Incidental Mutation 'R1667:Rnf207'
ID 187274
Institutional Source Beutler Lab
Gene Symbol Rnf207
Ensembl Gene ENSMUSG00000058498
Gene Name ring finger protein 207
Synonyms D330010C22Rik
MMRRC Submission 039703-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # R1667 (G1)
Quality Score 174
Status Validated
Chromosome 4
Chromosomal Location 152391476-152403450 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 152397672 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Lysine at position 361 (E361K)
Ref Sequence ENSEMBL: ENSMUSP00000075540 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076183] [ENSMUST00000130008] [ENSMUST00000170820]
AlphaFold Q3V3A7
Predicted Effect probably benign
Transcript: ENSMUST00000076183
AA Change: E361K

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000075540
Gene: ENSMUSG00000058498
AA Change: E361K

DomainStartEndE-ValueType
RING 25 63 1.16e-5 SMART
Pfam:zf-B_box 93 145 3.6e-11 PFAM
Pfam:DUF3583 204 378 1.2e-10 PFAM
coiled coil region 422 461 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000108688
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123133
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127565
Predicted Effect probably benign
Transcript: ENSMUST00000130008
SMART Domains Protein: ENSMUSP00000127196
Gene: ENSMUSG00000058498

DomainStartEndE-ValueType
RING 25 63 5.6e-8 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134269
Predicted Effect probably benign
Transcript: ENSMUST00000170820
AA Change: E326K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000129400
Gene: ENSMUSG00000058498
AA Change: E326K

