Incidental Mutation 'R1457:Slx1b'
ID 158576
Institutional Source Beutler Lab
Gene Symbol Slx1b
Ensembl Gene ENSMUSG00000059772
Gene Name SLX1 structure-specific endonuclease subunit homolog B (S. cerevisiae)
Synonyms 4833422P03Rik, Giyd2, 1110030E23Rik, 2410170E21Rik
MMRRC Submission 039512-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1457 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 126689468-126695784 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 126692796 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 63 (V63E)
Ref Sequence ENSEMBL: ENSMUSP00000118182 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106369] [ENSMUST00000130498] [ENSMUST00000142337] [ENSMUST00000144897]
AlphaFold Q8BX32
Predicted Effect noncoding transcript
Transcript: ENSMUST00000052145
Predicted Effect noncoding transcript
Transcript: ENSMUST00000084586
Predicted Effect probably benign
Transcript: ENSMUST00000106369
SMART Domains Protein: ENSMUSP00000101977
Gene: ENSMUSG00000047721

Pfam:BolA 10 54 4.7e-12 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000122029
Predicted Effect probably benign
Transcript: ENSMUST00000130498
SMART Domains Protein: ENSMUSP00000114873
Gene: ENSMUSG00000047721

Pfam:BolA 12 79 1.2e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000142337
SMART Domains Protein: ENSMUSP00000117927
Gene: ENSMUSG00000059772

Pfam:GIY-YIG 10 58 1.5e-10 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144571
Predicted Effect probably damaging
Transcript: ENSMUST00000144897
AA Change: V63E

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000118182
Gene: ENSMUSG00000059772
AA Change: V63E

