Incidental Mutation 'R5923:4921513I03Rik'
ID 461684
Institutional Source Beutler Lab
Gene Symbol 4921513I03Rik
Ensembl Gene ENSMUSG00000044544
Gene Name RIKEN cDNA 4921513I03 gene
Synonyms
MMRRC Submission 043241-MU
Accession Numbers
Essential gene? Not available question?
Stock # R5923 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 120601637-120614791 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to G at 120614675 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000089781 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092143]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000056994
SMART Domains Protein: ENSMUSP00000059458
Gene: ENSMUSG00000044544

DomainStartEndE-ValueType
low complexity region 62 74 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000092143
SMART Domains Protein: ENSMUSP00000089781
Gene: ENSMUSG00000051236

DomainStartEndE-ValueType
Pfam:SelR 41 161 1.9e-56 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139961
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219219
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.4%
  • 10x: 97.3%
  • 20x: 91.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 A G 11: 110,051,378 (GRCm39) V106A probably benign Het
Arnt2 G T 7: 83,911,741 (GRCm39) T577K probably benign Het
Bod1l G A 5: 41,974,762 (GRCm39) T2184I probably damaging Het
Brpf3 G A 17: 29,025,610 (GRCm39) V228I possibly damaging Het
Cacna1d T C 14: 29,833,105 (GRCm39) N890S probably damaging Het
Cacna1s T A 1: 136,004,560 (GRCm39) M120K possibly damaging Het
Cdr2 A G 7: 120,581,224 (GRCm39) Y18H probably damaging Het
Cilp2 A G 8: 70,335,525 (GRCm39) F491S probably damaging Het
Cubn A T 2: 13,490,889 (GRCm39) S185T possibly damaging Het
Dst T C 1: 34,220,840 (GRCm39) S2215P probably benign Het
Echdc3 A G 2: 6,194,383 (GRCm39) V224A possibly damaging Het
Hivep3 G T 4: 119,953,490 (GRCm39) S602I possibly damaging Het
Itga2 T C 13: 115,021,055 (GRCm39) S99G probably benign Het
Kat6a A G 8: 23,429,495 (GRCm39) T1617A probably benign Het
Map1b T C 13: 99,569,661 (GRCm39) E1020G unknown Het
Nbeal1 T C 1: 60,287,554 (GRCm39) F933L probably damaging Het
Ntrk3 A T 7: 78,101,676 (GRCm39) I419N possibly damaging Het
Nup188 A G 2: 30,194,102 (GRCm39) I136V probably benign Het
Or8b38 T A 9: 37,973,154 (GRCm39) D179E probably benign Het
Plcb4 A T 2: 135,803,734 (GRCm39) K536* probably null Het
Polk A T 13: 96,631,923 (GRCm39) I270N probably damaging Het
Prl6a1 A T 13: 27,500,346 (GRCm39) M106L probably benign Het
Scap G T 9: 110,212,648 (GRCm39) D1027Y probably damaging Het
Spg11 A T 2: 121,923,959 (GRCm39) H787Q probably damaging Het
Tatdn3 T C 1: 190,781,507 (GRCm39) D215G probably damaging Het
Tbcd G A 11: 121,470,978 (GRCm39) C665Y probably benign Het
Tmc8 C T 11: 117,674,638 (GRCm39) R118C probably damaging Het
Ttn T A 2: 76,642,901 (GRCm39) H13245L probably damaging Het
Unc79 T C 12: 103,078,727 (GRCm39) S1631P probably damaging Het
Vmn1r12 G A 6: 57,136,020 (GRCm39) G39D probably benign Het
Vmn2r24 A G 6: 123,792,751 (GRCm39) S693G probably damaging Het
Zc3h3 G T 15: 75,657,413 (GRCm39) R593S probably damaging Het
Zfp598 T C 17: 24,896,523 (GRCm39) L200P probably damaging Het
Other mutations in 4921513I03Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02132:4921513I03Rik APN 10 120,614,635 (GRCm39) unclassified probably benign
R0062:4921513I03Rik UTSW 10 120,614,511 (GRCm39) unclassified probably benign
R0062:4921513I03Rik UTSW 10 120,614,511 (GRCm39) unclassified probably benign
R1694:4921513I03Rik UTSW 10 120,614,533 (GRCm39) unclassified probably benign
R5740:4921513I03Rik UTSW 10 120,614,413 (GRCm39) unclassified probably benign
X0022:4921513I03Rik UTSW 10 120,614,705 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- GAGCCTTTCTTCATTCGAGTCG -3'
(R):5'- ACACCTGGCAGTTGGAAATGG -3'

Sequencing Primer
(F):5'- GAGTCGTACTTTCTTACATGTCTG -3'
(R):5'- AGTGGAGGCGTTTCCCAATC -3'
Posted On 2017-02-28