Incidental Mutation 'IGL02822:1110057P08Rik'
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ID361039
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1110057P08Rik
Ensembl Gene ENSMUSG00000068067
Gene NameRIKEN cDNA 1110057P08 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #IGL02822
Quality Score
Status
Chromosome16
Chromosomal Location89174735-89175199 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 89174795 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Arginine at position 2 (C2R)
Ref Sequence ENSEMBL: ENSMUSP00000086498 (fasta)
Predicted Effect unknown
Transcript: ENSMUST00000089097
AA Change: C2R
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931428F04Rik T C 8: 105,284,698 Y268C probably damaging Het
Aldh1a7 A G 19: 20,702,266 V382A possibly damaging Het
Asap2 T C 12: 21,265,910 V943A probably damaging Het
Bod1l C T 5: 41,794,345 V2908M possibly damaging Het
Casd1 C T 6: 4,630,017 T471I probably damaging Het
Col20a1 T C 2: 180,996,807 Y405H probably damaging Het
Evi5l T C 8: 4,187,248 I117T probably damaging Het
Fbxw5 A G 2: 25,503,010 N164S probably benign Het
Fga A G 3: 83,031,482 E388G probably damaging Het
Fgfr1 A G 8: 25,557,802 T55A probably benign Het
Gdpd4 T C 7: 97,971,924 V148A possibly damaging Het
Gm15448 T A 7: 3,816,918 T549S possibly damaging Het
Gm609 T C 16: 45,442,605 Y57C probably damaging Het
Gsap T A 5: 21,217,444 V137D probably damaging Het
Hsdl2 A G 4: 59,601,379 H117R possibly damaging Het
Htr4 T A 18: 62,428,184 probably benign Het
Ifitm1 T C 7: 140,968,278 V8A possibly damaging Het
Ikbkap A G 4: 56,774,520 probably null Het
Kdelr1 A G 7: 45,873,864 probably benign Het
Klra6 G T 6: 130,016,710 Y199* probably null Het
Mmp21 C T 7: 133,676,099 D333N possibly damaging Het
Mocs1 T C 17: 49,439,569 F189S probably damaging Het
Myo18b C T 5: 112,775,345 A1849T probably damaging Het
Naca C A 10: 128,039,345 probably benign Het
Nbea A T 3: 56,019,447 H778Q possibly damaging Het
Nlrp4c C T 7: 6,065,727 P209L probably damaging Het
Olfr125 T C 17: 37,835,643 Y215H possibly damaging Het
Olfr1254 A G 2: 89,789,100 L84P possibly damaging Het
Olfr1491 A G 19: 13,705,655 D276G probably benign Het
Osbpl9 A G 4: 109,072,921 S258P probably damaging Het
Pclaf A G 9: 65,901,593 E108G possibly damaging Het
Pla2r1 C A 2: 60,455,173 C699F probably damaging Het
Pnkp A G 7: 44,862,424 Y120C probably damaging Het
Psme4 T A 11: 30,848,204 probably benign Het
Rad54l2 A G 9: 106,710,407 S720P probably damaging Het
Rasa1 T C 13: 85,252,514 H301R probably damaging Het
Spg11 C A 2: 122,074,534 W1316L probably damaging Het
Ube2t C T 1: 134,973,950 probably benign Het
Vmn2r94 T A 17: 18,243,620 I803F probably benign Het
Other mutations in 1110057P08Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01503:1110057P08Rik APN 16 89174869 nonsense probably null
IGL02584:1110057P08Rik APN 16 89174856 missense unknown
R6060:1110057P08Rik UTSW 16 89169742 splice site probably null
Posted On2015-12-18