Incidental Mutation 'R0009:Gm4847'
ID 40448
Institutional Source Beutler Lab
Gene Symbol Gm4847
Ensembl Gene ENSMUSG00000051081
Gene Name predicted gene 4847
Synonyms
MMRRC Submission 038304-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.091) question?
Stock # R0009 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 166456540-166475262 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 166458055 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 433 (V433I)
Ref Sequence ENSEMBL: ENSMUSP00000039839 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046662]
AlphaFold G3X946
Predicted Effect probably benign
Transcript: ENSMUST00000046662
AA Change: V433I

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000039839
Gene: ENSMUSG00000051081
AA Change: V433I

DomainStartEndE-ValueType
Pfam:FMO-like 3 533 1.4e-235 PFAM
Pfam:Pyr_redox_2 4 241 5.2e-11 PFAM
Pfam:Pyr_redox_3 7 221 6.7e-15 PFAM
Pfam:NAD_binding_8 8 92 1.6e-7 PFAM
Pfam:K_oxygenase 77 333 5.2e-9 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.7%
Validation Efficiency 100% (68/68)
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A1bg T G 15: 60,791,482 (GRCm39) probably benign Het
Abcg4 T G 9: 44,188,946 (GRCm39) probably benign Het
Afm C A 5: 90,693,243 (GRCm39) probably benign Het
Ahrr G A 13: 74,431,143 (GRCm39) probably benign Het
Aplnr T A 2: 84,967,620 (GRCm39) probably null Het
Arih2 T A 9: 108,488,926 (GRCm39) H264L probably damaging Het
Atp1a1 A T 3: 101,487,151 (GRCm39) I886N possibly damaging Het
Bmf A T 2: 118,380,103 (GRCm39) V14E probably damaging Het
Ccdc116 T C 16: 16,961,903 (GRCm39) E15G probably damaging Het
Ccdc175 T C 12: 72,182,739 (GRCm39) N427D possibly damaging Het
Cfap53 A G 18: 74,432,247 (GRCm39) H45R probably benign Het
Chd3 A G 11: 69,240,732 (GRCm39) L1569P probably damaging Het
Cntn2 G A 1: 132,443,918 (GRCm39) Q457* probably null Het
Coro1a A T 7: 126,300,585 (GRCm39) probably benign Het
Cracr2b T A 7: 141,043,672 (GRCm39) L91Q probably damaging Het
Ctdspl T C 9: 118,849,114 (GRCm39) probably null Het
Dip2b T A 15: 100,067,193 (GRCm39) L565Q probably damaging Het
Dip2c T A 13: 9,671,939 (GRCm39) C1004S probably damaging Het
Dnah11 A T 12: 118,009,257 (GRCm39) I2135N possibly damaging Het
Dnah14 A G 1: 181,596,972 (GRCm39) probably benign Het
Dnase1 T C 16: 3,856,810 (GRCm39) V147A probably damaging Het
Dusp8 T C 7: 141,635,791 (GRCm39) probably benign Het
Fer1l6 T C 15: 58,534,636 (GRCm39) Y1828H probably damaging Het
Flvcr1 A G 1: 190,740,388 (GRCm39) V544A probably benign Het
Fsd1l T C 4: 53,687,209 (GRCm39) V311A probably benign Het
Glud1 G A 14: 34,056,225 (GRCm39) G300S probably benign Het
Gstm3 T G 3: 107,875,156 (GRCm39) Y62S probably damaging Het
Gtse1 C T 15: 85,746,636 (GRCm39) P151S probably benign Het
Herc2 T C 7: 55,857,560 (GRCm39) S4048P probably benign Het
Hp1bp3 T A 4: 137,948,994 (GRCm39) I19K probably benign Het
Htr7 C A 19: 36,018,940 (GRCm39) probably benign Het
Il1a C T 2: 129,150,994 (GRCm39) D10N probably damaging Het
