Incidental Mutation 'R6093:4932414N04Rik'
ID 486025
Institutional Source Beutler Lab
Gene Symbol 4932414N04Rik
Ensembl Gene ENSMUSG00000079324
Gene Name RIKEN cDNA 4932414N04 gene
Synonyms
MMRRC Submission 044250-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6093 (G1)
Quality Score 225.009
Status Not validated
Chromosome 2
Chromosomal Location 68487135-68578876 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 68490214 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000135792 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055930] [ENSMUST00000125621] [ENSMUST00000128259]
AlphaFold Q8CEQ9
Predicted Effect probably benign
Transcript: ENSMUST00000055930
SMART Domains Protein: ENSMUSP00000059809
Gene: ENSMUSG00000079324

DomainStartEndE-ValueType
coiled coil region 154 241 N/A INTRINSIC
Pfam:DUF3496 265 361 8.5e-12 PFAM
internal_repeat_1 456 597 1.76e-26 PROSPERO
internal_repeat_1 601 737 1.76e-26 PROSPERO
Predicted Effect noncoding transcript
Transcript: ENSMUST00000112332
Predicted Effect silent
Transcript: ENSMUST00000125621
Predicted Effect probably benign
Transcript: ENSMUST00000128259
SMART Domains Protein: ENSMUSP00000135792
Gene: ENSMUSG00000079324

DomainStartEndE-ValueType
internal_repeat_1 5 39 6.02e-5 PROSPERO
internal_repeat_1 209 242 6.02e-5 PROSPERO
low complexity region 286 297 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.8%
  • 20x: 93.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot11 C T 4: 106,617,327 (GRCm39) G240R probably damaging Het
Adgrl3 A C 5: 81,794,369 (GRCm39) R531S probably benign Het
Ahctf1 T C 1: 179,590,517 (GRCm39) D1252G probably benign Het
Ano1 T C 7: 144,165,114 (GRCm39) N648S possibly damaging Het
Antxr2 C A 5: 98,178,319 (GRCm39) L30F probably damaging Het
Apol9a T A 15: 77,288,620 (GRCm39) N249I probably benign Het
Atp2a1 A G 7: 126,046,093 (GRCm39) V977A probably damaging Het
Clmn T C 12: 104,738,215 (GRCm39) T968A probably benign Het
Clstn2 A T 9: 97,340,263 (GRCm39) I703N probably damaging Het
Cnot1 T C 8: 96,475,522 (GRCm39) T1051A probably benign Het
Csde1 A G 3: 102,960,218 (GRCm39) Y615C probably damaging Het
Dcaf17 A G 2: 70,912,356 (GRCm39) K314E possibly damaging Het
Dnah10 A T 5: 124,830,238 (GRCm39) I711F probably benign Het
Duox1 G T 2: 122,177,755 (GRCm39) R1513L probably benign Het
Exph5 A G 9: 53,283,917 (GRCm39) T333A possibly damaging Het
Fmnl2 A G 2: 53,004,880 (GRCm39) D658G probably damaging Het
Gcgr T A 11: 120,428,947 (GRCm39) L395Q probably damaging Het
Gm10801 C CGTA 2: 98,494,152 (GRCm39) probably null Het
Greb1 C T 12: 16,734,487 (GRCm39) C1501Y probably benign Het
Iqgap2 A G 13: 95,765,471 (GRCm39) V1533A probably damaging Het
Kcnc3 A C 7: 44,240,932 (GRCm39) D208A probably benign Het
Kctd14 A G 7: 97,104,160 (GRCm39) probably benign Het
Mcm5 C A 8: 75,836,374 (GRCm39) D13E probably benign Het
Med23 A G 10: 24,754,341 (GRCm39) I221V probably benign Het
Msantd5f6 T C 4: 73,320,258 (GRCm39) I174V probably benign Het
