Incidental Mutation 'R6910:Gm17655'
ID 538972
Institutional Source Beutler Lab
Gene Symbol Gm17655
Ensembl Gene ENSMUSG00000090963
Gene Name predicted gene, 17655
Synonyms
MMRRC Submission 045002-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R6910 (G1)
Quality Score 211.009
Status Validated
Chromosome 5
Chromosomal Location 110194007-110195416 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 110195039 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 248 (R248*)
Ref Sequence ENSEMBL: ENSMUSP00000148155 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167969] [ENSMUST00000210275]
AlphaFold A0A1B0GT13
Predicted Effect probably benign
Transcript: ENSMUST00000167969
SMART Domains Protein: ENSMUSP00000128849
Gene: ENSMUSG00000090963

DomainStartEndE-ValueType
ZnF_C2H2 4 26 1.47e-3 SMART
ZnF_C2H2 32 54 3.63e-3 SMART
ZnF_C2H2 60 82 1.38e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000210275
AA Change: R248*
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.4%
  • 20x: 98.2%
Validation Efficiency 100% (37/37)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cfap54 A G 10: 92,672,374 (GRCm39) S2899P probably benign Het
Chil5 A G 3: 105,926,977 (GRCm39) W82R probably damaging Het
Dennd3 A G 15: 73,426,965 (GRCm39) T781A probably benign Het
Epha2 A G 4: 141,048,824 (GRCm39) D597G probably damaging Het
Gcn1 A G 5: 115,744,597 (GRCm39) T1598A probably benign Het
Glp2r A G 11: 67,621,497 (GRCm39) F162S probably benign Het
Gnptab G A 10: 88,267,258 (GRCm39) G450S probably damaging Het
Gpatch2l G A 12: 86,290,958 (GRCm39) R47H probably damaging Het
Hapln2 A G 3: 87,931,135 (GRCm39) Y127H probably damaging Het
Hdac4 G T 1: 91,909,875 (GRCm39) T463K probably damaging Het
Ift80 A C 3: 68,835,068 (GRCm39) S458A probably benign Het
Lama1 A G 17: 68,098,459 (GRCm39) D1846G possibly damaging Het
Map3k8 A G 18: 4,340,801 (GRCm39) I171T probably benign Het
Micu1 A G 10: 59,576,489 (GRCm39) E115G probably damaging Het
Mrpl39 A G 16: 84,532,080 (GRCm39) V9A unknown Het
Ncoa7 T G 10: 30,570,117 (GRCm39) I281L possibly damaging Het
Nms A G 1: 38,980,976 (GRCm39) E54G probably benign Het
Nrip1 G A 16: 76,091,305 (GRCm39) A84V probably damaging Het
Or10ak9 T A 4: 118,726,335 (GRCm39) M119K probably damaging Het
Or11g27 G A 14: 50,771,330 (GRCm39) V154M probably benign Het
Pcdhga10 T A 18: 37,881,285 (GRCm39) S349T probably damaging Het
R3hcc1 G A 14: 69,935,024 (GRCm39) P454L probably damaging Het
Rsrc1 C T 3: 66,901,982 (GRCm39) P44L unknown Het
Ryr3 T C 2: 112,788,520 (GRCm39) D170G probably damaging Het
Sanbr A G 11: 23,570,447 (GRCm39) V151A probably damaging Het
Scp2 C A 4: 107,962,283 (GRCm39) G81C probably damaging Het
Sez6 A G 11: 77,844,695 (GRCm39) T173A possibly damaging Het
Syne1 T C 10: 4,998,887 (GRCm39) H8142R probably benign Het
Tcof1 G C 18: 60,962,123 (GRCm39) A702G possibly damaging Het
Tnfrsf11a A G 1: 105,772,272 (GRCm39) T520A probably damaging Het
Tpm1 A G 9: 66,939,256 (GRCm39) S170P probably damaging Het
Try5 T C 6: 41,288,733 (GRCm39) D54G possibly damaging Het
Vmn2r-ps158 T C 7: 42,673,475 (GRCm39) F178L probably benign Het
Zan T C 5: 137,417,342 (GRCm39) E3041G unknown Het
Zfp1001 A T 2: 150,165,987 (GRCm39) Q56L probably benign Het
Zfp616 A T 11: 73,975,828 (GRCm39) H699L probably damaging Het
Other mutations in Gm17655
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6041:Gm17655 UTSW 5 110,195,439 (GRCm39) missense possibly damaging 0.62
R6829:Gm17655 UTSW 5 110,194,792 (GRCm39) missense probably damaging 1.00
R9722:Gm17655 UTSW 5 110,194,226 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- CAAGAAGCAAAAGATTTACTGCATTGA -3'
(R):5'- CCTTTGCAGGACACCATACT -3'

Sequencing Primer
(F):5'- TGCATTGATTACATTCATAACGTTTC -3'
(R):5'- GTGGTAAAGCCTTTGCACAAC -3'
Posted On 2018-11-06