Incidental Mutation 'IGL02713:Cyp2d10'
ID 304670
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp2d10
Ensembl Gene ENSMUSG00000094806
Gene Name cytochrome P450, family 2, subfamily d, polypeptide 10
Synonyms P450-2D, Cyp2d
Accession Numbers
Essential gene? Probably non essential (E-score: 0.089) question?
Stock # IGL02713
Quality Score
Status
Chromosome 15
Chromosomal Location 82287047-82291396 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to C at 82290283 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000155572 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072776] [ENSMUST00000229628] [ENSMUST00000229911] [ENSMUST00000230198] [ENSMUST00000230248] [ENSMUST00000230843]
AlphaFold P24456
Predicted Effect probably benign
Transcript: ENSMUST00000072776
SMART Domains Protein: ENSMUSP00000072555
Gene: ENSMUSG00000094806

DomainStartEndE-ValueType
transmembrane domain 4 26 N/A INTRINSIC
Pfam:p450 37 497 6e-143 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000102440
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183705
Predicted Effect probably benign
Transcript: ENSMUST00000229628
Predicted Effect probably benign
Transcript: ENSMUST00000229911
Predicted Effect probably benign
Transcript: ENSMUST00000230198
Predicted Effect probably benign
Transcript: ENSMUST00000230248
Predicted Effect probably benign
Transcript: ENSMUST00000230843
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acan A G 7: 78,749,992 (GRCm39) T1588A possibly damaging Het
Apeh A T 9: 107,962,871 (GRCm39) L700Q probably damaging Het
Arid1b T C 17: 5,393,286 (GRCm39) I2272T probably damaging Het
Best3 T G 10: 116,860,434 (GRCm39) F565V probably benign Het
Birc6 A G 17: 74,886,319 (GRCm39) N521S probably benign Het
Cd209f T A 8: 4,153,732 (GRCm39) R191S probably benign Het
Clec4e A T 6: 123,263,263 (GRCm39) Y63* probably null Het
Cracdl C A 1: 37,663,218 (GRCm39) K893N possibly damaging Het
Cyp26c1 C T 19: 37,681,667 (GRCm39) T490M probably damaging Het
Cyp2b9 T A 7: 25,872,945 (GRCm39) H29Q probably benign Het
Dgat1 C A 15: 76,387,734 (GRCm39) R291L probably damaging Het
Dyrk1a C A 16: 94,486,204 (GRCm39) probably benign Het
Esp4 T C 17: 40,913,297 (GRCm39) F55L probably benign Het
Fam227a G A 15: 79,520,997 (GRCm39) probably benign Het
Ggt1 T C 10: 75,410,178 (GRCm39) Y37H probably damaging Het
Grsf1 A T 5: 88,820,589 (GRCm39) I64K probably damaging Het
Itga6 C T 2: 71,647,057 (GRCm39) T89I possibly damaging Het
Jph2 T C 2: 163,217,837 (GRCm39) T280A probably damaging Het
Lipm A G 19: 34,078,570 (GRCm39) M1V probably null Het
Nbeal1 C T 1: 60,274,396 (GRCm39) A513V possibly damaging Het
Or10a3 G A 7: 108,480,060 (GRCm39) T251I probably damaging Het
Or10a48 A T 7: 108,424,801 (GRCm39) M135K probably damaging Het
Or10q1b A T 19: 13,682,553 (GRCm39) I121F possibly damaging Het
Or13a28 A T 7: 140,217,829 (GRCm39) I72F probably damaging Het
Or5ak25 T A 2: 85,268,981 (GRCm39) I174F probably damaging Het
Or8b101 C T 9: 38,020,623 (GRCm39) P214S probably damaging Het
Orc6 A G 8: 86,034,215 (GRCm39) E146G probably benign Het
Patl2 A G 2: 121,956,328 (GRCm39) S179P probably benign Het
Pdzd8 C A 19: 59,333,890 (GRCm39) G44C probably damaging Het
Phox2b A G 5: 67,253,938 (GRCm39) probably benign Het
Ppp4r3b T G 11: 29,138,445 (GRCm39) H264Q probably damaging Het
Ptprk T C 10: 28,468,807 (GRCm39) I1409T possibly damaging Het
Pum1 T A 4: 130,493,323 (GRCm39) I842N probably damaging Het
Rnf123 G A 9: 107,945,501 (GRCm39) R390* probably null Het