Il22ra2 A T 10: 19,500,206 (GRCm39) N39I probably damaging Het
Kcnn4 T C 7: 24,078,680 (GRCm39) C267R possibly damaging Het
Larp1 A G 11: 57,946,299 (GRCm39) K879R possibly damaging Het
Lcn5 T A 2: 25,551,417 (GRCm39) probably benign Het
Lep T A 6: 29,068,971 (GRCm39) C7* probably null Het
Magi2 A T 5: 20,816,053 (GRCm39) Y747F probably benign Het
Mast4 T C 13: 102,878,566 (GRCm39) T1223A probably damaging Het
Mcc C T 18: 44,579,000 (GRCm39) E803K probably damaging Het
Mtmr4 T C 11: 87,502,334 (GRCm39) I796T probably benign Het
Myef2 A T 2: 124,950,898 (GRCm39) D312E probably benign Het
Myl3 A C 9: 110,596,997 (GRCm39) D119A probably damaging Het
Myo19 T A 11: 84,778,995 (GRCm39) probably null Het
Naa15 T G 3: 51,377,640 (GRCm39) H763Q probably damaging Het
Pde5a C T 3: 122,618,551 (GRCm39) probably benign Het
Plpp2 C T 10: 79,363,078 (GRCm39) R184H probably benign Het
Rab19 T G 6: 39,366,621 (GRCm39) L179V probably damaging Het
Rims2 T A 15: 39,398,362 (GRCm39) M1087K probably damaging Het
Riox2 C A 16: 59,309,730 (GRCm39) D361E probably benign Het
Sh3rf1 T A 8: 61,679,327 (GRCm39) V123E probably damaging Het
Slc35e1 A T 8: 73,238,553 (GRCm39) N318K probably damaging Het
Slc9a2 A T 1: 40,802,762 (GRCm39) E604V probably benign Het
Srp72 T C 5: 77,135,732 (GRCm39) S221P probably damaging Het
Tbx19 A T 1: 164,988,089 (GRCm39) S15T possibly damaging Het
Tcea2 A G 2: 181,327,610 (GRCm39) T112A probably benign Het
Tesk1 T A 4: 43,445,368 (GRCm39) D230E probably damaging Het
Tm4sf5 C T 11: 70,401,538 (GRCm39) A179V probably damaging Het
Tnr G T 1: 159,679,986 (GRCm39) G320V probably damaging Het
Trappc11 A T 8: 47,956,355 (GRCm39) C874S possibly damaging Het
Trpm3 T A 19: 22,891,810 (GRCm39) Y885N probably damaging Het
Unc5a T A 13: 55,150,692 (GRCm39) C505S probably damaging Het
Vmn1r28 G A 6: 58,242,702 (GRCm39) A182T probably benign Het
Xpo5 T C 17: 46,515,712 (GRCm39) probably benign Het
Zfp637 C A 6: 117,822,629 (GRCm39) H252Q probably damaging Het
Zfp646 T A 7: 127,479,903 (GRCm39) D693E probably damaging Het
Other mutations in Gm4847
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00726:Gm4847 APN 1 166,457,961 (GRCm39) missense possibly damaging 0.55
IGL00943:Gm4847 APN 1 166,469,922 (GRCm39) missense probably benign 0.01
IGL00948:Gm4847 APN 1 166,457,907 (GRCm39) missense probably benign 0.01
IGL01146:Gm4847 APN 1 166,462,521 (GRCm39) missense probably damaging 1.00
IGL01345:Gm4847 APN 1 166,462,541 (GRCm39) missense probably damaging 1.00
IGL01654:Gm4847 APN 1 166,465,917 (GRCm39) missense probably damaging 1.00
IGL01817:Gm4847 APN 1 166,462,471 (GRCm39) missense probably damaging 1.00
IGL02028:Gm4847 APN 1 166,469,765 (GRCm39) missense probably benign 0.23
IGL02031:Gm4847 APN 1 166,462,578 (GRCm39) missense probably damaging 1.00
IGL02412:Gm4847 APN 1 166,469,307 (GRCm39) missense probably damaging 0.98
IGL03278:Gm4847 APN 1 166,462,605 (GRCm39) missense probably benign 0.06
Disturbance UTSW 1 166,467,677 (GRCm39) missense probably damaging 1.00
ruckus UTSW 1 166,457,824 (GRCm39) missense probably benign 0.07
