Incidental Mutation 'IGL02416:Slco6b1'
ID 292463
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slco6b1
Ensembl Gene ENSMUSG00000045463
Gene Name solute carrier organic anion transporter family, member 6b1
Synonyms 1700022M03Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL02416
Quality Score
Status
Chromosome 1
Chromosomal Location 96849643-96924962 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 96852058 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
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamdec1 T C 14: 68,810,282 (GRCm39) N227S probably null Het
Adgrf5 T G 17: 43,755,871 (GRCm39) probably null Het
Arid2 G A 15: 96,247,936 (GRCm39) G116D possibly damaging Het
Arsa T A 15: 89,358,991 (GRCm39) H225L probably damaging Het
Atf6 T A 1: 170,574,726 (GRCm39) K571* probably null Het
Bicdl1 A C 5: 115,801,944 (GRCm39) L38R probably damaging Het
Cct4 T C 11: 22,952,868 (GRCm39) S515P probably damaging Het
Celsr3 A C 9: 108,709,318 (GRCm39) D1388A probably damaging Het
Clca3a2 T C 3: 144,790,777 (GRCm39) T432A probably benign Het
Des T A 1: 75,339,372 (GRCm39) probably null Het
Dock11 T A X: 35,283,739 (GRCm39) V1119E probably damaging Het
Dysf A G 6: 84,169,896 (GRCm39) N1763S possibly damaging Het
Emilin1 A G 5: 31,075,132 (GRCm39) S458G possibly damaging Het
Fhdc1 T G 3: 84,352,535 (GRCm39) M897L probably benign Het
Foxj1 T C 11: 116,222,829 (GRCm39) S325G probably benign Het
Gm5407 A G 16: 49,117,250 (GRCm39) noncoding transcript Het
Gm6576 T C 15: 27,026,073 (GRCm39) noncoding transcript Het
Hells G A 19: 38,953,071 (GRCm39) S743N probably benign Het
Ighv2-9-1 A T 12: 113,733,731 (GRCm39) L30Q probably damaging Het
Iqgap1 A T 7: 80,375,786 (GRCm39) L1363H probably damaging Het
Lrp2 T C 2: 69,299,977 (GRCm39) D3025G probably damaging Het
Mef2d C T 3: 88,063,809 (GRCm39) R79C probably damaging Het
Mical1 G T 10: 41,360,806 (GRCm39) probably null Het
Micu2 A T 14: 58,161,422 (GRCm39) V300E probably damaging Het
Mmgt2 T C 11: 62,555,703 (GRCm39) L17P probably damaging Het
Or4p21 A G 2: 88,277,174 (GRCm39) I36T probably benign Het
Or7c19 T A 8: 85,957,662 (GRCm39) C179* probably null Het
Or7e177 A T 9: 20,211,541 (GRCm39) E15V probably benign Het
Pigb A G 9: 72,924,714 (GRCm39) S482P probably benign Het
Pkd1l2 T A 8: 117,767,574 (GRCm39) T1239S possibly damaging Het
Pou1f1 T C 16: 65,328,842 (GRCm39) I187T probably damaging Het
Prox1 C T 1: 189,893,327 (GRCm39) A373T probably benign Het
Rabgap1 T C 2: 37,451,962 (GRCm39) I954T probably benign Het
Scube3 T G 17: 28,383,110 (GRCm39) C429W probably damaging Het
Strc A T 2: 121,199,539 (GRCm39) I1300N probably damaging Het
Tdrd6 T A 17: 43,935,629 (GRCm39) R1806S probably benign Het
Trpm8 T A 1: 88,288,438 (GRCm39) L860Q probably damaging Het
Vmn1r8 A G 6: 57,013,605 (GRCm39) R219G probably damaging Het
Wdr48 A G 9: 119,753,826 (GRCm39) S649G probably 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
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
R4281:Slco6b1 UTSW 1 96,925,115 (GRCm39) unclassified 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
Posted On 2015-04-16