Incidental Mutation 'R4281:Slco6b1'
ID 322878
Institutional Source Beutler Lab
Gene Symbol Slco6b1
Ensembl Gene ENSMUSG00000045463
Gene Name solute carrier organic anion transporter family, member 6b1
Synonyms 1700022M03Rik
MMRRC Submission 041649-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # R4281 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 96849643-96924962 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 96925115 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000167383
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178359
SMART Domains Protein: ENSMUSP00000136663
Gene: ENSMUSG00000045463

DomainStartEndE-ValueType
Pfam:MFS_1 103 481 1.6e-12 PFAM
Pfam:OATP 108 668 9.7e-128 PFAM
Pfam:Kazal_2 511 552 5.1e-8 PFAM
transmembrane domain 670 692 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180888
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency 92% (44/48)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arl6ip1 AAAATAAATAAATAAATAAATAAATA AAAATAAATAAATAAATAAATAAATAAATA 7: 117,721,122 (GRCm39) probably benign Het
B9d2 A G 7: 25,380,851 (GRCm39) T14A possibly damaging Het
Cavin3 A C 7: 105,130,981 (GRCm39) probably null Het
Defa27 A G 8: 21,805,632 (GRCm39) N24S probably benign Het
Defb40 A G 8: 19,028,093 (GRCm39) S14P probably damaging Het
Dnaaf11 A T 15: 66,252,378 (GRCm39) H429Q probably benign Het
Dnmt3a G A 12: 3,951,665 (GRCm39) G681R probably damaging Het
Evc2 T C 5: 37,495,938 (GRCm39) V16A probably benign Het
Fam210b T C 2: 172,193,468 (GRCm39) Y94H probably damaging Het
Gimap8 A C 6: 48,635,754 (GRCm39) R506S probably benign Het
Gmip T A 8: 70,266,251 (GRCm39) probably benign Het
Gpr39 G A 1: 125,605,728 (GRCm39) V219I probably benign Het
Gsn A G 2: 35,188,883 (GRCm39) Y434C probably damaging Het
Gtf2a1l A G 17: 89,019,065 (GRCm39) N383S possibly damaging Het
Hepacam2 G A 6: 3,475,938 (GRCm39) T329I probably damaging Het
Iqgap3 T C 3: 88,006,167 (GRCm39) V526A probably benign Het
Magea14 T C X: 51,057,867 (GRCm39) Y273C probably damaging Het
Mark4 T C 7: 19,167,371 (GRCm39) K456R probably benign Het
Nox4 A G 7: 86,946,732 (GRCm39) I143V possibly damaging Het
Or11h7 T C 14: 50,891,029 (GRCm39) C112R probably benign Het
Or12j3 A G 7: 139,953,385 (GRCm39) I46T probably benign Het
Pcdh18 A G 3: 49,710,982 (GRCm39) L111P possibly damaging Het
Pnma5 T C X: 72,079,036 (GRCm39) M549V probably benign Het
Pnpla6 T C 8: 3,571,513 (GRCm39) L148P probably damaging Het
Ppp4r3c1 A T X: 88,976,105 (GRCm39) W31R probably damaging Het
Prkdc A G 16: 15,623,963 (GRCm39) probably null Het
Rars1 T C 11: 35,712,051 (GRCm39) E275G probably damaging Het
Rasa3 A G 8: 13,638,946 (GRCm39) V287A probably benign Het
Rimbp2 C T 5: 128,865,404 (GRCm39) R641Q possibly damaging Het
Sned1 A T 1: 93,213,577 (GRCm39) R426* probably null Het
Tmem132a C G 19: 10,839,090 (GRCm39) E451Q possibly damaging Het
Tmem229b-ps A G 10: 53,351,474 (GRCm39) noncoding transcript Het
Trim33 T A 3: 103,236,402 (GRCm39) V504D probably damaging Het
Usp47 A T 7: 111,709,200 (GRCm39) E1315D probably benign Het
Zbtb24 T C 10: 41,340,916 (GRCm39) S649P probably benign Het
Zfp28 A T 7: 6,396,700 (GRCm39) Q378H probably benign Het
Zfp612 A G 8: 110,816,691 (GRCm39) I594V probably damaging Het
Zfp692 T C 11: 58,205,091 (GRCm39) F447L probably damaging Het
Zranb3 A C 1: 127,891,614 (GRCm39) S787R possibly damaging Het
Other mutations in Slco6b1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00434:Slco6b1 APN 1 96,916,375 (GRCm39) exon noncoding transcript
IGL02110:Slco6b1 APN 1 96,915,607 (GRCm39) exon noncoding transcript
IGL02416:Slco6b1 APN 1 96,852,058 (GRCm39) exon noncoding transcript
IGL03406:Slco6b1 APN 1 96,875,310 (GRCm39) exon noncoding transcript
R0147:Slco6b1 UTSW 1 96,915,562 (GRCm39) exon noncoding transcript
R0277:Slco6b1 UTSW 1 96,916,398 (GRCm39) exon noncoding transcript
R0513:Slco6b1 UTSW 1 96,924,909 (GRCm39) unclassified noncoding transcript
R1401:Slco6b1 UTSW 1 96,857,610 (GRCm39) splice site noncoding transcript
R1823:Slco6b1 UTSW 1 96,888,901 (GRCm39) exon noncoding transcript
R1888:Slco6b1 UTSW 1 96,849,786 (GRCm39) splice site noncoding transcript
R4125:Slco6b1 UTSW 1 96,915,622 (GRCm39) exon noncoding transcript
R4282:Slco6b1 UTSW 1 96,925,115 (GRCm39) unclassified noncoding transcript
R4576:Slco6b1 UTSW 1 96,916,422 (GRCm39) exon noncoding transcript
R4850:Slco6b1 UTSW 1 96,839,558 (GRCm39) unclassified noncoding transcript
R5222:Slco6b1 UTSW 1 96,925,216 (GRCm39) unclassified noncoding transcript
R5389:Slco6b1 UTSW 1 96,916,309 (GRCm39) exon noncoding transcript
R5801:Slco6b1 UTSW 1 96,875,356 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- CCTCCAAGGAAGCATCTTGC -3'
(R):5'- ACGTTGGCTTCCTTCACTAG -3'

Sequencing Primer
(F):5'- GCATTGTATCTGATAACTGCGATGAG -3'
(R):5'- ACGTTCCCTGCAAAGGTTAG -3'
Posted On 2015-06-20