Incidental Mutation 'IGL01149:4632415L05Rik'
ID50805
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4632415L05Rik
Ensembl Gene ENSMUSG00000048106
Gene NameRIKEN cDNA 4632415L05 gene
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.312) question?
Stock #IGL01149
Quality Score
Status
Chromosome3
Chromosomal Location19894886-19895962 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 19895112 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000055285 (fasta)
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000059704
SMART Domains Protein: ENSMUSP00000055285
Gene: ENSMUSG00000048106

DomainStartEndE-ValueType
low complexity region 55 103 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000198527
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy1 A C 11: 7,137,385 N420H probably damaging Het
Avp T C 2: 130,580,673 probably benign Het
B3galnt2 A T 13: 13,980,685 I216F probably benign Het
Cdc42bpa T C 1: 180,074,572 S465P probably damaging Het
Cdc42bpg T A 19: 6,312,205 probably benign Het
Cdcp2 T C 4: 107,107,111 F386S probably benign Het
Cdh4 A G 2: 179,874,144 T372A probably damaging Het
Clspn T G 4: 126,573,178 M612R probably damaging Het
Dll4 T C 2: 119,331,109 C391R probably damaging Het
Dll4 T C 2: 119,332,745 Y616H probably damaging Het
Exoc1 A G 5: 76,542,244 probably benign Het
F830045P16Rik A G 2: 129,460,312 probably benign Het
Fhod1 A G 8: 105,347,807 V16A probably benign Het
Fign T C 2: 63,979,760 R389G possibly damaging Het
Gm13941 T A 2: 111,101,137 E50V unknown Het
Gm436 T C 4: 144,673,779 D143G probably benign Het
Kit C T 5: 75,610,876 T231M probably damaging Het
Neu3 T C 7: 99,813,880 H212R probably benign Het
Nup214 G T 2: 32,034,700 S1747I probably damaging Het
Olfr1289 T C 2: 111,484,101 S252P probably damaging Het
Olfr735 G T 14: 50,345,614 A276E probably damaging Het
Olfr870 G T 9: 20,171,530 L14I probably damaging Het
Secisbp2 T C 13: 51,676,455 probably benign Het
Slc26a10 G A 10: 127,174,177 probably benign Het
Slc7a6 T C 8: 106,179,600 S155P probably damaging Het
Slf1 A T 13: 77,112,648 I173N probably damaging Het
Tedc1 C T 12: 113,163,188 R357* probably null Het
Tkfc A G 19: 10,600,651 L38P probably damaging Het
Tubgcp4 A G 2: 121,184,783 D324G probably benign Het
Zfyve16 T C 13: 92,508,283 H1137R probably damaging Het
Other mutations in 4632415L05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5271:4632415L05Rik UTSW 3 19895147 exon noncoding transcript
Posted OnJun 21, 2013