Incidental Mutation 'IGL02646:1700013G24Rik'
ID 301939
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700013G24Rik
Ensembl Gene ENSMUSG00000041399
Gene Name RIKEN cDNA 1700013G24 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL02646
Quality Score
Status
Chromosome 4
Chromosomal Location 137180607-137182772 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 137182101 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 85 (Y85*)
Ref Sequence ENSEMBL: ENSMUSP00000043461 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048893]
AlphaFold Q9DAC6
Predicted Effect probably null
Transcript: ENSMUST00000048893
AA Change: Y85*
SMART Domains Protein: ENSMUSP00000043461
Gene: ENSMUSG00000041399
AA Change: Y85*

DomainStartEndE-ValueType
low complexity region 44 65 N/A INTRINSIC
low complexity region 181 203 N/A INTRINSIC
SCOP:d1i50b_ 216 261 3e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg2 A G 6: 58,662,681 (GRCm39) I508V probably benign Het
Adgrb2 T C 4: 129,913,075 (GRCm39) probably null Het
Api5 T A 2: 94,260,184 (GRCm39) H24L possibly damaging Het
Apoh T C 11: 108,302,968 (GRCm39) V311A probably benign Het
Atp2a3 C A 11: 72,866,165 (GRCm39) H262N probably benign Het
Brca2 G T 5: 150,484,255 (GRCm39) V2994L possibly damaging Het
Brd1 A T 15: 88,585,080 (GRCm39) V918D probably damaging Het
Calr3 T G 8: 73,197,304 (GRCm39) D43A possibly damaging Het
Cdh16 T C 8: 105,348,737 (GRCm39) probably null Het
Cep192 T C 18: 67,995,548 (GRCm39) S2033P probably damaging Het
Dnah7a G A 1: 53,564,194 (GRCm39) T1955M probably damaging Het
Dock10 T A 1: 80,551,840 (GRCm39) Y665F probably damaging Het
Dync1i1 A G 6: 5,767,034 (GRCm39) D86G probably benign Het
Eri2 T C 7: 119,385,331 (GRCm39) D390G possibly damaging Het
Fank1 C T 7: 133,481,758 (GRCm39) probably benign Het
Hoxb7 A T 11: 96,177,570 (GRCm39) Y6F possibly damaging Het
Hspg2 A C 4: 137,279,159 (GRCm39) S3081R possibly damaging Het
Kcnt1 T A 2: 25,790,892 (GRCm39) probably benign Het
Med13 A G 11: 86,174,212 (GRCm39) I1762T probably benign Het
Mia2 A G 12: 59,155,622 (GRCm39) D445G probably damaging Het
Or8h9 T C 2: 86,789,697 (GRCm39) Y35C probably damaging Het
Plcg2 A T 8: 118,330,622 (GRCm39) I827F possibly damaging Het
Poglut3 A G 9: 53,295,551 (GRCm39) D51G probably benign Het
Rnls C A 19: 33,115,684 (GRCm39) probably benign Het
Scn1a A T 2: 66,129,962 (GRCm39) probably null Het
Sec22b T A 3: 97,828,561 (GRCm39) V208E possibly damaging Het
Slc8a3 A T 12: 81,361,868 (GRCm39) I317N probably damaging Het
Snx33 A G 9: 56,834,043 (GRCm39) Y9H probably damaging Het
Stard9 C A 2: 120,529,473 (GRCm39) T1910N probably damaging Het
Tas2r122 T A 6: 132,688,753 (GRCm39) I47F probably damaging Het
Tedc1 T G 12: 113,120,921 (GRCm39) L118V possibly damaging Het
Tln2 A T 9: 67,163,278 (GRCm39) S1090T probably benign Het
Tpcn2 T C 7: 144,812,311 (GRCm39) D511G probably benign Het
Usp21 T C 1: 171,110,669 (GRCm39) probably benign Het
Vmn2r17 T A 5: 109,600,946 (GRCm39) L748Q probably damaging Het
Zp2 T C 7: 119,734,564 (GRCm39) D495G possibly damaging Het
Other mutations in 1700013G24Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01547:1700013G24Rik APN 4 137,182,573 (GRCm39) missense possibly damaging 0.82
R0526:1700013G24Rik UTSW 4 137,182,535 (GRCm39) missense possibly damaging 0.92
R1449:1700013G24Rik UTSW 4 137,182,666 (GRCm39) missense possibly damaging 0.94
R3743:1700013G24Rik UTSW 4 137,182,348 (GRCm39) missense probably damaging 0.96
R5357:1700013G24Rik UTSW 4 137,182,463 (GRCm39) missense possibly damaging 0.90
R6265:1700013G24Rik UTSW 4 137,181,986 (GRCm39) missense probably damaging 1.00
R6586:1700013G24Rik UTSW 4 137,182,639 (GRCm39) missense possibly damaging 0.90
R6720:1700013G24Rik UTSW 4 137,181,997 (GRCm39) missense possibly damaging 0.94
R6988:1700013G24Rik UTSW 4 137,181,890 (GRCm39) missense probably damaging 1.00
R7640:1700013G24Rik UTSW 4 137,181,905 (GRCm39) missense probably damaging 0.99
R7825:1700013G24Rik UTSW 4 137,182,654 (GRCm39) missense probably damaging 1.00
R8905:1700013G24Rik UTSW 4 137,182,553 (GRCm39) missense probably benign
R9536:1700013G24Rik UTSW 4 137,182,623 (GRCm39) missense probably damaging 0.99
Z1176:1700013G24Rik UTSW 4 137,182,303 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16