Incidental Mutation 'IGL02034:Gm17019'
ID 184444
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17019
Ensembl Gene ENSMUSG00000091897
Gene Name predicted gene 17019
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL02034
Quality Score
Status
Chromosome 5
Chromosomal Location 15078964-15083012 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 15080266 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 182 (I182T)
Ref Sequence ENSEMBL: ENSMUSP00000127520 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000167908]
AlphaFold K7N6W5
Predicted Effect possibly damaging
Transcript: ENSMUST00000167908
AA Change: I182T

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000127520
Gene: ENSMUSG00000091897
AA Change: I182T

DomainStartEndE-ValueType
Pfam:Takusan 50 134 1.1e-30 PFAM
low complexity region 247 254 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bcor A G X: 11,905,498 (GRCm39) S1556P possibly damaging Het
Brd10 A G 19: 29,694,259 (GRCm39) S1745P possibly damaging Het
Ccdc6 T A 10: 70,004,978 (GRCm39) I241N probably benign Het
Cd81 T C 7: 142,619,986 (GRCm39) I48T probably damaging Het
Cfap52 A G 11: 67,837,118 (GRCm39) probably null Het
Cfap54 T C 10: 92,897,347 (GRCm39) M264V probably damaging Het
Cmya5 G A 13: 93,221,043 (GRCm39) probably benign Het
Csn2 A G 5: 87,843,941 (GRCm39) probably benign Het
Cyfip1 G A 7: 55,548,101 (GRCm39) R567Q probably damaging Het
Ehbp1 A G 11: 22,235,486 (GRCm39) probably null Het
Ermp1 G A 19: 29,623,359 (GRCm39) probably benign Het
Erv3 C T 2: 131,697,934 (GRCm39) V142I possibly damaging Het
Fzd2 A G 11: 102,495,730 (GRCm39) N58S probably damaging Het
Gcm2 G A 13: 41,259,269 (GRCm39) R67C probably damaging Het
Gpr45 T C 1: 43,072,478 (GRCm39) *374Q probably null Het
Haus8 T C 8: 71,708,202 (GRCm39) N165S probably damaging Het
Hoxd4 T A 2: 74,558,750 (GRCm39) L191Q probably damaging Het
I830077J02Rik A G 3: 105,834,565 (GRCm39) probably benign Het
Lpl T C 8: 69,333,424 (GRCm39) L7P possibly damaging Het
Lrp1b T A 2: 41,158,382 (GRCm39) K1612* probably null Het
Myh14 G T 7: 44,265,717 (GRCm39) A1546D possibly damaging Het
Nbea A G 3: 55,875,577 (GRCm39) S1698P probably damaging Het
Or10p22 A T 10: 128,826,570 (GRCm39) Q263L probably benign Het
Or4c112 C T 2: 88,854,015 (GRCm39) V111M probably benign Het
Or52e7 C A 7: 104,684,597 (GRCm39) T64N probably benign Het
Or5p51 G A 7: 107,444,385 (GRCm39) T185I probably benign Het
Otog A T 7: 45,945,417 (GRCm39) K40* probably null Het
Rgma C A 7: 73,067,181 (GRCm39) H145Q probably damaging Het
Rpgrip1l A T 8: 91,977,776 (GRCm39) probably null Het
Ssxb2 T A X: 8,324,743 (GRCm39) probably benign Het
Tmem175 C T 5: 108,790,002 (GRCm39) T118I probably damaging Het
Wdhd1 A G 14: 47,498,808 (GRCm39) V542A probably benign Het
Zfp977 G A 7: 42,230,136 (GRCm39) P130S probably damaging Het
Other mutations in Gm17019
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3617:Gm17019 UTSW 5 15,081,081 (GRCm39) missense possibly damaging 0.88
R5175:Gm17019 UTSW 5 15,082,817 (GRCm39) missense possibly damaging 0.92
R5520:Gm17019 UTSW 5 15,082,819 (GRCm39) missense possibly damaging 0.77
R7424:Gm17019 UTSW 5 15,079,386 (GRCm39) missense probably damaging 1.00
R7758:Gm17019 UTSW 5 15,079,300 (GRCm39) makesense probably null
R7762:Gm17019 UTSW 5 15,081,006 (GRCm39) missense probably benign 0.00
R7842:Gm17019 UTSW 5 15,081,049 (GRCm39) missense possibly damaging 0.58
R8898:Gm17019 UTSW 5 15,081,798 (GRCm39) missense possibly damaging 0.88
R9127:Gm17019 UTSW 5 15,081,113 (GRCm39) nonsense probably null
R9739:Gm17019 UTSW 5 15,082,841 (GRCm39) nonsense probably null
Z1176:Gm17019 UTSW 5 15,083,011 (GRCm39) start gained probably benign
Z1177:Gm17019 UTSW 5 15,082,945 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07