Incidental Mutation 'R8753:Cpox'
ID 664001
Institutional Source Beutler Lab
Gene Symbol Cpox
Ensembl Gene ENSMUSG00000022742
Gene Name coproporphyrinogen oxidase
Synonyms clone 560, nct, Cpo, M100835, cac
MMRRC Submission 068619-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R8753 (G1)
Quality Score 225.009
Status Validated
Chromosome 16
Chromosomal Location 58490571-58500754 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 58498391 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 408 (M408K)
Ref Sequence ENSEMBL: ENSMUSP00000055455 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000060077]
AlphaFold P36552
Predicted Effect probably damaging
Transcript: ENSMUST00000060077
AA Change: M408K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000055455
Gene: ENSMUSG00000022742
AA Change: M408K

DomainStartEndE-ValueType
low complexity region 57 81 N/A INTRINSIC
low complexity region 94 105 N/A INTRINSIC
Pfam:Coprogen_oxidas 140 442 7.6e-142 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 95% (59/62)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is the sixth enzyme of the heme biosynthetic pathway. The encoded enzyme is soluble and found in the intermembrane space of mitochondria. This enzyme catalyzes the stepwise oxidative decarboxylation of coproporphyrinogen III to protoporphyrinogen IX, a precursor of heme. Defects in this gene are a cause of hereditary coproporphyria (HCP).[provided by RefSeq, Oct 2009]
PHENOTYPE: Mice homozygous for a spontaneous allele develop cataracts. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 T C 2: 25,332,706 (GRCm39) Y1496H probably damaging Het
Acan G A 7: 78,748,516 (GRCm39) E1096K possibly damaging Het
Adprhl1 T C 8: 13,272,118 (GRCm39) K1547E possibly damaging Het
Ampd2 C A 3: 107,987,432 (GRCm39) V134L probably benign Het
Arf4 T A 14: 26,374,114 (GRCm39) probably benign Het
Boc A T 16: 44,320,775 (GRCm39) M295K Het
C2cd3 T A 7: 100,049,024 (GRCm39) probably null Het
Calcrl C G 2: 84,178,659 (GRCm39) G223A probably benign Het
Calcrl C A 2: 84,178,661 (GRCm39) M222I probably benign Het
Ccdc88b T C 19: 6,833,213 (GRCm39) E278G probably damaging Het
Ccz1 A G 5: 143,925,050 (GRCm39) C469R probably benign Het
Cdc40 C T 10: 40,717,480 (GRCm39) D404N probably damaging Het
Clpx G A 9: 65,223,958 (GRCm39) G251S probably damaging Het
Col6a3 C G 1: 90,695,328 (GRCm39) probably benign Het
Crybb3 A G 5: 113,226,247 (GRCm39) probably null Het
Cubn A T 2: 13,313,377 (GRCm39) C3064* probably null Het
Cxcl3 CCTGCTGCTGCTGCTG CCTGCTGCTGCTG 5: 90,934,071 (GRCm39) probably benign Het
Cyp4a31 A T 4: 115,432,158 (GRCm39) S432C probably benign Het
Ddias A T 7: 92,508,668 (GRCm39) F416I probably damaging Het
Dlat G T 9: 50,560,967 (GRCm39) A360E probably damaging Het
Dnttip2 A G 3: 122,074,398 (GRCm39) T612A probably damaging Het
Fnip1 A G 11: 54,400,867 (GRCm39) T1089A probably damaging Het
Gm12117 A T 11: 33,225,953 (GRCm39) L128M probably benign Het
Gtf2h5 C CA 17: 6,134,833 (GRCm39) probably null Het
Ibtk T C 9: 85,610,819 (GRCm39) T285A probably benign Het
Ifi206 A T 1: 173,301,223 (GRCm39) N818K unknown Het
Itga10 T G 3: 96,558,471 (GRCm39) L305R probably damaging Het
Khnyn T C 14: 56,125,223 (GRCm39) Y461H possibly damaging Het
Macroh2a2 T C 10: 61,585,113 (GRCm39) D177G possibly damaging Het
Mbtps1 T C 8: 120,235,601 (GRCm39) S1026G possibly damaging Het
Msantd4 A G 9: 4,385,013 (GRCm39) E246G probably damaging Het
N4bp1 T C 8: 87,575,085 (GRCm39) I737V probably damaging Het
Nav2 T G 7: 49,102,320 (GRCm39) S373A probably benign Het
Nbea T C 3: 55,534,329 (GRCm39) Y2936C probably damaging Het
Nbeal1 A T 1: 60,307,542 (GRCm39) I1685F probably damaging Het
Nt5c3 C G 6: 56,860,677 (GRCm39) G293R probably damaging Het
Or4f14c A T 2: 111,940,802 (GRCm39) V265E probably benign Het
