Incidental Mutation 'IGL01443:4930572O03Rik'
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ID84331
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 #IGL01443
Quality Score
Status
Chromosome5
Chromosomal Location15652286-15657059 bp(-) (GRCm38)
Type of Mutationmakesense
DNA Base Change (assembly) A to G at 15652644 bp
ZygosityHeterozygous
Amino Acid Change Stop codon to Glutamine at position 212 (*212Q)
Ref Sequence ENSEMBL: ENSMUSP00000090370 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092696]
Predicted Effect probably null
Transcript: ENSMUST00000092696
AA Change: *212Q
SMART Domains Protein: ENSMUSP00000090370
Gene: ENSMUSG00000069720
AA Change: *212Q

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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts2 A G 11: 50,803,863 E1159G possibly damaging Het
Adgrl3 A G 5: 81,465,287 Y189C probably damaging Het
AW554918 G A 18: 25,344,955 G446R probably damaging Het
Baiap3 A G 17: 25,245,147 F884S possibly damaging Het
Cd101 T C 3: 101,003,571 T924A probably benign Het
Cdk12 T A 11: 98,245,469 V1183E unknown Het
Clcc1 T C 3: 108,670,903 M240T probably benign Het
Dnmbp C A 19: 43,902,870 A153S probably damaging Het
Dus4l T C 12: 31,652,410 probably benign Het
Dyrk1a A G 16: 94,685,084 E430G probably benign Het
Erc1 T C 6: 119,824,471 K195R probably damaging Het
Evpl T C 11: 116,222,454 E1470G probably damaging Het
Extl3 A T 14: 65,077,470 S88T probably damaging Het
Fam135b A T 15: 71,463,364 H660Q probably benign Het
Fat1 G A 8: 45,040,576 G3920S probably damaging Het
Fbxo38 A G 18: 62,533,670 V144A probably damaging Het
Grwd1 C T 7: 45,830,410 probably null Het
Hdlbp T C 1: 93,431,074 T252A probably damaging Het
Igkv3-1 A G 6: 70,704,104 S96G possibly damaging Het
Igkv4-68 G T 6: 69,304,937 F83L probably damaging Het
Klhl31 T C 9: 77,650,260 V86A possibly damaging Het
Lypd3 G A 7: 24,636,638 G17R probably benign Het
Manba T A 3: 135,544,828 D405E probably damaging Het
Map3k19 A G 1: 127,838,507 S227P probably benign Het
Nras T A 3: 103,062,435 C118S probably benign Het
Olfr659 A G 7: 104,671,071 D123G probably damaging Het
Pde8a T C 7: 81,324,181 F629L probably damaging Het
Phtf2 A G 5: 20,782,267 probably benign Het
Pik3c2a A T 7: 116,418,194 F109L probably benign Het
Plod3 G A 5: 136,990,221 R320H probably benign Het
Ppib T C 9: 66,065,597 F152L probably damaging Het
Rbm19 T C 5: 120,143,438 probably benign Het
Rgs12 T A 5: 34,975,219 S628R probably benign Het
Ripk1 A G 13: 34,015,268 D201G probably damaging Het
St14 G T 9: 31,100,193 S434* probably null Het
Tbc1d9 A G 8: 83,239,931 D387G probably damaging Het
Trio A G 15: 27,838,775 probably benign Het
Ttn G A 2: 76,713,871 R32924C probably damaging Het
Vmn1r181 T C 7: 23,984,581 V157A possibly damaging Het
Zfp473 C T 7: 44,739,563 D45N 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
IGL01789:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL01790:4930572O03Rik APN 5 15656886 utr 5 prime probably benign
IGL01791:4930572O03Rik 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 On2013-11-11