Incidental Mutation 'IGL01863:Slc2a13'
ID 178421
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc2a13
Ensembl Gene ENSMUSG00000036298
Gene Name solute carrier family 2 (facilitated glucose transporter), member 13
Synonyms A630029G22Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01863
Quality Score
Status
Chromosome 15
Chromosomal Location 91151899-91457464 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 91400695 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 176 (I176V)
Ref Sequence ENSEMBL: ENSMUSP00000104906 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109283]
AlphaFold Q3UHK1
Predicted Effect probably benign
Transcript: ENSMUST00000109283
AA Change: I176V

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000104906
Gene: ENSMUSG00000036298
AA Change: I176V

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
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afg1l T A 10: 42,215,907 (GRCm39) I326F possibly damaging Het
Aimp1 T C 3: 132,377,853 (GRCm39) T171A probably benign Het
Ash1l T A 3: 88,892,813 (GRCm39) L1564* probably null Het
Atp1a1 G T 3: 101,499,205 (GRCm39) Y131* probably null Het
Celsr2 T C 3: 108,301,338 (GRCm39) E2686G probably benign Het
Cyp4f18 A G 8: 72,743,770 (GRCm39) V395A possibly damaging Het
Dnaaf11 A T 15: 66,268,823 (GRCm39) probably benign Het
Ephb2 T C 4: 136,387,088 (GRCm39) Q713R probably benign Het
Esf1 A T 2: 139,962,599 (GRCm39) M824K probably benign Het
Fat4 T C 3: 39,024,768 (GRCm39) probably benign Het
Gem A G 4: 11,705,980 (GRCm39) I23V probably benign Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm5862 A C 5: 26,227,769 (GRCm39) W41G probably benign Het
Il6st A G 13: 112,640,744 (GRCm39) E779G possibly damaging Het
Lama3 T A 18: 12,552,993 (GRCm39) probably benign Het
Lipi A C 16: 75,347,114 (GRCm39) I435R probably damaging Het
Odad2 T C 18: 7,222,617 (GRCm39) T551A probably damaging Het
Omg C T 11: 79,393,050 (GRCm39) M269I probably benign Het
Optn A T 2: 5,026,298 (GRCm39) probably benign Het
Or5ae2 T C 7: 84,505,619 (GRCm39) L14P probably damaging Het
Pex1 A G 5: 3,656,066 (GRCm39) T298A probably benign Het
Rab27b T A 18: 70,122,625 (GRCm39) R111S probably damaging Het
Rhbdf1 T G 11: 32,163,484 (GRCm39) E329D probably benign Het
Slc30a1 T A 1: 191,641,196 (GRCm39) C281S probably damaging Het
Slc4a7 T A 14: 14,762,430 (GRCm38) C509S probably damaging Het
Slfn9 T C 11: 82,872,151 (GRCm39) R862G probably benign Het
Tbc1d2 A G 4: 46,607,064 (GRCm39) I782T possibly damaging Het
Tent5c C T 3: 100,379,980 (GRCm39) D259N probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Vps33b T C 7: 79,924,059 (GRCm39) probably null Het
Wrap73 A G 4: 154,229,790 (GRCm39) I54V probably benign 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
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
R9396:Slc2a13 UTSW 15 91,227,915 (GRCm39) missense probably benign 0.00
Posted On 2014-05-07