Incidental Mutation 'IGL02285:Gm7808'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7808
Ensembl Gene ENSMUSG00000091460
Gene Namepredicted pseudogene 7808
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02285
Quality Score
Chromosomal Location19927896-19928282 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to G at 19928051 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057596] [ENSMUST00000217347]
Predicted Effect probably benign
Transcript: ENSMUST00000057596
SMART Domains Protein: ENSMUSP00000058810
Gene: ENSMUSG00000051118

Pfam:7tm_4 31 308 3e-53 PFAM
Pfam:7tm_1 41 290 1.2e-24 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000082002
SMART Domains Protein: ENSMUSP00000136791
Gene: ENSMUSG00000091460

UBQ 1 72 3.73e-36 SMART
Ribosomal_L40e 77 128 1.02e-31 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000217347
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ago3 A G 4: 126,350,877 V672A possibly damaging Het
Arhgef28 A T 13: 98,051,028 V253D possibly damaging Het
Atg3 G A 16: 45,178,317 probably benign Het
Camsap1 T C 2: 25,929,802 D1557G probably damaging Het
Cdh7 A G 1: 110,138,191 T732A probably damaging Het
Col4a3bp A G 13: 96,616,482 H348R probably benign Het
Cyp3a13 T A 5: 137,909,967 I207F probably benign Het
Dock1 T G 7: 135,081,920 probably null Het
Drc7 A T 8: 95,071,233 probably benign Het
Drosha C A 15: 12,833,864 P18H unknown Het
Fbxl5 A G 5: 43,765,348 S243P possibly damaging Het
Filip1 A G 9: 79,820,126 C404R probably damaging Het
Gm1840 C T 8: 5,640,373 noncoding transcript Het
Gm5745 G A 9: 73,175,498 noncoding transcript Het
Hcn3 T C 3: 89,152,812 D175G probably damaging Het
Igkv1-117 A T 6: 68,121,535 M23L probably benign Het
Kif26a A G 12: 112,157,507 D182G probably damaging Het
Lmbr1 A G 5: 29,254,235 probably benign Het
Lypd4 T A 7: 24,865,440 Q91L probably damaging Het
Ncoa5 C T 2: 165,002,840 A37T probably damaging Het
Olfr600 G A 7: 103,346,038 R297* probably null Het
Olfr657 A G 7: 104,635,725 E17G probably benign Het
Olfr829 T A 9: 18,856,990 C122S possibly damaging Het
Ppp1r18 A G 17: 35,867,256 K8E probably damaging Het
Ppp3ca A G 3: 136,928,626 probably benign Het
Ptpn12 T A 5: 21,055,713 Q12L probably benign Het
Rpgrip1l A G 8: 91,232,907 F1122L possibly damaging Het
Rps15 G T 10: 80,293,762 M43I probably benign Het
Rrp15 T C 1: 186,721,395 probably benign Het
Sash1 A T 10: 8,740,334 M588K probably damaging Het
Slc12a7 A G 13: 73,795,595 probably benign Het
Slc25a13 A G 6: 6,042,643 V587A possibly damaging Het
Sugct T C 13: 17,672,596 D34G possibly damaging Het
Tdpoz2 T A 3: 93,652,291 I125F probably damaging Het
Trim52 T A 14: 106,107,268 L120Q probably damaging Het
Vmn1r85 T C 7: 13,084,784 I144M probably damaging Het
Vmn2r107 T C 17: 20,375,561 F792S probably damaging Het
Vsnl1 A G 12: 11,386,877 F34L probably damaging Het
Other mutations in Gm7808
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01614:Gm7808 APN 9 19928146 unclassified probably benign
IGL01878:Gm7808 APN 9 19928246 unclassified probably benign
IGL02120:Gm7808 APN 9 19928017 unclassified probably benign
R1718:Gm7808 UTSW 9 19928003 unclassified probably benign
R1900:Gm7808 UTSW 9 19928114 unclassified probably benign
Posted On2015-04-16