Sgca T A 11: 94,862,131 (GRCm39) N174Y probably damaging Het
Slc7a14 A T 3: 31,311,912 (GRCm39) L36Q probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Stard13 G A 5: 150,965,651 (GRCm39) Q935* probably null Het
Suds3 C T 5: 117,232,970 (GRCm39) probably null Het
Sv2b A T 7: 74,773,911 (GRCm39) L520Q possibly damaging Het
Tmem26 T C 10: 68,587,125 (GRCm39) F191S probably damaging Het
Other mutations in Cyp2d10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00490:Cyp2d10 APN 15 82,287,515 (GRCm39) missense possibly damaging 0.71
IGL00840:Cyp2d10 APN 15 82,288,691 (GRCm39) missense probably benign 0.40
IGL01293:Cyp2d10 APN 15 82,287,210 (GRCm39) missense possibly damaging 0.92
IGL01339:Cyp2d10 APN 15 82,288,042 (GRCm39) missense probably benign 0.33
IGL01871:Cyp2d10 APN 15 82,288,086 (GRCm39) missense probably damaging 1.00
IGL02132:Cyp2d10 APN 15 82,288,808 (GRCm39) intron probably benign
IGL02869:Cyp2d10 APN 15 82,288,069 (GRCm39) missense possibly damaging 0.84
R0102:Cyp2d10 UTSW 15 82,288,794 (GRCm39) missense probably benign 0.01
R0102:Cyp2d10 UTSW 15 82,288,794 (GRCm39) missense probably benign 0.01
R0279:Cyp2d10 UTSW 15 82,289,540 (GRCm39) missense possibly damaging 0.94
R0331:Cyp2d10 UTSW 15 82,291,227 (GRCm39) missense probably benign 0.12
R1344:Cyp2d10 UTSW 15 82,290,106 (GRCm39) critical splice donor site probably null
R1418:Cyp2d10 UTSW 15 82,290,106 (GRCm39) critical splice donor site probably null
R1465:Cyp2d10 UTSW 15 82,288,129 (GRCm39) splice site probably null
R1465:Cyp2d10 UTSW 15 82,288,129 (GRCm39) splice site probably null
R1706:Cyp2d10 UTSW 15 82,289,783 (GRCm39) missense probably damaging 0.96
R1712:Cyp2d10 UTSW 15 82,287,240 (GRCm39) missense probably damaging 1.00
R1940:Cyp2d10 UTSW 15 82,289,495 (GRCm39) missense probably benign 0.13
R1983:Cyp2d10 UTSW 15 82,290,200 (GRCm39) missense probably benign 0.15
R2056:Cyp2d10 UTSW 15 82,288,015 (GRCm39) missense probably damaging 1.00
R2058:Cyp2d10 UTSW 15 82,288,015 (GRCm39) missense probably damaging 1.00
R3707:Cyp2d10 UTSW 15 82,287,217 (GRCm39) missense possibly damaging 0.91
R3708:Cyp2d10 UTSW 15 82,287,217 (GRCm39) missense possibly damaging 0.91
R4042:Cyp2d10 UTSW 15 82,290,269 (GRCm39) missense probably benign 0.33
R4531:Cyp2d10 UTSW 15 82,289,462 (GRCm39) missense probably benign 0.31
R4694:Cyp2d10 UTSW 15 82,288,684 (GRCm39) missense probably damaging 1.00
R4869:Cyp2d10 UTSW 15 82,287,967 (GRCm39) missense probably benign 0.00
R5071:Cyp2d10 UTSW 15 82,287,954 (GRCm39) missense probably benign 0.07
R5072:Cyp2d10 UTSW 15 82,287,954 (GRCm39) missense probably benign 0.07
R5073:Cyp2d10 UTSW 15 82,287,954 (GRCm39) missense probably benign 0.07
R5074:Cyp2d10 UTSW 15 82,287,954 (GRCm39) missense probably benign 0.07
R5746:Cyp2d10 UTSW 15 82,289,472 (GRCm39) missense probably benign 0.38
R7096:Cyp2d10 UTSW 15 82,289,462 (GRCm39) missense probably benign
R7212:Cyp2d10 UTSW 15 82,288,447 (GRCm39) critical splice acceptor site probably null
R7324:Cyp2d10 UTSW 15 82,287,961 (GRCm39) missense probably damaging 0.97
R7487:Cyp2d10 UTSW 15 82,288,793 (GRCm39) missense probably benign 0.00
R7915:Cyp2d10 UTSW 15 82,288,628 (GRCm39) critical splice donor site probably null
R9071:Cyp2d10 UTSW 15 82,288,361 (GRCm39) missense probably damaging 0.99
R9460:Cyp2d10 UTSW 15 82,289,470 (GRCm39) missense probably benign 0.00
X0063:Cyp2d10 UTSW 15 82,290,201 (GRCm39) missense probably benign 0.01
Posted On 2015-04-16