Incidental Mutation 'R6293:Gm9964'
ID 508567
Institutional Source Beutler Lab
Gene Symbol Gm9964
Ensembl Gene ENSMUSG00000055072
Gene Name predicted gene 9964
Synonyms
MMRRC Submission 044462-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.298) question?
Stock # R6293 (G1)
Quality Score 127.008
Status Validated
Chromosome 11
Chromosomal Location 79187005-79187732 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 79187420 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Methionine at position 9 (K9M)
Ref Sequence ENSEMBL: ENSMUSP00000063892 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000068448]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000068448
AA Change: K9M
SMART Domains Protein: ENSMUSP00000063892
Gene: ENSMUSG00000055072
AA Change: K9M

DomainStartEndE-ValueType
low complexity region 20 61 N/A INTRINSIC
transmembrane domain 83 105 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 96.4%
Validation Efficiency 98% (54/55)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 A G 3: 121,935,395 (GRCm39) D323G probably damaging Het
Abcb1b T C 5: 8,903,493 (GRCm39) I1048T probably benign Het
Adgra3 G A 5: 50,118,189 (GRCm39) P1120S probably benign Het
Alkbh8 G T 9: 3,347,841 (GRCm39) L211F possibly damaging Het
Ankrd27 T C 7: 35,307,885 (GRCm39) S375P possibly damaging Het
Apoc1 T A 7: 19,425,817 (GRCm39) T68S probably damaging Het
Arfgef2 T A 2: 166,715,508 (GRCm39) Y1318N possibly damaging Het
Camsap2 C A 1: 136,215,658 (GRCm39) R345L probably damaging Het
Ccdc38 C T 10: 93,398,659 (GRCm39) Q46* probably null Het
Cdk12 T A 11: 98,115,379 (GRCm39) M840K unknown Het
Cfap251 A C 5: 123,460,511 (GRCm39) N1158H probably damaging Het
Col12a1 A T 9: 79,521,640 (GRCm39) N2772K probably benign Het
Dthd1 A G 5: 63,000,193 (GRCm39) D505G probably damaging Het
Elf1 C T 14: 79,798,226 (GRCm39) H38Y probably damaging Het
Gcnt2 T A 13: 41,072,173 (GRCm39) V272D probably damaging Het
Gpr155 A G 2: 73,204,341 (GRCm39) S158P possibly damaging Het
Haus5 C T 7: 30,358,401 (GRCm39) W298* probably null Het
Hmcn2 T C 2: 31,225,463 (GRCm39) I124T probably damaging Het
Hydin A G 8: 111,324,543 (GRCm39) S4635G possibly damaging Het
Lrch2 C T X: 146,263,553 (GRCm39) A369T probably damaging Homo
Lrrc8c A G 5: 105,754,612 (GRCm39) Y129C probably damaging Het
Mbtd1 C T 11: 93,823,058 (GRCm39) H493Y possibly damaging Het
Mcm3ap C G 10: 76,307,312 (GRCm39) Y418* probably null Het
Mpdz A G 4: 81,278,293 (GRCm39) L764P probably damaging Het
Myt1l A G 12: 29,877,627 (GRCm39) D426G unknown Het
Ndel1 C T 11: 68,727,101 (GRCm39) R192H probably damaging Het
Nudt21 T C 8: 94,755,506 (GRCm39) D134G probably damaging Het
Nup210l A T 3: 90,022,371 (GRCm39) H113L probably damaging Het
Nxf1 A G 19: 8,746,546 (GRCm39) K586E probably damaging Het
Or2ag15 T C 7: 106,340,613 (GRCm39) H176R probably damaging Het
Or4s2 A G 2: 88,473,624 (GRCm39) E171G possibly damaging Het
Osbpl8 A G 10: 111,108,099 (GRCm39) Y365C possibly damaging Het
Pkd2l2 A G 18: 34,560,497 (GRCm39) Y368C probably damaging Het
Pkn2 A G 3: 142,515,465 (GRCm39) F649L probably benign Het
Pla2g4a T C 1: 149,755,798 (GRCm39) Y205C probably damaging Het
Prex2 A G 1: 11,232,522 (GRCm39) N863S probably benign Het
Prkdc A G 16: 15,605,019 (GRCm39) K2979R probably benign Het
Ptk6 T C 2: 180,840,253 (GRCm39) Y251C probably damaging Het
Rapgef6 T A 11: 54,525,607 (GRCm39) W334R probably damaging Het
Rbm11 A T 16: 75,393,655 (GRCm39) probably null Het
Rhbdl1 A G 17: 26,053,943 (GRCm39) L309P probably damaging Het
Rhbg G A 3: 88,153,133 (GRCm39) R274* probably null Het
Rpp30 A G 19: 36,081,845 (GRCm39) *269W probably null Het
Rsf1 GGCG GGCGACGGCCGCG 7: 97,229,113 (GRCm39) probably benign Homo
Slc44a1 A G 4: 53,561,099 (GRCm39) K605R probably damaging Het
Slco2a1 A G 9: 102,927,346 (GRCm39) S80G probably benign Het
Tmem50b A T 16: 91,380,164 (GRCm39) M71K probably damaging Het
Ttn G A 2: 76,579,673 (GRCm39) T23740M probably damaging Het
Tyro3 A G 2: 119,638,481 (GRCm39) T303A possibly damaging Het
Uba3 A T 6: 97,173,869 (GRCm39) D105E probably damaging Het
Vmn1r21 T C 6: 57,821,255 (GRCm39) D63G probably benign Het
Vstm2b T A 7: 40,549,533 (GRCm39) I63N probably damaging Het
Ylpm1 C G 12: 85,062,051 (GRCm39) P651A unknown Het
Zscan22 T A 7: 12,640,834 (GRCm39) C359* probably null Het
Other mutations in Gm9964
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01090:Gm9964 APN 11 79,187,210 (GRCm39) missense unknown
IGL02456:Gm9964 APN 11 79,187,196 (GRCm39) missense probably damaging 0.99
R3967:Gm9964 UTSW 11 79,187,202 (GRCm39) missense unknown
R6310:Gm9964 UTSW 11 79,187,476 (GRCm39) start gained probably benign
R8198:Gm9964 UTSW 11 79,187,405 (GRCm39) missense unknown
Z1088:Gm9964 UTSW 11 79,187,234 (GRCm39) missense unknown
Z1176:Gm9964 UTSW 11 79,187,226 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTGGTATTGCACTGCCTGAG -3'
(R):5'- AAGCAAGGCCTGTCTTCAAC -3'

Sequencing Primer
(F):5'- ACTGCCTGAGTGGTTTGTTTG -3'
(R):5'- GGTTTGATTCCCCAGTAGCACAG -3'
Posted On 2018-03-15