DomainStartEndE-ValueType
RING 25 63 1.16e-5 SMART
Pfam:zf-B_box 93 145 1e-11 PFAM
low complexity region 236 242 N/A INTRINSIC
low complexity region 315 326 N/A INTRINSIC
coiled coil region 387 426 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145311
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142427
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146496
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143968
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135837
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.0%
Validation Efficiency 99% (76/77)
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra1 G A 7: 139,425,564 (GRCm39) A26T possibly damaging Het
Adgrg3 T A 8: 95,760,001 (GRCm39) Y73* probably null Het
Alk A T 17: 72,218,562 (GRCm39) V761E probably damaging Het
Ankrd13a T C 5: 114,924,794 (GRCm39) V93A possibly damaging Het
Anks1b T C 10: 90,347,046 (GRCm39) probably null Het
Arb2a T A 13: 77,907,635 (GRCm39) M1K probably null Het
Ascl1 T C 10: 87,328,655 (GRCm39) N99S probably benign Het
Atm A T 9: 53,412,232 (GRCm39) L972Q probably damaging Het
Atp2c1 A T 9: 105,309,996 (GRCm39) L566Q probably null Het
Bank1 T A 3: 135,799,057 (GRCm39) Y629F probably damaging Het
Bod1l G T 5: 41,974,118 (GRCm39) L2399I probably benign Het
Bub1b G A 2: 118,471,670 (GRCm39) G1010D probably benign Het
Ces1b G A 8: 93,783,532 (GRCm39) H563Y possibly damaging Het
Cfap70 T C 14: 20,454,225 (GRCm39) E853G probably benign Het
Cfh T C 1: 140,033,261 (GRCm39) E779G probably benign Het
Cox7c A G 13: 86,194,003 (GRCm39) S7P probably benign Het
Cyp2c67 A G 19: 39,632,034 (GRCm39) probably null Het
Dhx30 G T 9: 109,914,513 (GRCm39) L995I possibly damaging Het
Dhx30 G C 9: 109,914,514 (GRCm39) N957K possibly damaging Het
Dsc3 T C 18: 20,124,617 (GRCm39) T36A possibly damaging Het
Dstyk A G 1: 132,384,657 (GRCm39) D717G probably damaging Het
Dusp10 A G 1: 183,769,055 (GRCm39) D7G probably damaging Het
E230001N04Rik T G 17: 28,742,935 (GRCm39) noncoding transcript Het
Ece2 T C 16: 20,456,588 (GRCm39) S330P possibly damaging Het
Frmd5 ATAGTGGAATTGTTCAAACTC ATAGTGGAATTGTTCAAACTCTAGTGGAATTGTTCAAACTC 2: 121,379,211 (GRCm39) probably null Het
Gata3 T C 2: 9,882,360 (GRCm39) H14R possibly damaging Het
Ggta1 T A 2: 35,304,295 (GRCm39) I75F possibly damaging Het
Hcn1 A T 13: 117,739,609 (GRCm39) I124F unknown Het
Herpud1 A C 8: 95,115,994 (GRCm39) D53A probably damaging Het
Inhba T A 13: 16,201,209 (GRCm39) L257Q possibly damaging Het
Itga10 C T 3: 96,559,054 (GRCm39) probably benign Het
Jmy T A 13: 93,634,878 (GRCm39) S313C probably damaging Het
Lpo G A 11: 87,698,067 (GRCm39) probably benign Het
Lsg1 T C 16: 30,390,170 (GRCm39) E315G probably damaging Het
Lsm14a T A 7: 34,065,079 (GRCm39) T167S possibly damaging Het
Lsmem1 GTACATACATACATACATACATACATACA GTACATACATACATACATACATACATACATACA 12: 40,235,260 (GRCm39) probably null Het
Map3k2 T C 18: 32,336,845 (GRCm39) probably benign Het
Mapk12 A T 15: 89,024,344 (GRCm39) M81K probably damaging Het
Matn2 T A 15: 34,378,878 (GRCm39) C305S probably damaging Het
Mgam T C 6: 40,653,978 (GRCm39) Y844H possibly damaging Het
Mgat5b A G 11: 116,838,203 (GRCm39) R281G probably benign Het
Mon1b T G 8: 114,368,589 (GRCm39) C497G probably damaging Het
Mybbp1a A T 11: 72,336,043 (GRCm39) H452L probably benign Het
Mybl2 A G 2: 162,917,616 (GRCm39) T41A probably damaging Het
Ncoa5 A G 2: 164,843,623 (GRCm39) V540A probably damaging Het
Nup93 T A 8: 95,019,315 (GRCm39) V47E possibly damaging Het
Or10a4 A T 7: 106,696,977 (GRCm39) M102L probably benign Het
Or5j3 A G 2: 86,129,080 (GRCm39) M307V probably null Het
Orc6 T A 8: 86,031,914 (GRCm39) C100S possibly damaging Het
Otogl G T 10: 107,649,826 (GRCm39) Y1176* probably null Het
Patj A T 4: 98,301,264 (GRCm39) D183V probably damaging Het
Pik3r3 A G 4: 116,079,514 (GRCm39) T4A probably damaging Het
