Incidental Mutation 'IGL00896:Cyp2d11'
ID 29023
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp2d11
Ensembl Gene ENSMUSG00000068085
Gene Name cytochrome P450, family 2, subfamily d, polypeptide 11
Synonyms P450-2D, Cyp2d
Accession Numbers
Essential gene? Probably non essential (E-score: 0.119) question?
Stock # IGL00896
Quality Score
Status
Chromosome 15
Chromosomal Location 82273355-82278223 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to T at 82275275 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130338 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170255]
AlphaFold P24457
Predicted Effect probably benign
Transcript: ENSMUST00000170255
SMART Domains Protein: ENSMUSP00000130338
Gene: ENSMUSG00000068085

DomainStartEndE-ValueType
transmembrane domain 7 26 N/A INTRINSIC
Pfam:p450 37 497 7.7e-140 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183858
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam6a A G 12: 113,509,030 (GRCm39) T468A possibly damaging Het
Ankrd35 A G 3: 96,591,592 (GRCm39) E626G probably damaging Het
Arhgef4 A G 1: 34,850,777 (GRCm39) Y1812C possibly damaging Het
Aurkc T C 7: 7,005,513 (GRCm39) Y260H possibly damaging Het
Bltp1 A G 3: 37,093,611 (GRCm39) T4352A probably benign Het
Cpb1 A G 3: 20,306,193 (GRCm39) V329A probably benign Het
Dnase1 G A 16: 3,857,076 (GRCm39) S28N probably benign Het
Drgx C T 14: 32,327,171 (GRCm39) probably benign Het
Evpl C A 11: 116,113,410 (GRCm39) E1427* probably null Het
Gimap6 T C 6: 48,679,394 (GRCm39) N214S probably benign Het
Htr1f A T 16: 64,746,469 (GRCm39) H274Q probably benign Het
Ipo9 A T 1: 135,327,797 (GRCm39) V538E probably damaging Het
Lmf2 T C 15: 89,237,539 (GRCm39) K308E probably benign Het
Mog T A 17: 37,328,377 (GRCm39) probably null Het
Myo19 T C 11: 84,800,324 (GRCm39) V903A probably benign Het
Myt1l A G 12: 29,876,885 (GRCm39) T179A unknown Het
Nckap1 C T 2: 80,411,297 (GRCm39) V5M possibly damaging Het
Or1e23 T C 11: 73,407,167 (GRCm39) N286S probably damaging Het
Or51l4 T C 7: 103,404,213 (GRCm39) D193G probably damaging Het
Or9a2 A T 6: 41,749,047 (GRCm39) L62Q probably damaging Het
Pcdhb5 T G 18: 37,455,838 (GRCm39) probably null Het
Pcm1 C A 8: 41,729,160 (GRCm39) Q711K possibly damaging Het
Pde6a A G 18: 61,353,864 (GRCm39) D63G possibly damaging Het
Piezo1 T C 8: 123,224,609 (GRCm39) M711V possibly damaging Het
Rev1 G A 1: 38,138,021 (GRCm39) T88I probably damaging Het
Sntg1 A T 1: 8,665,634 (GRCm39) probably null Het
Sult2a1 T A 7: 13,566,565 (GRCm39) T137S probably benign Het
Txndc15 G A 13: 55,873,488 (GRCm39) A283T probably damaging Het
Zswim8 A G 14: 20,766,069 (GRCm39) E785G probably damaging Het
Other mutations in Cyp2d11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00418:Cyp2d11 APN 15 82,276,669 (GRCm39) missense probably benign 0.00
IGL02119:Cyp2d11 APN 15 82,274,265 (GRCm39) missense probably damaging 0.98
IGL02234:Cyp2d11 APN 15 82,274,340 (GRCm39) missense probably benign
IGL02347:Cyp2d11 APN 15 82,274,681 (GRCm39) missense probably benign 0.22
IGL02352:Cyp2d11 APN 15 82,278,121 (GRCm39) missense possibly damaging 0.50
