Incidental Mutation 'IGL03255:1600012P17Rik'
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ID414617
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1600012P17Rik
Ensembl Gene ENSMUSG00000047661
Gene NameRIKEN cDNA 1600012P17 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #IGL03255
Quality Score
Status
Chromosome1
Chromosomal Location158967701-158980463 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 158969351 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000062159
SMART Domains Protein: ENSMUSP00000057224
Gene: ENSMUSG00000047661

DomainStartEndE-ValueType
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

DomainStartEndE-ValueType
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