Incidental Mutation 'IGL01146:Sult6b2'
ID 51390
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Sult6b2
Ensembl Gene ENSMUSG00000048473
Gene Name sulfotransferase family 6B, member 2
Synonyms LOC330440, Gm766
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # IGL01146
Quality Score
Status
Chromosome 6
Chromosomal Location 142731507-142750192 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 142750034 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Aspartic acid at position 28 (G28D)
Ref Sequence ENSEMBL: ENSMUSP00000138527 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000111768] [ENSMUST00000156662]
AlphaFold B7ZWN4
Predicted Effect probably benign
Transcript: ENSMUST00000111768
AA Change: G28D

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000107398
Gene: ENSMUSG00000048473
AA Change: G28D

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 37 276 1.5e-64 PFAM
Pfam:Sulfotransfer_3 38 200 1.6e-10 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000156662
AA Change: G28D

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000138527
Gene: ENSMUSG00000048473
AA Change: G28D

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 74 157 5.6e-21 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810009J06Rik T C 6: 40,943,217 (GRCm39) I54T probably damaging Het
Acss2 T C 2: 155,403,957 (GRCm39) V701A possibly damaging Het
Adam6a A T 12: 113,507,840 (GRCm39) Y71F probably damaging Het
Arhgef37 A T 18: 61,651,081 (GRCm39) I148N possibly damaging Het
Bhlhe40 T C 6: 108,641,901 (GRCm39) S282P possibly damaging Het
Bmp2 A T 2: 133,403,220 (GRCm39) Q257L probably benign Het
C2cd4d A G 3: 94,271,770 (GRCm39) probably benign Het
Calcr T A 6: 3,700,144 (GRCm39) Y316F possibly damaging Het
Ccdc186 T C 19: 56,797,749 (GRCm39) E274G probably damaging Het
Cdc34b G T 11: 94,633,420 (GRCm39) D207Y probably benign Het
Chst5 C T 8: 112,617,314 (GRCm39) C102Y probably damaging Het
Cnbd2 T A 2: 156,154,534 (GRCm39) probably benign Het
Dnaaf9 C T 2: 130,612,591 (GRCm39) probably null Het
Dnm1l T C 16: 16,132,189 (GRCm39) D549G probably benign Het
Gm4847 T A 1: 166,462,521 (GRCm39) D323V probably damaging Het
Gm9843 G A 16: 76,200,255 (GRCm39) noncoding transcript Het
Gopc A G 10: 52,234,963 (GRCm39) V120A probably benign Het
Kmt2c T G 5: 25,513,510 (GRCm39) M3095L probably damaging Het
Man1a T C 10: 53,783,615 (GRCm39) E629G possibly damaging Het
Pde4b T A 4: 102,112,460 (GRCm39) S12T possibly damaging Het
Phf2 A T 13: 48,973,083 (GRCm39) L391Q unknown Het
Phf8-ps A G 17: 33,284,357 (GRCm39) L815S possibly damaging Het
Plekha7 G A 7: 115,756,708 (GRCm39) probably benign Het
Pmpcb T A 5: 21,945,476 (GRCm39) probably benign Het
Poc1a T C 9: 106,182,503 (GRCm39) Y285H probably benign Het
Polr1e T C 4: 45,031,369 (GRCm39) L387S probably damaging Het
Prr9 A T 3: 92,030,504 (GRCm39) C45* probably null Het
Rnf157 T C 11: 116,240,912 (GRCm39) H393R probably benign Het
Rps6ka4 A G 19: 6,808,496 (GRCm39) F554L probably damaging Het
Sez6l A G 5: 112,576,275 (GRCm39) S861P probably damaging Het
Sh3tc2 G T 18: 62,122,582 (GRCm39) D448Y probably damaging Het
Smg6 T G 11: 74,821,254 (GRCm39) Y508* probably null Het
Traf2 C A 2: 25,414,931 (GRCm39) C303F probably benign Het
Other mutations in Sult6b2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00436:Sult6b2 APN 6 142,743,563 (GRCm39) splice site probably benign
IGL00694:Sult6b2 APN 6 142,736,015 (GRCm39) missense possibly damaging 0.92
IGL01886:Sult6b2 APN 6 142,735,852 (GRCm39) critical splice donor site probably null
IGL02385:Sult6b2 APN 6 142,747,498 (GRCm39) missense probably benign 0.01
IGL02477:Sult6b2 APN 6 142,747,447 (GRCm39) missense probably damaging 1.00
R0088:Sult6b2 UTSW 6 142,743,675 (GRCm39) missense probably damaging 1.00
R2850:Sult6b2 UTSW 6 142,743,613 (GRCm39) missense probably benign 0.18
R4015:Sult6b2 UTSW 6 142,735,988 (GRCm39) missense possibly damaging 0.89
R4667:Sult6b2 UTSW 6 142,747,421 (GRCm39) nonsense probably null
R5172:Sult6b2 UTSW 6 142,743,657 (GRCm39) missense probably damaging 1.00
R5973:Sult6b2 UTSW 6 142,736,021 (GRCm39) missense probably benign 0.01
R6152:Sult6b2 UTSW 6 142,750,102 (GRCm39) missense probably benign 0.00
R6893:Sult6b2 UTSW 6 142,750,025 (GRCm39) missense possibly damaging 0.63
R7667:Sult6b2 UTSW 6 142,732,085 (GRCm39) missense probably benign 0.10
R7853:Sult6b2 UTSW 6 142,747,524 (GRCm39) missense not run
R8071:Sult6b2 UTSW 6 142,735,868 (GRCm39) missense probably damaging 1.00
R8225:Sult6b2 UTSW 6 142,750,055 (GRCm39) missense probably benign 0.00
R8344:Sult6b2 UTSW 6 142,736,022 (GRCm39) missense probably benign 0.13
Posted On 2013-06-21