Incidental Mutation 'R4368:4930449A18Rik'
ID 325839
Institutional Source Beutler Lab
Gene Symbol 4930449A18Rik
Ensembl Gene ENSMUSG00000074589
Gene Name RIKEN cDNA 4930449A18 gene
Synonyms
MMRRC Submission 041115-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.174) question?
Stock # R4368 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 59733170-59754238 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 59754199 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: ENSMUST00000192453
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.0%
  • 20x: 94.6%
Validation Efficiency 98% (46/47)
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2fm2 T C 3: 59,659,387 (GRCm39) F280S probably damaging Het
Adamts7 G A 9: 90,077,904 (GRCm39) probably null Het
Adgrv1 A C 13: 81,641,029 (GRCm39) S3335R unknown Het
Armc6 G A 8: 70,677,943 (GRCm39) L129F probably benign Het
B4galt3 C A 1: 171,101,613 (GRCm39) H196N probably damaging Het
Bltp1 C T 3: 37,042,296 (GRCm39) Q2761* probably null Het
Cdh19 G A 1: 110,817,442 (GRCm39) Q767* probably null Het
Cep120 G A 18: 53,818,957 (GRCm39) probably null Het
Dhx38 C T 8: 110,279,763 (GRCm39) V976I probably damaging Het
Efr3a T A 15: 65,738,629 (GRCm39) F753I possibly damaging Het
Hspb7 A T 4: 141,151,329 (GRCm39) E157V probably damaging Het
Irx6 A G 8: 93,405,029 (GRCm39) E299G probably damaging Het
Jhy T A 9: 40,828,440 (GRCm39) N489Y possibly damaging Het
Klhl22 T C 16: 17,607,137 (GRCm39) V481A possibly damaging Het
Mapk13 A G 17: 28,996,539 (GRCm39) probably null Het
Meis1 A T 11: 18,960,656 (GRCm39) probably benign Het
Nlrp14 A G 7: 106,797,012 (GRCm39) K301E probably benign Het
Nol10 T C 12: 17,429,293 (GRCm39) Y340H probably damaging Het
Or2k2 T C 4: 58,785,153 (GRCm39) S190G probably benign Het
Paqr3 T C 5: 97,256,150 (GRCm39) S75G probably damaging Het
Pdgfa T C 5: 138,972,061 (GRCm39) T113A probably damaging Het
Phactr2 A G 10: 13,129,564 (GRCm39) S235P probably damaging Het
Psph T G 5: 129,848,654 (GRCm39) K9T probably benign Het
Ptpn21 T C 12: 98,644,852 (GRCm39) Y1163C probably damaging Het
Scaf8 T C 17: 3,221,470 (GRCm39) L319P unknown Het
Slc4a7 C T 14: 14,733,775 (GRCm38) R62W probably damaging Het
Slc6a3 C A 13: 73,709,031 (GRCm39) C318* probably null Het
Speer3 C G 5: 13,846,394 (GRCm39) A238G possibly damaging Het
Taf1c A C 8: 120,326,055 (GRCm39) S602R possibly damaging Het
Tiam2 A G 17: 3,464,958 (GRCm39) D229G probably benign Het
Tor1a A G 2: 30,857,382 (GRCm39) probably benign Het
Trim45 T C 3: 100,830,502 (GRCm39) I92T probably damaging Het
Ttll8 G A 15: 88,798,384 (GRCm39) P784S possibly damaging Het
Tubg1 G T 11: 101,016,190 (GRCm39) probably null Het
Vmn1r178 A T 7: 23,593,447 (GRCm39) N92I probably damaging Het
Vmn2r87 A G 10: 130,315,676 (GRCm39) V130A probably benign Het
Wdr46 A G 17: 34,160,120 (GRCm39) probably benign Het
Yme1l1 A G 2: 23,050,223 (GRCm39) H18R possibly damaging Het
Zfp263 T A 16: 3,562,770 (GRCm39) probably benign Het
Zfp534 T C 4: 147,760,015 (GRCm39) D218G probably benign Het
Zscan12 T C 13: 21,553,553 (GRCm39) V459A probably benign Het
Other mutations in 4930449A18Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02536:4930449A18Rik APN 3 59,685,665 (GRCm39) exon noncoding transcript
R4243:4930449A18Rik UTSW 3 59,733,203 (GRCm39) exon noncoding transcript
R4245:4930449A18Rik UTSW 3 59,733,203 (GRCm39) exon noncoding transcript
R4466:4930449A18Rik UTSW 3 59,745,887 (GRCm39) exon noncoding transcript
R4755:4930449A18Rik UTSW 3 59,733,280 (GRCm39) exon noncoding transcript
R4842:4930449A18Rik UTSW 3 59,749,153 (GRCm39) exon noncoding transcript
R5214:4930449A18Rik UTSW 3 59,733,305 (GRCm39) splice site noncoding transcript
R5436:4930449A18Rik UTSW 3 59,754,114 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- TTTGCTAGTCAATGACTCCCAG -3'
(R):5'- CTCCATTTTATCAGCAACTAACACTGG -3'

Sequencing Primer
(F):5'- CAATGACTCCCAGTTACAGAGTTTGC -3'
(R):5'- TGCAATGATCTTTATGC -3'
Posted On 2015-07-06