Incidental Mutation 'R4920:1700092K14Rik'
ID 378522
Institutional Source Beutler Lab
Gene Symbol 1700092K14Rik
Ensembl Gene ENSMUSG00000078600
Gene Name RIKEN cDNA 1700092K14 gene
Synonyms
MMRRC Submission 042522-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.176) question?
Stock # R4920 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 114089084-114090025 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 114089871 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: ENSMUST00000106604
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.1%
  • 20x: 87.9%
Validation Efficiency 96% (55/57)
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy4 C T 14: 56,016,486 (GRCm39) D322N probably damaging Het
Apbb1ip A G 2: 22,709,696 (GRCm39) D51G unknown Het
Bmal1 A G 7: 112,884,321 (GRCm39) T120A probably damaging Het
Brca1 A T 11: 101,415,785 (GRCm39) V783D probably damaging Het
Ccdc141 T C 2: 76,998,907 (GRCm39) D58G probably damaging Het
Ccr9 G T 9: 123,608,504 (GRCm39) G62V probably damaging Het
Ces2b T C 8: 105,563,538 (GRCm39) Y422H probably benign Het
Cpa4 T C 6: 30,568,462 (GRCm39) probably null Het
Dennd3 A G 15: 73,412,574 (GRCm39) H412R probably benign Het
Dpy19l3 A T 7: 35,407,467 (GRCm39) probably benign Het
Dtwd2 G T 18: 49,831,507 (GRCm39) R167S possibly damaging Het
Dync1i2 G A 2: 71,077,668 (GRCm39) R243Q probably damaging Het
Ear2 G A 14: 44,340,582 (GRCm39) G80E probably damaging Het
Fam171b A G 2: 83,710,703 (GRCm39) K792E possibly damaging Het
Fam83b G A 9: 76,399,150 (GRCm39) T651I probably benign Het
Fcrl5 T G 3: 87,351,480 (GRCm39) F243V probably damaging Het
Galntl6 T C 8: 58,880,807 (GRCm39) I115M probably damaging Het
Glrx3 A G 7: 137,065,859 (GRCm39) D163G probably null Het
Gm14488 A T 2: 30,605,044 (GRCm39) noncoding transcript Het
Gm973 T C 1: 59,666,725 (GRCm39) S683P probably benign Het
Grhl3 T A 4: 135,286,415 (GRCm39) K89* probably null Het
Gsdmd T C 15: 75,736,206 (GRCm39) S112P probably damaging Het
Ighv14-3 A G 12: 114,023,877 (GRCm39) V6A probably benign Het
Lca5l T A 16: 95,980,035 (GRCm39) S32C probably damaging Het
Lrba T A 3: 86,571,765 (GRCm39) Y260* probably null Het
Lyst T C 13: 13,821,645 (GRCm39) S1340P possibly damaging Het
Mfsd13a T G 19: 46,355,655 (GRCm39) F59V probably damaging Het
Nek10 T A 14: 14,860,986 (GRCm38) L513M possibly damaging Het
Noa1 T C 5: 77,454,334 (GRCm39) probably null Het
Ofcc1 G A 13: 40,168,864 (GRCm39) T841I probably damaging Het
Pgm1 C T 4: 99,843,930 (GRCm39) T571M probably damaging Het
Pramel23 T C 4: 143,425,853 (GRCm39) D30G probably benign Het
Rfc1 C A 5: 65,445,271 (GRCm39) V460F probably damaging Het
Rrn3 A G 16: 13,608,503 (GRCm39) D182G probably benign Het
Sap25 T A 5: 137,640,507 (GRCm39) probably benign Het
Slc9a2 A G 1: 40,794,878 (GRCm39) I480V probably benign Het
Smo T C 6: 29,759,593 (GRCm39) S642P probably damaging Het
Tbc1d22a A C 15: 86,195,949 (GRCm39) I307L probably benign Het
Tent2 G A 13: 93,322,833 (GRCm39) Q39* probably null Het
Ubr3 A G 2: 69,783,212 (GRCm39) Q716R probably benign Het
Vmn2r96 A G 17: 18,802,918 (GRCm39) E276G probably benign Het
Zfp189 G A 4: 49,529,302 (GRCm39) C135Y probably damaging Het
Other mutations in 1700092K14Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4282:1700092K14Rik UTSW 11 114,089,970 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- ACCTTGAGTGGTCCTGAGTG -3'
(R):5'- CCCATAAGATCACAGGACGAGATAG -3'

Sequencing Primer
(F):5'- AGTGAGTATACAGATCTGTGCCTCC -3'
(R):5'- CGGCAAAGCAAACCGTCAGG -3'
Posted On 2016-04-15