Incidental Mutation 'IGL01984:Sult3a1'
ID181822
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 #IGL01984
Quality Score
Status
Chromosome10
Chromosomal Location33857721-33879532 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to T at 33879209 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Stop codon at position 257 (G257*)
Ref Sequence ENSEMBL: ENSMUSP00000151228 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092597] [ENSMUST00000218204]
Predicted Effect probably null
Transcript: ENSMUST00000092597
AA Change: G257*
SMART Domains Protein: ENSMUSP00000090259
Gene: ENSMUSG00000069668
AA Change: G257*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 283 1.8e-81 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000218204
AA Change: G257*
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933434E20Rik C T 3: 90,063,230 L24F probably benign Het
Adamts16 T C 13: 70,787,147 D442G probably damaging Het
Ankmy1 T C 1: 92,883,765 T634A probably damaging Het
Anxa3 A T 5: 96,834,771 probably benign Het
Ccnh T C 13: 85,206,151 L202P probably damaging Het
Clcn3 A T 8: 60,929,580 S325T probably damaging Het
Clec2d A T 6: 129,184,229 E96D possibly damaging Het
Csn1s1 A T 5: 87,676,510 probably benign Het
Dcun1d5 T A 9: 7,205,307 Y189N possibly damaging Het
Dnah7a T C 1: 53,702,015 probably null Het
Erg T G 16: 95,409,927 D15A probably damaging Het
Gm11639 T A 11: 104,738,308 D937E probably benign Het
Gm17018 C T 19: 45,577,030 H148Y probably benign Het
Gm21759 T A 5: 8,180,547 probably benign Het
Heatr5b C T 17: 78,796,497 R1083Q possibly damaging Het
Ints3 A G 3: 90,392,226 S1012P possibly damaging Het
Klhl3 C T 13: 58,011,243 probably benign Het
Lama4 T A 10: 39,075,529 probably null Het
Magi1 A T 6: 93,708,174 V740D probably damaging Het
Nme8 C A 13: 19,688,980 V165L probably damaging Het
Odf2l G T 3: 145,139,829 E5* probably null Het
Olfr115 T C 17: 37,623,661 probably benign Het
Olfr1297 A G 2: 111,621,582 L164S probably benign Het
Olfr683 A T 7: 105,143,716 D192E probably benign Het
Pcnx4 T C 12: 72,574,409 V1001A probably benign Het
Plaa A G 4: 94,571,685 probably null Het
Prkdc G A 16: 15,708,779 A1305T probably benign Het
Rnps1 T C 17: 24,424,397 probably benign Het
St8sia5 T C 18: 77,248,461 F197L probably benign Het
Svep1 A C 4: 58,068,877 Y2970D possibly damaging Het
Tns3 G T 11: 8,548,992 Y30* probably null Het
Ubr1 G T 2: 120,921,386 P791T probably damaging Het
Zfp592 T C 7: 81,038,644 V1039A probably benign Het
Other mutations in Sult3a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
IGL03367:Sult3a1 APN 10 33877346 missense probably benign 0.01
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 On2014-05-07