IGL02359:Cyp2d11 APN 15 82,278,121 (GRCm39) missense possibly damaging 0.50
IGL02876:Cyp2d11 APN 15 82,273,697 (GRCm39) missense possibly damaging 0.85
IGL03079:Cyp2d11 APN 15 82,275,167 (GRCm39) missense probably damaging 1.00
IGL03259:Cyp2d11 APN 15 82,274,221 (GRCm39) missense probably damaging 0.99
FR4340:Cyp2d11 UTSW 15 82,274,223 (GRCm39) frame shift probably null
R0066:Cyp2d11 UTSW 15 82,275,958 (GRCm39) missense probably benign
R0066:Cyp2d11 UTSW 15 82,275,958 (GRCm39) missense probably benign
R0101:Cyp2d11 UTSW 15 82,274,395 (GRCm39) splice site probably benign
R0125:Cyp2d11 UTSW 15 82,273,422 (GRCm39) missense probably benign 0.45
R0973:Cyp2d11 UTSW 15 82,273,730 (GRCm39) missense possibly damaging 0.80
R1466:Cyp2d11 UTSW 15 82,275,936 (GRCm39) missense probably benign 0.00
R1466:Cyp2d11 UTSW 15 82,275,936 (GRCm39) missense probably benign 0.00
R1525:Cyp2d11 UTSW 15 82,273,498 (GRCm39) missense probably damaging 0.98
R1708:Cyp2d11 UTSW 15 82,274,633 (GRCm39) missense probably benign 0.01
R1968:Cyp2d11 UTSW 15 82,273,749 (GRCm39) missense probably benign 0.01
R2117:Cyp2d11 UTSW 15 82,275,954 (GRCm39) missense probably damaging 0.99
R2223:Cyp2d11 UTSW 15 82,274,332 (GRCm39) missense probably benign 0.23
R2405:Cyp2d11 UTSW 15 82,273,467 (GRCm39) missense possibly damaging 0.88
R3745:Cyp2d11 UTSW 15 82,276,056 (GRCm39) missense probably benign 0.31
R4081:Cyp2d11 UTSW 15 82,276,002 (GRCm39) missense possibly damaging 0.86
R4496:Cyp2d11 UTSW 15 82,276,149 (GRCm39) splice site probably benign
R4732:Cyp2d11 UTSW 15 82,273,428 (GRCm39) missense probably benign 0.03
R4733:Cyp2d11 UTSW 15 82,273,428 (GRCm39) missense probably benign 0.03
R4880:Cyp2d11 UTSW 15 82,276,306 (GRCm39) missense probably benign 0.01
R4898:Cyp2d11 UTSW 15 82,275,224 (GRCm39) missense probably benign 0.03
R5045:Cyp2d11 UTSW 15 82,275,272 (GRCm39) critical splice acceptor site probably null
R5328:Cyp2d11 UTSW 15 82,275,972 (GRCm39) missense probably benign 0.04
R5356:Cyp2d11 UTSW 15 82,274,712 (GRCm39) missense probably benign 0.11
R5397:Cyp2d11 UTSW 15 82,276,279 (GRCm39) missense probably damaging 1.00
R5582:Cyp2d11 UTSW 15 82,276,319 (GRCm39) splice site probably null
R6862:Cyp2d11 UTSW 15 82,274,339 (GRCm39) missense probably benign
R7194:Cyp2d11 UTSW 15 82,275,969 (GRCm39) missense probably benign
R8097:Cyp2d11 UTSW 15 82,274,581 (GRCm39) critical splice donor site probably null
R8122:Cyp2d11 UTSW 15 82,276,744 (GRCm39) missense probably benign 0.27
R8152:Cyp2d11 UTSW 15 82,276,688 (GRCm39) missense probably benign
R8194:Cyp2d11 UTSW 15 82,274,638 (GRCm39) missense probably damaging 1.00
R8531:Cyp2d11 UTSW 15 82,273,429 (GRCm39) missense probably benign
R8894:Cyp2d11 UTSW 15 82,274,671 (GRCm39) missense probably benign 0.22
R8905:Cyp2d11 UTSW 15 82,275,102 (GRCm39) missense probably benign 0.00
R9112:Cyp2d11 UTSW 15 82,276,203 (GRCm39) missense possibly damaging 0.94
Z1088:Cyp2d11 UTSW 15 82,274,312 (GRCm39) missense probably damaging 0.99
Z1177:Cyp2d11 UTSW 15 82,276,700 (GRCm39) missense probably damaging 0.96
Posted On 2013-04-17