Incidental Mutation 'R4941:Proc'
ID 383146
Institutional Source Beutler Lab
Gene Symbol Proc
Ensembl Gene ENSMUSG00000024386
Gene Name protein C
Synonyms inactivator of coagulation factors Va, VIII, PC
MMRRC Submission 042539-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4941 (G1)
Quality Score 191
Status Validated
Chromosome 18
Chromosomal Location 32256179-32272623 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 32258166 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 260 (K260E)
Ref Sequence ENSEMBL: ENSMUSP00000132226 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000171765]
AlphaFold P33587
Predicted Effect possibly damaging
Transcript: ENSMUST00000171765
AA Change: K260E

PolyPhen 2 Score 0.597 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000132226
Gene: ENSMUSG00000024386
AA Change: K260E

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
GLA 24 86 6.66e-30 SMART
EGF_CA 87 131 1.25e-6 SMART
EGF 138 175 3.62e-3 SMART
low complexity region 201 210 N/A INTRINSIC
Tryp_SPc 211 444 2.6e-82 SMART
Meta Mutation Damage Score 0.6023 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.4%
  • 20x: 89.0%
Validation Efficiency 97% (112/116)
MGI Phenotype FUNCTION: This gene encodes the vitamin K-dependent protein C, which plays a vital role in the anticoagulation pathway. The encoded protein undergoes proteolytic processing including activation by thrombin-thrombomodulin complex to form the anticoagulant serine protease that degrades activated coagulation factors. A complete lack of the encoded protein in mice results in severe perinatal consumptive coagulopathy in the brain and liver, resulting in death within 24 hours after birth. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate the mature protein. [provided by RefSeq, Sep 2015]
PHENOTYPE: Inactivation of the locus results in death within 24 hours of birth due to consumptive coagulopathy. Thromboses and bleeding are observed in the brains and livers of homozygous mutant mice. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 98 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A4galt T A 15: 83,112,529 (GRCm39) I85F probably damaging Het
Abcc6 T A 7: 45,661,947 (GRCm39) I435F probably benign Het
Adam3 T C 8: 25,167,332 (GRCm39) probably benign Het
Adrb3 T C 8: 27,717,450 (GRCm39) Y333C probably damaging Het
Ago4 A T 4: 126,419,847 (GRCm39) D43E probably benign Het
Agt T A 8: 125,283,727 (GRCm39) Q464L probably benign Het
Amdhd1 A T 10: 93,367,463 (GRCm39) D230E probably damaging Het
Aplf A G 6: 87,645,405 (GRCm39) I33T probably damaging Het
Aplf A T 6: 87,623,331 (GRCm39) N249K probably benign Het
Arap2 A G 5: 62,906,821 (GRCm39) M66T probably benign Het
Atf4 T C 15: 80,140,434 (GRCm39) probably benign Het
Bahcc1 A C 11: 120,177,491 (GRCm39) H2068P probably benign Het
Bcor C T X: 11,906,725 (GRCm39) R1551Q probably damaging Het
Bltp1 A C 3: 36,971,851 (GRCm39) H528P probably damaging Het
Bltp1 G A 3: 36,974,050 (GRCm39) S600N probably benign Het
Catsper1 C A 19: 5,391,466 (GRCm39) A616D possibly damaging Het
Cdkn3 A G 14: 47,007,320 (GRCm39) D159G possibly damaging Het
Cep162 T C 9: 87,108,022 (GRCm39) probably benign Het
Clca3a1 T A 3: 144,721,414 (GRCm39) I386L probably damaging Het
Cldn10 G A 14: 119,025,725 (GRCm39) G53S possibly damaging Het
Cmtm3 T C 8: 105,070,460 (GRCm39) L73P probably damaging Het
Cnksr3 A C 10: 7,102,925 (GRCm39) L149R probably benign Het
Cope T C 8: 70,755,584 (GRCm39) probably null Het
Cpa6 T A 1: 10,479,562 (GRCm39) M224L probably benign Het
Cyp2d41-ps T C 15: 82,666,154 (GRCm39) noncoding transcript Het
Ddx55 T A 5: 124,706,779 (GRCm39) L592* probably null Het
Deup1 T C 9: 15,499,323 (GRCm39) M333V probably benign Het
Eif4a1 T C 11: 69,558,640 (GRCm39) probably benign Het