PIT4494001:Gm4847 UTSW 1 166,467,587 (GRCm39) missense probably damaging 1.00
R0009:Gm4847 UTSW 1 166,458,055 (GRCm39) missense probably benign 0.00
R0121:Gm4847 UTSW 1 166,469,857 (GRCm39) missense probably damaging 1.00
R0492:Gm4847 UTSW 1 166,457,961 (GRCm39) missense probably damaging 1.00
R0973:Gm4847 UTSW 1 166,457,824 (GRCm39) missense probably benign 0.07
R1136:Gm4847 UTSW 1 166,457,935 (GRCm39) missense probably damaging 0.98
R1522:Gm4847 UTSW 1 166,469,219 (GRCm39) missense probably damaging 1.00
R1730:Gm4847 UTSW 1 166,465,908 (GRCm39) missense possibly damaging 0.80
R1818:Gm4847 UTSW 1 166,465,788 (GRCm39) missense probably damaging 1.00
R1819:Gm4847 UTSW 1 166,465,788 (GRCm39) missense probably damaging 1.00
R2145:Gm4847 UTSW 1 166,462,472 (GRCm39) missense probably benign 0.00
R4628:Gm4847 UTSW 1 166,457,964 (GRCm39) missense probably damaging 1.00
R4850:Gm4847 UTSW 1 166,469,908 (GRCm39) missense probably damaging 1.00
R5065:Gm4847 UTSW 1 166,462,359 (GRCm39) missense probably damaging 0.99
R5068:Gm4847 UTSW 1 166,465,953 (GRCm39) missense possibly damaging 0.81
R5493:Gm4847 UTSW 1 166,457,890 (GRCm39) missense probably damaging 1.00
R5500:Gm4847 UTSW 1 166,462,611 (GRCm39) missense probably damaging 1.00
R5990:Gm4847 UTSW 1 166,470,942 (GRCm39) missense probably benign 0.00
R6018:Gm4847 UTSW 1 166,471,017 (GRCm39) missense probably damaging 1.00
R6178:Gm4847 UTSW 1 166,469,905 (GRCm39) missense probably damaging 1.00
R6190:Gm4847 UTSW 1 166,457,892 (GRCm39) missense probably damaging 0.98
R6220:Gm4847 UTSW 1 166,462,541 (GRCm39) missense probably damaging 1.00
R6654:Gm4847 UTSW 1 166,457,956 (GRCm39) missense probably damaging 1.00
R7634:Gm4847 UTSW 1 166,460,249 (GRCm39) missense probably benign
R7796:Gm4847 UTSW 1 166,469,819 (GRCm39) missense probably damaging 0.96
R7856:Gm4847 UTSW 1 166,462,395 (GRCm39) missense probably damaging 1.00
R7877:Gm4847 UTSW 1 166,467,575 (GRCm39) missense possibly damaging 0.48
R8130:Gm4847 UTSW 1 166,465,917 (GRCm39) missense probably damaging 1.00
R8361:Gm4847 UTSW 1 166,469,839 (GRCm39) missense possibly damaging 0.69
R8496:Gm4847 UTSW 1 166,469,761 (GRCm39) missense possibly damaging 0.84
R8935:Gm4847 UTSW 1 166,469,789 (GRCm39) missense probably damaging 1.00
R9023:Gm4847 UTSW 1 166,469,332 (GRCm39) missense probably damaging 1.00
R9055:Gm4847 UTSW 1 166,467,677 (GRCm39) missense probably damaging 1.00
R9310:Gm4847 UTSW 1 166,460,281 (GRCm39) missense probably benign
R9513:Gm4847 UTSW 1 166,462,541 (GRCm39) missense probably damaging 1.00
R9653:Gm4847 UTSW 1 166,467,582 (GRCm39) missense possibly damaging 0.92
X0018:Gm4847 UTSW 1 166,462,519 (GRCm39) missense probably benign 0.24
X0024:Gm4847 UTSW 1 166,460,284 (GRCm39) missense possibly damaging 0.87
Z1177:Gm4847 UTSW 1 166,462,342 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- GGTGAGATTGTTTGACCACACGGG -3'
(R):5'- GAGACCATATTGTGCCTAAGGGAGTTG -3'

Sequencing Primer
(F):5'- TTGACCACACGGGTTCTCAG -3'
(R):5'- TGTGCCTAAGGGAGTTGAAGAAAG -3'
Posted On 2013-05-23