Incidental Mutation 'R6649:Gm6902'
ID 527678
Institutional Source Beutler Lab
Gene Symbol Gm6902
Ensembl Gene ENSMUSG00000094682
Gene Name predicted gene 6902
Synonyms
MMRRC Submission 044770-MU
Accession Numbers
Essential gene? Not available question?
Stock # R6649 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 22972213-22974668 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 22973159 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Proline at position 123 (T123P)
Ref Sequence ENSEMBL: ENSMUSP00000140400 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000179072] [ENSMUST00000191169]
AlphaFold Q3UTA8
Predicted Effect possibly damaging
Transcript: ENSMUST00000179072
AA Change: T123P

PolyPhen 2 Score 0.819 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000136627
Gene: ENSMUSG00000094682
AA Change: T123P

DomainStartEndE-ValueType
S_TKc 27 275 5.54e-90 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000191169
AA Change: T123P

PolyPhen 2 Score 0.819 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000140400
Gene: ENSMUSG00000094682
AA Change: T123P

DomainStartEndE-ValueType
S_TKc 27 275 5.54e-90 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208529
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.3%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 T A 19: 43,800,941 (GRCm39) H627Q probably benign Het
Abra G A 15: 41,732,629 (GRCm39) L146F probably benign Het
Adamts7 T C 9: 90,073,990 (GRCm39) C857R probably damaging Het
Ankhd1 A T 18: 36,733,836 (GRCm39) probably null Het
Asb15 A G 6: 24,562,632 (GRCm39) N198S probably benign Het
Asb16 A T 11: 102,159,863 (GRCm39) Q72L possibly damaging Het
Atosa T G 9: 74,917,432 (GRCm39) L677R probably damaging Het
Bbox1 G T 2: 110,135,914 (GRCm39) H22N probably benign Het
Bcdin3d T C 15: 99,368,696 (GRCm39) T168A probably damaging Het
Bmp1 A T 14: 70,728,058 (GRCm39) W624R probably damaging Het
Cdh18 A T 15: 23,436,620 (GRCm39) Y492F possibly damaging Het
Cep290 A C 10: 100,354,393 (GRCm39) D848A probably benign Het
Cip2a A T 16: 48,837,829 (GRCm39) Q843L probably damaging Het
Cmya5 G C 13: 93,234,533 (GRCm39) S185C possibly damaging Het
Cops9 C T 1: 92,568,136 (GRCm39) probably benign Het
Cutal C T 2: 34,775,933 (GRCm39) T88I probably benign Het
Dlg4 G T 11: 69,914,779 (GRCm39) probably benign Het
Dnah7c C A 1: 46,688,500 (GRCm39) T1890K probably benign Het
Dnah7c A G 1: 46,688,511 (GRCm39) S1894G probably benign Het
Eef2 CCC CCCC 10: 81,014,602 (GRCm39) probably null Het
Erp44 T C 4: 48,205,130 (GRCm39) I288V probably null Het
Fat3 T C 9: 16,288,038 (GRCm39) D495G probably damaging Het
Fsip2 T C 2: 82,798,161 (GRCm39) V485A possibly damaging Het
Gm14496 A T 2: 181,639,269 (GRCm39) H453L possibly damaging Het
Gm17027 T C 14: 41,981,236 (GRCm39) T207A unknown Het
Gpat2 T G 2: 127,274,355 (GRCm39) W366G possibly damaging Het
Heatr6 A T 11: 83,650,191 (GRCm39) T216S probably benign Het
Hsd17b14 T C 7: 45,205,500 (GRCm39) V11A probably damaging Het
Jak2 T A 19: 29,266,110 (GRCm39) I517N probably benign Het
Kmt5b G A 19: 3,857,295 (GRCm39) G351R probably damaging Het
Mau2 G T 8: 70,484,166 (GRCm39) Q141K possibly damaging Het
Mfsd13a T C 19: 46,356,305 (GRCm39) F137L probably damaging Het
Mfsd13a A G 19: 46,360,704 (GRCm39) H394R probably benign Het
Mfsd14b A T 13: 65,214,599 (GRCm39) I451N probably damaging Het
Milr1 C T 11: 106,648,537 (GRCm39) H143Y probably benign Het
Mon2 T G 10: 122,874,385 (GRCm39) K321T possibly damaging Het
Nlrp9c T A 7: 26,070,747 (GRCm39) N945Y probably damaging Het
Nwd2 A G 5: 63,882,527 (GRCm39) R60G possibly damaging Het
Or2z2 A T 11: 58,346,394 (GRCm39) I127N probably damaging Het
Or52b2 T C 7: 104,986,914 (GRCm39) H3R probably benign Het
Or8g20 A G 9: 39,396,048 (GRCm39) V164A probably benign Het
Papola A T 12: 105,778,566 (GRCm39) I315L possibly damaging Het
Phf3 A T 1: 30,844,104 (GRCm39) S1618R possibly damaging Het
Phyhipl A G 10: 70,404,843 (GRCm39) F77L probably damaging Het
Ppp3cb A G 14: 20,581,094 (GRCm39) L110P probably damaging Het
Prss53 T G 7: 127,485,747 (GRCm39) E531A probably benign Het
Raf1 A T 6: 115,608,302 (GRCm39) H236Q probably benign Het
Ryr2 A G 13: 11,610,529 (GRCm39) V4099A probably damaging Het
Sfxn3 G A 19: 45,038,354 (GRCm39) probably null Het
Sh3pxd2b T C 11: 32,365,978 (GRCm39) probably null Het
Slco6c1 C T 1: 97,053,436 (GRCm39) S155N probably benign Het
Speer4f2 A G 5: 17,580,767 (GRCm39) T115A probably benign Het
Spry1 T C 3: 37,696,871 (GRCm39) I38T probably damaging Het
Tagap T C 17: 8,152,546 (GRCm39) V577A probably benign Het
Ubr4 C A 4: 139,200,935 (GRCm39) H4706Q possibly damaging Het
Vmn2r112 T A 17: 22,820,160 (GRCm39) L11Q probably null Het
Zfp60 T C 7: 27,448,151 (GRCm39) F273S probably benign Het
Zfp938 A T 10: 82,061,232 (GRCm39) Y463N probably damaging Het
Other mutations in Gm6902
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01102:Gm6902 APN 7 22,973,087 (GRCm39) missense probably benign 0.26
R7545:Gm6902 UTSW 7 22,973,087 (GRCm39) missense probably benign 0.26
R7810:Gm6902 UTSW 7 22,973,243 (GRCm39) missense probably benign 0.08
R8219:Gm6902 UTSW 7 22,973,143 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- AAACCTGCCAGCTTTTGTCCAG -3'
(R):5'- TCCCCACAAGTACCTCTGTG -3'

Sequencing Primer
(F):5'- TTGTCCAGGAATCACTTCAGCAG -3'
(R):5'- GTACCTCTGTGGCTGTAAAAATTCTC -3'
Posted On 2018-07-23