Incidental Mutation 'R3942:Slco1a7'
ID 312901
Institutional Source Beutler Lab
Gene Symbol Slco1a7
Ensembl Gene ENSMUSG00000084927
Gene Name solute carrier organic anion transporter family, member 1a7
Synonyms Gm5724
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # R3942 (G1)
Quality Score 225
Status Not validated
Chromosome 6
Chromosomal Location 141653844-141719536 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 141673440 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 366 (I366T)
Ref Sequence ENSEMBL: ENSMUSP00000117177 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000148411]
AlphaFold L7N264
Predicted Effect probably damaging
Transcript: ENSMUST00000148411
AA Change: I366T

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000117177
Gene: ENSMUSG00000084927
AA Change: I366T

DomainStartEndE-ValueType
Pfam:MFS_1 22 405 3.4e-26 PFAM
KAZAL 438 484 1.71e0 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 T C 13: 81,330,908 (GRCm39) N6049S probably damaging Het
Aph1a C T 3: 95,801,573 (GRCm39) R31W probably damaging Het
Atp10b T C 11: 43,063,581 (GRCm39) V172A probably damaging Het
Atp13a2 T C 4: 140,733,733 (GRCm39) S1041P probably damaging Het
Best3 T A 10: 116,824,579 (GRCm39) F15Y possibly damaging Het
Brinp3 C A 1: 146,627,599 (GRCm39) D277E probably damaging Het
Crb1 A C 1: 139,265,211 (GRCm39) L69R possibly damaging Het
Crcp T C 5: 130,063,791 (GRCm39) probably null Het
Dysf G A 6: 84,163,491 (GRCm39) probably null Het
Hps3 T C 3: 20,051,103 (GRCm39) Y859C probably damaging Het
Irx5 C A 8: 93,086,314 (GRCm39) N132K probably damaging Het
Itgb2 A G 10: 77,393,867 (GRCm39) T436A probably benign Het
Kit A G 5: 75,769,978 (GRCm39) D130G probably benign Het
Krt12 A G 11: 99,312,922 (GRCm39) S41P unknown Het
Lypd6b G T 2: 49,833,552 (GRCm39) S64I probably damaging Het
Mpc1 T A 17: 8,507,420 (GRCm39) probably null Het
Or4c109 T A 2: 88,818,455 (GRCm39) L30F probably benign Het
Or5b95 A T 19: 12,657,768 (GRCm39) M99L probably benign Het
Pard3b T A 1: 62,198,611 (GRCm39) I233N probably damaging Het
Pcdh1 A G 18: 38,332,511 (GRCm39) V164A probably benign Het
Pclo A G 5: 14,729,932 (GRCm39) probably benign Het
Pkhd1l1 T C 15: 44,455,422 (GRCm39) probably null Het
Spata31d1d T C 13: 59,875,276 (GRCm39) Q753R probably benign Het
Stxbp6 A G 12: 44,949,641 (GRCm39) probably null Het
Trav6-5 T C 14: 53,728,838 (GRCm39) S32P probably benign Het
Zp3r A C 1: 130,504,791 (GRCm39) D470E possibly damaging Het
Other mutations in Slco1a7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01023:Slco1a7 APN 6 141,700,155 (GRCm39) missense probably benign 0.14
IGL01347:Slco1a7 APN 6 141,700,192 (GRCm39) nonsense probably null
IGL01539:Slco1a7 APN 6 141,673,333 (GRCm39) missense possibly damaging 0.88
IGL01613:Slco1a7 APN 6 141,658,940 (GRCm39) missense possibly damaging 0.67
IGL02060:Slco1a7 APN 6 141,700,134 (GRCm39) missense probably benign 0.00
IGL02063:Slco1a7 APN 6 141,684,615 (GRCm39) missense probably benign 0.01
IGL02126:Slco1a7 APN 6 141,684,739 (GRCm39) missense probably benign 0.29
IGL02214:Slco1a7 APN 6 141,668,911 (GRCm39) missense possibly damaging 0.50
