Incidental Mutation 'IGL02970:Sult2a4'
ID 365789
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult2a4
Ensembl Gene ENSMUSG00000074377
Gene Name sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 4
Synonyms Gm5584
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02970
Quality Score
Status
Chromosome 7
Chromosomal Location 13643602-13723516 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 13643831 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130490 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108520] [ENSMUST00000165167]
AlphaFold L7N245
Predicted Effect probably benign
Transcript: ENSMUST00000108520
SMART Domains Protein: ENSMUSP00000104160
Gene: ENSMUSG00000074377

DomainStartEndE-ValueType
Pfam:Sulfotransfer_3 5 205 1.5e-10 PFAM
Pfam:Sulfotransfer_1 34 278 1.2e-82 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000165167
SMART Domains Protein: ENSMUSP00000130490
Gene: ENSMUSG00000074377

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 33 277 1.3e-82 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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700019A02Rik C T 1: 53,226,748 (GRCm39) G5S probably damaging Het
A2ml1 A T 6: 128,546,942 (GRCm39) F396I probably damaging Het
BC051019 T A 7: 109,315,262 (GRCm39) N331I probably benign Het
Crocc G A 4: 140,757,557 (GRCm39) S912L possibly damaging Het
Dcaf4 A G 12: 83,575,989 (GRCm39) D46G probably damaging Het
Dido1 C T 2: 180,331,208 (GRCm39) R80Q probably damaging Het
Dnase2b A G 3: 146,288,261 (GRCm39) V278A probably damaging Het
Drosha C T 15: 12,914,042 (GRCm39) L1106F probably damaging Het
Dsc3 C A 18: 20,101,317 (GRCm39) W692L probably damaging Het
F2 T A 2: 91,455,896 (GRCm39) Y579F possibly damaging Het
Fam43a C T 16: 30,419,922 (GRCm39) R169C probably damaging Het
Gm9772 A G 17: 22,225,540 (GRCm39) F120S probably damaging Het
Gsdma3 T C 11: 98,523,819 (GRCm39) S251P probably benign Het
Hycc2 T C 1: 58,578,776 (GRCm39) E258G probably damaging Het
Itgam G A 7: 127,685,215 (GRCm39) E443K probably benign Het
Kif18a T C 2: 109,118,233 (GRCm39) V16A probably damaging Het
Lrrn3 T G 12: 41,502,359 (GRCm39) S653R probably benign Het
Map1b A T 13: 99,567,242 (GRCm39) Y1826* probably null Het
Mbnl1 T C 3: 60,520,844 (GRCm39) F139S probably damaging Het
Micu3 T C 8: 40,835,171 (GRCm39) Y509H possibly damaging Het
Ncmap T C 4: 135,104,329 (GRCm39) T17A probably damaging Het
Oas1h T A 5: 120,999,698 (GRCm39) M61K possibly damaging Het
Otog T A 7: 45,945,291 (GRCm39) W2183R probably benign Het
Pcdh15 T C 10: 74,126,794 (GRCm39) probably benign Het
Plekho1 C T 3: 95,898,214 (GRCm39) V150I probably damaging Het
Ppargc1b A G 18: 61,431,837 (GRCm39) S1004P probably damaging Het
Prf1 T C 10: 61,135,957 (GRCm39) S78P probably benign Het
Prss12 A G 3: 123,276,411 (GRCm39) S347G probably benign Het
Rai1 T C 11: 60,076,559 (GRCm39) S208P probably damaging Het
Sgms1 A G 19: 32,137,165 (GRCm39) Y134H probably damaging Het
T C T 17: 8,654,217 (GRCm39) A134V probably damaging Het
Thoc5 A G 11: 4,854,201 (GRCm39) T187A probably damaging Het
Ticrr A G 7: 79,344,919 (GRCm39) S1595G probably benign Het
Tiprl A G 1: 165,064,315 (GRCm39) S30P probably damaging Het
Ttl T C 2: 128,917,990 (GRCm39) S151P probably damaging Het
Ttn T A 2: 76,583,334 (GRCm39) T22520S probably damaging Het
Usp54 G A 14: 20,627,540 (GRCm39) S420L probably damaging Het
Vmn1r62 T A 7: 5,678,567 (GRCm39) Y83N possibly damaging Het
Other mutations in Sult2a4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00557:Sult2a4 APN 7 13,718,870 (GRCm39) missense probably damaging 1.00
IGL00835:Sult2a4 APN 7 13,643,714 (GRCm39) missense probably benign 0.01
IGL02078:Sult2a4 APN 7 13,723,469 (GRCm39) missense probably benign 0.02
IGL02409:Sult2a4 APN 7 13,718,844 (GRCm39) nonsense probably null
IGL03201:Sult2a4 APN 7 13,665,692 (GRCm39) missense probably damaging 0.97
R0827:Sult2a4 UTSW 7 13,718,886 (GRCm39) missense probably benign 0.03
R1484:Sult2a4 UTSW 7 13,643,726 (GRCm39) missense probably benign
R1523:Sult2a4 UTSW 7 13,643,785 (GRCm39) nonsense probably null
R1613:Sult2a4 UTSW 7 13,723,420 (GRCm39) missense probably damaging 0.98
R2127:Sult2a4 UTSW 7 13,649,185 (GRCm39) missense probably damaging 0.99
R2372:Sult2a4 UTSW 7 13,649,225 (GRCm39) missense probably benign 0.15
R3161:Sult2a4 UTSW 7 13,723,396 (GRCm39) missense probably benign 0.17
R5181:Sult2a4 UTSW 7 13,722,316 (GRCm39) missense probably benign 0.04
R7124:Sult2a4 UTSW 7 13,722,320 (GRCm39) nonsense probably null
R7983:Sult2a4 UTSW 7 13,649,152 (GRCm39) missense probably damaging 1.00
R8214:Sult2a4 UTSW 7 13,723,401 (GRCm39) missense probably benign 0.10
R9508:Sult2a4 UTSW 7 13,723,437 (GRCm39) missense probably benign 0.01
X0028:Sult2a4 UTSW 7 13,722,166 (GRCm39) missense probably damaging 1.00
Posted On 2015-12-18