Incidental Mutation 'R5599:Sult2a6'
ID 438940
Institutional Source Beutler Lab
Gene Symbol Sult2a6
Ensembl Gene ENSMUSG00000070810
Gene Name sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 6
Synonyms Gm6957
MMRRC Submission 043151-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R5599 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 13956328-13988795 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 13988629 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 44 (K44*)
Ref Sequence ENSEMBL: ENSMUSP00000138842 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076576] [ENSMUST00000184731]
AlphaFold B2RVI8
Predicted Effect probably null
Transcript: ENSMUST00000076576
AA Change: K44*
SMART Domains Protein: ENSMUSP00000075884
Gene: ENSMUSG00000070810
AA Change: K44*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 278 1.2e-81 PFAM
Pfam:Sulfotransfer_3 35 205 2.2e-11 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000184731
AA Change: K44*
SMART Domains Protein: ENSMUSP00000138842
Gene: ENSMUSG00000070810
AA Change: K44*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 34 116 4.7e-20 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.1%
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: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd2 T A 7: 78,946,746 (GRCm39) probably null Het
Agpat3 T C 10: 78,110,103 (GRCm39) D282G probably benign Het
Ankhd1 G A 18: 36,693,860 (GRCm39) A24T probably damaging Het
Cracdl T C 1: 37,652,424 (GRCm39) N1128D possibly damaging Het
Cry1 A T 10: 84,980,114 (GRCm39) M398K probably benign Het
Dpp10 A G 1: 123,832,803 (GRCm39) I47T probably damaging Het
Fpr-rs6 C T 17: 20,402,375 (GRCm39) D329N probably benign Het
Gfm2 G A 13: 97,299,659 (GRCm39) A406T probably damaging Het
Gprc5c G T 11: 114,755,093 (GRCm39) V257L possibly damaging Het
Gxylt1 CTCATCCGGGTCAT CTCAT 15: 93,152,198 (GRCm39) probably benign Het
Hnrnpul1 G A 7: 25,454,097 (GRCm39) probably benign Het
Lbx1 T A 19: 45,223,519 (GRCm39) S50C probably damaging Het
Lims2 A G 18: 32,090,324 (GRCm39) N183S probably benign Het
Lrp1 T C 10: 127,429,738 (GRCm39) N444S probably damaging Het
Mast4 A T 13: 102,873,987 (GRCm39) C1626S probably damaging Het
Mgat5 A G 1: 127,325,303 (GRCm39) Y390C probably damaging Het
Nf2 T C 11: 4,732,269 (GRCm39) E553G probably damaging Het
Nfatc4 A T 14: 56,069,733 (GRCm39) T704S probably benign Het
Or4c3d A G 2: 89,882,563 (GRCm39) V35A probably benign Het
Or56a3 T C 7: 104,735,757 (GRCm39) probably null Het
Or7g29 T G 9: 19,286,925 (GRCm39) N84T possibly damaging Het
Or9m1b T G 2: 87,836,349 (GRCm39) I258L probably benign Het
Plekha7 T A 7: 115,776,117 (GRCm39) probably null Het
Polr1a T C 6: 71,944,346 (GRCm39) M1271T possibly damaging Het
Ppip5k2 A G 1: 97,668,323 (GRCm39) M595T probably damaging Het
Ppox A T 1: 171,105,033 (GRCm39) V412D probably damaging Het
Ppp1r12b A G 1: 134,793,645 (GRCm39) V573A probably benign Het
Prkcb T C 7: 122,181,701 (GRCm39) Y430H probably benign Het
Psmd6 A C 14: 14,120,144 (GRCm38) M65R probably benign Het
Rbm12 G A 2: 155,938,713 (GRCm39) R520* probably null Het
Rin3 T C 12: 102,356,188 (GRCm39) F830L probably damaging Het
Sema4b A G 7: 79,863,039 (GRCm39) K104R probably benign Het
Slitrk1 T C 14: 109,149,244 (GRCm39) D489G probably benign Het
Spef2 T C 15: 9,729,789 (GRCm39) T110A possibly damaging Het
Tasor A G 14: 27,201,886 (GRCm39) N1427D probably benign Het
Tbc1d2 C T 4: 46,629,912 (GRCm39) G252R probably benign Het
Tcstv2c A C 13: 120,616,458 (GRCm39) Q99P probably damaging Het
Tnxb G T 17: 34,909,176 (GRCm39) G1445V probably damaging Het
Tnxb T C 17: 34,909,179 (GRCm39) V1569A probably benign Het
Zcchc2 A G 1: 105,959,880 (GRCm39) D1163G probably damaging Het
Zfp365 C T 10: 67,745,197 (GRCm39) E194K probably damaging Het
Other mutations in Sult2a6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00959:Sult2a6 APN 7 13,988,634 (GRCm39) missense probably damaging 1.00
IGL01977:Sult2a6 APN 7 13,987,411 (GRCm39) missense probably benign 0.00
IGL02524:Sult2a6 APN 7 13,970,611 (GRCm39) missense possibly damaging 0.80
IGL03209:Sult2a6 APN 7 13,959,897 (GRCm39) missense probably benign 0.36
IGL03379:Sult2a6 APN 7 13,956,511 (GRCm39) missense probably benign 0.01
R1840:Sult2a6 UTSW 7 13,988,754 (GRCm39) missense probably benign 0.03
R1893:Sult2a6 UTSW 7 13,959,814 (GRCm39) missense probably benign 0.00
R2037:Sult2a6 UTSW 7 13,988,634 (GRCm39) missense probably damaging 0.99
R2331:Sult2a6 UTSW 7 13,959,795 (GRCm39) missense possibly damaging 0.94
R3871:Sult2a6 UTSW 7 13,988,701 (GRCm39) missense probably benign 0.16
R3921:Sult2a6 UTSW 7 13,988,668 (GRCm39) missense possibly damaging 0.83
R5761:Sult2a6 UTSW 7 13,984,283 (GRCm39) missense probably damaging 0.97
R6744:Sult2a6 UTSW 7 13,956,470 (GRCm39) missense probably damaging 1.00
R6956:Sult2a6 UTSW 7 13,988,748 (GRCm39) missense possibly damaging 0.50
R7152:Sult2a6 UTSW 7 13,956,445 (GRCm39) missense probably benign 0.36
R7869:Sult2a6 UTSW 7 13,988,737 (GRCm39) missense not run
R7990:Sult2a6 UTSW 7 13,959,795 (GRCm39) missense possibly damaging 0.94
R8347:Sult2a6 UTSW 7 13,959,883 (GRCm39) missense probably benign 0.15
R8369:Sult2a6 UTSW 7 13,987,327 (GRCm39) critical splice donor site probably null
R8391:Sult2a6 UTSW 7 13,956,516 (GRCm39) critical splice acceptor site probably null
R8414:Sult2a6 UTSW 7 13,984,357 (GRCm39) missense probably damaging 1.00
R9317:Sult2a6 UTSW 7 13,970,615 (GRCm39) nonsense probably null
R9654:Sult2a6 UTSW 7 13,956,445 (GRCm39) missense probably benign 0.06
Z1088:Sult2a6 UTSW 7 13,959,819 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- GTGGTGCCATAGATGATCACC -3'
(R):5'- CAGCATTTGCAATATGCTGAAC -3'

Sequencing Primer
(F):5'- GTGGTGCCATAGATGATCACCTTATC -3'
(R):5'- CATTTGCAATATGCTGAACTGGTG -3'
Posted On 2016-10-26