Incidental Mutation 'IGL01063:4930444P10Rik'
ID 50176
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930444P10Rik
Ensembl Gene ENSMUSG00000067795
Gene Name RIKEN cDNA 4930444P10 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # IGL01063
Quality Score
Status
Chromosome 1
Chromosomal Location 16136203-16163549 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 16148870 bp (GRCm39)
Zygosity Heterozygous
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]
AlphaFold D3YUR1
Predicted Effect probably null
Transcript: ENSMUST00000115367
AA Change: L92*
SMART Domains Protein: ENSMUSP00000111024
Gene: ENSMUSG00000067795
AA Change: L92*

DomainStartEndE-ValueType
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*

DomainStartEndE-ValueType
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*

DomainStartEndE-ValueType
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: 76,834,475 (GRCm39) V124I probably damaging Het
Abca7 T C 10: 79,847,131 (GRCm39) I1705T probably damaging Het
Ablim1 T A 19: 57,049,760 (GRCm39) I393F probably damaging Het
Adamts5 A G 16: 85,696,722 (GRCm39) L145P probably damaging Het
Ano6 T C 15: 95,846,310 (GRCm39) I537T probably damaging Het
AU018091 T C 7: 3,212,153 (GRCm39) I190V possibly damaging Het
Camk1 T A 6: 113,315,333 (GRCm39) D155V probably damaging Het
Cdh6 A C 15: 13,064,581 (GRCm39) I103S probably damaging Het
Cntnap1 A G 11: 101,072,614 (GRCm39) D537G probably benign Het
Col6a3 T C 1: 90,730,054 (GRCm39) K1144E probably damaging Het
Cpeb1 T A 7: 81,021,929 (GRCm39) E71D probably benign Het
Cps1 T C 1: 67,234,325 (GRCm39) L904P possibly damaging Het
Cyfip1 T A 7: 55,553,958 (GRCm39) F700I probably damaging Het
Dmp1 G A 5: 104,354,965 (GRCm39) M1I probably null Het
Efcab6 A T 15: 83,938,713 (GRCm39) M1K probably null Het
Extl2 A T 3: 115,821,131 (GRCm39) H312L possibly damaging Het
Fat4 C A 3: 38,944,728 (GRCm39) A1207D possibly damaging Het
Flnb T C 14: 7,926,518 (GRCm38) probably benign Het
Hdac10 G T 15: 89,008,071 (GRCm39) A593E possibly damaging Het
Hdhd2 T C 18: 77,052,969 (GRCm39) probably null Het
Kcnq2 A G 2: 180,751,582 (GRCm39) probably benign Het
Kdm7a A G 6: 39,142,064 (GRCm39) F405L probably damaging Het
Lypd6b C A 2: 49,833,642 (GRCm39) probably benign Het
Mki67 A T 7: 135,296,651 (GRCm39) D2794E possibly damaging Het
Mtmr14 T A 6: 113,243,287 (GRCm39) F40I probably damaging Het
Or2y3 G T 17: 38,393,544 (GRCm39) S108R possibly damaging Het
Or5p55 A T 7: 107,566,741 (GRCm39) I46F probably damaging Het
Or6d13 T A 6: 116,517,968 (GRCm39) C185S probably damaging Het
Or6x1 A T 9: 40,099,052 (GRCm39) I214F probably benign Het
Ppargc1a C A 5: 51,631,664 (GRCm39) V322L probably benign Het
Ppfibp1 T A 6: 146,931,195 (GRCm39) M917K probably benign Het
Prkg2 C T 5: 99,117,795 (GRCm39) probably null Het
Rfx4 A G 10: 84,704,246 (GRCm39) E296G possibly damaging Het
Rfx8 T A 1: 39,722,110 (GRCm39) K292* probably null Het
Scamp3 C A 3: 89,084,973 (GRCm39) probably benign Het
Scn4a A T 11: 106,221,190 (GRCm39) I823N possibly damaging Het
Sdk2 A G 11: 113,721,668 (GRCm39) V1316A probably damaging Het
Setd2 T C 9: 110,402,741 (GRCm39) V1794A probably damaging Het
Stard8 G T X: 98,116,694 (GRCm39) R983L probably damaging Het
Tbc1d23 A T 16: 57,013,038 (GRCm39) D311E probably benign Het
Tex21 T C 12: 76,245,592 (GRCm39) H568R probably benign Het
Tex35 T C 1: 156,932,667 (GRCm39) probably benign Het
Tgs1 T A 4: 3,591,292 (GRCm39) F442I possibly damaging Het
Traf2 C A 2: 25,414,931 (GRCm39) C303F probably benign Het
Trim56 A T 5: 137,143,354 (GRCm39) V54D possibly damaging Het
Yars2 C T 16: 16,124,406 (GRCm39) R338* probably null Het
Zfp668 A T 7: 127,465,454 (GRCm39) C577S probably damaging Het
Other mutations in 4930444P10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1777:4930444P10Rik UTSW 1 16,148,813 (GRCm39) missense possibly damaging 0.77
R4992:4930444P10Rik UTSW 1 16,151,101 (GRCm39) missense probably damaging 0.98
R4999:4930444P10Rik UTSW 1 16,139,022 (GRCm39) critical splice donor site probably null
R5229:4930444P10Rik UTSW 1 16,151,183 (GRCm39) utr 5 prime probably benign
R8870:4930444P10Rik UTSW 1 16,136,451 (GRCm39) nonsense probably null
R8966:4930444P10Rik UTSW 1 16,151,062 (GRCm39) missense possibly damaging 0.66
R9617:4930444P10Rik UTSW 1 16,139,051 (GRCm39) missense probably benign 0.06
Z1177:4930444P10Rik UTSW 1 16,152,246 (GRCm39) intron probably benign
Posted On 2013-06-21