Incidental Mutation 'IGL03255:1600012P17Rik'
List |< first << previous [record 534639 of 534640] next >> last >|
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1600012P17Rik
Ensembl Gene ENSMUSG00000047661
Gene NameRIKEN cDNA 1600012P17 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.095) question?
Stock #IGL03255
Quality Score
Chromosomal Location158967701-158980463 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 158969351 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000062159
SMART Domains Protein: ENSMUSP00000057224
Gene: ENSMUSG00000047661

signal peptide 1 37 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159892
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162474
SMART Domains Protein: ENSMUSP00000136450
Gene: ENSMUSG00000047661

signal peptide 1 37 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alpk3 A G 7: 81,092,562 D709G probably benign Het
AY761184 T C 8: 21,703,518 T29A possibly damaging Het
Capn3 G T 2: 120,489,708 R309L probably damaging Het
Card11 T C 5: 140,898,331 I398V possibly damaging Het
Cps1 T A 1: 67,145,801 Y162* probably null Het
Defa26 A T 8: 21,618,241 D20V probably damaging Het
Dnah8 T G 17: 30,741,381 L2244R probably damaging Het
Fhad1 T A 4: 141,972,880 N353I possibly damaging Het
Flt1 T A 5: 147,588,521 probably benign Het
Glyr1 G A 16: 5,048,757 probably null Het
Gm10220 A G 5: 26,116,901 S258P possibly damaging Het
Lama3 A T 18: 12,539,703 D845V probably damaging Het
Myh2 T A 11: 67,193,225 L1558Q probably damaging Het
Nelfb G T 2: 25,203,195 H482N probably benign Het
Olfr290 T C 7: 84,916,517 L246P possibly damaging Het
Olfr482 A G 7: 108,094,817 V251A probably damaging Het
Ppfia2 A G 10: 106,896,507 T972A possibly damaging Het
Slc5a4a G A 10: 76,150,512 V85M probably damaging Het
Slc6a12 T G 6: 121,354,287 C166G probably damaging Het
Tm7sf3 T C 6: 146,606,120 probably benign Het
Tmem94 G T 11: 115,792,068 probably benign Het
Tmod2 T C 9: 75,577,258 probably benign Het
Tmprss11c T A 5: 86,271,482 I73F probably damaging Het
Vmn1r10 A G 6: 57,113,926 M168V probably benign Het
Vmn2r77 T A 7: 86,811,923 M819K probably benign Het
Vmo1 C T 11: 70,514,410 probably null Het
Ywhab A G 2: 164,014,016 D104G probably benign Het
Other mutations in 1600012P17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02551:1600012P17Rik APN 1 158969048 unclassified noncoding transcript
R1865:1600012P17Rik UTSW 1 158969524 unclassified noncoding transcript
R2020:1600012P17Rik UTSW 1 158968912 unclassified noncoding transcript
R4739:1600012P17Rik UTSW 1 158969334 unclassified noncoding transcript
R4762:1600012P17Rik UTSW 1 158969556 unclassified noncoding transcript
Posted On2016-08-02