Incidental Mutation 'IGL01385:1700016C15Rik'
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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 #IGL01385
Quality Score
Chromosomal Location177729814-177753324 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 177741074 bp
Amino Acid Change Glycine to Arginine at position 46 (G46R)
Ref Sequence ENSEMBL: ENSMUSP00000016106 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000016106]
Predicted Effect probably benign
Transcript: ENSMUST00000016106
AA Change: G46R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000016106
Gene: ENSMUSG00000015962
AA Change: G46R

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


Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim1 A T 19: 57,068,914 S292R probably damaging Het
Adamts19 A G 18: 58,972,779 T749A probably damaging Het
Agap2 A T 10: 127,087,996 I747F unknown Het
Arhgap35 T A 7: 16,564,474 N222I probably damaging Het
Atp10b A G 11: 43,234,429 E1074G probably damaging Het
Brd3 T C 2: 27,464,089 T4A possibly damaging Het
Col6a6 A G 9: 105,783,666 S415P probably damaging Het
Dennd2a A G 6: 39,523,136 V165A probably damaging Het
Dnm1l T A 16: 16,341,453 E95V probably damaging Het
Dock9 A G 14: 121,580,583 Y1609H possibly damaging Het
Esm1 A C 13: 113,216,682 E166A possibly damaging Het
F2rl2 A C 13: 95,701,328 I294L probably benign Het
Gstt3 A G 10: 75,774,988 S187P probably benign Het
Katna1 T C 10: 7,752,810 C268R probably damaging Het
Mbd5 T A 2: 49,250,221 C66S possibly damaging Het
Naa35 G A 13: 59,601,066 E167K probably damaging Het
Olfr1330 T C 4: 118,893,551 L156S probably benign Het
Osbpl2 A G 2: 180,137,080 N2S probably benign Het
Parp6 T C 9: 59,630,612 probably benign Het
Pcdhb5 T A 18: 37,322,214 V549E probably benign Het
Pcnx4 T C 12: 72,573,746 L780P probably damaging Het
Plcb3 A T 19: 6,957,908 D851E probably benign Het
Ppfia2 A G 10: 106,913,699 S1149G probably damaging Het
Prkca A G 11: 107,978,352 V469A probably damaging Het
Ryr1 A T 7: 29,056,985 V3468D probably damaging Het
Stxbp4 A G 11: 90,540,248 V412A possibly damaging Het
Vmn1r238 G T 18: 3,122,770 Q215K possibly damaging Het
Wdr11 A G 7: 129,607,913 M482V probably benign Het
Wdr72 T C 9: 74,179,506 probably benign Het
Xirp2 T C 2: 67,509,677 L754P probably damaging Het
Zmym6 G A 4: 127,124,106 G1135S probably benign Het
Other mutations in 1700016C15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01542:1700016C15Rik APN 1 177743384 missense possibly damaging 0.94
IGL02329:1700016C15Rik APN 1 177743301 missense probably benign 0.05
N/A:1700016C15Rik UTSW 1 177733534 missense probably damaging 0.99
R0850:1700016C15Rik UTSW 1 177741005 missense probably benign
Posted On2013-11-05