Incidental Mutation 'IGL02353:Sult2a3'
ID 289560
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult2a3
Ensembl Gene ENSMUSG00000074375
Gene Name sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 3
Synonyms Gm6955
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02353
Quality Score
Status
Chromosome 7
Chromosomal Location 13801480-13856973 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 13855575 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 94 (R94*)
Ref Sequence ENSEMBL: ENSMUSP00000096407 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098809]
AlphaFold D3Z1W5
Predicted Effect probably null
Transcript: ENSMUST00000098809
AA Change: R94*
SMART Domains Protein: ENSMUSP00000096407
Gene: ENSMUSG00000074375
AA Change: R94*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 278 1.5e-83 PFAM
Pfam:Sulfotransfer_3 35 205 3.4e-11 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: This is one of seven sulfotransferase family 2A genes in a chromosome 7 A1 cluster. [provided by RefSeq, May 2010]
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh18a1 A T 19: 40,566,364 (GRCm39) V102D probably damaging Het
Car4 C T 11: 84,856,593 (GRCm39) P294S probably damaging Het
Casp6 C T 3: 129,704,175 (GRCm39) S87L probably damaging Het
Ccdc121rt1 T C 1: 181,338,190 (GRCm39) E254G possibly damaging Het
Ccnl1 A C 3: 65,856,141 (GRCm39) C255G probably damaging Het
Celf4 T C 18: 25,619,955 (GRCm39) I485M probably damaging Het
Cntln A G 4: 84,968,087 (GRCm39) R769G probably damaging Het
Cstdc1 A G 2: 148,625,387 (GRCm39) probably benign Het
Cyp2d12 T C 15: 82,443,171 (GRCm39) V360A probably benign Het
Dgki T C 6: 36,824,324 (GRCm39) E1068G probably damaging Het
Fbxl4 A G 4: 22,433,684 (GRCm39) N607S probably benign Het
Fgd4 T C 16: 16,279,909 (GRCm39) I383V probably damaging Het
Fgd6 C T 10: 93,974,258 (GRCm39) T1333I possibly damaging Het
Got1 A G 19: 43,512,882 (GRCm39) S5P probably damaging Het
Herc2 T A 7: 55,764,560 (GRCm39) N995K probably damaging Het
Kcnma1 A G 14: 23,641,681 (GRCm39) F159S probably damaging Het
Krt87 T C 15: 101,383,339 (GRCm39) S456G probably benign Het
Lhb T C 7: 45,070,718 (GRCm39) V32A possibly damaging Het
Mau2 A T 8: 70,472,288 (GRCm39) V602E probably damaging Het
Mpst C T 15: 78,294,285 (GRCm39) L6F probably damaging Het
Nlrp2 G A 7: 5,340,598 (GRCm39) T72I probably damaging Het
Or8g20 A G 9: 39,396,444 (GRCm39) I32T probably benign Het
Phldb2 T C 16: 45,569,142 (GRCm39) Y1239C probably damaging Het
Slc22a8 T C 19: 8,585,619 (GRCm39) F328S possibly damaging Het
Spns1 C T 7: 125,974,312 (GRCm39) R94Q probably damaging Het
Syt16 A G 12: 74,176,245 (GRCm39) N38S probably damaging Het
Tbc1d1 G A 5: 64,414,179 (GRCm39) R180Q probably damaging Het
Ush2a T C 1: 188,460,635 (GRCm39) I2632T probably benign Het
Vcam1 T A 3: 115,909,543 (GRCm39) I595F possibly damaging Het
Other mutations in Sult2a3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00583:Sult2a3 APN 7 13,856,905 (GRCm39) missense probably benign 0.03
IGL02360:Sult2a3 APN 7 13,855,575 (GRCm39) nonsense probably null
IGL02806:Sult2a3 APN 7 13,856,857 (GRCm39) missense probably damaging 1.00
IGL03252:Sult2a3 APN 7 13,801,559 (GRCm39) missense probably damaging 1.00
R0029:Sult2a3 UTSW 7 13,806,999 (GRCm39) missense probably benign 0.11
R1480:Sult2a3 UTSW 7 13,856,836 (GRCm39) missense possibly damaging 0.51
R1491:Sult2a3 UTSW 7 13,856,867 (GRCm39) missense probably benign 0.01
R4078:Sult2a3 UTSW 7 13,855,662 (GRCm39) missense possibly damaging 0.94
R4668:Sult2a3 UTSW 7 13,856,786 (GRCm39) missense probably damaging 1.00
R4928:Sult2a3 UTSW 7 13,845,482 (GRCm39) missense probably benign 0.06
R6311:Sult2a3 UTSW 7 13,845,482 (GRCm39) missense probably benign 0.00
R6749:Sult2a3 UTSW 7 13,816,629 (GRCm39) missense probably benign 0.00
R7030:Sult2a3 UTSW 7 13,801,493 (GRCm39) missense probably damaging 1.00
R7232:Sult2a3 UTSW 7 13,816,685 (GRCm39) missense possibly damaging 0.89
R7394:Sult2a3 UTSW 7 13,845,449 (GRCm39) missense probably benign 0.05
R7617:Sult2a3 UTSW 7 13,806,981 (GRCm39) missense probably benign 0.00
R8029:Sult2a3 UTSW 7 13,855,553 (GRCm39) missense probably damaging 1.00
R8097:Sult2a3 UTSW 7 13,816,635 (GRCm39) missense possibly damaging 0.93
R9154:Sult2a3 UTSW 7 13,806,981 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16