Incidental Mutation 'IGL01791:4930572O03Rik'
ID278924
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930572O03Rik
Ensembl Gene ENSMUSG00000069720
Gene NameRIKEN cDNA 4930572O03 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01791
Quality Score
Status
Chromosome5
Chromosomal Location15652286-15657059 bp(-) (GRCm38)
Type of Mutationutr 5 prime
DNA Base Change (assembly) C to A at 15656886 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000090370 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092696]
Predicted Effect probably benign
Transcript: ENSMUST00000092696
SMART Domains Protein: ENSMUSP00000090370
Gene: ENSMUSG00000069720

DomainStartEndE-ValueType
Pfam:Takusan 6 90 5.2e-29 PFAM
low complexity region 203 210 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178227
SMART Domains Protein: ENSMUSP00000136079
Gene: ENSMUSG00000094230

DomainStartEndE-ValueType
low complexity region 43 54 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap32 A G 9: 32,247,190 I174V probably damaging Het
Asb15 T A 6: 24,567,212 C511S probably damaging Het
Atr C T 9: 95,921,781 A1896V probably benign Het
B3gnt4 C T 5: 123,511,099 R176C probably damaging Het
Brf1 T C 12: 112,962,475 D557G probably benign Het
Catsperg2 T A 7: 29,704,665 probably null Het
Ccdc144b T C 3: 36,035,267 probably benign Het
Cdip1 A G 16: 4,768,865 I122T probably damaging Het
Ctrl C T 8: 105,932,567 E147K probably benign Het
Dennd2c T C 3: 103,166,425 V829A probably benign Het
Dync1h1 T A 12: 110,658,930 L3874Q probably damaging Het
Gm10521 T C 1: 171,896,397 S92P unknown Het
Gzf1 G A 2: 148,684,061 A151T probably benign Het
Hddc2 A G 10: 31,326,026 Y123C probably damaging Het
Hyal4 T C 6: 24,763,895 probably benign Het
Ighv16-1 T C 12: 114,068,969 N71S probably benign Het
Ing2 A T 8: 47,669,035 S159R probably benign Het
Itga1 A T 13: 114,987,661 N698K probably benign Het
Lemd2 A T 17: 27,190,728 I483N probably damaging Het
Lyst T C 13: 13,635,302 L519P probably damaging Het
Mapk10 T C 5: 102,996,648 N101S probably damaging Het
Nfatc4 A T 14: 55,832,238 E164V probably null Het
Nfkb2 T G 19: 46,309,839 probably benign Het
Nox3 A G 17: 3,682,943 V231A possibly damaging Het
Nup160 G A 2: 90,703,853 G674D probably damaging Het
Olfr364-ps1 A T 2: 37,146,536 D108V probably damaging Het
Olfr657 C T 7: 104,636,475 T267I possibly damaging Het
Otoa T G 7: 121,155,849 V998G probably benign Het
Pcnx3 A T 19: 5,673,267 M1300K probably benign Het
Pde4b A G 4: 102,590,930 probably benign Het
Rfc1 T A 5: 65,263,145 K1104I probably benign Het
Serpina1f G T 12: 103,693,502 Q174K probably damaging Het
Serping1 T C 2: 84,773,377 N107D possibly damaging Het
Surf6 A G 2: 26,899,747 S94P probably benign Het
Tctex1d4 T A 4: 117,128,597 S206T probably damaging Het
Tigd4 T A 3: 84,594,745 I323N probably damaging Het
Vmn2r28 T C 7: 5,488,162 D362G probably benign Het
Wdfy3 A G 5: 101,937,412 S739P probably damaging Het
Other mutations in 4930572O03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL00088:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL01443:4930572O03Rik APN 5 15652644 makesense probably null
IGL01789:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL01790:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL01792:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL01795:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL02344:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
Posted On2015-04-16