Incidental Mutation 'R5902:4932414N04Rik'
ID 501636
Institutional Source Beutler Lab
Gene Symbol 4932414N04Rik
Ensembl Gene ENSMUSG00000079324
Gene Name RIKEN cDNA 4932414N04 gene
Synonyms
MMRRC Submission 044100-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5902 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 68487135-68578876 bp(+) (GRCm39)
Type of Mutation start codon destroyed
DNA Base Change (assembly) A to G at 68539281 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 1 (M1V)
Ref Sequence ENSEMBL: ENSMUSP00000135792 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055930] [ENSMUST00000128259]
AlphaFold Q8CEQ9
Predicted Effect probably null
Transcript: ENSMUST00000055930
AA Change: M1V
SMART Domains Protein: ENSMUSP00000059809
Gene: ENSMUSG00000079324
AA Change: M1V

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 probably null
Transcript: ENSMUST00000128259
AA Change: M1V
SMART Domains Protein: ENSMUSP00000135792
Gene: ENSMUSG00000079324
AA Change: M1V

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
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.4%
  • 10x: 97.4%
  • 20x: 92.1%
Validation Efficiency 99% (81/82)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T A 11: 9,247,177 (GRCm39) L2308H probably damaging Het
Abcc8 T C 7: 45,764,463 (GRCm39) T1161A probably benign Het
Acin1 T A 14: 54,901,130 (GRCm39) T659S probably benign Het
Actl7a G T 4: 56,743,827 (GRCm39) R118L probably damaging Het
Acyp2 C T 11: 30,456,354 (GRCm39) E98K possibly damaging Het
Alkbh8 A G 9: 3,385,414 (GRCm39) K569E probably benign Het
Anxa3 A T 5: 96,960,712 (GRCm39) K39* probably null Het
Aoc2 A G 11: 101,220,072 (GRCm39) E659G probably damaging Het
Atg7 C T 6: 114,650,639 (GRCm39) T83M possibly damaging Het
AU022252 T C 4: 119,084,101 (GRCm39) D104G probably benign Het
Car6 T C 4: 150,271,956 (GRCm39) Y231C possibly damaging Het
Cdh10 T G 15: 18,985,341 (GRCm39) probably null Het
Cebpz A C 17: 79,233,366 (GRCm39) M787R probably benign Het
Chst2 A G 9: 95,287,662 (GRCm39) L228P probably damaging Het
Clic4 T C 4: 134,999,869 (GRCm39) K11R probably benign Het
Col6a3 C T 1: 90,729,921 (GRCm39) probably null Het
Commd7 T A 2: 153,463,737 (GRCm39) T144S probably damaging Het
Ctla2a T A 13: 61,082,834 (GRCm39) *138Y probably null Het
Dhx33 A T 11: 70,879,957 (GRCm39) V351D probably damaging Het
Dnah9 G A 11: 65,916,013 (GRCm39) T2313I probably benign Het
Dspp A T 5: 104,325,977 (GRCm39) D780V unknown Het
Dync1li1 A G 9: 114,546,929 (GRCm39) probably null Het
E2f3 C T 13: 30,169,250 (GRCm39) probably benign Het
Fan1 T C 7: 64,023,070 (GRCm39) probably null Het
Gart A G 16: 91,425,415 (GRCm39) S617P probably damaging Het
Ggcx A G 6: 72,406,979 (GRCm39) N705S possibly damaging Het
Gm4841 A T 18: 60,403,868 (GRCm39) V75E probably damaging Het
Greb1l A G 18: 10,538,302 (GRCm39) E1105G probably benign Het
Hr C A 14: 70,795,231 (GRCm39) Q288K probably benign Het