Or52z1 T A 7: 103,436,567 (GRCm39) I306F probably benign Het
Pcnx2 A T 8: 126,613,999 (GRCm39) V484E probably benign Het
Pcsk5 C T 19: 17,446,408 (GRCm39) R1195Q probably benign Het
Perm1 TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT 4: 156,302,525 (GRCm39) probably benign Het
Pitpnm3 A G 11: 71,942,704 (GRCm39) V861A probably benign Het
Pkd1 A G 17: 24,793,176 (GRCm39) Y1621C probably damaging Het
Polr3a C A 14: 24,513,702 (GRCm39) E846* probably null Het
Polr3e T C 7: 120,539,540 (GRCm39) V455A possibly damaging Het
Prr5l C T 2: 101,571,723 (GRCm39) G118D probably damaging Het
Pygl G T 12: 70,242,400 (GRCm39) N685K probably damaging Het
Rfx8 A G 1: 39,757,600 (GRCm39) V56A probably damaging Het
Sbf1 T C 15: 89,179,662 (GRCm39) D1341G probably benign Het
Selenon T C 4: 134,275,330 (GRCm39) T123A probably benign Het
Slc23a1 T G 18: 35,752,631 (GRCm39) K549Q probably benign Het
Slc7a13 T C 4: 19,841,443 (GRCm39) F430S probably damaging Het
Smarcc2 G A 10: 128,319,070 (GRCm39) V707M probably damaging Het
St18 A G 1: 6,916,015 (GRCm39) S887G probably damaging Het
T2 T C 17: 8,615,477 (GRCm39) probably benign Het
Tbc1d16 A G 11: 119,101,492 (GRCm39) L6P probably damaging Het
Tcf7l2 T C 19: 55,920,195 (GRCm39) L576P possibly damaging Het
Tnr A G 1: 159,677,936 (GRCm39) D107G probably benign Het
Trpv1 G T 11: 73,135,082 (GRCm39) K426N probably damaging Het
Vmn1r15 A T 6: 57,235,895 (GRCm39) L254F probably benign Het
Vmn1r219 A T 13: 23,347,191 (GRCm39) I127F probably damaging Het
Zc3h14 A T 12: 98,724,831 (GRCm39) E164D probably benign Het
Other mutations in Cpox
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02152:Cpox APN 16 58,494,787 (GRCm39) missense possibly damaging 0.87
IGL03031:Cpox APN 16 58,492,923 (GRCm39) missense probably damaging 1.00
IGL03034:Cpox APN 16 58,495,718 (GRCm39) missense probably damaging 0.98
scraggy UTSW 16 58,491,298 (GRCm39) missense probably damaging 1.00
R0413:Cpox UTSW 16 58,491,232 (GRCm39) missense possibly damaging 0.52
R0523:Cpox UTSW 16 58,495,608 (GRCm39) nonsense probably null
R0551:Cpox UTSW 16 58,495,753 (GRCm39) missense probably benign 0.11
R2064:Cpox UTSW 16 58,494,772 (GRCm39) missense probably benign 0.36
R4651:Cpox UTSW 16 58,491,050 (GRCm39) missense possibly damaging 0.92
R4701:Cpox UTSW 16 58,498,332 (GRCm39) nonsense probably null
R4782:Cpox UTSW 16 58,492,986 (GRCm39) missense probably damaging 1.00
R5285:Cpox UTSW 16 58,495,649 (GRCm39) missense probably damaging 1.00
R5287:Cpox UTSW 16 58,495,649 (GRCm39) missense probably damaging 1.00
R5313:Cpox UTSW 16 58,498,311 (GRCm39) nonsense probably null
R5346:Cpox UTSW 16 58,495,649 (GRCm39) missense probably damaging 1.00
R5354:Cpox UTSW 16 58,491,205 (GRCm39) missense probably damaging 0.99
R5404:Cpox UTSW 16 58,495,649 (GRCm39) missense probably damaging 1.00
R5476:Cpox UTSW 16 58,499,088 (GRCm39) missense probably damaging 0.99
R5853:Cpox UTSW 16 58,495,780 (GRCm39) missense probably damaging 0.99
R6026:Cpox UTSW 16 58,491,298 (GRCm39) missense probably damaging 1.00
R7059:Cpox UTSW 16 58,491,290 (GRCm39) missense probably damaging 1.00
R7061:Cpox UTSW 16 58,491,223 (GRCm39) missense possibly damaging 0.76
R7606:Cpox UTSW 16 58,494,812 (GRCm39) missense probably benign 0.16
R8779:Cpox UTSW 16 58,491,229 (GRCm39) missense probably damaging 1.00
R8793:Cpox UTSW 16 58,493,708 (GRCm39) missense probably damaging 1.00
R9667:Cpox UTSW 16 58,490,984 (GRCm39) missense possibly damaging 0.52
R9736:Cpox UTSW 16 58,494,746 (GRCm39) missense probably benign 0.00
RF059:Cpox UTSW 16 58,491,130 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GAAGGGCCACTCTTCGTTTTC -3'
(R):5'- CAGAATCCAATCTGGGCTTTATTC -3'

Sequencing Primer
(F):5'- CCTTAAGGATTTCTAGAAAGTTTCGC -3'
(R):5'- AATCTGGGCTTTATTCTCTCACAG -3'
Posted On 2021-03-08