Incidental Mutation 'IGL03367:Sult3a1'
ID420121
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult3a1
Ensembl Gene ENSMUSG00000069668
Gene Namesulfotransferase family 3A, member 1
SynonymsSultx2
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.223) question?
Stock #IGL03367
Quality Score
Status
Chromosome10
Chromosomal Location33857721-33879532 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 33877346 bp
ZygosityHeterozygous
Amino Acid Change Valine to Leucine at position 213 (V213L)
Ref Sequence ENSEMBL: ENSMUSP00000151228 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092597] [ENSMUST00000218204]
Predicted Effect probably benign
Transcript: ENSMUST00000092597
AA Change: V213L

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000090259
Gene: ENSMUSG00000069668
AA Change: V213L

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 283 1.8e-81 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217760
Predicted Effect probably benign
Transcript: ENSMUST00000218204
AA Change: V213L

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6030419C18Rik A G 9: 58,499,098 H97R probably damaging Het
Abcc5 A T 16: 20,392,811 probably benign Het
Adra1a G A 14: 66,637,989 V138I possibly damaging Het
Alpk3 A G 7: 81,094,990 I1278V probably benign Het
Asb6 A T 2: 30,824,679 I185N possibly damaging Het
Atg9a A G 1: 75,187,957 V121A probably benign Het
Cdc42bpb A G 12: 111,336,159 Y155H probably damaging Het
Ceacam15 A C 7: 16,675,587 S8A possibly damaging Het
Cep170b T A 12: 112,737,238 D615E probably benign Het
Cntn6 G T 6: 104,804,338 G462C probably damaging Het
Col8a2 A G 4: 126,312,198 D667G probably damaging Het
Cyp2c29 A G 19: 39,329,215 K382E probably damaging Het
Dgkd T C 1: 87,940,308 probably null Het
Dkk2 C T 3: 132,178,077 T246I probably damaging Het
Dnah5 T C 15: 28,234,327 L294P possibly damaging Het
Erbb2 G T 11: 98,422,875 probably null Het
Fn1 A G 1: 71,597,553 F2147L probably benign Het
Gm11149 G A 9: 49,546,346 probably benign Het
Gm13088 C T 4: 143,655,623 V168I possibly damaging Het
Gnrhr C T 5: 86,182,331 V277I probably benign Het
H2-T10 T A 17: 36,120,393 E129V possibly damaging Het
Hmgcr T C 13: 96,665,853 T108A probably damaging Het
Hnrnph3 A T 10: 63,017,229 I196N probably damaging Het
Kcnq5 T C 1: 21,403,065 K653E probably damaging Het
Lgi2 C A 5: 52,562,160 D100Y probably damaging Het
Mettl15 T A 2: 109,131,571 H231L probably benign Het
Mthfd1l A G 10: 4,106,536 probably benign Het
Pik3cg A G 12: 32,192,121 S997P probably benign Het
Pla2g1b T C 5: 115,472,114 C105R probably damaging Het
Ppil1 A T 17: 29,252,244 probably benign Het
Rbbp8 A G 18: 11,721,719 T334A probably benign Het
Slc15a4 T C 5: 127,601,941 Y445C probably damaging Het
Sox14 A C 9: 99,875,662 I8S probably damaging Het
Spice1 A G 16: 44,356,178 T44A probably damaging Het
Vkorc1l1 C A 5: 129,982,307 Y111* probably null Het
Wdr47 G T 3: 108,629,773 probably benign Het
Wdr90 A G 17: 25,847,791 probably benign Het
Other mutations in Sult3a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01984:Sult3a1 APN 10 33879209 nonsense probably null
IGL02269:Sult3a1 APN 10 33879263 missense probably benign 0.25
IGL02302:Sult3a1 APN 10 33866575 missense possibly damaging 0.81
IGL02947:Sult3a1 APN 10 33864050 missense possibly damaging 0.92
IGL02966:Sult3a1 APN 10 33877273 splice site probably benign
IGL03271:Sult3a1 APN 10 33864001 missense probably benign
R0539:Sult3a1 UTSW 10 33866523 missense probably damaging 1.00
R0627:Sult3a1 UTSW 10 33864014 missense probably benign 0.00
R0838:Sult3a1 UTSW 10 33879288 missense probably damaging 0.99
R1538:Sult3a1 UTSW 10 33870170 missense probably benign 0.29
R1604:Sult3a1 UTSW 10 33866620 missense probably damaging 1.00
R1622:Sult3a1 UTSW 10 33870250 missense probably benign 0.39
R3031:Sult3a1 UTSW 10 33877349 missense possibly damaging 0.70
R4933:Sult3a1 UTSW 10 33866554 missense probably damaging 1.00
R5943:Sult3a1 UTSW 10 33866641 missense probably damaging 0.99
R6440:Sult3a1 UTSW 10 33870202 missense possibly damaging 0.46
R7140:Sult3a1 UTSW 10 33877287 missense probably damaging 1.00
R7356:Sult3a1 UTSW 10 33866583 missense probably benign 0.25
R8342:Sult3a1 UTSW 10 33866521 missense probably damaging 1.00
Posted On2016-08-02