stim1 G A 7: 102,064,592 (GRCm39) V221I possibly damaging Het
Tbx18 T C 9: 87,609,432 (GRCm39) D201G probably damaging Het
Tcf25 A G 8: 124,127,831 (GRCm39) E630G probably benign Het
Tm7sf3 T C 6: 146,523,472 (GRCm39) N135S possibly damaging Het
Togaram1 A G 12: 65,014,429 (GRCm39) N560S probably damaging Het
Unc13d A G 11: 115,966,529 (GRCm39) probably null Het
Zfp445 A C 9: 122,681,581 (GRCm39) S787A probably benign Het
Zfp949 T C 9: 88,449,260 (GRCm39) W22R probably damaging Het
Other mutations in Slc2a13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00899:Slc2a13 APN 15 91,381,602 (GRCm39) missense probably benign
IGL01295:Slc2a13 APN 15 91,234,335 (GRCm39) critical splice acceptor site probably null
IGL01863:Slc2a13 APN 15 91,400,695 (GRCm39) missense probably benign 0.00
IGL02149:Slc2a13 APN 15 91,227,924 (GRCm39) missense probably benign
IGL02670:Slc2a13 APN 15 91,381,712 (GRCm39) missense probably damaging 0.99
IGL02692:Slc2a13 APN 15 91,205,861 (GRCm39) missense probably benign 0.23
IGL03307:Slc2a13 APN 15 91,160,317 (GRCm39) missense probably damaging 0.98
R0394:Slc2a13 UTSW 15 91,400,595 (GRCm39) missense probably damaging 1.00
R0624:Slc2a13 UTSW 15 91,234,215 (GRCm39) missense possibly damaging 0.89
R0698:Slc2a13 UTSW 15 91,205,870 (GRCm39) missense probably benign
R0702:Slc2a13 UTSW 15 91,205,870 (GRCm39) missense probably benign
R1052:Slc2a13 UTSW 15 91,296,363 (GRCm39) missense probably damaging 0.96
R2090:Slc2a13 UTSW 15 91,400,695 (GRCm39) missense probably benign 0.00
R2118:Slc2a13 UTSW 15 91,400,679 (GRCm39) missense probably damaging 0.99
R4445:Slc2a13 UTSW 15 91,234,223 (GRCm39) missense possibly damaging 0.46
R4896:Slc2a13 UTSW 15 91,296,415 (GRCm39) missense probably benign 0.20
R6028:Slc2a13 UTSW 15 91,160,319 (GRCm39) missense probably damaging 1.00
R6414:Slc2a13 UTSW 15 91,228,008 (GRCm39) missense probably benign 0.00
R6836:Slc2a13 UTSW 15 91,205,835 (GRCm39) missense probably benign 0.00
R6928:Slc2a13 UTSW 15 91,160,382 (GRCm39) missense probably damaging 1.00
R7353:Slc2a13 UTSW 15 91,205,807 (GRCm39) missense probably benign
R7423:Slc2a13 UTSW 15 91,456,883 (GRCm39) missense probably damaging 1.00
R7458:Slc2a13 UTSW 15 91,296,390 (GRCm39) missense probably benign 0.04
R7641:Slc2a13 UTSW 15 91,156,359 (GRCm39) makesense probably null
R7993:Slc2a13 UTSW 15 91,296,356 (GRCm39) nonsense probably null
R8057:Slc2a13 UTSW 15 91,400,619 (GRCm39) missense probably damaging 0.99
R8164:Slc2a13 UTSW 15 91,160,281 (GRCm39) missense probably damaging 0.96
R8520:Slc2a13 UTSW 15 91,457,105 (GRCm39) missense probably damaging 1.00
R8794:Slc2a13 UTSW 15 91,234,302 (GRCm39) missense probably damaging 1.00
R9061:Slc2a13 UTSW 15 91,234,333 (GRCm39) missense possibly damaging 0.85
R9185:Slc2a13 UTSW 15 91,227,906 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- ACCAATGTGTTACCCACCTC -3'
(R):5'- GAGTGTCATTCAGAGCTCCAATG -3'

Sequencing Primer
(F):5'- GAAAATTATGGTTTTCATGCAGATGG -3'
(R):5'- GTCATTCAGAGCTCCAATGTCAAATC -3'
Posted On 2022-04-18