Incidental Mutation 'R1937:Pamr1'
ID 213498
Institutional Source Beutler Lab
Gene Symbol Pamr1
Ensembl Gene ENSMUSG00000027188
Gene Name peptidase domain containing associated with muscle regeneration 1
Synonyms E430002G05Rik, RAMP
MMRRC Submission 039955-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R1937 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 102380357-102473386 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 102472617 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 639 (I639F)
Ref Sequence ENSEMBL: ENSMUSP00000028612 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028612]
AlphaFold Q8BU25
Predicted Effect possibly damaging
Transcript: ENSMUST00000028612
AA Change: I639F

PolyPhen 2 Score 0.802 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000028612
Gene: ENSMUSG00000027188
AA Change: I639F

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
EGF 84 126 1.18e1 SMART
CUB 128 236 1.07e-33 SMART
EGF 238 272 4.12e-7 SMART
CCP 280 342 1.3e-9 SMART
CCP 389 442 6.7e-3 SMART
Tryp_SPc 444 715 1.02e-34 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143071
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 97.0%
  • 10x: 95.7%
  • 20x: 93.5%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 106 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730480H06Rik C A 5: 48,531,777 (GRCm39) T35K probably benign Het
Abhd14a A G 9: 106,317,446 (GRCm39) probably benign Het
Abhd8 A G 8: 71,914,506 (GRCm39) F41L possibly damaging Het
Ace2 A T X: 162,939,524 (GRCm39) M123L possibly damaging Het
Actr5 T C 2: 158,477,949 (GRCm39) Y440H possibly damaging Het
Akr1c6 T A 13: 4,496,383 (GRCm39) N81K probably benign Het
Aqp11 T A 7: 97,386,725 (GRCm39) N157I possibly damaging Het
Arhgap10 T C 8: 78,071,282 (GRCm39) E568G probably damaging Het
Asb7 T A 7: 66,329,001 (GRCm39) Q13L probably benign Het
Atf7ip C A 6: 136,537,778 (GRCm39) A345E probably benign Het
Atp8a2 T C 14: 60,097,719 (GRCm39) K770E probably benign Het
Bpifb4 A T 2: 153,785,996 (GRCm39) I259F probably damaging Het
Cand1 A T 10: 119,038,925 (GRCm39) D1218E probably damaging Het
Capg A G 6: 72,535,236 (GRCm39) probably null Het
Cep290 C T 10: 100,333,815 (GRCm39) T289M possibly damaging Het
Cfap69 T C 5: 5,643,818 (GRCm39) Y548C probably damaging Het
Cfap97d1 A T 11: 101,877,989 (GRCm39) H17L probably damaging Het
Cimip2b T A 4: 43,427,586 (GRCm39) K220N probably damaging Het
Clock A G 5: 76,377,340 (GRCm39) L652P probably damaging Het
Col3a1 C T 1: 45,373,453 (GRCm39) probably benign Het
Coro7 T C 16: 4,446,596 (GRCm39) E843G probably benign Het
Crebrf T C 17: 26,961,442 (GRCm39) S188P probably damaging Het
Crppa G A 12: 36,440,367 (GRCm39) V92I probably benign Het
Cul1 T C 6: 47,485,289 (GRCm39) F307L probably benign Het
Cyb561d2 G A 9: 107,417,515 (GRCm39) R79W probably damaging Het
Cyp3a59 T C 5: 146,031,187 (GRCm39) S117P possibly damaging Het
Ddias A G 7: 92,507,830 (GRCm39) I695T probably benign Het
Dhx29 G A 13: 113,101,864 (GRCm39) G1311D probably benign Het
Dync2h1 A G 9: 7,139,159 (GRCm39) probably null Het
Ece2 T A 16: 20,436,616 (GRCm39) V146E probably damaging Het
Eml2 A G 7: 18,937,889 (GRCm39) K586E possibly damaging Het
Eps8l3 A G 3: 107,791,708 (GRCm39) E316G probably benign Het
Fam135b A T 15: 71,493,863 (GRCm39) L22H probably damaging Het
Focad T A 4: 88,319,318 (GRCm39) M1K probably null Het
Fryl A G 5: 73,290,710 (GRCm39) S65P probably damaging Het
Gm14190 C T 11: 99,581,556 (GRCm39) C4Y unknown Het
H2-T5 T A 17: 36,478,899 (GRCm39) T117S probably damaging Het
Ift74 T A 4: 94,550,883 (GRCm39) M345K probably benign Het
