Incidental Mutation 'R4036:4930544M13Rik'
ID 359705
Institutional Source Beutler Lab
Gene Symbol 4930544M13Rik
Ensembl Gene ENSMUSG00000051758
Gene Name RIKEN cDNA 4930544M13 gene
Synonyms
MMRRC Submission 040963-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.179) question?
Stock # R4036 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 114743773-114834358 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 114744205 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000063230
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181553
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224961
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.8%
  • 20x: 93.4%
Validation Efficiency 100% (33/33)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahctf1 T C 1: 179,590,181 (GRCm39) Q1364R possibly damaging Het
Anxa2 A G 9: 69,395,352 (GRCm39) N265S probably damaging Het
Bcan A G 3: 87,903,423 (GRCm39) probably null Het
Cntln A G 4: 84,924,725 (GRCm39) Y610C probably damaging Het
Cyp39a1 C A 17: 43,987,831 (GRCm39) A99E probably damaging Het
Drc1 A G 5: 30,504,526 (GRCm39) I223V probably benign Het
Eef2kmt A T 16: 5,063,135 (GRCm39) V335D probably damaging Het
Fanci T C 7: 79,094,570 (GRCm39) L1167P probably damaging Het
Glb1l3 A C 9: 26,740,343 (GRCm39) M329R probably damaging Het
Gns C A 10: 121,207,095 (GRCm39) T72N probably damaging Het
Hspa2 T C 12: 76,452,542 (GRCm39) V412A probably damaging Het
Klk1b8 A G 7: 43,447,511 (GRCm39) I9V probably null Het
Map4 A G 9: 109,861,283 (GRCm39) T216A possibly damaging Het
Metrn T C 17: 26,013,984 (GRCm39) T281A probably benign Het
Mid1-ps1 G A Y: 90,773,563 (GRCm39) noncoding transcript Het
Ndc1 G A 4: 107,268,269 (GRCm39) D602N probably benign Het
Nsd1 A G 13: 55,361,524 (GRCm39) D164G possibly damaging Het
Or5ac22 T A 16: 59,135,113 (GRCm39) H219L probably benign Het
Pcdha8 T C 18: 37,125,914 (GRCm39) M132T probably benign Het
Pomt2 A G 12: 87,158,296 (GRCm39) probably null Het
Prrt3 AGGGGG AGGGG 6: 113,474,641 (GRCm39) probably null Het
Rfx6 T A 10: 51,602,842 (GRCm39) H786Q probably damaging Het
Scn4a A C 11: 106,212,883 (GRCm39) L1374R possibly damaging Het
Slc16a9 C T 10: 70,110,786 (GRCm39) T124M probably damaging Het
Slc46a2 A T 4: 59,913,818 (GRCm39) F368L probably damaging Het
St18 T A 1: 6,898,010 (GRCm39) I604K probably damaging Het
Ttn A G 2: 76,548,497 (GRCm39) V31935A possibly damaging Het
Urb1 T C 16: 90,584,974 (GRCm39) H549R probably benign Het
Vmn1r219 A G 13: 23,347,272 (GRCm39) M154V probably benign Het
Zfp575 G A 7: 24,285,440 (GRCm39) S67L possibly damaging Het
Other mutations in 4930544M13Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4831:4930544M13Rik UTSW 13 114,744,183 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- GGCTTTACATGTGTGGCCAC -3'
(R):5'- TGCATCAAGGCTGCCACATG -3'

Sequencing Primer
(F):5'- GTGGCCACACTCATGCC -3'
(R):5'- GCTGCCACATGCCACCAAG -3'
Posted On 2015-12-02