Incidental Mutation 'R6677:Sult5a1'
ID 527314
Institutional Source Beutler Lab
Gene Symbol Sult5a1
Ensembl Gene ENSMUSG00000000739
Gene Name sulfotransferase family 5A, member 1
Synonyms Sultx1
MMRRC Submission 044796-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # R6677 (G1)
Quality Score 225.009
Status Validated
Chromosome 8
Chromosomal Location 123869582-123885170 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 123876017 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 100 (F100L)
Ref Sequence ENSEMBL: ENSMUSP00000122415 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000755] [ENSMUST00000122819] [ENSMUST00000127664] [ENSMUST00000137998] [ENSMUST00000146007]
AlphaFold Q91X36
Predicted Effect probably benign
Transcript: ENSMUST00000000755
AA Change: F100L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000000755
Gene: ENSMUSG00000000739
AA Change: F100L

DomainStartEndE-ValueType
Pfam:Sulfotransfer_1 36 283 5e-78 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000122819
AA Change: F100L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000123501
Gene: ENSMUSG00000000739
AA Change: F100L

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
AA Change: F100L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000122415
Gene: ENSMUSG00000000739
AA Change: F100L

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: 99.7%
  • 10x: 98.4%
  • 20x: 95.7%
Validation Efficiency 100% (31/31)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc12 G T 8: 87,261,381 (GRCm39) H713Q possibly damaging Het
Akap9 A G 5: 4,079,869 (GRCm39) T1874A probably benign Het
Atl1 A G 12: 70,000,218 (GRCm39) I289M probably damaging Het
Atp12a A G 14: 56,618,311 (GRCm39) D654G probably damaging Het
Bbox1 C A 2: 110,135,770 (GRCm39) D70Y probably damaging Het
Blzf1 A T 1: 164,130,181 (GRCm39) V50D possibly damaging Het
Ccdc168 G T 1: 44,097,859 (GRCm39) R1080S probably benign Het
Cfap65 C A 1: 74,943,844 (GRCm39) D1556Y probably damaging Het
Chrm2 A T 6: 36,501,027 (GRCm39) N295Y probably damaging Het
Clca3b T A 3: 144,529,145 (GRCm39) E843V probably benign Het
Enpp3 T A 10: 24,653,855 (GRCm39) N701Y possibly damaging Het
Fbxo30 G T 10: 11,166,380 (GRCm39) L367F possibly damaging Het
Gm4841 A T 18: 60,403,652 (GRCm39) F147Y probably damaging Het
Itprid2 A G 2: 79,485,445 (GRCm39) T500A possibly damaging Het
Lama1 G A 17: 68,102,228 (GRCm39) V1951I probably benign Het
Mgat4b A G 11: 50,123,898 (GRCm39) probably null Het
Mpp3 A G 11: 101,899,444 (GRCm39) V359A probably benign Het
Nhsl1 T A 10: 18,401,610 (GRCm39) D911E probably damaging Het
Or13a23-ps1 T G 7: 140,118,465 (GRCm39) F12V probably damaging Het
Polr1b T C 2: 128,962,131 (GRCm39) probably benign Het
Qrfprl A T 6: 65,433,229 (GRCm39) I350F probably benign Het
Rnd2 C T 11: 101,359,825 (GRCm39) L57F probably damaging Het
Saxo2 T C 7: 82,284,484 (GRCm39) R125G probably benign Het
Scn8a A G 15: 100,866,953 (GRCm39) D103G probably damaging Het
Sfxn2 A T 19: 46,570,967 (GRCm39) N9I possibly damaging Het
Shroom1 G A 11: 53,354,343 (GRCm39) A88T possibly damaging Het
Slc24a5 G T 2: 124,922,615 (GRCm39) A126S possibly damaging Het
Syne1 T C 10: 4,990,942 (GRCm39) Q579R possibly damaging Het
Vmn1r113 G A 7: 20,521,903 (GRCm39) G232S probably benign Het
Zic5 C G 14: 122,702,566 (GRCm39) R55P unknown 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
R5578:Sult5a1 UTSW 8 123,869,860 (GRCm39) nonsense probably null
R5623:Sult5a1 UTSW 8 123,884,181 (GRCm39) missense probably damaging 1.00
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'- AACTCCCAGCTGTGTAGACC -3'
(R):5'- TTAGGCAGAAGTAGCCACAC -3'

Sequencing Primer
(F):5'- AGCTGTGTAGACCCTGCCTC -3'
(R):5'- GAAGTAGCCACACCCCAAC -3'
Posted On 2018-07-23