Incidental Mutation 'R0145:Slc7a13'
ID 261797
Institutional Source Beutler Lab
Gene Symbol Slc7a13
Ensembl Gene ENSMUSG00000041052
Gene Name solute carrier family 7, (cationic amino acid transporter, y+ system) member 13
Synonyms AGT-1, XAT2, 0610009O04Rik, AGT1
MMRRC Submission 038430-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R0145 (G1) of strain 722
Quality Score 86
Status Not validated
Chromosome 4
Chromosomal Location 19818727-19842213 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) G to A at 19818782 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000036228 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035890]
AlphaFold Q91WN3
Predicted Effect probably benign
Transcript: ENSMUST00000035890
SMART Domains Protein: ENSMUSP00000036228
Gene: ENSMUSG00000041052

DomainStartEndE-ValueType
Pfam:AA_permease_2 17 440 3.3e-44 PFAM
Pfam:AA_permease 21 454 3.7e-19 PFAM
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 93.7%
  • 20x: 82.1%
Validation Efficiency 96% (109/113)
Allele List at MGI
Other mutations in this stock
Total: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik A G 10: 100,437,783 (GRCm39) E64G probably damaging Het
Actr6 A T 10: 89,564,040 (GRCm39) Y77* probably null Het
Aldoart1 A T 4: 72,769,576 (GRCm39) S411T probably benign Het
Aqp1 C T 6: 55,323,672 (GRCm39) R234C probably damaging Het
Arsb G A 13: 93,998,795 (GRCm39) G368R possibly damaging Het
Asxl3 G A 18: 22,586,662 (GRCm39) A151T probably damaging Het
Bcas3 T C 11: 85,250,436 (GRCm39) probably benign Het
Bmpr2 AACACA AACA 1: 59,906,739 (GRCm39) probably null Het
Bst1 A G 5: 43,976,414 (GRCm39) Y49C probably damaging Het
Btrc T A 19: 45,411,612 (GRCm39) L12Q probably damaging Het
Cd248 T C 19: 5,119,051 (GRCm39) F300L possibly damaging Het
Cdk11b G T 4: 155,726,076 (GRCm39) probably benign Het
Cfap410 T C 10: 77,819,390 (GRCm39) S196P probably benign Het
Cfap44 A T 16: 44,288,735 (GRCm39) D1495V probably damaging Het
Chil3 T A 3: 106,067,794 (GRCm39) I124F probably damaging Het
Cnot2 A T 10: 116,353,273 (GRCm39) S63T possibly damaging Het
Cox8a G T 19: 7,192,783 (GRCm39) H61N probably benign Het
Cpne9 T C 6: 113,277,562 (GRCm39) V427A probably damaging Het
Ctsll3 C A 13: 60,946,409 (GRCm39) G301C probably damaging Het
Cubn T A 2: 13,311,243 (GRCm39) D3094V probably damaging Het
Cyba A T 8: 123,153,977 (GRCm39) M65K possibly damaging Het
Cyp4f39 T A 17: 32,705,934 (GRCm39) S342T possibly damaging Het
Daam2 T C 17: 49,787,806 (GRCm39) I436V probably benign Het
Daglb T C 5: 143,460,363 (GRCm39) probably benign Het
Dnah7b T G 1: 46,262,338 (GRCm39) L2067R probably damaging Het
Ep300 T C 15: 81,500,328 (GRCm39) probably null Het
Esm1 A G 13: 113,353,230 (GRCm39) N171D probably damaging Het
Fbxl2 T C 9: 113,814,393 (GRCm39) E266G probably damaging Het
Ficd G T 5: 113,876,880 (GRCm39) A352S probably damaging Het
H2-Q2 A G 17: 35,564,152 (GRCm39) D302G probably benign Het
Hacd3 A T 9: 64,911,524 (GRCm39) probably benign Het
Kbtbd6 T A 14: 79,690,464 (GRCm39) N386K probably benign Het
Lct T C 1: 128,255,632 (GRCm39) M137V probably benign Het
Lilrb4b T G 10: 51,360,614 (GRCm39) N176K probably benign Het
Macf1 T A 4: 123,281,190 (GRCm39) H4340L probably damaging Het
Mcidas A G 13: 113,130,906 (GRCm39) D77G probably damaging Het
Mmrn1 C A 6: 60,949,994 (GRCm39) Q315K probably damaging Het
Mon2 C A 10: 122,849,417 (GRCm39) L1294F possibly damaging Het
Muc5ac A G 7: 141,349,012 (GRCm39) T483A possibly damaging Het
Nacc1 T C 8: 85,401,504 (GRCm39) probably benign Het
Nanos3 C T 8: 84,902,763 (GRCm39) R133Q probably damaging Het
Ngef A G 1: 87,468,370 (GRCm39) probably benign Het
Nol8 C T 13: 49,815,923 (GRCm39) A677V possibly damaging Het
Ogfod3 A T 11: 121,085,896 (GRCm39) probably benign Het
Or6c8 A T 10: 128,915,232 (GRCm39) V200E probably damaging Het
Or8i2 A C 2: 86,852,134 (GRCm39) Y251* probably null Het
Parpbp T C 10: 87,928,871 (GRCm39) Y523C possibly damaging Het
Pik3cg C A 12: 32,254,321 (GRCm39) L555F probably benign Het
Pkp3 T G 7: 140,669,676 (GRCm39) probably null Het
Pole G T 5: 110,472,291 (GRCm39) R1518L probably damaging Het
