Incidental Mutation 'R2048:Cyp2d26'
ID 266040
Institutional Source Beutler Lab
Gene Symbol Cyp2d26
Ensembl Gene ENSMUSG00000022445
Gene Name cytochrome P450, family 2, subfamily d, polypeptide 26
Synonyms 1300006E06Rik
MMRRC Submission 040055-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.090) question?
Stock # R2048 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 82674302-82678495 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 82676928 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000155850 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000006094] [ENSMUST00000006094] [ENSMUST00000229387] [ENSMUST00000229512]
AlphaFold no structure available at present
Predicted Effect silent
Transcript: ENSMUST00000006094
SMART Domains Protein: ENSMUSP00000006094
Gene: ENSMUSG00000022445

DomainStartEndE-ValueType
transmembrane domain 10 27 N/A INTRINSIC
Pfam:p450 37 497 3.5e-141 PFAM
Predicted Effect silent
Transcript: ENSMUST00000006094
SMART Domains Protein: ENSMUSP00000006094
Gene: ENSMUSG00000022445

DomainStartEndE-ValueType
transmembrane domain 10 27 N/A INTRINSIC
Pfam:p450 37 497 3.5e-141 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000229387
Predicted Effect probably benign
Transcript: ENSMUST00000229512
Predicted Effect noncoding transcript
Transcript: ENSMUST00000230125
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.2%
Validation Efficiency 98% (52/53)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam10 A G 9: 70,647,357 (GRCm39) D19G possibly damaging Het
Adhfe1 A G 1: 9,633,778 (GRCm39) K342R probably benign Het
Adk A G 14: 21,368,244 (GRCm39) N223S probably damaging Het
Aff4 A G 11: 53,289,212 (GRCm39) S454G probably benign Het
Ahnak T A 19: 8,984,420 (GRCm39) N1901K probably damaging Het
Camsap1 T C 2: 25,819,755 (GRCm39) T1578A probably benign Het
Ccdc63 A C 5: 122,268,350 (GRCm39) probably null Het
Ceacam1 G T 7: 25,176,113 (GRCm39) S27Y probably benign Het
Cit T C 5: 116,024,872 (GRCm39) probably null Het
Cntn4 A G 6: 106,414,825 (GRCm39) probably benign Het
Cyp3a13 A T 5: 137,908,237 (GRCm39) V204E probably damaging Het
Cyp51 G A 5: 4,136,636 (GRCm39) probably benign Het
Dipk1a T C 5: 108,057,886 (GRCm39) D179G probably damaging Het
Epb41l4b T G 4: 57,142,866 (GRCm39) E96D probably benign Het
Epg5 A G 18: 78,067,202 (GRCm39) E2221G probably damaging Het
Fbxo21 T A 5: 118,146,169 (GRCm39) N597K probably damaging Het
Fpr-rs4 CAGGAA CA 17: 18,242,596 (GRCm39) probably null Het
Fsip1 C A 2: 118,072,197 (GRCm39) E195D probably damaging Het
Gm10152 T C 7: 144,317,049 (GRCm39) F35L unknown Het
Gtpbp6 A C 5: 110,254,931 (GRCm39) V87G probably damaging Het
Hal A G 10: 93,327,002 (GRCm39) T176A probably damaging Het
Il12rb2 G T 6: 67,337,529 (GRCm39) N117K probably benign Het
Kalrn A G 16: 34,072,680 (GRCm39) V734A probably benign Het
Klf7 A G 1: 64,117,913 (GRCm39) V228A possibly damaging Het
Kng1 A G 16: 22,877,354 (GRCm39) Y54C probably damaging Het
Lpcat2 T G 8: 93,596,471 (GRCm39) N169K possibly damaging Het
Magohb A T 6: 131,266,385 (GRCm39) S40R probably damaging Het
Mgam A G 6: 40,633,363 (GRCm39) D186G possibly damaging Het
Mycbp2 A G 14: 103,469,960 (GRCm39) probably null Het
Myh15 A G 16: 48,975,928 (GRCm39) D1332G probably damaging Het
Myh9 G A 15: 77,655,332 (GRCm39) T1208M possibly damaging Het
Ncor2 C T 5: 125,161,996 (GRCm39) R426H unknown Het
Nradd T C 9: 110,450,697 (GRCm39) E160G probably benign Het
Or10u4 G A 10: 129,801,861 (GRCm39) S230L probably damaging Het
Or2a54 T A 6: 43,093,312 (GRCm39) M212K probably benign Het
Otog A T 7: 45,937,063 (GRCm39) T1591S probably damaging Het
Oxsr1 A G 9: 119,076,140 (GRCm39) S389P probably benign Het
Pde3a A G 6: 141,434,732 (GRCm39) probably benign Het
Pi4k2b A T 5: 52,905,773 (GRCm39) I105L probably benign Het