Hus1 T C 11: 8,960,669 (GRCm39) probably benign Het
Ifi47 C A 11: 48,986,213 (GRCm39) probably null Het
Irf2bp1 T C 7: 18,738,372 (GRCm39) V4A probably benign Het
Kprp C T 3: 92,731,835 (GRCm39) C405Y unknown Het
Lacc1 T C 14: 77,272,239 (GRCm39) I186V possibly damaging Het
Lifr A G 15: 7,220,231 (GRCm39) T954A probably benign Het
Lonrf2 T C 1: 38,846,174 (GRCm39) M333V probably benign Het
Mthfd1 A T 12: 76,337,826 (GRCm39) H400L probably benign Het
Myh4 A G 11: 67,141,733 (GRCm39) K864R possibly damaging Het
Nup50 C T 15: 84,819,641 (GRCm39) A305V probably benign Het
Or4a74 T A 2: 89,439,595 (GRCm39) I284L probably damaging Het
Or4k44 C T 2: 111,367,739 (GRCm39) M298I probably benign Het
Pax4 G T 6: 28,447,126 (GRCm39) Q3K probably benign Het
Pced1b T G 15: 97,282,970 (GRCm39) Y336* probably null Het
Postn C A 3: 54,279,510 (GRCm39) N329K probably benign Het
Prickle1 T C 15: 93,408,553 (GRCm39) E82G probably null Het
Prtn3 T C 10: 79,718,766 (GRCm39) Y241H probably damaging Het
Rasgrf2 A T 13: 92,068,011 (GRCm39) I260K probably damaging Het
Sh3glb1 T C 3: 144,418,431 (GRCm39) N44S possibly damaging Het
Sis A T 3: 72,867,589 (GRCm39) probably null Het
Slc4a9 A G 18: 36,662,386 (GRCm39) probably null Het
Slc4a9 A T 18: 36,664,560 (GRCm39) D406V probably damaging Het
Slc8a1 C T 17: 81,715,511 (GRCm39) G841R probably damaging Het
Smn1 C T 13: 100,263,412 (GRCm39) P60L probably benign Het
Snai1 G A 2: 167,383,930 (GRCm39) C241Y probably damaging Het
Spock3 A G 8: 63,808,336 (GRCm39) D411G unknown Het
Szt2 T A 4: 118,248,700 (GRCm39) T607S probably benign Het
Tcap A T 11: 98,274,673 (GRCm39) M1L probably benign Het
Tex29 A T 8: 11,905,723 (GRCm39) probably benign Het
Tex29 C A 8: 11,904,276 (GRCm39) probably benign Het
Tex29 C T 8: 11,904,277 (GRCm39) probably benign Het
Tln2 T C 9: 67,269,999 (GRCm39) T467A probably benign Het
Trim34a C T 7: 103,910,328 (GRCm39) Q377* probably null Het
Ube2q1 T A 3: 89,683,487 (GRCm39) L144* probably null Het
Vps13c A G 9: 67,841,729 (GRCm39) E1917G probably benign Het
Wdr19 T A 5: 65,384,482 (GRCm39) N525K probably benign Het
Wdr3 A T 3: 100,051,807 (GRCm39) probably benign Het
Wnt5b T A 6: 119,425,199 (GRCm39) H6L probably benign Het
Yju2 A G 17: 56,269,077 (GRCm39) T62A probably damaging Het
Zdbf2 T C 1: 63,345,685 (GRCm39) S1355P possibly damaging Het
Zfp11 T A 5: 129,734,976 (GRCm39) I162F probably damaging Het
Zpbp T C 11: 11,365,332 (GRCm39) T172A probably benign 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
R6002:4932414N04Rik UTSW 2 68,492,768 (GRCm39) splice site probably null
R6029:4932414N04Rik UTSW 2 68,524,370 (GRCm39) splice site probably null
R6093:4932414N04Rik UTSW 2 68,490,214 (GRCm39) splice site probably benign
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 PCR Primer
(F):5'- GGTATGGAGAGCTGTAGCAC -3'
(R):5'- TCTCTAAGTTGAGAACACCTATGTG -3'

Sequencing Primer
(F):5'- AGAAACCTGAAGGATCCTGTC -3'
(R):5'- CACCTATGTGTACAATTAGAGTTCC -3'
Posted On 2017-12-01