Incidental Mutation 'R8255:Sult3a2'
ID 640613
Institutional Source Beutler Lab
Gene Symbol Sult3a2
Ensembl Gene ENSMUSG00000090298
Gene Name sulfotransferase family 3A, member 2
Synonyms Gm4794
MMRRC Submission 067681-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.130) question?
Stock # R8255 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 33642420-33662700 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 33655747 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Methionine at position 77 (I77M)
Ref Sequence ENSEMBL: ENSMUSP00000127159 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000165904]
AlphaFold G5E904
Predicted Effect probably benign
Transcript: ENSMUST00000165904
AA Change: I77M

PolyPhen 2 Score 0.043 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000127159
Gene: ENSMUSG00000090298
AA Change: I77M

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 283 8.9e-80 PFAM
Pfam:Sulfotransfer_3 37 207 6.8e-9 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 100% (46/46)
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik A T 13: 77,415,850 (GRCm39) T648S possibly damaging Het
Abca12 T A 1: 71,359,058 (GRCm39) I583F probably benign Het
Abca4 A T 3: 121,948,926 (GRCm39) M1732L probably benign Het
Ank2 A G 3: 126,740,398 (GRCm39) S1742P unknown Het
Birc6 G A 17: 74,969,775 (GRCm39) A4273T probably damaging Het
Chd5 A G 4: 152,463,880 (GRCm39) T1450A probably damaging Het
Dhx32 T C 7: 133,339,120 (GRCm39) N305S probably benign Het
Dnah7c T C 1: 46,698,589 (GRCm39) S2174P probably damaging Het
Fat2 T A 11: 55,161,101 (GRCm39) I3210F probably benign Het
Gm12888 A G 4: 121,181,994 (GRCm39) S33P probably damaging Het
Gpaa1 T C 15: 76,217,438 (GRCm39) L292P probably damaging Het
Gzmg T A 14: 56,395,753 (GRCm39) R69W probably damaging Het
Hat1 A G 2: 71,239,347 (GRCm39) D40G probably damaging Het
Hcrtr2 T A 9: 76,140,203 (GRCm39) I362F probably damaging Het
Hmmr T C 11: 40,598,262 (GRCm39) E650G probably damaging Het
Ifi35 A T 11: 101,348,608 (GRCm39) M180L probably benign Het
Ifi44 A T 3: 151,451,619 (GRCm39) H162Q probably benign Het
Il1rl2 T C 1: 40,404,471 (GRCm39) F531L probably damaging Het
Ipcef1 T G 10: 6,870,007 (GRCm39) K182T probably benign Het
Med27 C A 2: 29,414,376 (GRCm39) probably null Het
Med31 G A 11: 72,106,294 (GRCm39) probably benign Het
Moxd1 A G 10: 24,099,700 (GRCm39) T67A probably benign Het
Myh3 A G 11: 66,985,848 (GRCm39) E1266G probably damaging Het
Nkx2-4 C A 2: 146,925,924 (GRCm39) E313* probably null Het
Nol6 G T 4: 41,120,168 (GRCm39) R487S probably benign Het
Or2v1 C A 11: 49,025,307 (GRCm39) A96D probably benign Het
Or2z8 T A 8: 72,811,607 (GRCm39) F28I possibly damaging Het
Or4k15c C T 14: 50,321,329 (GRCm39) V270I noncoding transcript Het
Or5p51 A G 7: 107,444,368 (GRCm39) S191P probably damaging Het
Rnf135 A G 11: 80,084,713 (GRCm39) D162G probably benign Het
Sdr42e1 G T 8: 118,390,502 (GRCm39) N46K probably benign Het
Skor2 T C 18: 76,946,664 (GRCm39) S129P unknown Het
Slc7a11 A T 3: 50,382,177 (GRCm39) I190N probably damaging Het
Smc5 A T 19: 23,186,290 (GRCm39) F1056I Het
Son A T 16: 91,461,824 (GRCm39) Q2243L unknown Het
Sult1a1 T A 7: 126,274,280 (GRCm39) I101F possibly damaging Het
Tas1r1 A T 4: 152,116,774 (GRCm39) S287T probably benign Het
Thbs3 A C 3: 89,132,565 (GRCm39) T836P probably benign Het
Tlcd3b G A 7: 126,423,275 (GRCm39) V6M probably benign Het
Tmem161b C A 13: 84,370,537 (GRCm39) probably benign Het
Tnfrsf8 A T 4: 145,041,653 (GRCm39) M1K probably null Het
Vmn1r121 T G 7: 20,831,679 (GRCm39) N254H probably benign Het
Vmn1r179 C T 7: 23,628,436 (GRCm39) A209V probably benign Het
Wdr31 A T 4: 62,381,634 (GRCm39) S66T probably benign Het
Zbtb18 T C 1: 177,275,003 (GRCm39) V121A probably damaging Het
Zfp30 T A 7: 29,488,826 (GRCm39) M82K probably benign Het
Zzef1 A G 11: 72,765,955 (GRCm39) Q1494R probably benign Het
Other mutations in Sult3a2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02510:Sult3a2 APN 10 33,642,435 (GRCm39) missense probably benign 0.01
IGL03106:Sult3a2 APN 10 33,655,769 (GRCm39) missense probably benign 0.25
H8441:Sult3a2 UTSW 10 33,642,474 (GRCm39) missense probably benign 0.00
R0002:Sult3a2 UTSW 10 33,655,803 (GRCm39) missense possibly damaging 0.95
R0602:Sult3a2 UTSW 10 33,658,044 (GRCm39) missense probably benign 0.04
R1170:Sult3a2 UTSW 10 33,653,188 (GRCm39) missense possibly damaging 0.87
R1510:Sult3a2 UTSW 10 33,658,026 (GRCm39) missense probably benign 0.03
R1572:Sult3a2 UTSW 10 33,657,973 (GRCm39) missense probably damaging 1.00
R1725:Sult3a2 UTSW 10 33,655,705 (GRCm39) missense probably benign 0.00
R4601:Sult3a2 UTSW 10 33,658,083 (GRCm39) missense probably benign 0.00
R5570:Sult3a2 UTSW 10 33,654,268 (GRCm39) missense probably damaging 1.00
R6529:Sult3a2 UTSW 10 33,655,733 (GRCm39) missense probably damaging 1.00
R7996:Sult3a2 UTSW 10 33,644,254 (GRCm39) missense probably damaging 1.00
R8531:Sult3a2 UTSW 10 33,653,239 (GRCm39) missense probably damaging 1.00
R8982:Sult3a2 UTSW 10 33,658,069 (GRCm39) missense probably damaging 0.97
R9018:Sult3a2 UTSW 10 33,655,689 (GRCm39) missense probably benign 0.03
R9504:Sult3a2 UTSW 10 33,642,436 (GRCm39) missense probably benign 0.01
R9546:Sult3a2 UTSW 10 33,655,670 (GRCm39) missense possibly damaging 0.62
V1024:Sult3a2 UTSW 10 33,642,474 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GATAGCAGTTGTGTTATAACAGCAG -3'
(R):5'- TAACACTGGGCATATTGAAGCATG -3'

Sequencing Primer
(F):5'- GCAGTTGTGTTATAACAGCAGAATAC -3'
(R):5'- CTGGGCATATTGAAGCATGCTTAAAG -3'
Posted On 2020-07-28