Incidental Mutation 'IGL01542:1700016C15Rik'
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 #IGL01542
Quality Score
Chromosomal Location177729814-177753324 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 177743384 bp
Amino Acid Change Threonine to Alanine at position 95 (T95A)
Ref Sequence ENSEMBL: ENSMUSP00000016106 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000016106]
Predicted Effect possibly damaging
Transcript: ENSMUST00000016106
AA Change: T95A

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000016106
Gene: ENSMUSG00000015962
AA Change: T95A

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


Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arap3 G A 18: 37,990,836 R377C probably damaging Het
Arhgap20 A G 9: 51,838,887 M316V probably benign Het
Chd7 T G 4: 8,859,285 N2458K possibly damaging Het
Clock T C 5: 76,231,475 E538G possibly damaging Het
Clpb G A 7: 101,787,505 V596I probably damaging Het
Col9a3 T C 2: 180,609,316 probably benign Het
D130043K22Rik G A 13: 24,876,037 probably null Het
Drd4 T C 7: 141,293,831 probably benign Het
Fam228b A T 12: 4,763,055 I105N probably damaging Het
Gm20939 A T 17: 94,874,293 probably benign Het
Gm4952 A G 19: 12,618,407 T54A possibly damaging Het
Hbs1l T C 10: 21,307,756 V132A probably benign Het
Kpna2 T A 11: 106,991,201 E266D probably benign Het
Lars T C 18: 42,214,827 E977G probably benign Het
Lrrn4 T C 2: 132,879,472 T142A probably benign Het
Myo19 T C 11: 84,909,546 L919P probably damaging Het
Nhlrc1 A T 13: 47,014,131 F217I probably damaging Het
Olfr1495 T C 19: 13,768,537 F65S probably damaging Het
Plch1 T C 3: 63,731,649 I468V probably damaging Het
Rergl T A 6: 139,493,498 probably null Het
Sctr A G 1: 120,044,769 probably benign Het
Sdhb T C 4: 140,972,967 V126A probably benign Het
Smad3 C T 9: 63,655,586 R214Q probably damaging Het
Tdrd9 T C 12: 112,046,989 M1219T possibly damaging Het
Tmem167b A T 3: 108,558,906 N75K possibly damaging Het
Vmn2r83 T C 10: 79,479,012 S365P probably benign Het
Vps16 T C 2: 130,438,394 F153L probably damaging Het
Other mutations in 1700016C15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01385:1700016C15Rik APN 1 177741074 missense probably benign
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
R7739:1700016C15Rik UTSW 1 177743262 missense probably damaging 0.97
Z1176:1700016C15Rik UTSW 1 177741017 missense possibly damaging 0.95
Posted On2013-12-03