Prkab1 T C 5: 116,156,144 (GRCm39) probably benign Het
Prrc2a T C 17: 35,374,796 (GRCm39) T1285A probably benign Het
Pus1 C A 5: 110,922,720 (GRCm39) V222L probably benign Het
Rab11fip1 A G 8: 27,633,352 (GRCm39) L1118P probably damaging Het
Ranbp2 T A 10: 58,315,868 (GRCm39) I2196N probably damaging Het
Rims3 T C 4: 120,744,223 (GRCm39) L151P probably damaging Het
Rnf130 A G 11: 49,962,046 (GRCm39) D164G possibly damaging Het
Rps6ka2 C A 17: 7,529,585 (GRCm39) L293I probably benign Het
Ruvbl1 A G 6: 88,461,441 (GRCm39) T269A possibly damaging Het
Sema4a A T 3: 88,358,729 (GRCm39) I10N probably damaging Het
Serpinb6e A T 13: 34,025,043 (GRCm39) S83T probably benign Het
Slc12a9 C A 5: 137,313,550 (GRCm39) W803L probably damaging Het
Slc3a2 A G 19: 8,685,437 (GRCm39) S188P probably damaging Het
Spart A T 3: 55,035,092 (GRCm39) K493* probably null Het
Spata31e2 A G 1: 26,726,413 (GRCm39) M32T probably benign Het
Sun1 T C 5: 139,227,166 (GRCm39) V574A probably damaging Het
Supt6 A G 11: 78,099,062 (GRCm39) V1603A probably benign Het
Tgm5 A G 2: 120,908,062 (GRCm39) V38A possibly damaging Het
Tm6sf2 T C 8: 70,530,518 (GRCm39) probably benign Het
Tnfaip2 T A 12: 111,412,292 (GRCm39) V231E possibly damaging Het
Tube1 T A 10: 39,021,598 (GRCm39) M281K possibly damaging Het
Tubgcp3 A G 8: 12,707,561 (GRCm39) Y143H probably benign Het
Tyrp1 A G 4: 80,759,015 (GRCm39) Y296C probably damaging Het
Utp4 A G 8: 107,621,301 (GRCm39) N26S probably benign Het
Vgf T A 5: 137,060,336 (GRCm39) probably benign Het
Zfat T C 15: 68,058,948 (GRCm39) K196E possibly damaging Het
Zfp366 G T 13: 99,366,048 (GRCm39) S403I probably damaging Het
Zfp462 G A 4: 55,010,529 (GRCm39) G832R probably damaging Het
Zfp955a T A 17: 33,461,430 (GRCm39) Q234L probably damaging Het
Zup1 T C 10: 33,819,709 (GRCm39) T202A probably damaging Het
Other mutations in Slc7a13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01769:Slc7a13 APN 4 19,839,527 (GRCm39) missense probably benign 0.00
IGL02491:Slc7a13 APN 4 19,841,404 (GRCm39) missense probably damaging 0.98
IGL02541:Slc7a13 APN 4 19,839,212 (GRCm39) splice site probably benign
IGL02814:Slc7a13 APN 4 19,839,387 (GRCm39) missense probably benign
R0305:Slc7a13 UTSW 4 19,839,401 (GRCm39) missense probably benign 0.12
R0468:Slc7a13 UTSW 4 19,841,500 (GRCm39) missense probably benign 0.04
R0522:Slc7a13 UTSW 4 19,824,010 (GRCm39) missense probably benign 0.02
R0848:Slc7a13 UTSW 4 19,818,866 (GRCm39) missense probably benign 0.00
R1240:Slc7a13 UTSW 4 19,819,212 (GRCm39) missense probably damaging 1.00
R1623:Slc7a13 UTSW 4 19,824,031 (GRCm39) missense possibly damaging 0.84
R1830:Slc7a13 UTSW 4 19,819,046 (GRCm39) missense probably benign 0.33
R1903:Slc7a13 UTSW 4 19,839,254 (GRCm39) missense probably benign 0.01
R1952:Slc7a13 UTSW 4 19,841,578 (GRCm39) missense probably benign
R2229:Slc7a13 UTSW 4 19,839,399 (GRCm39) missense probably benign 0.43
R2887:Slc7a13 UTSW 4 19,819,052 (GRCm39) missense possibly damaging 0.69
R4175:Slc7a13 UTSW 4 19,819,492 (GRCm39) missense probably null 0.99
R4233:Slc7a13 UTSW 4 19,819,070 (GRCm39) missense probably damaging 0.97
R4764:Slc7a13 UTSW 4 19,819,390 (GRCm39) missense probably benign 0.08
R4941:Slc7a13 UTSW 4 19,841,467 (GRCm39) missense probably damaging 1.00
R5355:Slc7a13 UTSW 4 19,839,267 (GRCm39) missense probably benign 0.43
R6221:Slc7a13 UTSW 4 19,839,305 (GRCm39) missense probably benign 0.00
R6641:Slc7a13 UTSW 4 19,839,534 (GRCm39) missense probably damaging 1.00
R7237:Slc7a13 UTSW 4 19,839,364 (GRCm39) missense probably benign
R8188:Slc7a13 UTSW 4 19,819,082 (GRCm39) missense probably benign 0.03
R8384:Slc7a13 UTSW 4 19,823,984 (GRCm39) missense probably damaging 1.00
R8753:Slc7a13 UTSW 4 19,841,443 (GRCm39) missense probably damaging 0.99
R8830:Slc7a13 UTSW 4 19,819,189 (GRCm39) missense probably benign 0.01
R9140:Slc7a13 UTSW 4 19,819,487 (GRCm39) missense possibly damaging 0.72
R9663:Slc7a13 UTSW 4 19,818,818 (GRCm39) missense possibly damaging 0.84
R9764:Slc7a13 UTSW 4 19,819,033 (GRCm39) missense probably benign 0.19
Predicted Primers
Posted On 2015-02-04