Incidental Mutation 'IGL01063:4930444P10Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930444P10Rik
Ensembl Gene ENSMUSG00000067795
Gene NameRIKEN cDNA 4930444P10 gene
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.069) question?
Stock #IGL01063
Quality Score
Chromosomal Location16065979-16093325 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 16078646 bp
Amino Acid Change Leucine to Stop codon at position 61 (L61*)
Ref Sequence ENSEMBL: ENSMUSP00000119257 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115367] [ENSMUST00000145070] [ENSMUST00000151004]
Predicted Effect probably null
Transcript: ENSMUST00000115367
AA Change: L92*
SMART Domains Protein: ENSMUSP00000111024
Gene: ENSMUSG00000067795
AA Change: L92*

low complexity region 93 100 N/A INTRINSIC
low complexity region 172 184 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000145070
AA Change: L61*
SMART Domains Protein: ENSMUSP00000137853
Gene: ENSMUSG00000067795
AA Change: L61*

low complexity region 62 69 N/A INTRINSIC
low complexity region 141 153 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000151004
AA Change: L61*
SMART Domains Protein: ENSMUSP00000119257
Gene: ENSMUSG00000067795
AA Change: L61*

low complexity region 62 69 N/A INTRINSIC
low complexity region 141 153 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110038F14Rik G A 15: 76,950,275 V124I probably damaging Het
Abca7 T C 10: 80,011,297 I1705T probably damaging Het
Ablim1 T A 19: 57,061,328 I393F probably damaging Het
Adamts5 A G 16: 85,899,834 L145P probably damaging Het
Ano6 T C 15: 95,948,429 I537T probably damaging Het
AU018091 T C 7: 3,162,313 I190V possibly damaging Het
Camk1 T A 6: 113,338,372 D155V probably damaging Het
Cdh6 A C 15: 13,064,495 I103S probably damaging Het
Cntnap1 A G 11: 101,181,788 D537G probably benign Het
Col6a3 T C 1: 90,802,332 K1144E probably damaging Het
Cpeb1 T A 7: 81,372,181 E71D probably benign Het
Cps1 T C 1: 67,195,166 L904P possibly damaging Het
Cyfip1 T A 7: 55,904,210 F700I probably damaging Het
Dmp1 G A 5: 104,207,099 M1I probably null Het
Efcab6 A T 15: 84,054,512 M1K probably null Het
Extl2 A T 3: 116,027,482 H312L possibly damaging Het
Fat4 C A 3: 38,890,579 A1207D possibly damaging Het
Flnb T C 14: 7,926,518 probably benign Het
Hdac10 G T 15: 89,123,868 A593E possibly damaging Het
Hdhd2 T C 18: 76,965,273 probably null Het
Kcnq2 A G 2: 181,109,789 probably benign Het
Kdm7a A G 6: 39,165,130 F405L probably damaging Het
Lypd6b C A 2: 49,943,630 probably benign Het
Mki67 A T 7: 135,694,922 D2794E possibly damaging Het
Mtmr14 T A 6: 113,266,326 F40I probably damaging Het
Olfr131 G T 17: 38,082,653 S108R possibly damaging Het
Olfr213 T A 6: 116,541,007 C185S probably damaging Het
Olfr476 A T 7: 107,967,534 I46F probably damaging Het
Olfr986 A T 9: 40,187,756 I214F probably benign Het
Ppargc1a C A 5: 51,474,322 V322L probably benign Het
Ppfibp1 T A 6: 147,029,697 M917K probably benign Het
Prkg2 C T 5: 98,969,936 probably null Het
Rfx4 A G 10: 84,868,382 E296G possibly damaging Het
Rfx8 T A 1: 39,682,950 K292* probably null Het
Scamp3 C A 3: 89,177,666 probably benign Het
Scn4a A T 11: 106,330,364 I823N possibly damaging Het
Sdk2 A G 11: 113,830,842 V1316A probably damaging Het
Setd2 T C 9: 110,573,673 V1794A probably damaging Het
Stard8 G T X: 99,073,088 R983L probably damaging Het
Tbc1d23 A T 16: 57,192,675 D311E probably benign Het
Tex21 T C 12: 76,198,818 H568R probably benign Het
Tex35 T C 1: 157,105,097 probably benign Het
Tgs1 T A 4: 3,591,292 F442I possibly damaging Het
Traf2 C A 2: 25,524,919 C303F probably benign Het
Trim56 A T 5: 137,114,500 V54D possibly damaging Het
Yars2 C T 16: 16,306,542 R338* probably null Het
Zfp668 A T 7: 127,866,282 C577S probably damaging Het
Other mutations in 4930444P10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1777:4930444P10Rik UTSW 1 16078589 missense possibly damaging 0.77
R4992:4930444P10Rik UTSW 1 16080877 missense probably damaging 0.98
R4999:4930444P10Rik UTSW 1 16068798 critical splice donor site probably null
R5229:4930444P10Rik UTSW 1 16080959 utr 5 prime probably benign
Z1177:4930444P10Rik UTSW 1 16082022 intron probably benign
Posted On2013-06-21