Incidental Mutation 'R7317:Gm4553'
ID 563471
Institutional Source Beutler Lab
Gene Symbol Gm4553
Ensembl Gene ENSMUSG00000090471
Gene Name predicted gene 4553
Synonyms
MMRRC Submission 045369-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.110) question?
Stock # R7317 (G1)
Quality Score 214.458
Status Not validated
Chromosome 7
Chromosomal Location 141718433-141719476 bp(-) (GRCm39)
Type of Mutation small deletion (16 aa in frame mutation)
DNA Base Change (assembly) ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC to ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC at 141719157 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147863 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168049] [ENSMUST00000210925]
AlphaFold A0A1B0GSA9
Predicted Effect probably benign
Transcript: ENSMUST00000168049
SMART Domains Protein: ENSMUSP00000131778
Gene: ENSMUSG00000090471

DomainStartEndE-ValueType
low complexity region 18 238 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000210925
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam22 G A 5: 8,140,202 (GRCm39) P832L probably benign Het
Adamts17 C T 7: 66,490,304 (GRCm39) R129* probably null Het
Alg5 G T 3: 54,656,752 (GRCm39) R321L probably benign Het
Amotl1 T A 9: 14,486,515 (GRCm39) T460S probably benign Het
Ankrd50 T C 3: 38,537,332 (GRCm39) E7G possibly damaging Het
Ap3b2 T C 7: 81,110,776 (GRCm39) T1000A unknown Het
Arap2 G A 5: 62,807,067 (GRCm39) T1200M probably damaging Het
Asb2 A T 12: 103,299,616 (GRCm39) I272N probably damaging Het
Bicd2 T C 13: 49,531,784 (GRCm39) L342P probably damaging Het
C1qtnf6 T A 15: 78,409,206 (GRCm39) I214F probably damaging Het
Cdc42bpg T A 19: 6,364,534 (GRCm39) H587Q probably benign Het
Cfap70 T A 14: 20,450,502 (GRCm39) I1010F possibly damaging Het
Chd1 A T 17: 15,962,536 (GRCm39) K764N possibly damaging Het
Cluh A G 11: 74,556,530 (GRCm39) D956G possibly damaging Het
Ehbp1l1 T C 19: 5,770,730 (GRCm39) D243G probably benign Het
Ercc4 T C 16: 12,939,977 (GRCm39) V169A probably benign Het
Erich6 T C 3: 58,544,305 (GRCm39) E94G probably benign Het
Fubp3 A G 2: 31,494,624 (GRCm39) probably null Het
Gabbr1 C T 17: 37,380,305 (GRCm39) T736I probably damaging Het
Garre1 A G 7: 33,963,072 (GRCm39) V200A probably benign Het
Gm14496 T A 2: 181,637,613 (GRCm39) M229K possibly damaging Het
Gspt1 T C 16: 11,040,521 (GRCm39) T596A probably benign Het
H1f4 A G 13: 23,806,350 (GRCm39) I44T probably damaging Het
Htr5b T A 1: 121,438,157 (GRCm39) Y358F probably damaging Het
Il18r1 A T 1: 40,513,992 (GRCm39) Y66F possibly damaging Het
Il18rap A G 1: 40,564,536 (GRCm39) T189A probably damaging Het
Irag2 G A 6: 145,104,424 (GRCm39) G164R possibly damaging Het
Itgav G T 2: 83,625,327 (GRCm39) A771S probably benign Het
Klf11 T C 12: 24,705,518 (GRCm39) V324A possibly damaging Het
Krtap15-1 T C 16: 88,626,193 (GRCm39) C87R probably benign Het
Mapk8ip3 C T 17: 25,120,692 (GRCm39) G807D probably benign Het
Mbd5 A G 2: 49,169,755 (GRCm39) D1642G probably benign Het
Med15 G T 16: 17,489,507 (GRCm39) Q356K unknown Het
Mmp3 A G 9: 7,446,937 (GRCm39) Y39C probably damaging Het
Mon2 A G 10: 122,849,851 (GRCm39) S1149P probably damaging Het
Msh3 A G 13: 92,422,512 (GRCm39) I548T probably damaging Het
Noc2l T A 4: 156,323,673 (GRCm39) V179E possibly damaging Het
Or4b1b A T 2: 90,112,748 (GRCm39) M57K probably damaging Het
Or5k3 T G 16: 58,969,684 (GRCm39) M157R possibly damaging Het
Or5p64 G T 7: 107,854,425 (GRCm39) Q307K probably benign Het
Oxa1l A T 14: 54,598,312 (GRCm39) M1L probably benign Het
Pcdhb10 A T 18: 37,546,079 (GRCm39) Q385L possibly damaging Het
Pdzd2 T C 15: 12,592,329 (GRCm39) K105R probably damaging Het
