Incidental Mutation 'IGL02329:1700016C15Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700016C15Rik
Ensembl Gene ENSMUSG00000015962
Gene NameRIKEN cDNA 1700016C15 gene
Accession Numbers

Genbank: NM_027077; MGI: 1916678

Is this an essential gene? Not available question?
Stock #IGL02329
Quality Score
Chromosomal Location177729814-177753324 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 177743301 bp
Amino Acid Change Glutamine to Leucine at position 67 (Q67L)
Ref Sequence ENSEMBL: ENSMUSP00000016106 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000016106]
Predicted Effect probably benign
Transcript: ENSMUST00000016106
AA Change: Q67L

PolyPhen 2 Score 0.053 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000016106
Gene: ENSMUSG00000015962
AA Change: Q67L

low complexity region 75 86 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI


Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atg2a T C 19: 6,249,929 probably null Het
Bfsp1 T C 2: 143,862,646 T96A probably benign Het
Btnl1 A G 17: 34,382,265 E322G possibly damaging Het
Cand2 T C 6: 115,789,607 V391A probably damaging Het
Ccdc169 A G 3: 55,171,281 M188V probably benign Het
Cngb1 T C 8: 95,242,359 I1174V probably benign Het
Cpeb4 T C 11: 31,872,316 V10A possibly damaging Het
Cpt1b T C 15: 89,423,739 T206A probably benign Het
Dapk3 T C 10: 81,190,165 S97P probably benign Het
Drc3 T C 11: 60,370,578 L185P probably damaging Het
Efr3b T C 12: 3,992,923 probably null Het
Erbb3 T A 10: 128,573,219 I742F probably damaging Het
Fktn A G 4: 53,720,181 Y65C probably benign Het
Fstl5 G A 3: 76,588,995 G355D probably damaging Het
Grm8 A T 6: 27,363,116 I800N probably damaging Het
Gss C T 2: 155,567,853 R221H probably benign Het
H2-M10.4 A T 17: 36,460,467 V273D probably damaging Het
Large1 C A 8: 73,048,317 W255L possibly damaging Het
Meig1 T C 2: 3,409,251 K71E probably damaging Het
Mtor A G 4: 148,534,939 N1760D probably benign Het
Ncapd2 A T 6: 125,189,818 N24K probably damaging Het
Nphp3 A C 9: 104,025,968 S715R probably benign Het
Papolg T G 11: 23,891,869 H18P probably damaging Het
Psd T C 19: 46,319,659 H667R possibly damaging Het
Rita1 C T 5: 120,609,793 A147T probably damaging Het
Rtp1 T C 16: 23,431,193 S103P probably damaging Het
Snx21 T C 2: 164,792,390 probably benign Het
Tiam1 G T 16: 89,800,036 H301N probably benign Het
Trcg1 A T 9: 57,240,393 I11F possibly damaging Het
Trpm6 A G 19: 18,854,217 K1482R probably benign Het
Tyw1 G T 5: 130,267,080 G116V probably benign Het
Zfp341 T C 2: 154,632,304 C343R possibly damaging Het
Other mutations in 1700016C15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01385:1700016C15Rik APN 1 177741074 missense probably benign
IGL01542:1700016C15Rik APN 1 177743384 missense possibly damaging 0.94
N/A:1700016C15Rik UTSW 1 177733534 missense probably damaging 0.99
R0850:1700016C15Rik UTSW 1 177741005 missense probably benign
R7739:1700016C15Rik UTSW 1 177743262 missense probably damaging 0.97
Z1176:1700016C15Rik UTSW 1 177741017 missense possibly damaging 0.95
Posted On2015-04-16