Incidental Mutation 'R5578:Sult5a1'
ID 437303
Institutional Source Beutler Lab
Gene Symbol Sult5a1
Ensembl Gene ENSMUSG00000000739
Gene Name sulfotransferase family 5A, member 1
Synonyms Sultx1
MMRRC Submission 043133-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # R5578 (G1)
Quality Score 225
Status Not validated
Chromosome 8
Chromosomal Location 123869582-123885170 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 123869860 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 262 (Y262*)
Ref Sequence ENSEMBL: ENSMUSP00000000755 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000755] [ENSMUST00000122819] [ENSMUST00000127664] [ENSMUST00000137998] [ENSMUST00000146007]
AlphaFold Q91X36
Predicted Effect probably null
Transcript: ENSMUST00000000755
AA Change: Y262*
SMART Domains Protein: ENSMUSP00000000755
Gene: ENSMUSG00000000739
AA Change: Y262*

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 283 5e-78 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000122819
SMART Domains Protein: ENSMUSP00000123501
Gene: ENSMUSG00000000739

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 169 2.5e-36 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000127664
SMART Domains Protein: ENSMUSP00000118564
Gene: ENSMUSG00000092329

DomainStartEndE-ValueType
Pfam:Glycos_transf_2 104 287 7.4e-31 PFAM
Pfam:Glyco_transf_7C 261 331 4.9e-8 PFAM
RICIN 406 531 9.28e-27 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000137998
SMART Domains Protein: ENSMUSP00000122415
Gene: ENSMUSG00000000739

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 219 2.5e-57 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000146007
SMART Domains Protein: ENSMUSP00000116815
Gene: ENSMUSG00000000739

DomainStartEndE-ValueType
SCOP:d1j99a_ 11 48 8e-9 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acap2 A G 16: 30,926,932 (GRCm39) S521P probably benign Het
Aqp11 A G 7: 97,386,665 (GRCm39) F177S probably damaging Het
Arhgap40 G T 2: 158,373,126 (GRCm39) G128V probably damaging Het
Aspm A T 1: 139,398,455 (GRCm39) K1011I probably damaging Het
Cachd1 A G 4: 100,722,203 (GRCm39) T89A probably benign Het
Cep89 ACTCCTCCTCCTCCTCCTCCTCCTC ACTCCTCCTCCTCCTCCTCCTC 7: 35,109,067 (GRCm39) probably benign Het
Cfhr2 A T 1: 139,758,806 (GRCm39) C81* probably null Het
Chd7 A G 4: 8,847,149 (GRCm39) T1631A probably benign Het
Clca4b T A 3: 144,638,196 (GRCm39) D22V probably benign Het
Csnk2a1-ps3 A G 1: 156,352,800 (GRCm39) M334V probably benign Het
Cybb C G X: 9,316,989 (GRCm39) D246H probably benign Het
Cyp39a1 T A 17: 43,991,031 (GRCm39) N113K possibly damaging Het
Dnah11 A T 12: 117,982,537 (GRCm39) V2544D probably damaging Het
Dnai3 A T 3: 145,802,983 (GRCm39) Y69* probably null Het
Esr1 A C 10: 4,919,164 (GRCm39) Q418P probably damaging Het
Fam89a T A 8: 125,467,968 (GRCm39) K115* probably null Het
Fstl4 T A 11: 53,056,608 (GRCm39) V455D probably damaging Het
Gm20730 T A 6: 43,058,474 (GRCm39) M113L probably benign Het
H2ac21 T C 3: 96,127,554 (GRCm39) V108A probably damaging Het
Hk3 C T 13: 55,159,994 (GRCm39) V327M probably damaging Het
Itm2c T A 1: 85,830,774 (GRCm39) V57E possibly damaging Het
Lrba T C 3: 86,664,814 (GRCm39) Y565H probably benign Het
Mab21l1 C T 3: 55,691,435 (GRCm39) Q341* probably null Het
Mdm2 C T 10: 117,538,192 (GRCm39) E69K possibly damaging Het
Mdn1 A T 4: 32,728,167 (GRCm39) I2709F probably benign Het
Mpp7 T C 18: 7,355,101 (GRCm39) N442D probably benign Het
Ncoa3 A G 2: 165,896,248 (GRCm39) I384V probably benign Het
Pm20d1 A G 1: 131,743,760 (GRCm39) N475S probably benign Het
Rhpn2 A G 7: 35,070,135 (GRCm39) D131G probably damaging Het
S1pr5 T A 9: 21,155,847 (GRCm39) Y193F probably damaging Het
Sdk1 A T 5: 141,598,880 (GRCm39) K182* probably null Het
Slx4 T A 16: 3,804,726 (GRCm39) E696V probably damaging Het
Smyd4 C T 11: 75,295,602 (GRCm39) P753S probably benign Het
Stambp T G 6: 83,538,782 (GRCm39) D206A probably benign Het
Taar1 A T 10: 23,796,718 (GRCm39) I139F possibly damaging Het
Tchh A T 3: 93,351,618 (GRCm39) R353* probably null Het
Thnsl2 C T 6: 71,115,749 (GRCm39) V153I probably benign Het
Trmt5 C T 12: 73,331,837 (GRCm39) probably null Het
Trpa1 T A 1: 14,957,232 (GRCm39) Y728F probably damaging Het
Usp19 T C 9: 108,370,639 (GRCm39) V126A probably benign Het
Vcan A G 13: 89,839,622 (GRCm39) V1974A probably benign Het
Vmn2r120 T A 17: 57,829,514 (GRCm39) H461L probably benign Het
Zfp445 T C 9: 122,682,402 (GRCm39) Y513C probably benign Het
Zfp84 A C 7: 29,474,856 (GRCm39) M43L possibly damaging Het
Other mutations in Sult5a1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4284:Sult5a1 UTSW 8 123,875,969 (GRCm39) missense probably damaging 1.00
R5223:Sult5a1 UTSW 8 123,872,161 (GRCm39) missense probably damaging 1.00
R5623:Sult5a1 UTSW 8 123,884,181 (GRCm39) missense probably damaging 1.00
R6677:Sult5a1 UTSW 8 123,876,017 (GRCm39) missense probably benign
R7572:Sult5a1 UTSW 8 123,872,117 (GRCm39) missense probably benign 0.01
R7792:Sult5a1 UTSW 8 123,872,180 (GRCm39) missense probably benign 0.12
R9334:Sult5a1 UTSW 8 123,875,146 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACCAGTAGCATAGCACAGTAGG -3'
(R):5'- ACCAGTCACTAGATTAGGCCTC -3'

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