Pilrb1 T C 5: 137,853,153 (GRCm39) R217G possibly damaging Het
Poteg A T 8: 27,946,774 (GRCm39) I159L probably benign Het
Ppargc1a A G 5: 51,705,858 (GRCm39) F75S probably damaging Het
Ptk2b T G 14: 66,409,954 (GRCm39) D466A probably benign Het
Ptpn21 A G 12: 98,655,785 (GRCm39) V394A possibly damaging Het
Rsf1 GCG GCGACGGCGACG 7: 97,229,114 (GRCm39) probably benign Het
Shisa3 G A 5: 67,768,651 (GRCm39) E184K possibly damaging Het
Slc4a2 A G 5: 24,636,557 (GRCm39) H283R probably damaging Het
Slc9a3 A G 13: 74,311,860 (GRCm39) S603G probably damaging Het
Tas2r124 A G 6: 132,731,858 (GRCm39) I56V possibly damaging Het
Tbcd G T 11: 121,431,762 (GRCm39) C470F probably damaging Het
Thsd1 A G 8: 22,749,333 (GRCm39) R674G probably benign Het
Zbtb11 T A 16: 55,818,372 (GRCm39) C599S probably damaging Het
Zfp541 A G 7: 15,812,252 (GRCm39) R302G possibly damaging Het
Other mutations in Cyp2d26
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00559:Cyp2d26 APN 15 82,675,244 (GRCm39) missense probably benign 0.31
IGL00670:Cyp2d26 APN 15 82,675,942 (GRCm39) missense probably benign
IGL01646:Cyp2d26 APN 15 82,675,619 (GRCm39) missense probably benign 0.00
IGL01915:Cyp2d26 APN 15 82,674,450 (GRCm39) missense probably benign 0.06
IGL01940:Cyp2d26 APN 15 82,676,758 (GRCm39) missense probably benign 0.00
IGL02127:Cyp2d26 APN 15 82,675,307 (GRCm39) missense probably benign 0.09
IGL02452:Cyp2d26 APN 15 82,676,827 (GRCm39) missense probably benign 0.00
IGL03216:Cyp2d26 APN 15 82,677,462 (GRCm39) missense probably benign
IGL03377:Cyp2d26 APN 15 82,674,755 (GRCm39) missense possibly damaging 0.47
R0149:Cyp2d26 UTSW 15 82,676,968 (GRCm39) missense probably damaging 1.00
R0848:Cyp2d26 UTSW 15 82,674,434 (GRCm39) missense probably benign 0.00
R1165:Cyp2d26 UTSW 15 82,678,242 (GRCm39) missense probably damaging 1.00
R1217:Cyp2d26 UTSW 15 82,677,068 (GRCm39) splice site probably benign
R1780:Cyp2d26 UTSW 15 82,678,208 (GRCm39) missense probably damaging 1.00
R2152:Cyp2d26 UTSW 15 82,676,907 (GRCm39) critical splice donor site probably null
R2397:Cyp2d26 UTSW 15 82,678,236 (GRCm39) missense probably damaging 1.00
R4702:Cyp2d26 UTSW 15 82,676,648 (GRCm39) intron probably benign
R5157:Cyp2d26 UTSW 15 82,675,190 (GRCm39) missense probably benign 0.01
R5444:Cyp2d26 UTSW 15 82,676,739 (GRCm39) missense probably benign 0.18
R6017:Cyp2d26 UTSW 15 82,674,774 (GRCm39) missense possibly damaging 0.68
R6223:Cyp2d26 UTSW 15 82,675,918 (GRCm39) missense probably benign 0.04
R6390:Cyp2d26 UTSW 15 82,676,825 (GRCm39) missense possibly damaging 0.68
R6473:Cyp2d26 UTSW 15 82,675,968 (GRCm39) missense probably benign 0.02
R6858:Cyp2d26 UTSW 15 82,678,284 (GRCm39) missense probably damaging 1.00
R6912:Cyp2d26 UTSW 15 82,675,320 (GRCm39) missense probably benign 0.16
R6936:Cyp2d26 UTSW 15 82,676,741 (GRCm39) missense probably benign 0.14
R6960:Cyp2d26 UTSW 15 82,674,446 (GRCm39) missense probably damaging 0.98
R7053:Cyp2d26 UTSW 15 82,676,801 (GRCm39) missense probably benign 0.00
R7113:Cyp2d26 UTSW 15 82,674,403 (GRCm39) missense probably benign 0.02
R7126:Cyp2d26 UTSW 15 82,678,209 (GRCm39) missense probably benign 0.00
R7272:Cyp2d26 UTSW 15 82,676,764 (GRCm39) missense probably benign
R7771:Cyp2d26 UTSW 15 82,675,947 (GRCm39) missense probably benign
R8695:Cyp2d26 UTSW 15 82,676,907 (GRCm39) critical splice donor site probably benign
R9466:Cyp2d26 UTSW 15 82,674,424 (GRCm39) missense probably benign 0.01
R9489:Cyp2d26 UTSW 15 82,674,672 (GRCm39) missense probably benign 0.00
R9605:Cyp2d26 UTSW 15 82,674,672 (GRCm39) missense probably benign 0.00
R9656:Cyp2d26 UTSW 15 82,677,059 (GRCm39) missense probably benign 0.03
X0021:Cyp2d26 UTSW 15 82,674,718 (GRCm39) missense probably benign 0.04
Predicted Primers
Posted On 2015-02-05