Jag1 C G 2: 136,925,393 (GRCm39) V1070L possibly damaging Het
Kcng1 T C 2: 168,104,941 (GRCm39) T302A probably benign Het
Kif20b T C 19: 34,930,278 (GRCm39) V1221A possibly damaging Het
Kif23 A T 9: 61,853,892 (GRCm39) probably null Het
Lpxn T G 19: 12,802,274 (GRCm39) S200A probably benign Het
Meiob A G 17: 25,037,305 (GRCm39) H61R probably benign Het
Mfhas1 C T 8: 36,056,799 (GRCm39) L425F probably damaging Het
Myo3a A T 2: 22,401,126 (GRCm39) S632C probably damaging Het
Naip2 T C 13: 100,298,362 (GRCm39) E558G probably benign Het
Naip2 C T 13: 100,298,368 (GRCm39) G556D probably benign Het
Nbeal1 T A 1: 60,307,100 (GRCm39) Y374* probably null Het
Notch3 T C 17: 32,372,826 (GRCm39) S582G probably benign Het
Nphs1 A T 7: 30,173,798 (GRCm39) Q985L probably damaging Het
Oas1c T A 5: 120,941,049 (GRCm39) H248L probably benign Het
Or5c1 A T 2: 37,221,896 (GRCm39) N46Y probably damaging Het
Or5g26 T C 2: 85,494,341 (GRCm39) I146V probably benign Het
Or5h25 A T 16: 58,930,157 (GRCm39) M272K probably benign Het
Or8g35 A G 9: 39,381,333 (GRCm39) S230P possibly damaging Het
Panx1 G T 9: 14,918,980 (GRCm39) T293K possibly damaging Het
Papss1 G T 3: 131,305,632 (GRCm39) V226F probably benign Het
Pax1 G T 2: 147,209,809 (GRCm39) G301V possibly damaging Het
Pdlim5 C A 3: 141,950,742 (GRCm39) R557L possibly damaging Het
Pdyn C A 2: 129,531,729 (GRCm39) M20I probably benign Het
Pelp1 G A 11: 70,284,541 (GRCm39) probably null Het
Pkd2 T C 5: 104,626,790 (GRCm39) V324A probably damaging Het
Pkdrej A G 15: 85,703,368 (GRCm39) I856T probably benign Het
Polr1a T C 6: 71,913,536 (GRCm39) probably null Het
Pot1a A T 6: 25,753,323 (GRCm39) D404E probably benign Het
Ppp2r2a A T 14: 67,253,878 (GRCm39) I430N possibly damaging Het
Prob1 C T 18: 35,787,279 (GRCm39) R325Q possibly damaging Het
Prrc2a T C 17: 35,376,884 (GRCm39) D742G probably damaging Het
Psmc1 C T 12: 100,081,102 (GRCm39) P54S probably benign Het
Rab22a A G 2: 173,530,004 (GRCm39) T61A probably damaging Het
Rims1 T A 1: 22,358,754 (GRCm39) K184N probably damaging Het
Rnf213 G A 11: 119,322,511 (GRCm39) R1376H probably damaging Het
Ryr2 T C 13: 11,683,848 (GRCm39) E3072G probably damaging Het
Serpina1b T C 12: 103,698,420 (GRCm39) K143R probably benign Het
Slc22a15 T G 3: 101,787,505 (GRCm39) probably null Het
Slc25a14 G A X: 47,740,840 (GRCm39) V210I probably benign Het
Slc25a48 A C 13: 56,596,811 (GRCm39) T31P probably damaging Het
Slc9a3 C T 13: 74,314,175 (GRCm39) probably null Het
Slx4 T C 16: 3,805,030 (GRCm39) *105W probably null Het
Smc6 A G 12: 11,349,399 (GRCm39) N794S probably benign Het
Spata18 G A 5: 73,834,307 (GRCm39) R387Q probably damaging Het
Sphkap C A 1: 83,245,162 (GRCm39) E1486* probably null Het
Srsf6 C T 2: 162,776,403 (GRCm39) probably benign Het
St8sia1 C T 6: 142,909,398 (GRCm39) A33T probably damaging Het
Tet2 T C 3: 133,194,399 (GRCm39) T12A possibly damaging Het
Tmem144 G T 3: 79,732,611 (GRCm39) S222R probably damaging Het
Tnrc6c A G 11: 117,646,849 (GRCm39) D1450G possibly damaging Het
Top1 A T 2: 160,512,042 (GRCm39) K27N unknown Het
Tox2 A G 2: 163,067,476 (GRCm39) H30R probably benign Het
Tra2b T C 16: 22,065,993 (GRCm39) probably benign Het
Trio A T 15: 27,833,142 (GRCm39) V1165E probably damaging Het
Troap T A 15: 98,975,269 (GRCm39) S145R probably damaging Het
Ttc34 G A 4: 154,950,139 (GRCm39) A1031T possibly damaging Het
Ttc6 C T 12: 57,663,109 (GRCm39) P302S probably benign Het
Ubiad1 A G 4: 148,528,468 (GRCm39) L147P probably damaging Het
Ugt2b35 G T 5: 87,149,141 (GRCm39) V131F probably damaging Het
Utp25 A T 1: 192,804,401 (GRCm39) D200E probably damaging Het