GIYc 10 112 1.14e-3 SMART
low complexity region 152 163 N/A INTRINSIC
low complexity region 194 205 N/A INTRINSIC
low complexity region 214 229 N/A INTRINSIC
low complexity region 250 270 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155012
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206275
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.8%
  • 10x: 94.7%
  • 20x: 87.3%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit mouse embryonic fibroblasts that are more sensitive to DNA interstrand corsslinking agents with increased cell death, chromatide breaks, radial structures and impaired resolution of Holliday junctions. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010300C02Rik A T 1: 37,626,012 (GRCm38) Y268* probably null Het
Abca14 A T 7: 120,289,460 (GRCm38) I1210F probably benign Het
Ankrd17 T C 5: 90,285,846 (GRCm38) H688R possibly damaging Het
Arhgap24 T A 5: 102,664,106 (GRCm38) N66K probably damaging Het
Atp1a1 C T 3: 101,590,466 (GRCm38) G335D probably damaging Het
Cacna1g C T 11: 94,459,555 (GRCm38) R488H possibly damaging Het
Cacna1h A T 17: 25,397,620 (GRCm38) V149E probably damaging Het
Cd22 G T 7: 30,873,170 (GRCm38) P338Q probably benign Het
Cntln G T 4: 85,096,839 (GRCm38) M1122I probably benign Het
Cntrl A G 2: 35,122,756 (GRCm38) N302S probably benign Het
Cog8 T C 8: 107,052,896 (GRCm38) R250G probably damaging Het
Creld2 T C 15: 88,823,753 (GRCm38) C232R probably damaging Het
Cyp2b23 G A 7: 26,673,149 (GRCm38) P347L probably damaging Het
Dnah5 T C 15: 28,403,542 (GRCm38) probably null Het
Eml6 C T 11: 30,024,459 (GRCm38) V40I probably damaging Het
Epb42 C T 2: 121,029,967 (GRCm38) probably null Het
Fcrla A G 1: 170,921,004 (GRCm38) L190P probably damaging Het
Galnt18 A T 7: 111,779,428 (GRCm38) Y40* probably null Het
Gdf7 A T 12: 8,298,073 (GRCm38) M416K probably damaging Het
Gm11232 T A 4: 71,756,919 (GRCm38) probably null Het
Gpam T A 19: 55,088,176 (GRCm38) N198Y probably damaging Het
Grip1 C T 10: 119,986,350 (GRCm38) S327F possibly damaging Het
Hey2 C T 10: 30,834,356 (GRCm38) A134T probably benign Het
Kat6a T C 8: 22,938,652 (GRCm38) I1341T probably benign Het
Kcnd3 T C 3: 105,668,186 (GRCm38) L542P probably benign Het
Lars G A 18: 42,210,050 (GRCm38) R1101C probably damaging Het
Lman2 T C 13: 55,351,251 (GRCm38) D234G probably benign Het
Map3k19 A C 1: 127,817,898 (GRCm38) I1273R probably damaging Het
Matn1 T A 4: 130,950,019 (GRCm38) F180I possibly damaging Het
Meikin T A 11: 54,370,941 (GRCm38) L61* probably null Het
Mroh2b G T 15: 4,925,684 (GRCm38) D720Y probably damaging Het
Myh13 T C 11: 67,331,046 (GRCm38) I199T probably damaging Het
Myh4 T A 11: 67,248,461 (GRCm38) S535T probably damaging Het
Myo5a T C 9: 75,213,065 (GRCm38) M1715T probably damaging Het
Nat8 A T 6: 85,830,989 (GRCm38) V54D probably damaging Het
Nbea A G 3: 56,085,327 (GRCm38) V286A probably damaging Het
Ndnf A G 6: 65,704,014 (GRCm38) K426E possibly damaging Het
Nup210l T A 3: 90,190,972 (GRCm38) N1410K possibly damaging Het
Oca2 A T 7: 56,321,521 (GRCm38) T399S probably damaging Het
Olfr1045 A G 2: 86,198,252 (GRCm38) S167P probably damaging Het
Olfr118 A T 17: 37,672,925 (GRCm38) K301* probably null Het
Olfr250 G A 9: 38,368,196 (GRCm38) V217I probably benign Het
Olfr366 A C 2: 37,219,659 (GRCm38) T57P possibly damaging Het
Olfr644 A T 7: 104,068,459 (GRCm38) C191S probably damaging Het
Olfr652 T A 7: 104,565,071 (GRCm38) N283K probably damaging Het
Otogl A C 10: 107,878,152 (GRCm38) probably null Het
Pde4b C T 4: 102,605,176 (GRCm38) T511I probably damaging Het
Proser3 A G 7: 30,539,747 (GRCm38) probably null Het
Psmd12 G A 11: 107,479,646 (GRCm38) V24M probably damaging Het
Rbm17 A T 2: 11,593,461 (GRCm38) M170K probably benign Het
Rims2 C T 15: 39,511,314 (GRCm38) T1064I possibly damaging Het
Ripor3 C T 2: 167,992,653 (GRCm38) V281M probably damaging Het
Rreb1 C A 13: 37,946,928 (GRCm38) Q1353K possibly damaging Het
Sgo2a A G 1: 58,015,806 (GRCm38) D383G probably benign Het
Sik3 C T 9: 46,221,148 (GRCm38) T1346M probably damaging Het
Son A G 16: 91,657,086 (GRCm38) D907G probably damaging Het
Src G A 2: 157,469,212 (GRCm38) V401M probably damaging Het
St3gal4 T C 9: 35,054,757 (GRCm38) K24E possibly damaging Het
Stat6 A G 10: 127,658,245 (GRCm38) K647R probably damaging Het
Tbl1xr1 G A 3: 22,193,169 (GRCm38) probably null Het
Tlk2 G A 11: 105,256,952 (GRCm38) probably null Het
Tmbim6 T A 15: 99,401,615 (GRCm38) I3K probably benign Het
Tmeff2 A T 1: 51,181,867 (GRCm38) I334F probably damaging Het
Ttn T C 2: 76,840,315 (GRCm38) probably null Het
Ubl7 T A 9: 57,914,611 (GRCm38) I81N probably damaging Het
Ugt1a10 A G 1: 88,055,711 (GRCm38) Y77C probably damaging Het
Uqcrfs1 A G 13: 30,540,907 (GRCm38) C217R probably damaging Het
Usp50 T C 2: 126,761,634 (GRCm38) T331A probably benign Het
Vmn1r65 A G 7: 6,009,157 (GRCm38) V26A probably benign Het
Wdfy3 A C 5: 101,917,579 (GRCm38) V1241G possibly damaging Het
Wtap A C 17: 12,981,744 (GRCm38) probably null Het
Zbtb40 C A 4: 136,984,837 (GRCm38) A1187S possibly damaging Het
Zfp57 T C 17: 37,006,098 (GRCm38) S20P probably damaging Het
Zfp592 A G 7: 81,024,479 (GRCm38) D397G probably damaging Het
Zfp747 A T 7: 127,374,504 (GRCm38) S165T probably benign Het
Zfp949 C T 9: 88,569,838 (GRCm38) T487I probably damaging Het
Zscan4d A G 7: 11,164,994 (GRCm38) C119R probably damaging Het
Other mutations in Slx1b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0437:Slx1b UTSW 7 126,692,581 (GRCm38) missense probably benign 0.02
R0601:Slx1b UTSW 7 126,692,640 (GRCm38) missense probably damaging 1.00
R0714:Slx1b UTSW 7 126,692,448 (GRCm38) missense probably damaging 0.98
R3975:Slx1b UTSW 7 126,691,807 (GRCm38) missense probably damaging 1.00
R4757:Slx1b UTSW 7 126,692,529 (GRCm38) missense probably benign
R4950:Slx1b UTSW 7 126,691,767 (GRCm38) utr 3 prime probably benign
R6194:Slx1b UTSW 7 126,692,331 (GRCm38) missense possibly damaging 0.80
R7334:Slx1b UTSW 7 126,692,527 (GRCm38) missense probably damaging 0.99
R9664:Slx1b UTSW 7 126,692,526 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2014-03-14