Incidental Mutation 'R2196:Sult2a8'
ID 238359
Institutional Source Beutler Lab
Gene Symbol Sult2a8
Ensembl Gene ENSMUSG00000030378
Gene Name sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 8
Synonyms 2810007J24Rik, mL-STL
MMRRC Submission 040198-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R2196 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 14144611-14180694 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 14161778 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 23 (I23L)
Ref Sequence ENSEMBL: ENSMUSP00000128428 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063509] [ENSMUST00000125941] [ENSMUST00000168252] [ENSMUST00000209425] [ENSMUST00000209972] [ENSMUST00000211800] [ENSMUST00000210396]
AlphaFold Q8BGL3
Predicted Effect probably benign
Transcript: ENSMUST00000063509
AA Change: I23L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000066897
Gene: ENSMUSG00000030378
AA Change: I23L

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 275 1.6e-73 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000125941
AA Change: I23L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000116469
Gene: ENSMUSG00000030378
AA Change: I23L

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 189 4e-47 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000168252
AA Change: I23L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000128428
Gene: ENSMUSG00000030378
AA Change: I23L

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 275 1.6e-73 PFAM
Pfam:Sulfotransfer_3 36 205 6.3e-10 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000209425
AA Change: I23L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Predicted Effect probably benign
Transcript: ENSMUST00000209972
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210366
Predicted Effect probably benign
Transcript: ENSMUST00000211800
AA Change: I23L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Predicted Effect probably benign
Transcript: ENSMUST00000210396
AA Change: I23L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actn2 T A 13: 12,290,065 (GRCm39) T734S probably damaging Het
Acvr2a A T 2: 48,760,324 (GRCm39) T27S possibly damaging Het
Ankhd1 T A 18: 36,781,432 (GRCm39) N2161K probably damaging Het
Apba3 A G 10: 81,107,542 (GRCm39) Y350C probably damaging Het
Bnipl T A 3: 95,157,181 (GRCm39) R47S possibly damaging Het
Cacna1b C T 2: 24,651,800 (GRCm39) M126I probably damaging Het
Cep112 G A 11: 108,461,187 (GRCm39) E329K probably damaging Het
Cep55 T A 19: 38,057,558 (GRCm39) Y187N probably damaging Het
Cngb3 T C 4: 19,415,690 (GRCm39) I400T possibly damaging Het
Csad T C 15: 102,096,028 (GRCm39) N142D probably benign Het
Dars1 A T 1: 128,306,595 (GRCm39) I195N probably damaging Het
Dmxl1 T A 18: 50,050,698 (GRCm39) L2454Q probably benign Het
Emc1 A T 4: 139,093,841 (GRCm39) E650D probably benign Het
Enam A G 5: 88,650,603 (GRCm39) D704G probably damaging Het
Fat1 T A 8: 45,477,683 (GRCm39) I2220N probably damaging Het
Fat4 T C 3: 39,035,566 (GRCm39) S3073P probably benign Het
Fbxl4 T C 4: 22,403,624 (GRCm39) M399T probably benign Het
Gcsh G A 8: 117,715,909 (GRCm39) T58M possibly damaging Het
Ghrhr T C 6: 55,356,726 (GRCm39) Y108H probably damaging Het
Gm5431 A T 11: 48,780,058 (GRCm39) I566N probably damaging Het
Gnb5 A T 9: 75,234,511 (GRCm39) D70V probably damaging Het
Grin2c G T 11: 115,141,492 (GRCm39) S875R probably benign Het
Itch A C 2: 155,044,141 (GRCm39) Q482P probably benign Het
Krt87 T C 15: 101,336,314 (GRCm39) E113G probably damaging Het
Map4 A G 9: 109,900,116 (GRCm39) E934G probably damaging Het