Myo19 T C 11: 84,776,535 (GRCm39) F64L probably damaging Het
Ncapd3 T G 9: 26,967,454 (GRCm39) S597A probably damaging Het
Neb A T 2: 52,141,782 (GRCm39) Y72* probably null Het
Nrip1 C T 16: 76,091,652 (GRCm39) probably benign Het
Or5h26 T A 16: 58,988,330 (GRCm39) M59L probably damaging Het
Otx1 A T 11: 21,949,406 (GRCm39) L24H probably damaging Het
Phkb T A 8: 86,668,958 (GRCm39) D328E probably damaging Het
Phyh G T 2: 4,923,896 (GRCm39) A6S possibly damaging Het
Pole A T 5: 110,459,956 (GRCm39) Q1120L probably benign Het
Rbmxl1 T C 8: 79,232,572 (GRCm39) Y257C probably damaging Het
Smurf2 A T 11: 106,759,449 (GRCm39) H69Q possibly damaging Het
Tmem167b A T 3: 108,469,439 (GRCm39) M1K probably null Het
Tmod4 A T 3: 95,032,929 (GRCm39) T22S probably benign Het
Triml1 T C 8: 43,593,755 (GRCm39) I149M probably benign Het
Vmn2r108 T C 17: 20,701,402 (GRCm39) T33A probably benign Het
Vmn2r76 T A 7: 85,877,469 (GRCm39) R525* probably null Het
Zfp109 A T 7: 23,928,558 (GRCm39) W292R probably benign Het
Zfp292 C T 4: 34,811,902 (GRCm39) A381T probably damaging Het
Zfp791 C T 8: 85,840,135 (GRCm39) probably null Het
Other mutations in 4932414N04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00160:4932414N04Rik APN 2 68,563,219 (GRCm39) missense probably benign 0.02
IGL01384:4932414N04Rik APN 2 68,575,749 (GRCm39) missense possibly damaging 0.53
IGL02170:4932414N04Rik APN 2 68,561,467 (GRCm39) missense probably benign 0.02
IGL02650:4932414N04Rik APN 2 68,571,881 (GRCm39) missense probably benign 0.00
IGL02707:4932414N04Rik APN 2 68,561,474 (GRCm39) missense possibly damaging 0.71
IGL02737:4932414N04Rik APN 2 68,566,904 (GRCm39) missense possibly damaging 0.53
IGL03351:4932414N04Rik APN 2 68,561,427 (GRCm39) missense probably benign
R0328:4932414N04Rik UTSW 2 68,574,624 (GRCm39) missense possibly damaging 0.53
R0362:4932414N04Rik UTSW 2 68,563,261 (GRCm39) missense probably benign 0.00
R0638:4932414N04Rik UTSW 2 68,547,572 (GRCm39) missense probably benign 0.18
R1201:4932414N04Rik UTSW 2 68,546,626 (GRCm39) missense possibly damaging 0.53
R1381:4932414N04Rik UTSW 2 68,561,430 (GRCm39) missense probably benign 0.18
R1456:4932414N04Rik UTSW 2 68,546,558 (GRCm39) missense possibly damaging 0.86
R2001:4932414N04Rik UTSW 2 68,571,800 (GRCm39) missense probably benign
R2051:4932414N04Rik UTSW 2 68,541,392 (GRCm39) missense possibly damaging 0.72
R2228:4932414N04Rik UTSW 2 68,559,935 (GRCm39) missense probably benign 0.00
R2292:4932414N04Rik UTSW 2 68,562,483 (GRCm39) missense probably benign 0.00
R2357:4932414N04Rik UTSW 2 68,569,844 (GRCm39) missense possibly damaging 0.86
R2484:4932414N04Rik UTSW 2 68,541,819 (GRCm39) missense possibly damaging 0.85
R3035:4932414N04Rik UTSW 2 68,575,762 (GRCm39) missense probably benign 0.00
R3916:4932414N04Rik UTSW 2 68,562,329 (GRCm39) missense possibly damaging 0.71
R3950:4932414N04Rik UTSW 2 68,494,747 (GRCm39) critical splice donor site probably null
