Incidental Mutation 'R2877:4930522L14Rik'
ID 260598
Institutional Source Beutler Lab
Gene Symbol 4930522L14Rik
Ensembl Gene ENSMUSG00000072762
Gene Name RIKEN cDNA 4930522L14 gene
Synonyms Gm42152
MMRRC Submission 040465-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # R2877 (G1)
Quality Score 217
Status Validated
Chromosome 5
Chromosomal Location 109883856-109899752 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to C at 109886811 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000108166 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100937] [ENSMUST00000112547]
AlphaFold E9QAG4
Predicted Effect probably benign
Transcript: ENSMUST00000100937
SMART Domains Protein: ENSMUSP00000098497
Gene: ENSMUSG00000072762

DomainStartEndE-ValueType
KRAB 4 64 5.37e-15 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000112547
SMART Domains Protein: ENSMUSP00000108166
Gene: ENSMUSG00000072762

DomainStartEndE-ValueType
KRAB 4 66 7.19e-16 SMART
ZnF_C2H2 103 125 2.75e-3 SMART
ZnF_C2H2 131 153 1.72e-4 SMART
ZnF_C2H2 159 181 7.9e-4 SMART
ZnF_C2H2 187 209 1.04e-3 SMART
ZnF_C2H2 215 237 1.1e-2 SMART
ZnF_C2H2 243 265 3.89e-3 SMART
ZnF_C2H2 271 294 3.69e-4 SMART
ZnF_C2H2 300 322 5.9e-3 SMART
ZnF_C2H2 328 350 1.56e-2 SMART
ZnF_C2H2 356 378 1.18e-2 SMART
ZnF_C2H2 384 406 9.08e-4 SMART
ZnF_C2H2 412 434 1.98e-4 SMART
ZnF_C2H2 440 462 2.61e-4 SMART
ZnF_C2H2 468 491 1.38e-3 SMART
ZnF_C2H2 497 519 3.39e-3 SMART
ZnF_C2H2 525 547 1.4e-4 SMART
ZnF_C2H2 553 576 1.95e-3 SMART
ZnF_C2H2 582 604 5.14e-3 SMART
ZnF_C2H2 610 632 1.67e-2 SMART
ZnF_C2H2 638 660 1.72e-4 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
Validation Efficiency 96% (66/69)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 C T 11: 9,241,889 (GRCm39) L1251F possibly damaging Het
Accsl A T 2: 93,689,755 (GRCm39) M384K probably damaging Het
Adss1 A C 12: 112,600,623 (GRCm39) K197N probably damaging Het
Alg11 A G 8: 22,555,374 (GRCm39) N170D possibly damaging Het
Ambn T C 5: 88,608,559 (GRCm39) probably benign Het
Anapc7 T C 5: 122,566,219 (GRCm39) Y43H probably benign Het
Anxa10 T A 8: 62,513,373 (GRCm39) I255F probably damaging Het
Atg2b A T 12: 105,630,268 (GRCm39) Y374* probably null Het
Axl T A 7: 25,465,949 (GRCm39) M563L probably damaging Het
Carmil2 A G 8: 106,422,055 (GRCm39) E1108G probably damaging Het
Casp1 T C 9: 5,303,110 (GRCm39) M188T probably damaging Het
Chd3 A T 11: 69,251,998 (GRCm39) C87* probably null Het
Col6a3 G A 1: 90,703,321 (GRCm39) T2475I unknown Het
Creb3l4 A T 3: 90,149,615 (GRCm39) S83R probably damaging Het
Cyp2a4 G A 7: 26,011,612 (GRCm39) E278K possibly damaging Het
Dync1li2 A C 8: 105,156,047 (GRCm39) Y265D probably damaging Het
Eif3f G A 7: 108,534,019 (GRCm39) probably null Het
Eipr1 C T 12: 28,810,091 (GRCm39) T22I possibly damaging Het
Fbxo48 A G 11: 16,903,382 (GRCm39) K3E possibly damaging Het
Fbxw13 A G 9: 109,010,534 (GRCm39) F368S probably damaging Het
