Incidental Mutation 'IGL02555:2010109I03Rik'
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ID298486
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2010109I03Rik
Ensembl Gene ENSMUSG00000063522
Gene NameRIKEN cDNA 2010109I03 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.028) question?
Stock #IGL02555
Quality Score
Status
Chromosome15
Chromosomal Location74876987-74897021 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) G to T at 74881608 bp
ZygosityHeterozygous
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

DomainStartEndE-ValueType
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