Incidental Mutation 'R7637:Gm40460'
ID 590014
Institutional Source Beutler Lab
Gene Symbol Gm40460
Ensembl Gene ENSMUSG00000110324
Gene Name predicted gene, 40460
Synonyms
MMRRC Submission 045695-MU
Accession Numbers
Essential gene? Not available question?
Stock # R7637 (G1)
Quality Score 101.592
Status Not validated
Chromosome 7
Chromosomal Location 141794081-141794815 bp(-) (GRCm39)
Type of Mutation small deletion (10 aa in frame mutation)
DNA Base Change (assembly) ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG to ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG at 141794450 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147331 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000211591]
AlphaFold A0A1B0GR10
Predicted Effect probably benign
Transcript: ENSMUST00000211591
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (51/51)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca6 T A 11: 110,109,778 (GRCm39) Q651L probably benign Het
Adam8 C T 7: 139,565,343 (GRCm39) V624I probably damaging Het
Cltc T C 11: 86,621,158 (GRCm39) H287R probably damaging Het
Cmya5 T C 13: 93,219,720 (GRCm39) K3243R possibly damaging Het
Dock5 G A 14: 68,023,789 (GRCm39) T1124M possibly damaging Het
Fam8a1 A T 13: 46,824,723 (GRCm39) M237L probably benign Het
Fars2 G T 13: 36,388,758 (GRCm39) K82N probably benign Het
Gm57858 T A 3: 36,101,025 (GRCm39) Q49L probably damaging Het
Gnat3 A G 5: 18,208,770 (GRCm39) D158G Het
Grhl2 A C 15: 37,328,574 (GRCm39) N400T probably damaging Het
Grin2c A T 11: 115,147,085 (GRCm39) probably null Het
Hipk4 A G 7: 27,222,973 (GRCm39) Y11C probably damaging Het
Hspa9 G T 18: 35,071,740 (GRCm39) A620E not run Het
Igkv12-89 A G 6: 68,812,083 (GRCm39) S29P probably benign Het
Itga8 A T 2: 12,113,998 (GRCm39) D1039E probably damaging Het
Itgae A T 11: 73,004,457 (GRCm39) D248V probably damaging Het
Kmt2c T C 5: 25,520,093 (GRCm39) K2006E probably damaging Het
Litafd C T 16: 8,501,510 (GRCm39) P59L unknown Het
Mdga1 C T 17: 30,051,353 (GRCm39) G934R probably benign Het
Mov10 T C 3: 104,703,201 (GRCm39) N896S probably benign Het
Ndufb6 A T 4: 40,273,080 (GRCm39) probably null Het
Nlk T C 11: 78,481,831 (GRCm39) probably null Het
Notch2 T A 3: 98,053,939 (GRCm39) S2201T probably damaging Het
Or5i1 A T 2: 87,613,778 (GRCm39) D298V probably damaging Het
Pank1 A C 19: 34,799,388 (GRCm39) probably null Het
Pdlim3 T C 8: 46,362,102 (GRCm39) F126S probably damaging Het
Pds5a C A 5: 65,795,947 (GRCm39) G648C probably benign Het
Plekhh3 T C 11: 101,055,153 (GRCm39) I567V unknown Het
Ppfia2 T C 10: 106,701,264 (GRCm39) probably null Het
Prl3d1 A G 13: 27,284,052 (GRCm39) D207G probably damaging Het
Prss23 T A 7: 89,159,454 (GRCm39) D205V probably benign Het
Pygl C T 12: 70,244,569 (GRCm39) probably null Het
Qsox2 A G 2: 26,111,032 (GRCm39) F111S probably damaging Het
Sart3 T C 5: 113,909,413 (GRCm39) N95S probably benign Het
Scpep1 A G 11: 88,820,046 (GRCm39) F414S probably damaging Het
Selenbp1 C A 3: 94,844,659 (GRCm39) Y105* probably null Het
Sirpa A G 2: 129,458,365 (GRCm39) D327G probably benign Het
Sowahc G A 10: 59,058,005 (GRCm39) R47H probably damaging Het
Szt2 T C 4: 118,251,025 (GRCm39) Y361C probably damaging Het
Taf3 A G 2: 9,945,804 (GRCm39) V600A probably benign Het
Tie1 T C 4: 118,330,175 (GRCm39) I1042M probably damaging Het
Tmem132e T A 11: 82,325,342 (GRCm39) L114Q probably damaging Het
Tmx3 A G 18: 90,555,233 (GRCm39) T317A probably damaging Het
Tppp3 A G 8: 106,194,924 (GRCm39) V69A probably benign Het
Tpr T C 1: 150,299,267 (GRCm39) Y1156H probably damaging Het
Trank1 A C 9: 111,194,364 (GRCm39) D796A possibly damaging Het
Tsc2 G A 17: 24,826,466 (GRCm39) P928S probably benign Het
Unc80 G T 1: 66,711,843 (GRCm39) V2722F possibly damaging Het
Vmn1r199 G T 13: 22,566,845 (GRCm39) L46F probably benign Het
Vps13a A T 19: 16,727,513 (GRCm39) H196Q probably benign Het
Wnt10a T A 1: 74,832,633 (GRCm39) C75* probably null Het
Zfp335 A G 2: 164,734,459 (GRCm39) probably null Het
Other mutations in Gm40460
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6822:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7016:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R7053:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R7083:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7087:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R7110:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R7184:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7224:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R7367:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R7411:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R7481:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R7491:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7553:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7643:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7663:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R7785:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R7871:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R7895:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R8054:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R8355:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R8389:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R8501:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R8509:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R8705:Gm40460 UTSW 7 141,794,734 (GRCm39) missense unknown
R8736:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R8815:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R8815:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R8862:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R8884:Gm40460 UTSW 7 141,794,555 (GRCm39) nonsense probably null
R8892:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R8915:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R8939:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R9034:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R9040:Gm40460 UTSW 7 141,794,171 (GRCm39) small deletion probably benign
R9122:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R9142:Gm40460 UTSW 7 141,794,499 (GRCm39) missense unknown
R9172:Gm40460 UTSW 7 141,794,447 (GRCm39) small deletion probably benign
R9217:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R9292:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R9314:Gm40460 UTSW 7 141,794,447 (GRCm39) small deletion probably benign
R9401:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R9556:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R9562:Gm40460 UTSW 7 141,794,701 (GRCm39) missense unknown
R9642:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R9731:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
R9741:Gm40460 UTSW 7 141,794,450 (GRCm39) small deletion probably benign
R9793:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
RF040:Gm40460 UTSW 7 141,794,554 (GRCm39) small deletion probably benign
Z1177:Gm40460 UTSW 7 141,794,643 (GRCm39) missense unknown
Z1177:Gm40460 UTSW 7 141,794,509 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGAACCTCAGATCTTGCACTG -3'
(R):5'- AAGGGAGGCTGTAGTTCCTG -3'

Sequencing Primer
(F):5'- AGCAGCAGGGCTTACAGC -3'
(R):5'- TCCTGTGGGGGCTGCAAG -3'
Posted On 2019-10-24