Incidental Mutation 'R0723:4931423N10Rik'
ID218672
Institutional Source Beutler Lab
Gene Symbol 4931423N10Rik
Ensembl Gene ENSMUSG00000026774
Gene NameRIKEN cDNA 4931423N10 gene
Synonyms
MMRRC Submission 038905-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.092) question?
Stock #R0723 (G1)
Quality Score38
Status Validated
Chromosome2
Chromosomal Location23207476-23267129 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 23256924 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000110150 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028113] [ENSMUST00000114505]
Predicted Effect probably benign
Transcript: ENSMUST00000028113
SMART Domains Protein: ENSMUSP00000028113
Gene: ENSMUSG00000026774

DomainStartEndE-ValueType
Blast:ANK 62 92 7e-15 BLAST
ANK 96 125 6.71e-2 SMART
ANK 129 158 1.3e1 SMART
ANK 162 191 1.01e-5 SMART
ANK 195 224 2.88e-1 SMART
ANK 228 257 1.93e-2 SMART
ANK 261 290 1.09e3 SMART
low complexity region 341 352 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114505
SMART Domains Protein: ENSMUSP00000110150
Gene: ENSMUSG00000026774

DomainStartEndE-ValueType
Blast:ANK 62 92 4e-15 BLAST
ANK 96 125 6.71e-2 SMART
ANK 137 166 2.88e-1 SMART
ANK 170 199 1.93e-2 SMART
ANK 203 232 1.09e3 SMART
low complexity region 282 293 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.7%
  • 20x: 96.0%
Validation Efficiency 99% (69/70)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700022I11Rik T A 4: 42,971,691 N341K probably damaging Het
4930433I11Rik A T 7: 40,993,056 T141S probably benign Het
8030411F24Rik T C 2: 148,783,362 I72T probably damaging Het
Acbd5 T G 2: 23,069,596 V54G probably damaging Het
Acin1 A T 14: 54,665,451 S255T probably damaging Het
Adcy2 A G 13: 68,999,129 L56P probably damaging Het
Akap6 G T 12: 53,141,902 C2033F probably damaging Het
Ano5 A G 7: 51,587,758 I777V probably benign Het
Arhgef28 A G 13: 97,939,479 V1349A probably benign Het
Bank1 T C 3: 136,054,403 probably null Het
C2cd5 T C 6: 143,041,555 probably benign Het
Cadps2 A G 6: 23,287,698 V1161A probably damaging Het
Car8 A T 4: 8,169,703 D268E probably benign Het
Ckap5 T A 2: 91,555,331 S175T probably damaging Het
Clk4 T A 11: 51,275,493 Y67* probably null Het
Copg2 T C 6: 30,815,982 I473V possibly damaging Het
Cyp2s1 C T 7: 25,809,548 V43I probably benign Het
Ddx54 A G 5: 120,623,638 D493G probably benign Het
Efemp2 T C 19: 5,480,050 S140P probably damaging Het
Fam214a G A 9: 75,009,451 G444E probably damaging Het
Fat1 C A 8: 45,026,749 T2944K probably damaging Het
Fgfr1 T A 8: 25,557,768 D43E probably damaging Het
Fry G A 5: 150,496,360 A996T probably damaging Het
Fyb2 G A 4: 105,015,866 V784I probably benign Het
Gm6507 T A 6: 89,185,162 noncoding transcript Het
Gm7964 T C 7: 83,756,166 noncoding transcript Het
Gucy2c T C 6: 136,727,801 probably null Het
Hdac10 A T 15: 89,126,418 L259Q probably damaging Het
Hoxd9 A T 2: 74,698,828 D258V probably damaging Het
Hs3st3b1 T C 11: 63,921,575 T105A probably benign Het
Hsd17b7 A G 1: 169,956,026 L271P probably damaging Het
Ifnlr1 T A 4: 135,701,213 probably benign Het
Kif22 A T 7: 127,033,906 M121K probably damaging Het
Kl G A 5: 150,953,101 D129N probably damaging Het
Mettl13 A T 1: 162,534,430 I648N probably damaging Het
Mlh1 C T 9: 111,271,472 R18H probably damaging Het
Mtmr14 T C 6: 113,270,512 probably benign Het
Myo15 C A 11: 60,478,977 N854K possibly damaging Het
Myo1h T C 5: 114,319,680 I84T probably benign Het
Myo9a A T 9: 59,871,100 S1380C probably benign Het
Myof A G 19: 37,981,260 V318A probably damaging Het
N4bp2l2 A G 5: 150,662,432 S28P probably damaging Het
Narfl G A 17: 25,781,821 V406M probably damaging Het
Nbr1 C T 11: 101,576,319 Q570* probably null Het
Nhp2 C T 11: 51,619,923 Q36* probably null Het
Olfr23 T G 11: 73,940,270 V8G probably benign Het
Olfr884 G T 9: 38,047,827 V202L probably benign Het
Poc1b T A 10: 99,129,595 W129R probably damaging Het
Rapgef2 C T 3: 79,079,174 E1018K probably benign Het
Rgs12 T C 5: 35,024,366 probably benign Het
Rufy2 G A 10: 62,998,094 V280I probably benign Het
Snx2 A G 18: 53,210,372 I281V probably benign Het
Spag5 C A 11: 78,319,584 probably benign Het
Stxbp5 A T 10: 9,768,873 I961N probably damaging Het
Tet2 T C 3: 133,467,284 E1739G probably benign Het
Tmod2 A G 9: 75,595,055 F50S possibly damaging Het
Tnfsf13b T G 8: 10,007,166 probably null Het
Ttn T C 2: 76,786,335 K16525E possibly damaging Het
Txnrd2 T C 16: 18,440,879 probably benign Het
Ubr1 A T 2: 120,881,101 Y1437* probably null Het
Vwf C A 6: 125,566,262 D170E probably benign Het
Wdr95 C G 5: 149,574,048 I230M probably damaging Het
Xirp2 C T 2: 67,512,215 S1600F probably damaging Het
Zfp12 A G 5: 143,244,883 K322E probably damaging Het
Other mutations in 4931423N10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00694:4931423N10Rik APN 2 23230168 missense probably damaging 0.99
IGL02141:4931423N10Rik APN 2 23230200 missense probably damaging 1.00
IGL02377:4931423N10Rik APN 2 23212655 intron probably benign
IGL03328:4931423N10Rik APN 2 23212805 missense possibly damaging 0.71
R0467:4931423N10Rik UTSW 2 23212820 missense possibly damaging 0.85
R1169:4931423N10Rik UTSW 2 23256982 missense possibly damaging 0.53
R1507:4931423N10Rik UTSW 2 23208074 missense probably damaging 0.98
R4965:4931423N10Rik UTSW 2 23245115 missense probably benign 0.40
R5198:4931423N10Rik UTSW 2 23212461 missense probably damaging 1.00
R5619:4931423N10Rik UTSW 2 23257005 critical splice donor site probably null
R5677:4931423N10Rik UTSW 2 23212718 missense probably damaging 0.98
R5715:4931423N10Rik UTSW 2 23207977 missense possibly damaging 0.86
R6123:4931423N10Rik UTSW 2 23230122 missense possibly damaging 0.93
R6263:4931423N10Rik UTSW 2 23266733 unclassified probably benign
R6858:4931423N10Rik UTSW 2 23212664 missense possibly damaging 0.51
R7427:4931423N10Rik UTSW 2 23256994 missense probably benign
R7577:4931423N10Rik UTSW 2 23207825 missense probably benign
Predicted Primers
Posted On2014-08-19