Incidental Mutation 'IGL01121:2700046A07Rik'
ID 53190
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2700046A07Rik
Ensembl Gene ENSMUSG00000041789
Gene Name RIKEN cDNA 2700046A07 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # IGL01121
Quality Score
Status
Chromosome 18
Chromosomal Location 62884745-62889418 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 62888219 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000048109
SMART Domains Protein: ENSMUSP00000046498
Gene: ENSMUSG00000041789

DomainStartEndE-ValueType
low complexity region 41 55 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000067450
SMART Domains Protein: ENSMUSP00000064287
Gene: ENSMUSG00000041789

DomainStartEndE-ValueType
low complexity region 41 55 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930432E11Rik A T 7: 29,273,426 (GRCm39) noncoding transcript Het
Alg3 T C 16: 20,429,397 (GRCm39) E31G probably damaging Het
Arhgap29 A G 3: 121,803,512 (GRCm39) E764G probably damaging Het
Atp5mf C A 5: 145,121,378 (GRCm39) V68L probably benign Het
Birc6 T A 17: 74,938,033 (GRCm39) I2645K probably benign Het
Capn11 A G 17: 45,950,058 (GRCm39) S369P probably benign Het
Car4 A T 11: 84,855,172 (GRCm39) probably null Het
Ccdc185 C T 1: 182,576,222 (GRCm39) V156I probably benign Het
Cpsf2 G T 12: 101,954,965 (GRCm39) E245D probably damaging Het
Dnah11 T C 12: 118,014,430 (GRCm39) D2019G probably benign Het
Dscc1 A G 15: 54,945,721 (GRCm39) probably benign Het
Dzip3 T C 16: 48,765,244 (GRCm39) D490G probably benign Het
E2f8 G A 7: 48,517,569 (GRCm39) Q745* probably null Het
Fat3 T A 9: 15,909,697 (GRCm39) T2102S probably benign Het
Fgf7 C T 2: 125,930,152 (GRCm39) probably benign Het
Fstl4 T C 11: 52,705,464 (GRCm39) F47L probably benign Het
Gm15097 A T X: 148,587,324 (GRCm39) R129S possibly damaging Het
Gm4297 C T X: 24,418,854 (GRCm39) D200N probably benign Het
Itgb5 G T 16: 33,740,359 (GRCm39) D490Y probably benign Het
Kansl1 A G 11: 104,226,422 (GRCm39) S912P probably benign Het
Kcnq3 A T 15: 65,877,826 (GRCm39) probably benign Het
Kctd6 A G 14: 8,222,656 (GRCm38) H166R possibly damaging Het
Kel T C 6: 41,679,343 (GRCm39) D140G probably benign Het
Lrif1 C A 3: 106,642,980 (GRCm39) S177* probably null Het
Lrp1 A T 10: 127,419,722 (GRCm39) C962* probably null Het
Lypd5 A T 7: 24,050,976 (GRCm39) Y29F probably benign Het
Mmrn1 A G 6: 60,952,928 (GRCm39) D403G possibly damaging Het
Nhsl1 T G 10: 18,387,458 (GRCm39) V244G probably damaging Het
Or6c35 T C 10: 129,168,804 (GRCm39) I18T probably benign Het
Ptprd A T 4: 75,872,438 (GRCm39) probably benign Het
Rcan2 A T 17: 44,328,775 (GRCm39) I69L probably damaging Het
Rprd2 A G 3: 95,683,862 (GRCm39) L373P probably damaging Het
Slc10a4 T C 5: 73,164,929 (GRCm39) C174R probably damaging Het
Tas2r134 C T 2: 51,518,001 (GRCm39) T160I probably damaging Het
Tbc1d19 T A 5: 54,054,404 (GRCm39) L464* probably null Het
Tmem45a2 C T 16: 56,861,153 (GRCm39) D225N possibly damaging Het
Unc79 G A 12: 103,131,890 (GRCm39) C2139Y probably damaging Het
Vmn2r101 G T 17: 19,809,936 (GRCm39) G241C probably damaging Het
Vmn2r91 T C 17: 18,356,766 (GRCm39) V811A possibly damaging Het
Wdr11 T C 7: 129,229,746 (GRCm39) Y844H probably benign Het
Wdr70 T C 15: 7,902,655 (GRCm39) K656E possibly damaging Het
Zfp579 C A 7: 4,996,246 (GRCm39) C555F possibly damaging Het
Other mutations in 2700046A07Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0855:2700046A07Rik UTSW 18 62,886,414 (GRCm39) splice site noncoding transcript
Posted On 2013-06-21