Fbxw19 A T 9: 109,315,038 (GRCm39) W175R probably damaging Het
Fibcd1 G A 2: 31,728,678 (GRCm39) P60S probably benign Het
Foxa3 A T 7: 18,748,805 (GRCm39) M107K probably benign Het
Foxj2 G A 6: 122,819,791 (GRCm39) D560N probably damaging Het
Gfm2 A G 13: 97,289,757 (GRCm39) R181G possibly damaging Het
Gpr25 C T 1: 136,188,553 (GRCm39) G20D possibly damaging Het
Grin1 A G 2: 25,187,641 (GRCm39) V594A probably damaging Het
Itpripl1 A G 2: 126,983,534 (GRCm39) V196A probably benign Het
Kcns1 A G 2: 164,006,682 (GRCm39) I427T probably damaging Het
Kiz T C 2: 146,731,476 (GRCm39) V322A possibly damaging Het
Mslnl G A 17: 25,961,908 (GRCm39) V128M probably damaging Het
Muc19 T A 15: 91,777,200 (GRCm39) noncoding transcript Het
Naa16 A G 14: 79,580,738 (GRCm39) M592T probably benign Het
Naa80 A T 9: 107,460,367 (GRCm39) E87D possibly damaging Het
Ncapd3 T A 9: 26,955,783 (GRCm39) probably null Het
Nebl C A 2: 17,439,740 (GRCm39) D178Y probably damaging Het
Nedd1 T A 10: 92,549,988 (GRCm39) N99I possibly damaging Het
Nuak1 T C 10: 84,211,209 (GRCm39) D293G possibly damaging Het
Or5b123 A T 19: 13,596,996 (GRCm39) I157F probably damaging Het
Or5m9b T C 2: 85,905,675 (GRCm39) M197T possibly damaging Het
Palb2 A G 7: 121,713,652 (GRCm39) V877A probably damaging Het
Rassf6 C T 5: 90,754,664 (GRCm39) V205I probably damaging Het
Rbak A G 5: 143,159,860 (GRCm39) Y398H probably damaging Het
Rcbtb1 A G 14: 59,448,041 (GRCm39) probably benign Het
Robo4 CGG CG 9: 37,322,786 (GRCm39) probably null Het
Smpdl3a C A 10: 57,685,181 (GRCm39) T317K probably damaging Het
Speer4e1 C T 5: 14,987,130 (GRCm39) V92M probably damaging Het
Syne2 A G 12: 76,047,605 (GRCm39) I4009V probably benign Het
Tarbp1 G A 8: 127,154,571 (GRCm39) L1474F probably damaging Het
Tchh A G 3: 93,351,535 (GRCm39) E325G unknown Het
Trpc4 T C 3: 54,198,761 (GRCm39) S562P probably damaging Het
Ttn T C 2: 76,567,409 (GRCm39) D27828G probably damaging Het
Ulk4 T C 9: 121,089,105 (GRCm39) D258G probably benign Het
Vmn1r215 A G 13: 23,260,731 (GRCm39) H257R probably benign Het
Vmn2r56 A C 7: 12,444,954 (GRCm39) M433R probably benign Het
Vmn2r76 C A 7: 85,875,201 (GRCm39) C592F probably benign Het
Zcchc8 C T 5: 123,838,766 (GRCm39) V591I probably benign Het
Znhit6 G C 3: 145,282,409 (GRCm39) G96A probably benign Het
Other mutations in 4930522L14Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02622:4930522L14Rik APN 5 109,887,101 (GRCm39) missense possibly damaging 0.86
R0164:4930522L14Rik UTSW 5 109,884,713 (GRCm39) missense probably damaging 0.96
R0164:4930522L14Rik UTSW 5 109,884,713 (GRCm39) missense probably damaging 0.96
R0432:4930522L14Rik UTSW 5 109,884,785 (GRCm39) missense probably damaging 1.00
R0463:4930522L14Rik UTSW 5 109,884,926 (GRCm39) unclassified probably benign
R0891:4930522L14Rik UTSW 5 109,884,156 (GRCm39) missense possibly damaging 0.47
