Incidental Mutation 'IGL01307:Cyp2c37'
ID 73483
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cyp2c37
Ensembl Gene ENSMUSG00000042248
Gene Name cytochrome P450, family 2. subfamily c, polypeptide 37
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.107) question?
Stock # IGL01307
Quality Score
Status
Chromosome 19
Chromosomal Location 39980868-40000687 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 39981023 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 47 (V47A)
Ref Sequence ENSEMBL: ENSMUSP00000045362 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049178]
AlphaFold P56654
Predicted Effect probably benign
Transcript: ENSMUST00000049178
AA Change: V47A

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000045362
Gene: ENSMUSG00000042248
AA Change: V47A

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
Pfam:p450 30 487 5e-160 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T A 11: 9,247,159 (GRCm39) M2302K possibly damaging Het
Actl9 A G 17: 33,653,152 (GRCm39) E404G probably damaging Het
Adamts12 A T 15: 11,237,632 (GRCm39) I314L possibly damaging Het
Card6 C A 15: 5,129,484 (GRCm39) M637I possibly damaging Het
Ccdc122 G A 14: 77,329,516 (GRCm39) probably benign Het
Cdh10 A G 15: 18,899,886 (GRCm39) D71G probably benign Het
Cdk15 A T 1: 59,326,955 (GRCm39) Y214F probably benign Het
Cdon A G 9: 35,368,860 (GRCm39) K365E probably benign Het
Ddc T A 11: 11,789,462 (GRCm39) D271V probably damaging Het
Dnah6 G A 6: 73,042,708 (GRCm39) A3290V probably damaging Het
Dtl A T 1: 191,302,811 (GRCm39) S20T possibly damaging Het
Egf A C 3: 129,533,642 (GRCm39) I66S probably damaging Het
Eif4a3 T C 11: 119,184,387 (GRCm39) K268E probably damaging Het
Fbxl16 A T 17: 26,038,338 (GRCm39) probably benign Het
Fez2 C T 17: 78,689,029 (GRCm39) probably benign Het
Fras1 C A 5: 96,929,551 (GRCm39) T3985K probably benign Het
Gbp4 T C 5: 105,284,887 (GRCm39) M1V probably null Het
Gpnmb A G 6: 49,022,299 (GRCm39) D143G probably benign Het
Grm5 A T 7: 87,724,220 (GRCm39) T837S probably damaging Het
Hmcn1 T C 1: 150,620,752 (GRCm39) T1153A possibly damaging Het
Hp C T 8: 110,302,415 (GRCm39) V178I probably benign Het
Macf1 A T 4: 123,276,922 (GRCm39) V4061E probably damaging Het
Msto1 C A 3: 88,820,993 (GRCm39) R34L probably benign Het
Mtf2 C T 5: 108,254,756 (GRCm39) T519M probably damaging Het
Myo3a T A 2: 22,448,301 (GRCm39) N25K probably damaging Het
Ncapd2 A G 6: 125,145,582 (GRCm39) V1355A possibly damaging Het
Nhlrc2 C A 19: 56,540,231 (GRCm39) Y73* probably null Het
Nwd2 A T 5: 63,965,626 (GRCm39) S1737C possibly damaging Het
Or1p1 T A 11: 74,180,254 (GRCm39) C261S possibly damaging Het
Osmr A G 15: 6,873,908 (GRCm39) V163A probably damaging Het
Palm3 T C 8: 84,756,074 (GRCm39) S529P possibly damaging Het
Pcnt A G 10: 76,247,422 (GRCm39) Y1037H probably damaging Het
Pkhd1l1 T C 15: 44,393,425 (GRCm39) I1920T possibly damaging Het
Plekha7 A G 7: 115,744,479 (GRCm39) probably benign Het
Psd C T 19: 46,303,097 (GRCm39) G762R probably damaging Het
Psmb8 A G 17: 34,418,210 (GRCm39) T51A probably benign Het
Rbm12 A C 2: 155,937,302 (GRCm39) probably benign Het
Rictor T A 15: 6,804,085 (GRCm39) probably null Het
Slc24a5 G A 2: 124,922,800 (GRCm39) G158S probably damaging Het
Spata31f1a G T 4: 42,850,963 (GRCm39) L398I probably benign Het
Stag1 A G 9: 100,833,841 (GRCm39) probably benign Het
Tln2 A G 9: 67,302,749 (GRCm39) M74T probably benign Het
Trim24 C A 6: 37,942,570 (GRCm39) D957E possibly damaging Het
Trpa1 A T 1: 14,966,771 (GRCm39) M531K probably benign Het
Ttn A G 2: 76,736,637 (GRCm39) Y4376H possibly damaging Het
Twsg1 T C 17: 66,255,646 (GRCm39) probably benign Het
Usp34 T A 11: 23,367,676 (GRCm39) V1671E probably damaging Het
Vwa5b2 A G 16: 20,423,020 (GRCm39) D1006G probably benign Het
Other mutations in Cyp2c37
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00465:Cyp2c37 APN 19 39,990,441 (GRCm39) missense probably benign 0.00
IGL01959:Cyp2c37 APN 19 39,984,277 (GRCm39) nonsense probably null
IGL02580:Cyp2c37 APN 19 39,982,942 (GRCm39) missense probably damaging 1.00
IGL02611:Cyp2c37 APN 19 39,982,309 (GRCm39) missense probably benign 0.00
R0124:Cyp2c37 UTSW 19 39,982,546 (GRCm39) missense probably damaging 1.00
R0391:Cyp2c37 UTSW 19 39,982,950 (GRCm39) missense probably damaging 1.00
R0420:Cyp2c37 UTSW 19 39,984,238 (GRCm39) missense probably benign 0.00
R0782:Cyp2c37 UTSW 19 39,982,269 (GRCm39) missense probably benign 0.00
R1413:Cyp2c37 UTSW 19 39,982,542 (GRCm39) missense probably benign 0.21
R1637:Cyp2c37 UTSW 19 39,990,426 (GRCm39) nonsense probably null
R1688:Cyp2c37 UTSW 19 39,982,887 (GRCm39) splice site probably null
R2258:Cyp2c37 UTSW 19 39,984,303 (GRCm39) missense possibly damaging 0.49
R4353:Cyp2c37 UTSW 19 39,988,989 (GRCm39) missense possibly damaging 0.66
R4640:Cyp2c37 UTSW 19 40,000,276 (GRCm39) missense possibly damaging 0.67
R4965:Cyp2c37 UTSW 19 40,000,206 (GRCm39) missense possibly damaging 0.79
R5053:Cyp2c37 UTSW 19 39,990,331 (GRCm39) missense probably benign 0.00
R5645:Cyp2c37 UTSW 19 39,982,596 (GRCm39) missense probably benign 0.04
R5847:Cyp2c37 UTSW 19 40,000,176 (GRCm39) missense probably damaging 0.98
R6487:Cyp2c37 UTSW 19 39,983,025 (GRCm39) missense probably benign
R6631:Cyp2c37 UTSW 19 39,998,287 (GRCm39) missense probably damaging 1.00
R7062:Cyp2c37 UTSW 19 39,983,990 (GRCm39) splice site probably null
R7937:Cyp2c37 UTSW 19 39,982,202 (GRCm39) missense probably damaging 1.00
R9640:Cyp2c37 UTSW 19 40,000,180 (GRCm39) missense probably benign 0.01
R9779:Cyp2c37 UTSW 19 39,998,323 (GRCm39) missense probably benign 0.09
R9784:Cyp2c37 UTSW 19 39,988,943 (GRCm39) missense possibly damaging 0.85
Posted On 2013-10-07