IGL02630:Slco1a7 APN 6 141,668,836 (GRCm39) missense probably damaging 1.00
R0966:Slco1a7 UTSW 6 141,673,299 (GRCm39) missense probably benign 0.00
R1082:Slco1a7 UTSW 6 141,657,859 (GRCm39) missense probably damaging 1.00
R1433:Slco1a7 UTSW 6 141,711,429 (GRCm39) missense probably benign 0.00
R1571:Slco1a7 UTSW 6 141,700,135 (GRCm39) nonsense probably null
R1765:Slco1a7 UTSW 6 141,700,084 (GRCm39) splice site probably benign
R2055:Slco1a7 UTSW 6 141,671,181 (GRCm39) missense probably benign 0.33
R2174:Slco1a7 UTSW 6 141,673,319 (GRCm39) nonsense probably null
R2495:Slco1a7 UTSW 6 141,711,503 (GRCm39) missense probably benign 0.02
R2857:Slco1a7 UTSW 6 141,690,264 (GRCm39) missense probably benign 0.35
R3551:Slco1a7 UTSW 6 141,654,322 (GRCm39) missense probably benign 0.20
R3824:Slco1a7 UTSW 6 141,700,100 (GRCm39) missense possibly damaging 0.50
R3912:Slco1a7 UTSW 6 141,673,362 (GRCm39) missense probably damaging 0.97
R4161:Slco1a7 UTSW 6 141,654,322 (GRCm39) missense probably benign 0.20
R4168:Slco1a7 UTSW 6 141,684,673 (GRCm39) missense probably benign 0.03
R4395:Slco1a7 UTSW 6 141,657,844 (GRCm39) missense probably benign 0.02
R4720:Slco1a7 UTSW 6 141,668,948 (GRCm39) missense probably damaging 1.00
R4732:Slco1a7 UTSW 6 141,668,905 (GRCm39) missense probably benign 0.01
R4733:Slco1a7 UTSW 6 141,668,905 (GRCm39) missense probably benign 0.01
R4794:Slco1a7 UTSW 6 141,713,288 (GRCm39) missense probably benign 0.11
R5062:Slco1a7 UTSW 6 141,713,180 (GRCm39) missense possibly damaging 0.46
R5389:Slco1a7 UTSW 6 141,686,193 (GRCm39) missense probably benign 0.12
R5419:Slco1a7 UTSW 6 141,681,826 (GRCm39) splice site probably null
R5423:Slco1a7 UTSW 6 141,690,188 (GRCm39) missense probably damaging 1.00
R5704:Slco1a7 UTSW 6 141,658,980 (GRCm39) missense probably benign 0.00
R5973:Slco1a7 UTSW 6 141,700,182 (GRCm39) missense probably benign 0.01
R6041:Slco1a7 UTSW 6 141,684,764 (GRCm39) missense probably benign 0.11
R6284:Slco1a7 UTSW 6 141,671,119 (GRCm39) missense probably damaging 1.00
R6395:Slco1a7 UTSW 6 141,668,818 (GRCm39) splice site probably null
R6993:Slco1a7 UTSW 6 141,711,468 (GRCm39) missense possibly damaging 0.94
R7149:Slco1a7 UTSW 6 141,690,178 (GRCm39) missense probably damaging 1.00
R7159:Slco1a7 UTSW 6 141,719,504 (GRCm39) start codon destroyed probably damaging 1.00
R7627:Slco1a7 UTSW 6 141,690,271 (GRCm39) missense probably damaging 1.00
R7784:Slco1a7 UTSW 6 141,658,919 (GRCm39) critical splice donor site probably null
R7873:Slco1a7 UTSW 6 141,673,448 (GRCm39) missense probably benign 0.44
R8670:Slco1a7 UTSW 6 141,711,468 (GRCm39) missense possibly damaging 0.94
R8720:Slco1a7 UTSW 6 141,668,852 (GRCm39) missense probably benign 0.01
R9124:Slco1a7 UTSW 6 141,668,830 (GRCm39) missense possibly damaging 0.81
R9238:Slco1a7 UTSW 6 141,686,153 (GRCm39) missense probably damaging 0.98
R9381:Slco1a7 UTSW 6 141,711,490 (GRCm39) missense probably benign 0.00
X0020:Slco1a7 UTSW 6 141,700,091 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TACCCTTCATAAGAGGCAGTTAAG -3'
(R):5'- CCCAGAGCTGAGTCAAATTCC -3'

Sequencing Primer
(F):5'- GCAGTTAAGCCAGCAACTTG -3'
(R):5'- GAGCTGAGTCAAATTCCCAATATAC -3'
Posted On 2015-04-30