Incidental Mutation 'R1332:4933415A04Rik'
ID 156747
Institutional Source Beutler Lab
Gene Symbol 4933415A04Rik
Ensembl Gene ENSMUSG00000045877
Gene Name RIKEN cDNA 4933415A04 gene
Synonyms
MMRRC Submission 039397-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.107) question?
Stock # R1332 (G1)
Quality Score 155
Status Not validated
Chromosome 11
Chromosomal Location 43477867-43479875 bp(+) (GRCm39)
Type of Mutation small insertion (6 aa in frame mutation)
DNA Base Change (assembly) T to TNNNNNNNNNNNNNNNNNN at 43478256 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000062657 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050574] [ENSMUST00000056256]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000050574
SMART Domains Protein: ENSMUSP00000058111
Gene: ENSMUSG00000044707

DomainStartEndE-ValueType
CYCLIN 43 135 7.96e-14 SMART
Cyclin_C 144 281 2.52e-22 SMART
CYCLIN 153 247 1.58e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000056256
SMART Domains Protein: ENSMUSP00000062657
Gene: ENSMUSG00000045877

DomainStartEndE-ValueType
transmembrane domain 30 62 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.1%
  • 20x: 93.0%
Validation Efficiency 100% (35/35)
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd14b A T 9: 106,329,195 (GRCm39) I42F probably damaging Het
Apbb1 A T 7: 105,214,750 (GRCm39) I498N possibly damaging Het
Asah2 A G 19: 32,022,341 (GRCm39) I231T probably damaging Het
Bid C T 6: 120,874,216 (GRCm39) A110T possibly damaging Het
Caskin2 C T 11: 115,694,171 (GRCm39) probably benign Het
Ccdc141 T C 2: 76,844,784 (GRCm39) T1428A probably damaging Het
Cd22 A C 7: 30,569,912 (GRCm39) W477G possibly damaging Het
Cox16 T C 12: 81,519,064 (GRCm39) D89G probably damaging Het
Dnah17 A G 11: 117,934,041 (GRCm39) I3511T possibly damaging Het
Dpy19l4 A T 4: 11,276,901 (GRCm39) Y333N probably damaging Het
Eya2 T C 2: 165,529,528 (GRCm39) probably benign Het
Fras1 A G 5: 96,855,167 (GRCm39) D1892G probably benign Het
Hlf G T 11: 90,231,679 (GRCm39) S265* probably null Het
Immt T C 6: 71,823,256 (GRCm39) probably benign Het
Lair1 T C 7: 4,013,595 (GRCm39) E36G possibly damaging Het
Lrfn5 T C 12: 61,904,314 (GRCm39) probably benign Het
Nos1ap T C 1: 170,177,001 (GRCm39) N134S probably damaging Het
Ogfod1 T C 8: 94,784,727 (GRCm39) C344R probably damaging Het
Or6c212 A G 10: 129,559,116 (GRCm39) L99S probably damaging Het
Pkhd1l1 G A 15: 44,368,943 (GRCm39) V863I probably damaging Het
Pmfbp1 T G 8: 110,256,898 (GRCm39) I534S probably damaging Het
Prex2 A G 1: 11,274,315 (GRCm39) D1329G probably damaging Het
Rasal2 T C 1: 157,003,391 (GRCm39) T423A probably benign Het
Rif1 T A 2: 51,968,326 (GRCm39) W170R probably benign Het
Scarb2 C T 5: 92,599,205 (GRCm39) probably null Het
Stard9 C A 2: 120,504,117 (GRCm39) S221R probably damaging Het
Tlr3 A C 8: 45,851,774 (GRCm39) N374K probably damaging Het
Uck1 T C 2: 32,149,666 (GRCm39) D71G probably damaging Het
Vcan C T 13: 89,841,174 (GRCm39) E497K probably damaging Het
Vmn2r86 G A 10: 130,282,739 (GRCm39) L626F probably damaging Het
Vmn2r89 A G 14: 51,692,559 (GRCm39) T121A probably benign Het
Wdr64 T C 1: 175,622,706 (GRCm39) S828P possibly damaging Het
Zfp334 A T 2: 165,222,776 (GRCm39) H422Q probably damaging Het
Other mutations in 4933415A04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0106:4933415A04Rik UTSW 11 43,478,200 (GRCm39) unclassified probably benign
R0541:4933415A04Rik UTSW 11 43,478,227 (GRCm39) frame shift probably null
R7709:4933415A04Rik UTSW 11 43,478,237 (GRCm39) frame shift probably null
R7782:4933415A04Rik UTSW 11 43,478,239 (GRCm39) frame shift probably null
R7804:4933415A04Rik UTSW 11 43,478,241 (GRCm39) small deletion probably benign
R7852:4933415A04Rik UTSW 11 43,478,253 (GRCm39) frame shift probably null
R7868:4933415A04Rik UTSW 11 43,478,257 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- CGATAGGGCTTTTCTGAGCAGATGG -3'
(R):5'- GGCTGACTTGCTAAGAGATGTCCAG -3'

Sequencing Primer
(F):5'- CAGATGGATGTCTCATGGAAAC -3'
(R):5'- GGACATCTGGTCCTGAGAATC -3'
Posted On 2014-02-11