Incidental Mutation 'IGL00896:Sult2a1'
ID 27751
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult2a1
Ensembl Gene ENSMUSG00000078798
Gene Name sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 1
Synonyms Std, Sth1, mSTa1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # IGL00896
Quality Score
Status
Chromosome 7
Chromosomal Location 13530171-13571334 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 13566565 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 137 (T137S)
Ref Sequence ENSEMBL: ENSMUSP00000104162 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108522]
AlphaFold P52843
Predicted Effect probably benign
Transcript: ENSMUST00000108522
AA Change: T137S

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000104162
Gene: ENSMUSG00000078798
AA Change: T137S

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 278 4.6e-83 PFAM
Pfam:Sulfotransfer_3 35 205 5.8e-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
Adam6a A G 12: 113,509,030 (GRCm39) T468A possibly damaging Het
Ankrd35 A G 3: 96,591,592 (GRCm39) E626G probably damaging Het
Arhgef4 A G 1: 34,850,777 (GRCm39) Y1812C possibly damaging Het
Aurkc T C 7: 7,005,513 (GRCm39) Y260H possibly damaging Het
Bltp1 A G 3: 37,093,611 (GRCm39) T4352A probably benign Het
Cpb1 A G 3: 20,306,193 (GRCm39) V329A probably benign Het
Cyp2d11 G T 15: 82,275,275 (GRCm39) probably benign Het
Dnase1 G A 16: 3,857,076 (GRCm39) S28N probably benign Het
Drgx C T 14: 32,327,171 (GRCm39) probably benign Het
Evpl C A 11: 116,113,410 (GRCm39) E1427* probably null Het
Gimap6 T C 6: 48,679,394 (GRCm39) N214S probably benign Het
Htr1f A T 16: 64,746,469 (GRCm39) H274Q probably benign Het
Ipo9 A T 1: 135,327,797 (GRCm39) V538E probably damaging Het
Lmf2 T C 15: 89,237,539 (GRCm39) K308E probably benign Het
Mog T A 17: 37,328,377 (GRCm39) probably null Het
Myo19 T C 11: 84,800,324 (GRCm39) V903A probably benign Het
Myt1l A G 12: 29,876,885 (GRCm39) T179A unknown Het
Nckap1 C T 2: 80,411,297 (GRCm39) V5M possibly damaging Het
Or1e23 T C 11: 73,407,167 (GRCm39) N286S probably damaging Het
Or51l4 T C 7: 103,404,213 (GRCm39) D193G probably damaging Het
Or9a2 A T 6: 41,749,047 (GRCm39) L62Q probably damaging Het
Pcdhb5 T G 18: 37,455,838 (GRCm39) probably null Het
Pcm1 C A 8: 41,729,160 (GRCm39) Q711K possibly damaging Het
Pde6a A G 18: 61,353,864 (GRCm39) D63G possibly damaging Het
Piezo1 T C 8: 123,224,609 (GRCm39) M711V possibly damaging Het
Rev1 G A 1: 38,138,021 (GRCm39) T88I probably damaging Het
Sntg1 A T 1: 8,665,634 (GRCm39) probably null Het
Txndc15 G A 13: 55,873,488 (GRCm39) A283T probably damaging Het
Zswim8 A G 14: 20,766,069 (GRCm39) E785G probably damaging Het
Other mutations in Sult2a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00990:Sult2a1 APN 7 13,537,961 (GRCm39) missense probably benign
IGL01322:Sult2a1 APN 7 13,566,604 (GRCm39) nonsense probably null
IGL02558:Sult2a1 APN 7 13,566,520 (GRCm39) missense probably benign 0.03
IGL03033:Sult2a1 APN 7 13,566,635 (GRCm39) splice site probably benign
IGL03199:Sult2a1 APN 7 13,566,585 (GRCm39) missense probably damaging 1.00
R1633:Sult2a1 UTSW 7 13,535,351 (GRCm39) missense probably benign 0.01
R1903:Sult2a1 UTSW 7 13,569,900 (GRCm39) missense possibly damaging 0.94
R2295:Sult2a1 UTSW 7 13,569,884 (GRCm39) critical splice donor site probably null
R4207:Sult2a1 UTSW 7 13,535,472 (GRCm39) missense probably benign 0.00
R5444:Sult2a1 UTSW 7 13,569,944 (GRCm39) missense possibly damaging 0.80
R6233:Sult2a1 UTSW 7 13,566,600 (GRCm39) missense probably damaging 1.00
R6317:Sult2a1 UTSW 7 13,569,945 (GRCm39) missense probably benign 0.00
R6853:Sult2a1 UTSW 7 13,535,412 (GRCm39) missense possibly damaging 0.50
R7098:Sult2a1 UTSW 7 13,549,978 (GRCm39) splice site probably null
R8948:Sult2a1 UTSW 7 13,530,342 (GRCm39) missense probably damaging 0.99
R8950:Sult2a1 UTSW 7 13,530,342 (GRCm39) missense probably damaging 0.99
R9207:Sult2a1 UTSW 7 13,566,627 (GRCm39) missense probably benign 0.40
Z1088:Sult2a1 UTSW 7 13,537,961 (GRCm39) missense probably benign
Z1088:Sult2a1 UTSW 7 13,535,360 (GRCm39) missense probably benign 0.00
Z1088:Sult2a1 UTSW 7 13,535,339 (GRCm39) missense probably benign
Z1176:Sult2a1 UTSW 7 13,537,961 (GRCm39) missense probably benign
Z1176:Sult2a1 UTSW 7 13,535,360 (GRCm39) missense probably benign 0.00
Z1176:Sult2a1 UTSW 7 13,535,339 (GRCm39) missense probably benign
Z1176:Sult2a1 UTSW 7 13,569,892 (GRCm39) missense probably damaging 1.00
Z1177:Sult2a1 UTSW 7 13,535,360 (GRCm39) missense probably benign 0.00
Z1177:Sult2a1 UTSW 7 13,535,339 (GRCm39) missense probably benign
Z1177:Sult2a1 UTSW 7 13,530,288 (GRCm39) frame shift probably null
Z1177:Sult2a1 UTSW 7 13,537,961 (GRCm39) missense probably benign
Posted On 2013-04-17