Eif4g3 A C 4: 137,897,876 (GRCm39) D1026A probably damaging Het
Eif5b T C 1: 38,090,280 (GRCm39) V1153A probably damaging Het
Ercc8 G T 13: 108,297,301 (GRCm39) probably benign Het
Fam227a C A 15: 79,524,204 (GRCm39) probably null Het
Fat1 A G 8: 45,489,312 (GRCm39) I3505V probably benign Het
Fat3 T G 9: 16,286,448 (GRCm39) E1025A probably damaging Het
Fat4 C T 3: 39,011,601 (GRCm39) R2234W probably damaging Het
Fer1l4 G T 2: 155,887,009 (GRCm39) F634L probably damaging Het
Fetub G A 16: 22,756,624 (GRCm39) V162I probably benign Het
Fgd4 T C 16: 16,302,402 (GRCm39) Q51R probably benign Het
Fgfr2 T C 7: 129,800,175 (GRCm39) H140R probably benign Het
Flt3 T A 5: 147,293,185 (GRCm39) probably null Het
Gabrb1 A G 5: 72,294,121 (GRCm39) N465S probably damaging Het
Gapdhs T C 7: 30,432,691 (GRCm39) I206V probably benign Het
Gkn3 C T 6: 87,360,507 (GRCm39) A163T probably damaging Het
Glp2r T C 11: 67,637,529 (GRCm39) probably null Het
Gm4956 T A 1: 21,368,306 (GRCm39) noncoding transcript Het
Gtf2a1l A T 17: 89,022,350 (GRCm39) D447V probably damaging Het
Hsd3b5 A G 3: 98,526,379 (GRCm39) W356R probably damaging Het
Idh2 A T 7: 79,745,847 (GRCm39) V335D probably damaging Het
Isyna1 T C 8: 71,048,146 (GRCm39) I184T probably damaging Het
Kcnh2 A G 5: 24,536,085 (GRCm39) S320P probably damaging Het
Klk14 G A 7: 43,341,501 (GRCm39) C51Y probably damaging Het
Kpna6 A G 4: 129,541,825 (GRCm39) F524S probably damaging Het
Lap3 A T 5: 45,663,539 (GRCm39) M338L probably benign Het
Lins1 T C 7: 66,359,198 (GRCm39) probably benign Het
Llgl1 C T 11: 60,600,394 (GRCm39) P581L probably benign Het
Lrrc43 A G 5: 123,639,126 (GRCm39) D385G probably benign Het
Maf T C 8: 116,433,532 (GRCm39) D24G unknown Het
Nell1 T C 7: 49,712,386 (GRCm39) S69P probably benign Het
Nkapd1 G T 9: 50,518,809 (GRCm39) Q268K probably benign Het
Or13p4 C T 4: 118,547,089 (GRCm39) V187I possibly damaging Het
Or2h1 C T 17: 37,404,484 (GRCm39) G94E probably damaging Het
Or2j6 T A 7: 139,980,792 (GRCm39) M56L probably benign Het
Or51af1 T C 7: 103,141,458 (GRCm39) D209G probably damaging Het
Or5an10 A G 19: 12,276,260 (GRCm39) S79P possibly damaging Het
Or8g54 T C 9: 39,707,160 (GRCm39) M163T possibly damaging Het
Oxld1 T C 11: 120,347,862 (GRCm39) T112A probably benign Het
Parp14 T C 16: 35,666,403 (GRCm39) N1210S probably benign Het
Pcdhb10 C A 18: 37,545,887 (GRCm39) T321K probably benign Het
Pcdhb8 C T 18: 37,489,059 (GRCm39) L246F probably benign Het
Pcdhga1 T A 18: 37,795,659 (GRCm39) I221K probably benign Het
Pcdhga9 T A 18: 37,871,185 (GRCm39) V338E probably damaging Het
Pdcd11 T C 19: 47,108,325 (GRCm39) S1231P probably damaging Het
Pde6c A T 19: 38,140,013 (GRCm39) L325F probably damaging Het
Pnpla7 T A 2: 24,887,276 (GRCm39) probably null Het
Pparg T A 6: 115,467,071 (GRCm39) V478E probably damaging Het
Ppib T C 9: 65,967,672 (GRCm39) V42A probably benign Het
Ppox T C 1: 171,105,166 (GRCm39) M341V probably damaging Het
Ptpro C T 6: 137,369,763 (GRCm39) P525L probably damaging Het
Rnf14 C A 18: 38,441,435 (GRCm39) A275E probably damaging Het
Scnn1b C T 7: 121,511,231 (GRCm39) P306L probably damaging Het
Sec14l5 A G 16: 4,994,364 (GRCm39) E386G probably damaging Het
Sftpa1 T A 14: 40,854,509 (GRCm39) I32N probably damaging Het
Slc26a5 A G 5: 22,025,384 (GRCm39) I408T probably damaging Het
Slc7a13 A G 4: 19,841,467 (GRCm39) Y438C probably damaging Het
Spire1 T C 18: 67,652,384 (GRCm39) E231G possibly damaging Het
Stab1 T A 14: 30,873,528 (GRCm39) I1014F probably benign Het
Steap2 T C 5: 5,727,651 (GRCm39) Y228C probably damaging Het
Tmem131l T C 3: 83,806,546 (GRCm39) T1487A probably benign Het
Tmem171 A G 13: 98,828,803 (GRCm39) F116L possibly damaging Het
Tmem215 T C 4: 40,474,520 (GRCm39) V199A probably damaging Het