Mkx A G 18: 7,000,675 (GRCm39) L89P probably damaging Het
Myo15a T A 11: 60,400,847 (GRCm39) Y2982* probably null Het
Nedd4 C T 9: 72,632,356 (GRCm39) L397F possibly damaging Het
Nom1 A G 5: 29,641,019 (GRCm39) D353G probably benign Het
Notch1 A T 2: 26,353,816 (GRCm39) L1937* probably null Het
Nrxn2 A T 19: 6,540,139 (GRCm39) D820V probably damaging Het
Nup210 A T 6: 91,032,226 (GRCm39) N47K probably benign Het
Or1j12 T A 2: 36,342,600 (GRCm39) M1K probably null Het
Or4p21 G A 2: 88,277,054 (GRCm39) T76I probably benign Het
Or6d14 A T 6: 116,533,578 (GRCm39) Q64L probably damaging Het
Pcolce2 A T 9: 95,576,742 (GRCm39) I338F probably damaging Het
Pkd1 T C 17: 24,799,046 (GRCm39) M2755T possibly damaging Het
Plekhg4 TAGTCGATGCCCGAGTC TAGTC 8: 106,103,084 (GRCm39) probably benign Het
Rab3a T C 8: 71,209,872 (GRCm39) S51P probably benign Het
Scn10a G A 9: 119,438,070 (GRCm39) A1933V probably benign Het
Serpina1c T A 12: 103,862,370 (GRCm39) Y315F probably damaging Het
Slc29a4 A C 5: 142,698,650 (GRCm39) I104L possibly damaging Het
Spag16 G A 1: 69,897,681 (GRCm39) V144I possibly damaging Het
Spata22 A G 11: 73,236,660 (GRCm39) K322R probably benign Het
Thoc1 T A 18: 9,986,300 (GRCm39) V344D probably damaging Het
Tnn G C 1: 159,924,798 (GRCm39) Y1185* probably null Het
Trpc4 A G 3: 54,209,614 (GRCm39) I660V probably benign Het
Urb1 A G 16: 90,571,144 (GRCm39) Y1222H probably benign Het
Usp4 A G 9: 108,250,885 (GRCm39) E531G probably benign Het
Vmn2r93 C T 17: 18,525,428 (GRCm39) S362L probably damaging Het
Zfhx3 G T 8: 109,526,885 (GRCm39) E927D probably damaging Het
Zfp644 A T 5: 106,786,469 (GRCm39) M1K probably null Het
Zp2 T C 7: 119,737,529 (GRCm39) H252R probably benign Het
Other mutations in Sult2a8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01558:Sult2a8 APN 7 14,159,377 (GRCm39) nonsense probably null
IGL01904:Sult2a8 APN 7 14,159,382 (GRCm39) missense probably damaging 1.00
IGL02060:Sult2a8 APN 7 14,159,326 (GRCm39) missense probably damaging 1.00
IGL02532:Sult2a8 APN 7 14,150,183 (GRCm39) missense probably benign 0.01
IGL02663:Sult2a8 APN 7 14,159,368 (GRCm39) missense possibly damaging 0.52
IGL02803:Sult2a8 APN 7 14,145,630 (GRCm39) utr 3 prime probably benign
R1070:Sult2a8 UTSW 7 14,147,698 (GRCm39) missense probably damaging 0.99
R1251:Sult2a8 UTSW 7 14,159,350 (GRCm39) nonsense probably null
R1465:Sult2a8 UTSW 7 14,150,208 (GRCm39) missense probably benign 0.00
R1465:Sult2a8 UTSW 7 14,150,208 (GRCm39) missense probably benign 0.00
R1799:Sult2a8 UTSW 7 14,157,451 (GRCm39) missense probably damaging 1.00
R4233:Sult2a8 UTSW 7 14,147,608 (GRCm39) missense probably benign 0.01
R4713:Sult2a8 UTSW 7 14,159,402 (GRCm39) missense probably benign 0.02
R4964:Sult2a8 UTSW 7 14,159,457 (GRCm39) missense probably damaging 0.98
R5114:Sult2a8 UTSW 7 14,147,584 (GRCm39) missense probably benign 0.01
R5330:Sult2a8 UTSW 7 14,147,679 (GRCm39) missense possibly damaging 0.53
R5439:Sult2a8 UTSW 7 14,159,439 (GRCm39) missense probably damaging 1.00
R5662:Sult2a8 UTSW 7 14,161,765 (GRCm39) missense probably benign 0.13
R7353:Sult2a8 UTSW 7 14,147,640 (GRCm39) missense possibly damaging 0.95
R7366:Sult2a8 UTSW 7 14,150,254 (GRCm39) splice site probably null
R7832:Sult2a8 UTSW 7 14,147,596 (GRCm39) missense probably benign 0.02
R9499:Sult2a8 UTSW 7 14,157,487 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTTGAGTGAGTAAAGACACTGCC -3'
(R):5'- GAAACACTGATCATTGTGTCCTC -3'

Sequencing Primer
(F):5'- GACACTGCCATAGTTCTGGAG -3'
(R):5'- GTGTCCTCACTATAAAATTGAGACTC -3'
Posted On 2014-10-02