Pex1 A T 5: 3,668,875 (GRCm39) D582V probably damaging Het
Pheta1 A T 5: 121,991,336 (GRCm39) T233S possibly damaging Het
Pi4ka A G 16: 17,223,496 (GRCm39) probably null Het
Pigw T C 11: 84,768,066 (GRCm39) N421S probably benign Het
Plek T C 11: 16,944,739 (GRCm39) K97R probably benign Het
R3hcc1l C T 19: 42,571,979 (GRCm39) R753* probably null Het
R3hdml G A 2: 163,344,367 (GRCm39) W252* probably null Het
Septin12 T C 16: 4,809,599 (GRCm39) K238E probably damaging Het
Sgce G A 6: 4,691,615 (GRCm39) T320I probably benign Het
Sidt2 A T 9: 45,854,988 (GRCm39) C562* probably null Het
Skint8 T C 4: 111,796,717 (GRCm39) C274R possibly damaging Het
Slc13a5 A T 11: 72,135,953 (GRCm39) M529K probably damaging Het
Smg8 T G 11: 86,976,391 (GRCm39) S397R possibly damaging Het
Spock3 G T 8: 63,566,590 (GRCm39) R68L possibly damaging Het
Stau2 T A 1: 16,530,553 (GRCm39) H122L unknown Het
Tent5a G C 9: 85,206,670 (GRCm39) A376G possibly damaging Het
Tert G A 13: 73,790,495 (GRCm39) R858H probably damaging Het
Tgm3 G A 2: 129,890,211 (GRCm39) R658Q probably benign Het
Tmc4 A G 7: 3,672,918 (GRCm39) I455T probably benign Het
Tmtc4 G A 14: 123,215,593 (GRCm39) P18S probably benign Het
Tnc A G 4: 63,890,959 (GRCm39) I1641T probably damaging Het
Trav14-3 A T 14: 54,000,951 (GRCm39) N54I probably damaging Het
Ttll13 A C 7: 79,903,911 (GRCm39) K280Q probably damaging Het
Unc5c T A 3: 141,495,703 (GRCm39) M524K probably benign Het
Unc93a A G 17: 13,335,171 (GRCm39) F292L probably benign Het
Uso1 A G 5: 92,321,851 (GRCm39) N248S possibly damaging Het
Usp5 A G 6: 124,803,281 (GRCm39) L73P probably damaging Het
Utp20 T A 10: 88,598,797 (GRCm39) I60F possibly damaging Het
Vmn2r94 T A 17: 18,463,882 (GRCm39) I803F probably benign Het
Other mutations in Gm4553
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00323:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00324:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00325:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00329:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00332:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00336:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00337:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00338:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00339:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL00340:Gm4553 APN 7 141,718,964 (GRCm39) missense unknown
IGL01348:Gm4553 APN 7 141,718,909 (GRCm39) missense unknown
R0468:Gm4553 UTSW 7 141,719,362 (GRCm39) missense unknown
R0568:Gm4553 UTSW 7 141,719,357 (GRCm39) missense unknown
R0932:Gm4553 UTSW 7 141,719,423 (GRCm39) missense unknown
R4988:Gm4553 UTSW 7 141,718,729 (GRCm39) unclassified probably benign
R5050:Gm4553 UTSW 7 141,718,773 (GRCm39) missense unknown
R7372:Gm4553 UTSW 7 141,719,157 (GRCm39) small deletion probably benign
R7709:Gm4553 UTSW 7 141,719,384 (GRCm39) missense unknown
R7901:Gm4553 UTSW 7 141,718,602 (GRCm39) small deletion probably benign
R8179:Gm4553 UTSW 7 141,718,594 (GRCm39) missense unknown
R8296:Gm4553 UTSW 7 141,719,458 (GRCm39) missense unknown
R8510:Gm4553 UTSW 7 141,719,025 (GRCm39) small deletion probably benign
R8549:Gm4553 UTSW 7 141,719,157 (GRCm39) small deletion probably benign
R9288:Gm4553 UTSW 7 141,719,025 (GRCm39) small deletion probably benign
R9335:Gm4553 UTSW 7 141,719,157 (GRCm39) small deletion probably benign
R9497:Gm4553 UTSW 7 141,719,298 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- AGCAACCGGGCTTACAACAG -3'
(R):5'- AGCTGTTGCAAGCCTGTGTG -3'

Sequencing Primer
(F):5'- GGGCTTACAACAGCTGGAC -3'
(R):5'- CAAGCCTGTGTGCTGCTG -3'
Posted On 2019-06-26