R1289:4930522L14Rik UTSW 5 109,884,756 (GRCm39) nonsense probably null
R1637:4930522L14Rik UTSW 5 109,886,858 (GRCm39) missense probably benign 0.01
R1764:4930522L14Rik UTSW 5 109,884,655 (GRCm39) missense probably benign 0.22
R1793:4930522L14Rik UTSW 5 109,884,144 (GRCm39) missense probably damaging 1.00
R1860:4930522L14Rik UTSW 5 109,884,098 (GRCm39) missense probably damaging 1.00
R1899:4930522L14Rik UTSW 5 109,884,664 (GRCm39) missense probably benign 0.04
R2135:4930522L14Rik UTSW 5 109,885,509 (GRCm39) missense probably benign 0.00
R2143:4930522L14Rik UTSW 5 109,884,616 (GRCm39) missense probably damaging 1.00
R3847:4930522L14Rik UTSW 5 109,884,190 (GRCm39) splice site probably null
R4431:4930522L14Rik UTSW 5 109,884,440 (GRCm39) missense possibly damaging 0.47
R4578:4930522L14Rik UTSW 5 109,884,537 (GRCm39) nonsense probably null
R4611:4930522L14Rik UTSW 5 109,885,259 (GRCm39) missense probably benign 0.00
R4776:4930522L14Rik UTSW 5 109,884,739 (GRCm39) missense probably benign 0.22
R4921:4930522L14Rik UTSW 5 109,885,662 (GRCm39) missense probably benign 0.25
R4937:4930522L14Rik UTSW 5 109,884,067 (GRCm39) missense probably benign 0.12
R4952:4930522L14Rik UTSW 5 109,887,063 (GRCm39) critical splice donor site probably null
R4980:4930522L14Rik UTSW 5 109,885,292 (GRCm39) missense probably damaging 1.00
R5079:4930522L14Rik UTSW 5 109,885,196 (GRCm39) missense probably benign
R5088:4930522L14Rik UTSW 5 109,883,939 (GRCm39) missense probably damaging 1.00
R5143:4930522L14Rik UTSW 5 109,887,064 (GRCm39) critical splice donor site probably null
R5183:4930522L14Rik UTSW 5 109,887,171 (GRCm39) missense probably damaging 1.00
R5461:4930522L14Rik UTSW 5 109,884,643 (GRCm39) missense possibly damaging 0.74
R5498:4930522L14Rik UTSW 5 109,885,413 (GRCm39) missense probably benign 0.05
R5576:4930522L14Rik UTSW 5 109,885,570 (GRCm39) missense probably benign 0.00
R6081:4930522L14Rik UTSW 5 109,887,097 (GRCm39) missense probably damaging 1.00
R6387:4930522L14Rik UTSW 5 109,884,881 (GRCm39) missense possibly damaging 0.88
R6509:4930522L14Rik UTSW 5 109,885,250 (GRCm39) nonsense probably null
R6585:4930522L14Rik UTSW 5 109,885,534 (GRCm39) missense probably damaging 1.00
R7309:4930522L14Rik UTSW 5 109,884,819 (GRCm39) missense probably damaging 1.00
R7740:4930522L14Rik UTSW 5 109,885,370 (GRCm39) nonsense probably null
R7877:4930522L14Rik UTSW 5 109,884,230 (GRCm39) missense probably damaging 1.00
R8526:4930522L14Rik UTSW 5 109,885,655 (GRCm39) missense possibly damaging 0.92
R8884:4930522L14Rik UTSW 5 109,885,354 (GRCm39) missense probably damaging 0.98
R9047:4930522L14Rik UTSW 5 109,885,420 (GRCm39) missense
R9432:4930522L14Rik UTSW 5 109,884,917 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GCTGGAATGTGGCTATGATTCAA -3'
(R):5'- CTCAAGAAGAATGGGCTTTGCTGA -3'

Sequencing Primer
(F):5'- ATATCTGTGAAGGCATTGTTTCC -3'
(R):5'- TTGGAGACCTACAGGAACCTCATTG -3'
Posted On 2015-01-23