Vmn1r167 G A 7: 23,204,452 (GRCm39) T188I probably benign Het
Vmn1r46 G T 6: 89,953,716 (GRCm39) M188I probably benign Het
Vmn2r115 T A 17: 23,578,388 (GRCm39) N620K probably damaging Het
Vmn2r66 A G 7: 84,644,344 (GRCm39) S689P probably damaging Het
Wipf2 C T 11: 98,783,236 (GRCm39) R221* probably null Het
Zbtb16 T C 9: 48,571,078 (GRCm39) S563G probably benign Het
Zfp319 T C 8: 96,055,199 (GRCm39) T335A probably damaging Het
Zfp418 A G 7: 7,185,401 (GRCm39) R455G possibly damaging Het
Other mutations in Pamr1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00503:Pamr1 APN 2 102,472,617 (GRCm39) missense possibly damaging 0.80
IGL00741:Pamr1 APN 2 102,416,966 (GRCm39) missense possibly damaging 0.62
IGL00928:Pamr1 APN 2 102,469,686 (GRCm39) missense probably benign 0.01
IGL01328:Pamr1 APN 2 102,472,482 (GRCm39) missense probably benign 0.00
IGL02621:Pamr1 APN 2 102,464,688 (GRCm39) missense probably benign 0.03
IGL02732:Pamr1 APN 2 102,472,486 (GRCm39) missense probably benign 0.03
R0020:Pamr1 UTSW 2 102,472,423 (GRCm39) missense probably benign 0.19
R0743:Pamr1 UTSW 2 102,440,252 (GRCm39) missense probably damaging 1.00
R1068:Pamr1 UTSW 2 102,472,590 (GRCm39) missense probably damaging 1.00
R1127:Pamr1 UTSW 2 102,469,698 (GRCm39) missense possibly damaging 0.81
R1711:Pamr1 UTSW 2 102,471,197 (GRCm39) missense probably benign 0.28
R1912:Pamr1 UTSW 2 102,472,645 (GRCm39) missense probably damaging 1.00
R1926:Pamr1 UTSW 2 102,471,342 (GRCm39) splice site probably null
R2021:Pamr1 UTSW 2 102,464,880 (GRCm39) missense probably benign 0.00
R2023:Pamr1 UTSW 2 102,464,880 (GRCm39) missense probably benign 0.00
R4718:Pamr1 UTSW 2 102,472,681 (GRCm39) missense probably damaging 1.00
R4934:Pamr1 UTSW 2 102,472,549 (GRCm39) missense probably benign 0.21
R5268:Pamr1 UTSW 2 102,417,029 (GRCm39) missense probably damaging 0.98
R5450:Pamr1 UTSW 2 102,469,662 (GRCm39) missense probably damaging 0.98
R5864:Pamr1 UTSW 2 102,464,693 (GRCm39) missense possibly damaging 0.91
R6112:Pamr1 UTSW 2 102,441,953 (GRCm39) missense probably damaging 1.00
R6286:Pamr1 UTSW 2 102,471,293 (GRCm39) nonsense probably null
R6327:Pamr1 UTSW 2 102,472,519 (GRCm39) missense probably damaging 1.00
R6831:Pamr1 UTSW 2 102,445,276 (GRCm39) missense probably damaging 0.97
R6834:Pamr1 UTSW 2 102,445,276 (GRCm39) missense probably damaging 0.97
R6980:Pamr1 UTSW 2 102,472,549 (GRCm39) missense probably benign 0.21
R7000:Pamr1 UTSW 2 102,441,968 (GRCm39) missense probably damaging 1.00
R7073:Pamr1 UTSW 2 102,471,280 (GRCm39) missense probably benign 0.00
R7255:Pamr1 UTSW 2 102,441,929 (GRCm39) missense probably damaging 1.00
R7357:Pamr1 UTSW 2 102,417,049 (GRCm39) nonsense probably null
R7851:Pamr1 UTSW 2 102,416,945 (GRCm39) missense probably benign 0.02
R8745:Pamr1 UTSW 2 102,441,924 (GRCm39) missense probably damaging 1.00
R8766:Pamr1 UTSW 2 102,380,538 (GRCm39) start codon destroyed probably null 0.90
R8817:Pamr1 UTSW 2 102,464,766 (GRCm39) missense probably benign 0.05
R8964:Pamr1 UTSW 2 102,464,811 (GRCm39) missense possibly damaging 0.65
R8977:Pamr1 UTSW 2 102,441,963 (GRCm39) missense probably damaging 0.96
R9081:Pamr1 UTSW 2 102,441,933 (GRCm39) missense probably damaging 1.00
R9139:Pamr1 UTSW 2 102,464,766 (GRCm39) missense probably benign 0.19
X0067:Pamr1 UTSW 2 102,469,680 (GRCm39) nonsense probably null
Z1088:Pamr1 UTSW 2 102,464,791 (GRCm39) missense possibly damaging 0.84
Predicted Primers PCR Primer
(F):5'- CGCTGTTCTGAAGCTCCTAG -3'
(R):5'- TGTCTTGTCATAGCTCCAGC -3'

Sequencing Primer
(F):5'- GCTGTTCTGAAGCTCCTAGACAAAG -3'
(R):5'- CTGACCAGCCCCACCAAATG -3'
Posted On 2014-07-14