R3951:4932414N04Rik UTSW 2 68,494,747 (GRCm39) critical splice donor site probably null
R3952:4932414N04Rik UTSW 2 68,494,747 (GRCm39) critical splice donor site probably null
R4091:4932414N04Rik UTSW 2 68,575,722 (GRCm39) missense possibly damaging 0.73
R4118:4932414N04Rik UTSW 2 68,566,857 (GRCm39) missense probably benign
R4153:4932414N04Rik UTSW 2 68,498,941 (GRCm39) intron probably benign
R4210:4932414N04Rik UTSW 2 68,490,222 (GRCm39) start gained probably benign
R4614:4932414N04Rik UTSW 2 68,575,804 (GRCm39) missense probably benign 0.01
R4818:4932414N04Rik UTSW 2 68,571,810 (GRCm39) missense probably benign
R5202:4932414N04Rik UTSW 2 68,562,308 (GRCm39) missense probably benign
R5466:4932414N04Rik UTSW 2 68,541,733 (GRCm39) missense probably benign 0.11
R5585:4932414N04Rik UTSW 2 68,571,770 (GRCm39) missense probably benign 0.00
R5602:4932414N04Rik UTSW 2 68,578,712 (GRCm39) makesense probably null
R5846:4932414N04Rik UTSW 2 68,562,377 (GRCm39) missense unknown
R5902:4932414N04Rik UTSW 2 68,539,281 (GRCm39) start codon destroyed probably null
R6002:4932414N04Rik UTSW 2 68,492,768 (GRCm39) splice site probably null
R6029:4932414N04Rik UTSW 2 68,524,370 (GRCm39) splice site probably null
R6168:4932414N04Rik UTSW 2 68,571,827 (GRCm39) missense possibly damaging 0.86
R6300:4932414N04Rik UTSW 2 68,561,453 (GRCm39) missense possibly damaging 0.96
R6322:4932414N04Rik UTSW 2 68,559,843 (GRCm39) missense probably benign 0.00
R6533:4932414N04Rik UTSW 2 68,546,662 (GRCm39) nonsense probably null
R6547:4932414N04Rik UTSW 2 68,490,251 (GRCm39) utr 5 prime probably benign
R7309:4932414N04Rik UTSW 2 68,546,530 (GRCm39) missense probably benign 0.29
R7400:4932414N04Rik UTSW 2 68,496,547 (GRCm39) missense unknown
R7454:4932414N04Rik UTSW 2 68,518,648 (GRCm39) missense unknown
R7481:4932414N04Rik UTSW 2 68,494,575 (GRCm39) missense unknown
R7498:4932414N04Rik UTSW 2 68,498,012 (GRCm39) missense unknown
R7523:4932414N04Rik UTSW 2 68,569,673 (GRCm39) missense probably benign 0.01
R7523:4932414N04Rik UTSW 2 68,492,824 (GRCm39) missense unknown
R7583:4932414N04Rik UTSW 2 68,569,670 (GRCm39) missense probably damaging 0.98
R7701:4932414N04Rik UTSW 2 68,561,548 (GRCm39) missense possibly damaging 0.60
R7746:4932414N04Rik UTSW 2 68,559,339 (GRCm39) missense probably benign 0.33
R7778:4932414N04Rik UTSW 2 68,569,855 (GRCm39) missense possibly damaging 0.73
R7985:4932414N04Rik UTSW 2 68,494,693 (GRCm39) missense unknown
R8525:4932414N04Rik UTSW 2 68,559,378 (GRCm39) missense possibly damaging 0.83
R8765:4932414N04Rik UTSW 2 68,566,956 (GRCm39) missense possibly damaging 0.85
R8906:4932414N04Rik UTSW 2 68,562,498 (GRCm39) missense possibly damaging 0.85
R9406:4932414N04Rik UTSW 2 68,498,019 (GRCm39) missense unknown
R9627:4932414N04Rik UTSW 2 68,487,834 (GRCm39) unclassified probably benign
X0025:4932414N04Rik UTSW 2 68,559,360 (GRCm39) missense probably benign 0.06
Predicted Primers
Posted On 2017-08-16