Incidental Mutation 'IGL03113:Sult1d1'
ID 419268
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult1d1
Ensembl Gene ENSMUSG00000029273
Gene Name sulfotransferase family 1D, member 1
Synonyms 5033411P13Rik, tyrosine-ester sulfotransferase, Sultn
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL03113
Quality Score
Status
Chromosome 5
Chromosomal Location 87702509-87716865 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 87707738 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 127 (Y127*)
Ref Sequence ENSEMBL: ENSMUSP00000108940 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113314]
AlphaFold Q3UZZ6
PDB Structure Crystal structure of mouse sulfotransferase SULT1D1 complex with PAP [X-RAY DIFFRACTION]
Crystal structure of mouse cytosolic sulfotransferase mSULT1D1 complex with PAP and p-nitrophenol [X-RAY DIFFRACTION]
Crystal structure of mouse cytosolic sulfotransferase mSULT1D1 complex with PAP and alpha-naphthol [X-RAY DIFFRACTION]
Crystal structure of mouse cytosolic sulfotransferase mSULT1D1 complex with PAPS [X-RAY DIFFRACTION]
Crystal structure of mouse cytosolic sulfotransferase mSULT1D1 complex with PAPS and p-nitrophenyl sulfate [X-RAY DIFFRACTION]
Crystal structure of mouse cytosolic sulfotransferase mSULT1D1 complex with PAPS/PAP and p-nitrophenol [X-RAY DIFFRACTION]
crystal structure of mouse cytosolic sulfotransferase mSULT1D1 complex with PAP and p-nitrophenol, obtained by two-step soaking method [X-RAY DIFFRACTION]
Predicted Effect probably null
Transcript: ENSMUST00000113314
AA Change: Y127*
SMART Domains Protein: ENSMUSP00000108940
Gene: ENSMUSG00000029273
AA Change: Y127*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 38 288 6e-95 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000166996
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased benzylic DNA adduct formation in the liver and kidney but increased formation in the colon. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Apof G A 10: 128,105,568 (GRCm39) V241M probably benign Het
Arhgef10 T A 8: 15,004,505 (GRCm39) I91N probably damaging Het
Arhgef17 G A 7: 100,578,938 (GRCm39) T670I probably benign Het
Barhl1 T C 2: 28,805,468 (GRCm39) D75G probably benign Het
Capn13 T C 17: 73,638,108 (GRCm39) T432A probably benign Het
Casd1 T A 6: 4,640,951 (GRCm39) Y691N probably damaging Het
Ccdc175 C A 12: 72,191,557 (GRCm39) V340L probably benign Het
Cdc5l A T 17: 45,744,348 (GRCm39) M5K possibly damaging Het
Cgn A G 3: 94,686,544 (GRCm39) F253L probably benign Het
Csmd1 T C 8: 16,078,712 (GRCm39) K2003R probably benign Het
Disp2 T A 2: 118,621,259 (GRCm39) probably null Het
Dnah7a T C 1: 53,472,163 (GRCm39) N3535D possibly damaging Het
Exoc3 G A 13: 74,341,232 (GRCm39) Q191* probably null Het
Fstl5 T A 3: 76,337,099 (GRCm39) Y219* probably null Het
Gad2 T A 2: 22,571,367 (GRCm39) L435Q probably benign Het
Gcnt3 A G 9: 69,941,983 (GRCm39) V195A probably damaging Het
Haus6 G A 4: 86,501,343 (GRCm39) Q843* probably null Het
Hivep2 T A 10: 14,006,395 (GRCm39) F998I probably damaging Het
Hsf5 A T 11: 87,548,190 (GRCm39) E624D probably benign Het
Klb A G 5: 65,540,813 (GRCm39) N969D probably benign Het
Klhl6 T A 16: 19,776,001 (GRCm39) S186C possibly damaging Het
Klk15 T C 7: 43,587,805 (GRCm39) F78L probably benign Het
Ldlr A G 9: 21,651,124 (GRCm39) E514G possibly damaging Het
Map9 T A 3: 82,267,285 (GRCm39) probably benign Het
Miga2 A T 2: 30,274,022 (GRCm39) I99F possibly damaging Het
Morc4 T C X: 138,758,605 (GRCm39) E189G probably benign Het
Nhlrc3 A T 3: 53,365,984 (GRCm39) Y170N possibly damaging Het
Or3a1b G A 11: 74,012,529 (GRCm39) R138Q probably benign Het
Or4c111 A G 2: 88,844,379 (GRCm39) F10L probably damaging Het
Or51b6b A T 7: 103,309,851 (GRCm39) V202D possibly damaging Het
Or52u1 A T 7: 104,237,940 (GRCm39) R310W probably benign Het
Or5o1 T A X: 48,815,939 (GRCm39) N291Y probably damaging Het
Or5w15 T C 2: 87,568,506 (GRCm39) Q54R probably benign Het
Or8g32 A C 9: 39,305,981 (GRCm39) K295T probably damaging Het
Pkd1l1 G A 11: 8,784,793 (GRCm39) T1997I probably benign Het
Poln A G 5: 34,274,206 (GRCm39) S377P probably benign Het
Rab22a T A 2: 173,503,265 (GRCm39) V26E probably damaging Het
Rhbdl3 T C 11: 80,244,439 (GRCm39) V382A possibly damaging Het
Slitrk3 G T 3: 72,957,723 (GRCm39) Q350K probably benign Het
Vmn1r73 A T 7: 11,490,527 (GRCm39) Y115F probably benign Het
Zfp128 T A 7: 12,624,314 (GRCm39) D227E probably benign Het
Other mutations in Sult1d1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02306:Sult1d1 APN 5 87,703,914 (GRCm39) splice site probably benign
IGL02566:Sult1d1 APN 5 87,712,670 (GRCm39) missense probably damaging 0.98
IGL03080:Sult1d1 APN 5 87,704,847 (GRCm39) missense probably benign 0.16
R0269:Sult1d1 UTSW 5 87,712,661 (GRCm39) missense probably damaging 1.00
R1473:Sult1d1 UTSW 5 87,712,598 (GRCm39) missense probably benign 0.13
R2105:Sult1d1 UTSW 5 87,707,661 (GRCm39) missense probably damaging 1.00
R2273:Sult1d1 UTSW 5 87,703,887 (GRCm39) missense probably damaging 1.00
R2919:Sult1d1 UTSW 5 87,707,614 (GRCm39) splice site probably benign
R4416:Sult1d1 UTSW 5 87,706,435 (GRCm39) missense probably damaging 1.00
R4648:Sult1d1 UTSW 5 87,713,954 (GRCm39) missense probably benign 0.00
R5031:Sult1d1 UTSW 5 87,707,703 (GRCm39) missense possibly damaging 0.77
R5108:Sult1d1 UTSW 5 87,711,728 (GRCm39) critical splice donor site probably null
R5905:Sult1d1 UTSW 5 87,707,685 (GRCm39) missense probably damaging 1.00
R5934:Sult1d1 UTSW 5 87,707,629 (GRCm39) frame shift probably null
R6028:Sult1d1 UTSW 5 87,707,685 (GRCm39) missense probably damaging 1.00
R8786:Sult1d1 UTSW 5 87,712,575 (GRCm39) missense probably benign
R9398:Sult1d1 UTSW 5 87,713,954 (GRCm39) missense probably benign 0.00
R9519:Sult1d1 UTSW 5 87,704,721 (GRCm39) missense probably damaging 0.98
R9795:Sult1d1 UTSW 5 87,712,655 (GRCm39) missense probably damaging 0.98
Posted On 2016-08-02