Tmem45a T C 16: 56,642,652 (GRCm39) N173S possibly damaging Het
Uqcrc2 C T 7: 120,242,301 (GRCm39) R148C probably benign Het
Vmn2r116 A G 17: 23,620,116 (GRCm39) K617E probably damaging Het
Xrcc6 T C 15: 81,924,013 (GRCm39) L229P probably damaging Het
Yju2 A G 17: 56,271,149 (GRCm39) D97G possibly damaging Het
Zfp184 A G 13: 22,133,891 (GRCm39) D46G probably damaging Het
Zfp790 T A 7: 29,528,916 (GRCm39) C534S possibly damaging Het
Zfp990 A T 4: 145,263,407 (GRCm39) N135I probably damaging Het
Other mutations in Proc
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00693:Proc APN 18 32,256,566 (GRCm39) missense probably benign 0.05
IGL01071:Proc APN 18 32,256,770 (GRCm39) missense probably damaging 1.00
IGL01287:Proc APN 18 32,256,873 (GRCm39) splice site probably benign
IGL01298:Proc APN 18 32,256,605 (GRCm39) missense probably benign 0.01
IGL01898:Proc APN 18 32,266,198 (GRCm39) critical splice donor site probably null
IGL01977:Proc APN 18 32,260,472 (GRCm39) missense probably benign 0.02
IGL02040:Proc APN 18 32,267,913 (GRCm39) missense probably benign 0.07
IGL02724:Proc APN 18 32,267,925 (GRCm39) missense probably damaging 1.00
IGL02852:Proc APN 18 32,258,208 (GRCm39) missense probably damaging 1.00
IGL02901:Proc APN 18 32,256,678 (GRCm39) missense possibly damaging 0.89
IGL03401:Proc APN 18 32,256,326 (GRCm39) missense possibly damaging 0.96
R0110:Proc UTSW 18 32,258,171 (GRCm39) missense probably benign 0.26
R0131:Proc UTSW 18 32,268,951 (GRCm39) missense probably benign 0.01
R0510:Proc UTSW 18 32,258,171 (GRCm39) missense probably benign 0.26
R0988:Proc UTSW 18 32,266,536 (GRCm39) missense probably benign
R1455:Proc UTSW 18 32,256,451 (GRCm39) missense probably damaging 1.00
R1463:Proc UTSW 18 32,266,491 (GRCm39) missense possibly damaging 0.69
R1546:Proc UTSW 18 32,260,463 (GRCm39) missense probably damaging 1.00
R1711:Proc UTSW 18 32,260,459 (GRCm39) missense probably benign 0.05
R3414:Proc UTSW 18 32,256,738 (GRCm39) missense probably benign 0.00
R3911:Proc UTSW 18 32,256,758 (GRCm39) missense probably damaging 1.00
R4276:Proc UTSW 18 32,268,967 (GRCm39) missense probably benign 0.00
R4598:Proc UTSW 18 32,256,512 (GRCm39) missense probably damaging 1.00
R4623:Proc UTSW 18 32,260,526 (GRCm39) missense probably benign 0.32
R4758:Proc UTSW 18 32,256,863 (GRCm39) missense probably damaging 0.97
R5917:Proc UTSW 18 32,260,513 (GRCm39) missense probably benign 0.07
R6349:Proc UTSW 18 32,266,486 (GRCm39) missense probably benign 0.00
R6636:Proc UTSW 18 32,256,813 (GRCm39) missense probably benign 0.00
R6735:Proc UTSW 18 32,256,701 (GRCm39) missense probably benign 0.01
R7110:Proc UTSW 18 32,266,441 (GRCm39) missense probably benign 0.30
R7310:Proc UTSW 18 32,268,952 (GRCm39) missense probably benign 0.03
R7409:Proc UTSW 18 32,260,513 (GRCm39) missense probably benign 0.03
R7597:Proc UTSW 18 32,256,689 (GRCm39) missense probably damaging 1.00
R7598:Proc UTSW 18 32,268,929 (GRCm39) missense probably benign 0.00
R7604:Proc UTSW 18 32,267,831 (GRCm39) splice site probably null
R7738:Proc UTSW 18 32,260,532 (GRCm39) nonsense probably null
R7921:Proc UTSW 18 32,256,470 (GRCm39) missense probably damaging 1.00
R8425:Proc UTSW 18 32,256,411 (GRCm39) missense probably damaging 1.00
R9074:Proc UTSW 18 32,268,950 (GRCm39) missense possibly damaging 0.67
R9382:Proc UTSW 18 32,256,336 (GRCm39) missense probably damaging 1.00
R9690:Proc UTSW 18 32,256,371 (GRCm39) missense probably damaging 1.00
X0021:Proc UTSW 18 32,256,560 (GRCm39) missense probably damaging 0.96
Z1176:Proc UTSW 18 32,268,032 (GRCm39) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- GCCTAGATCTGAGATGAACACC -3'
(R):5'- GTTTGAGAAACACCGGAAGC -3'

Sequencing Primer
(F):5'- GATCTGAGATGAACACCAGAAAATC -3'
(R):5'- GCCCCTTAGGATTCAGAGATC -3'
Posted On 2016-04-27