Incidental Mutation 'R6105:Sult4a1'
ID 485484
Institutional Source Beutler Lab
Gene Symbol Sult4a1
Ensembl Gene ENSMUSG00000018865
Gene Name sulfotransferase family 4A, member 1
Synonyms BR-STL-1, Sultx3, 2400007A17Rik
MMRRC Submission 044255-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6105 (G1)
Quality Score 225.009
Status Not validated
Chromosome 15
Chromosomal Location 83960298-83989955 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 83970821 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 195 (K195*)
Ref Sequence ENSEMBL: ENSMUSP00000155695 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000082365] [ENSMUST00000229826]
AlphaFold P63046
Predicted Effect probably null
Transcript: ENSMUST00000082365
AA Change: K195*
SMART Domains Protein: ENSMUSP00000080973
Gene: ENSMUSG00000018865
AA Change: K195*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 45 277 1.1e-60 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000229826
AA Change: K195*
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 94.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the sulfotransferase family. The encoded protein is a brain-specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. Polymorphisms in this gene may be associated with susceptibility to schizophrenia. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T C 11: 9,347,812 (GRCm39) M3555T probably damaging Het
Adam9 A T 8: 25,460,775 (GRCm39) C570S probably damaging Het
Adh6b T A 3: 138,063,471 (GRCm39) I350K possibly damaging Het
Ahnak G A 19: 8,981,463 (GRCm39) V916I probably benign Het
Aldh4a1 C T 4: 139,365,806 (GRCm39) P266S possibly damaging Het
Cnot7 C T 8: 40,963,078 (GRCm39) R32Q probably benign Het
Cyb5a G A 18: 84,889,718 (GRCm39) R49Q possibly damaging Het
Fbxo6 A T 4: 148,233,979 (GRCm39) I39N probably damaging Het
Glul T A 1: 153,782,177 (GRCm39) Y137* probably null Het
Ipo8 A G 6: 148,700,168 (GRCm39) Y570H probably damaging Het
Kif2b A G 11: 91,466,814 (GRCm39) S490P probably benign Het
Kxd1 A T 8: 70,972,589 (GRCm39) N33K probably benign Het
Man2a2 T C 7: 80,016,749 (GRCm39) D355G probably damaging Het
Map6 T C 7: 98,917,314 (GRCm39) V29A probably damaging Het
Mtmr3 T C 11: 4,435,432 (GRCm39) D1116G probably damaging Het
Or4p23 T A 2: 88,577,184 (GRCm39) H16L probably benign Het
Or8b52 A G 9: 38,576,916 (GRCm39) S75P probably damaging Het
Or8d2b T C 9: 38,788,604 (GRCm39) L44P possibly damaging Het
Pak1ip1 T A 13: 41,158,361 (GRCm39) L78Q probably damaging Het
Phf10 C T 17: 15,174,387 (GRCm39) probably null Het
Pikfyve A G 1: 65,303,504 (GRCm39) probably null Het
Pkd1l3 A G 8: 110,367,478 (GRCm39) D1225G probably damaging Het
Postn A G 3: 54,279,641 (GRCm39) probably null Het
Slc22a30 T C 19: 8,315,232 (GRCm39) probably null Het
Specc1l T C 10: 75,084,466 (GRCm39) S730P probably damaging Het
Steap2 T A 5: 5,725,891 (GRCm39) I378F possibly damaging Het
Tgfb1i1 T A 7: 127,847,589 (GRCm39) probably null Het
Thbs4 G T 13: 92,911,993 (GRCm39) Q246K possibly damaging Het
Tnfsf10 A G 3: 27,389,698 (GRCm39) Y253C probably damaging Het
Tnpo3 G T 6: 29,588,042 (GRCm39) C125* probably null Het
Trappc8 A G 18: 20,979,504 (GRCm39) probably null Het
Trpm6 C T 19: 18,831,112 (GRCm39) R1326* probably null Het
Vmn2r19 A C 6: 123,293,054 (GRCm39) E365D possibly damaging Het
Vps18 A G 2: 119,119,543 (GRCm39) Y8C probably damaging Het
Zc3hav1l A G 6: 38,270,012 (GRCm39) V279A probably benign Het
Zfp111 T C 7: 23,902,791 (GRCm39) probably null Het
Zfp618 A T 4: 63,051,478 (GRCm39) Q753L probably benign Het
Zkscan17 A T 11: 59,394,401 (GRCm39) C67S probably damaging Het
Other mutations in Sult4a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01322:Sult4a1 APN 15 83,970,817 (GRCm39) missense possibly damaging 0.93
IGL01826:Sult4a1 APN 15 83,974,247 (GRCm39) missense probably damaging 1.00
mum UTSW 15 83,974,159 (GRCm39) critical splice donor site probably null
R0305:Sult4a1 UTSW 15 83,970,868 (GRCm39) missense probably damaging 1.00
R1416:Sult4a1 UTSW 15 83,970,847 (GRCm39) missense probably benign 0.15
R1664:Sult4a1 UTSW 15 83,970,818 (GRCm39) missense probably benign 0.04
R4630:Sult4a1 UTSW 15 83,989,779 (GRCm39) missense possibly damaging 0.81
R5524:Sult4a1 UTSW 15 83,974,159 (GRCm39) critical splice donor site probably null
R7313:Sult4a1 UTSW 15 83,970,814 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCCATGACATCACTGGACAC -3'
(R):5'- AGTTTCCTTCCCAGCAGCTG -3'

Sequencing Primer
(F):5'- GCCTGTCTCAAAAGATGCCC -3'
(R):5'- CAGCAGCTGGGCAGGAG -3'
Posted On 2017-08-16