Pla2g4d G A 2: 120,100,631 (GRCm39) probably benign Het
Pla2r1 A G 2: 60,250,601 (GRCm39) I1407T probably benign Het
Pramel13 A T 4: 144,119,606 (GRCm39) C320* probably null Het
Prex2 A T 1: 11,256,981 (GRCm39) H1231L probably benign Het
Prkca A G 11: 107,874,772 (GRCm39) V390A probably damaging Het
Psmd13 T A 7: 140,470,522 (GRCm39) W255R probably damaging Het
Rec8 T A 14: 55,856,253 (GRCm39) N37K probably damaging Het
Serpina3f T A 12: 104,183,699 (GRCm39) L187Q probably damaging Het
Skint11 A T 4: 114,051,978 (GRCm39) T109S probably damaging Het
Slc7a8 A G 14: 54,962,306 (GRCm39) S443P probably damaging Het
Slc8b1 T A 5: 120,659,147 (GRCm39) F197Y probably benign Het
Sox2 T C 3: 34,704,568 (GRCm39) Y2H probably damaging Het
Speg T A 1: 75,387,193 (GRCm39) probably benign Het
Tlr3 T C 8: 45,853,874 (GRCm39) N149D probably benign Het
Trim60 A C 8: 65,454,116 (GRCm39) D44E probably benign Het
Ugt1a7c A G 1: 88,023,657 (GRCm39) Y272C probably damaging Het
Vmn1r4 T A 6: 56,933,738 (GRCm39) Y81N probably damaging Het
Vmn2r73 A T 7: 85,506,889 (GRCm39) C808S probably benign Het
Ythdf3 T C 3: 16,259,056 (GRCm39) I412T possibly damaging Het
Zfp672 T C 11: 58,206,921 (GRCm39) T467A possibly damaging Het
Zfp985 A T 4: 147,668,407 (GRCm39) Q425L possibly damaging Het
Other mutations in Rnf207
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01643:Rnf207 APN 4 152,402,718 (GRCm39) splice site probably benign
IGL02325:Rnf207 APN 4 152,396,237 (GRCm39) missense probably damaging 0.97
IGL02451:Rnf207 APN 4 152,396,869 (GRCm39) missense probably benign 0.25
felonius UTSW 4 152,396,237 (GRCm39) missense probably damaging 0.98
perjury UTSW 4 152,397,672 (GRCm39) missense probably benign 0.00
R0311:Rnf207 UTSW 4 152,400,236 (GRCm39) missense probably damaging 1.00
R0462:Rnf207 UTSW 4 152,397,829 (GRCm39) missense possibly damaging 0.78
R0671:Rnf207 UTSW 4 152,391,925 (GRCm39) missense probably benign 0.00
R0845:Rnf207 UTSW 4 152,396,521 (GRCm39) splice site probably benign
R1544:Rnf207 UTSW 4 152,398,328 (GRCm39) splice site probably benign
R4052:Rnf207 UTSW 4 152,395,894 (GRCm39) missense probably benign 0.41
R4335:Rnf207 UTSW 4 152,400,062 (GRCm39) splice site probably benign
R4649:Rnf207 UTSW 4 152,396,612 (GRCm39) missense probably benign 0.06
R5033:Rnf207 UTSW 4 152,397,666 (GRCm39) missense probably benign 0.00
R5268:Rnf207 UTSW 4 152,398,346 (GRCm39) missense probably damaging 1.00
R5603:Rnf207 UTSW 4 152,396,851 (GRCm39) missense probably damaging 1.00
R5938:Rnf207 UTSW 4 152,402,385 (GRCm39) intron probably benign
R6147:Rnf207 UTSW 4 152,400,112 (GRCm39) missense probably damaging 1.00
R6181:Rnf207 UTSW 4 152,393,305 (GRCm39) missense probably benign 0.00
R6866:Rnf207 UTSW 4 152,396,989 (GRCm39) missense possibly damaging 0.81
R7166:Rnf207 UTSW 4 152,396,237 (GRCm39) missense probably damaging 0.98
R7177:Rnf207 UTSW 4 152,396,634 (GRCm39) missense probably benign 0.43
R7354:Rnf207 UTSW 4 152,398,548 (GRCm39) missense probably damaging 0.96
R7893:Rnf207 UTSW 4 152,395,895 (GRCm39) missense probably damaging 0.99
R8200:Rnf207 UTSW 4 152,398,492 (GRCm39) critical splice donor site probably null
R8789:Rnf207 UTSW 4 152,391,924 (GRCm39) missense probably benign 0.04
R9520:Rnf207 UTSW 4 152,396,234 (GRCm39) missense probably damaging 1.00
R9609:Rnf207 UTSW 4 152,402,222 (GRCm39) missense probably damaging 0.99
R9666:Rnf207 UTSW 4 152,397,717 (GRCm39) missense probably damaging 1.00
R9758:Rnf207 UTSW 4 152,397,666 (GRCm39) missense probably benign 0.06
R9766:Rnf207 UTSW 4 152,400,402 (GRCm39) missense probably damaging 1.00
X0026:Rnf207 UTSW 4 152,400,499 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGATTCACAGTGACTCTGCACCCC -3'
(R):5'- AGACTTCAAGGCATCGTCACGC -3'

Sequencing Primer
(F):5'- GAGTTAAGGAGCACCCAGTCTC -3'
(R):5'- GCCGCATCGCCTAAGAC -3'
Posted On 2014-05-09