Incidental Mutation 'IGL03406:Slco6b1'
ID421605
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slco6b1
Ensembl Gene ENSMUSG00000045463
Gene Namesolute carrier organic anion transporter family, member 6b1
Synonyms1700022M03Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.095) question?
Stock #IGL03406
Quality Score
Status
Chromosome1
Chromosomal Location96906176-96997577 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to C at 96947585 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700012P22Rik A G 4: 144,423,844 Y56H probably damaging Het
A530016L24Rik T A 12: 112,496,883 probably null Het
Adcy7 C T 8: 88,318,319 R228* probably null Het
Cdcp1 T C 9: 123,185,313 H132R probably benign Het
Cyp4a32 T C 4: 115,602,303 I78T probably benign Het
Fap A T 2: 62,542,122 probably benign Het
Gad1-ps C T 10: 99,444,779 noncoding transcript Het
Gli3 T C 13: 15,648,581 I296T probably damaging Het
H2-Q2 T C 17: 35,342,825 V97A probably benign Het
Hr T A 14: 70,563,420 probably null Het
Itgax C T 7: 128,149,198 T1133I possibly damaging Het
L3mbtl2 G A 15: 81,681,993 R339H probably damaging Het
Mast4 T C 13: 102,737,107 K1726E possibly damaging Het
Nlrc5 T C 8: 94,476,855 Y528H probably benign Het
Nmnat3 G A 9: 98,399,477 G44D probably damaging Het
Nol8 A T 13: 49,661,568 D366V probably damaging Het
Olfr539 C A 7: 140,667,511 L68M probably damaging Het
Pde4d A T 13: 109,954,591 probably benign Het
Ptpn22 C A 3: 103,912,016 N795K probably benign Het
Rabgap1l A T 1: 160,722,169 V289D probably damaging Het
Slc50a1 T C 3: 89,270,101 D40G possibly damaging Het
Smarcad1 T A 6: 65,092,526 F530Y probably damaging Het
Spag6 A G 2: 18,742,873 probably benign Het
Supt16 A T 14: 52,178,141 I379N possibly damaging Het
Tmem154 A G 3: 84,684,260 N39S probably benign Het
Ubash3b T A 9: 41,037,479 Y180F probably damaging Het
Usp48 T A 4: 137,639,295 D921E possibly damaging Het
Zdhhc20 T C 14: 57,839,099 T366A probably benign Het
Zfp456 A T 13: 67,366,331 C419S probably damaging Het
Zfp69 T C 4: 120,931,084 T345A probably benign Het
Other mutations in Slco6b1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00434:Slco6b1 APN 1 96988650 exon noncoding transcript
IGL02110:Slco6b1 APN 1 96987882 exon noncoding transcript
IGL02416:Slco6b1 APN 1 96924333 exon noncoding transcript
R0147:Slco6b1 UTSW 1 96987837 exon noncoding transcript
R0277:Slco6b1 UTSW 1 96988673 exon noncoding transcript
R0513:Slco6b1 UTSW 1 96997184 unclassified noncoding transcript
R1401:Slco6b1 UTSW 1 96929885 splice site noncoding transcript
R1823:Slco6b1 UTSW 1 96961176 exon noncoding transcript
R1888:Slco6b1 UTSW 1 96922061 splice site noncoding transcript
R4125:Slco6b1 UTSW 1 96987897 exon noncoding transcript
R4281:Slco6b1 UTSW 1 96997390 unclassified noncoding transcript
R4282:Slco6b1 UTSW 1 96997390 unclassified noncoding transcript
R4576:Slco6b1 UTSW 1 96988697 exon noncoding transcript
R4850:Slco6b1 UTSW 1 96911833 unclassified noncoding transcript
R5222:Slco6b1 UTSW 1 96997491 unclassified noncoding transcript
R5389:Slco6b1 UTSW 1 96988584 exon noncoding transcript
R5801:Slco6b1 UTSW 1 96947631 exon noncoding transcript
Posted On2016-08-02