Incidental Mutation 'R6759:4933427I04Rik'
ID 531132
Institutional Source Beutler Lab
Gene Symbol 4933427I04Rik
Ensembl Gene ENSMUSG00000073761
Gene Name Riken cDNA 4933427I04 gene
Synonyms
MMRRC Submission 044875-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # R6759 (G1)
Quality Score 225.009
Status Validated
Chromosome 4
Chromosomal Location 123753472-123756958 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) G to T at 123753879 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000095506 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097896]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000097896
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137546
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.9%
Validation Efficiency 98% (49/50)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2900026A02Rik T C 5: 113,331,692 (GRCm39) S841G probably benign Het
Aak1 A G 6: 86,921,399 (GRCm39) T199A probably damaging Het
Acnat2 C A 4: 49,380,254 (GRCm39) V375L probably benign Het
Aldh1a7 T C 19: 20,677,320 (GRCm39) T434A possibly damaging Het
Aldh3a2 T C 11: 61,156,088 (GRCm39) T63A probably benign Het
Anxa2 T C 9: 69,391,103 (GRCm39) S97P probably damaging Het
Apip T C 2: 102,922,191 (GRCm39) S186P probably benign Het
Apob A G 12: 8,061,049 (GRCm39) K3177R probably benign Het
Atm C T 9: 53,429,859 (GRCm39) W392* probably null Het
Atp8b1 T A 18: 64,679,161 (GRCm39) R773S probably benign Het
Bicdl2 T A 17: 23,885,718 (GRCm39) probably null Het
Bltp1 C T 3: 37,042,234 (GRCm39) T2740I possibly damaging Het
Cacng3 G A 7: 122,361,547 (GRCm39) probably null Het
Clca3a1 G T 3: 144,455,450 (GRCm39) L448M probably damaging Het
Clk4 A G 11: 51,166,401 (GRCm39) I94M possibly damaging Het
Cnot3 G T 7: 3,654,918 (GRCm39) V124F probably damaging Het
Cyp4a30b C T 4: 115,318,571 (GRCm39) A426V probably benign Het
Dact1 T A 12: 71,364,911 (GRCm39) L564* probably null Het
Dnah8 T A 17: 30,882,266 (GRCm39) probably null Het
Dock5 T A 14: 68,033,445 (GRCm39) T975S probably benign Het
Dock8 C A 19: 25,104,848 (GRCm39) H739Q probably damaging Het
Efr3b T A 12: 4,034,613 (GRCm39) N186Y probably damaging Het
Enam G A 5: 88,649,550 (GRCm39) G278D probably damaging Het
Fgl2 A G 5: 21,578,256 (GRCm39) D181G probably benign Het
Gfra3 G T 18: 34,828,926 (GRCm39) S156* probably null Het
Jam3 G C 9: 27,013,276 (GRCm39) T98S probably benign Het
Ltbp2 A T 12: 84,834,184 (GRCm39) I1435N probably damaging Het
Man2a1 G A 17: 64,932,383 (GRCm39) A157T probably benign Het
Mcm3ap T A 10: 76,337,148 (GRCm39) V1361E probably benign Het
Nobox A T 6: 43,284,538 (GRCm39) L36Q possibly damaging Het
Or2ag12 T A 7: 106,277,100 (GRCm39) M198L probably benign Het
Or51a10 A G 7: 103,699,334 (GRCm39) S76P probably damaging Het
Parp4 G A 14: 56,857,947 (GRCm39) V860I probably benign Het
Pim3 T A 15: 88,747,296 (GRCm39) probably null Het
Ptpn13 A T 5: 103,713,121 (GRCm39) N1748I possibly damaging Het
Rad51ap2 A G 12: 11,507,145 (GRCm39) T356A possibly damaging Het
Ranbp2 C T 10: 58,293,559 (GRCm39) R310* probably null Het
Rassf5 C T 1: 131,109,988 (GRCm39) V190I probably benign Het
Rgl1 T G 1: 152,409,281 (GRCm39) Q481P probably damaging Het
Rrp1b A G 17: 32,276,063 (GRCm39) T537A probably benign Het
Smok3c T A 5: 138,063,699 (GRCm39) S395R probably benign Het
St3gal1 A G 15: 66,983,195 (GRCm39) V187A possibly damaging Het
Strn4 A T 7: 16,556,978 (GRCm39) E145V probably damaging Het
Tex21 T A 12: 76,251,086 (GRCm39) probably null Het
Usp37 G A 1: 74,534,908 (GRCm39) R13* probably null Het
Uty G T Y: 1,174,735 (GRCm39) L222I probably damaging Homo
Wwp2 A G 8: 108,267,314 (GRCm39) T309A probably damaging Het
Zfp40 C T 17: 23,395,510 (GRCm39) R359H possibly damaging Het
Other mutations in 4933427I04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00979:4933427I04Rik APN 4 123,754,338 (GRCm39) missense probably damaging 0.97
IGL01518:4933427I04Rik APN 4 123,754,494 (GRCm39) missense probably benign 0.00
IGL02246:4933427I04Rik APN 4 123,754,655 (GRCm39) missense probably damaging 0.99
PIT4494001:4933427I04Rik UTSW 4 123,754,698 (GRCm39) missense probably benign
R0090:4933427I04Rik UTSW 4 123,754,775 (GRCm39) missense possibly damaging 0.66
R0299:4933427I04Rik UTSW 4 123,754,615 (GRCm39) missense possibly damaging 0.66
R0598:4933427I04Rik UTSW 4 123,754,681 (GRCm39) missense possibly damaging 0.46
R1775:4933427I04Rik UTSW 4 123,754,286 (GRCm39) missense possibly damaging 0.66
R2082:4933427I04Rik UTSW 4 123,754,769 (GRCm39) missense probably benign 0.05
R4581:4933427I04Rik UTSW 4 123,754,146 (GRCm39) missense possibly damaging 0.90
R4594:4933427I04Rik UTSW 4 123,754,331 (GRCm39) missense possibly damaging 0.66
R4841:4933427I04Rik UTSW 4 123,754,170 (GRCm39) missense probably benign 0.04
R6021:4933427I04Rik UTSW 4 123,754,509 (GRCm39) missense possibly damaging 0.90
R7660:4933427I04Rik UTSW 4 123,754,512 (GRCm39) missense possibly damaging 0.66
R8553:4933427I04Rik UTSW 4 123,754,327 (GRCm39) missense probably benign 0.03
R9333:4933427I04Rik UTSW 4 123,754,416 (GRCm39) missense probably benign 0.00
R9399:4933427I04Rik UTSW 4 123,754,413 (GRCm39) nonsense probably null
R9465:4933427I04Rik UTSW 4 123,754,317 (GRCm39) missense possibly damaging 0.83
Z1176:4933427I04Rik UTSW 4 123,754,668 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- TTGGCAGTCAAGTCTCAGGG -3'
(R):5'- CGCATTTTCACCCTGTATGGAAAAG -3'

Sequencing Primer
(F):5'- CAAGTCTCAGGGCAGGTCACTAG -3'
(R):5'- CCCTGTATGGAAAAGCTATTGCC -3'
Posted On 2018-08-01