Incidental Mutation 'R5431:C330018D20Rik'
ID 428075
Institutional Source Beutler Lab
Gene Symbol C330018D20Rik
Ensembl Gene ENSMUSG00000024592
Gene Name RIKEN cDNA C330018D20 gene
MMRRC Submission 042847-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.159) question?
Stock # R5431 (G1)
Quality Score 225
Status Not validated
Chromosome 18
Chromosomal Location 56955833-56975368 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 56957856 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 78 (F78L)
Ref Sequence ENSEMBL: ENSMUSP00000116181 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025488] [ENSMUST00000139243]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000025488
AA Change: F78L

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000025488
Gene: ENSMUSG00000024592
AA Change: F78L

Pfam:DUF836 31 105 9.7e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000139243
AA Change: F78L

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000116181
Gene: ENSMUSG00000024592
AA Change: F78L

Pfam:DUF836 31 105 1.6e-20 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310061N02Rik T C 16: 88,707,538 (GRCm38) S124G possibly damaging Het
4921539E11Rik T C 4: 103,270,848 (GRCm38) T27A probably benign Het
Aspg T A 12: 112,123,412 (GRCm38) N461K probably benign Het
B4galnt3 T A 6: 120,218,967 (GRCm38) T300S probably damaging Het
BC035044 A G 6: 128,885,007 (GRCm38) probably benign Het
Bmp5 C T 9: 75,893,709 (GRCm38) P374S probably damaging Het
Cds2 T A 2: 132,302,170 (GRCm38) S289T probably benign Het
Cerkl C T 2: 79,341,335 (GRCm38) C393Y probably damaging Het
Ciita C T 16: 10,523,792 (GRCm38) R1020C probably damaging Het
Dcaf13 C A 15: 39,123,224 (GRCm38) D130E probably benign Het
Dnal4 C T 15: 79,762,447 (GRCm38) G50R probably damaging Het
Elfn1 A G 5: 139,971,568 (GRCm38) N109S probably damaging Het
Ep400 A G 5: 110,676,554 (GRCm38) V2435A unknown Het
Fam178b T C 1: 36,632,485 (GRCm38) E185G probably damaging Het
Fam227b C A 2: 126,126,931 (GRCm38) L74F probably benign Het
Fam92b C A 8: 120,167,303 (GRCm38) probably null Het
Fgfr4 G A 13: 55,156,651 (GRCm38) V138I probably benign Het
Flnc A G 6: 29,456,384 (GRCm38) I2161V possibly damaging Het
Frmd5 T C 2: 121,562,909 (GRCm38) N235S probably damaging Het
Gad1-ps G A 10: 99,445,147 (GRCm38) noncoding transcript Het
Ggt6 A G 11: 72,437,738 (GRCm38) T355A possibly damaging Het
Gm14393 G A 2: 175,063,876 (GRCm38) T41I probably damaging Het
Gpr151 A C 18: 42,578,867 (GRCm38) S249A probably damaging Het
Gpr152 T A 19: 4,143,747 (GRCm38) V429D probably benign Het
Grm7 G A 6: 111,358,426 (GRCm38) M599I probably benign Het
Hdac4 T A 1: 91,972,790 (GRCm38) R54* probably null Het
Ice1 A G 13: 70,592,650 (GRCm38) L2146S probably damaging Het
Igfbpl1 C T 4: 45,815,588 (GRCm38) V183I probably benign Het
Kel G A 6: 41,698,420 (GRCm38) S299F probably benign Het
Kif14 T C 1: 136,496,695 (GRCm38) I1016T possibly damaging Het
Lhx3 T C 2: 26,201,118 (GRCm38) D395G probably damaging Het
Micu1 T C 10: 59,750,521 (GRCm38) Y140H possibly damaging Het
Myt1l G A 12: 29,832,332 (GRCm38) G509R unknown Het
Nbn C T 4: 15,986,593 (GRCm38) H665Y probably benign Het
Pkhd1 G T 1: 20,117,836 (GRCm38) T3416K probably benign Het
Plxnb1 T C 9: 109,100,772 (GRCm38) F232S probably damaging Het
Pus7l T C 15: 94,529,486 (GRCm38) N472D probably damaging Het
Rfx1 C T 8: 84,082,720 (GRCm38) Q225* probably null Het
Rnase2a T C 14: 51,255,563 (GRCm38) Y115C possibly damaging Het
Ryr1 T A 7: 29,109,812 (GRCm38) D386V probably benign Het
Sfi1 A ATCTTCCCAAAGCCAGTGC 11: 3,153,384 (GRCm38) probably benign Homo
Sgcz T A 8: 37,639,984 (GRCm38) T125S probably damaging Het
Sntb1 C G 15: 55,642,795 (GRCm38) G461R probably damaging Het
Syt2 A G 1: 134,740,957 (GRCm38) S36G probably benign Het
Tcaf3 A G 6: 42,597,185 (GRCm38) L31P probably damaging Het
Tenm3 C A 8: 48,367,377 (GRCm38) E142* probably null Het
Tgfbr2 G T 9: 116,131,601 (GRCm38) S94R probably damaging Het
Vmn2r12 A G 5: 109,091,818 (GRCm38) I293T probably damaging Het
Wrap73 G A 4: 154,145,274 (GRCm38) R34Q probably damaging Het
Zc3h14 A G 12: 98,780,065 (GRCm38) D511G possibly damaging Het
Zcchc11 T A 4: 108,491,412 (GRCm38) I297N probably damaging Het
Other mutations in C330018D20Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2857:C330018D20Rik UTSW 18 56,962,459 (GRCm38) missense probably benign 0.01
R5987:C330018D20Rik UTSW 18 56,957,896 (GRCm38) missense probably damaging 0.98
R6287:C330018D20Rik UTSW 18 56,962,335 (GRCm38) splice site probably null
R6378:C330018D20Rik UTSW 18 56,962,507 (GRCm38) missense probably damaging 0.99
R7619:C330018D20Rik UTSW 18 56,962,411 (GRCm38) missense probably damaging 1.00
R8445:C330018D20Rik UTSW 18 56,957,890 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2016-09-01