Incidental Mutation 'IGL02555:2010109I03Rik'
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Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2010109I03Rik
Ensembl Gene ENSMUSG00000063522
Gene NameRIKEN cDNA 2010109I03 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.028) question?
Stock #IGL02555
Quality Score
Chromosomal Location74876987-74897021 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) G to T at 74881608 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000076264 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077004]
Predicted Effect probably benign
Transcript: ENSMUST00000077004
SMART Domains Protein: ENSMUSP00000076264
Gene: ENSMUSG00000063522

signal peptide 1 20 N/A INTRINSIC
LU 21 100 6.96e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190826
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr1b G A 1: 36,701,747 R199C probably damaging Het
Adam9 T C 8: 24,966,736 N661D probably damaging Het
Amy1 C T 3: 113,564,892 E164K probably benign Het
Arid5b A C 10: 68,101,904 D221E probably benign Het
B3galt1 G T 2: 68,118,561 V207F probably benign Het
Begain A G 12: 109,034,189 S219P probably damaging Het
Clip1 A G 5: 123,621,794 probably null Het
Cps1 A G 1: 67,214,021 K1224R probably benign Het
Dnm1 A G 2: 32,328,038 Y449H probably damaging Het
Epas1 A T 17: 86,829,064 M755L probably benign Het
F13b T C 1: 139,517,186 C525R probably damaging Het
Fmnl2 A G 2: 53,126,851 probably null Het
Gm5346 A T 8: 43,625,268 C640S probably damaging Het
Ighv5-15 A G 12: 113,827,115 F3L probably benign Het
Inpp4a A G 1: 37,379,968 Q538R possibly damaging Het
Insrr A T 3: 87,813,817 M1092L probably damaging Het
Itgb8 C T 12: 119,189,881 V300M probably damaging Het
Kcnk5 A T 14: 20,141,985 H369Q probably benign Het
Olfr1023 G A 2: 85,887,398 M199I probably benign Het
Olfr1249 G A 2: 89,630,203 R232C probably damaging Het
Olfr1294 A G 2: 111,537,917 V124A probably damaging Het
Olfr24 T A 9: 18,755,473 H54L probably benign Het
Plxdc2 A G 2: 16,729,341 I417M probably benign Het
Polr1a G A 6: 71,920,457 E186K probably damaging Het
Ppp3cb A T 14: 20,530,953 F134L probably damaging Het
Prox2 C T 12: 85,095,260 W56* probably null Het
Scaf4 C T 16: 90,250,305 A395T unknown Het
Sh3tc2 G T 18: 61,990,237 A690S probably damaging Het
Slc34a1 T C 13: 55,401,168 S144P possibly damaging Het
Slc6a6 C T 6: 91,748,330 probably benign Het
Tubgcp3 A T 8: 12,639,595 M557K probably benign Het
Vmn2r103 A T 17: 19,811,611 D549V probably damaging Het
Washc2 T A 6: 116,209,100 N90K probably damaging Het
Other mutations in 2010109I03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01471:2010109I03Rik APN 15 74879900 missense probably benign
IGL02550:2010109I03Rik APN 15 74880755 missense probably damaging 1.00
R2905:2010109I03Rik UTSW 15 74879867 missense probably benign
R3547:2010109I03Rik UTSW 15 74881614 missense probably null 0.96
R4777:2010109I03Rik UTSW 15 74880683 missense probably benign
R6432:2010109I03Rik UTSW 15 74879964 missense probably benign 0.00
Posted On2015-04-16