Incidental Mutation 'R7624:Rundc1'
ID589339
Institutional Source Beutler Lab
Gene Symbol Rundc1
Ensembl Gene ENSMUSG00000035007
Gene NameRUN domain containing 1
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.799) question?
Stock #R7624 (G1)
Quality Score225.009
Status Validated
Chromosome11
Chromosomal Location101425085-101435673 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to C at 101433479 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Proline at position 337 (R337P)
Ref Sequence ENSEMBL: ENSMUSP00000042151 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040561]
Predicted Effect possibly damaging
Transcript: ENSMUST00000040561
AA Change: R337P

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000042151
Gene: ENSMUSG00000035007
AA Change: R337P

DomainStartEndE-ValueType
low complexity region 43 75 N/A INTRINSIC
coiled coil region 80 102 N/A INTRINSIC
coiled coil region 165 201 N/A INTRINSIC
low complexity region 327 338 N/A INTRINSIC
RUN 540 602 2.77e-21 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency 99% (69/70)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atm C A 9: 53,454,768 R2533L probably damaging Het
Caprin1 T A 2: 103,772,677 M514L possibly damaging Het
Ccdc78 A G 17: 25,787,152 E98G probably damaging Het
Cmya5 A T 13: 93,090,357 M2741K possibly damaging Het
Cnot1 T G 8: 95,751,819 R959S probably damaging Het
Col12a1 G T 9: 79,645,794 probably null Het
Col4a3 A G 1: 82,718,884 T177A probably benign Het
Cpa3 T C 3: 20,225,143 N211D possibly damaging Het
Cryba1 T C 11: 77,722,717 Y36C probably damaging Het
Ctnna1 T A 18: 35,244,844 I632N probably benign Het
D630045J12Rik T C 6: 38,149,563 N1504S probably damaging Het
Dgkz C A 2: 91,942,674 R346L probably damaging Het
Dnajc21 A T 15: 10,461,234 I210N probably damaging Het
Dnajc21 G A 15: 10,461,232 R211C probably benign Het
Dscam T C 16: 96,610,324 D1784G probably damaging Het
Eya3 A G 4: 132,672,951 T94A probably benign Het
Fan1 T A 7: 64,372,486 N340Y probably damaging Het
Fat3 T C 9: 15,959,869 D3742G possibly damaging Het
Ficd T C 5: 113,738,690 F309L probably benign Het
Gfra1 A T 19: 58,238,446 M451K probably benign Het
Gm43517 T A 12: 49,391,178 L318Q Het
Gsc A T 12: 104,473,051 V22E possibly damaging Het
Il4ra T C 7: 125,569,108 Y100H probably damaging Het
Ilf3 T C 9: 21,398,044 S486P probably benign Het
Itga10 T A 3: 96,652,953 H594Q probably benign Het
Kcnf1 T C 12: 17,176,136 D28G probably benign Het
Kiss1 A G 1: 133,329,422 K53R possibly damaging Het
Lcn5 A G 2: 25,661,414 I182V probably benign Het
Lcorl T C 5: 45,701,965 D269G probably benign Het
Letm2 A T 8: 25,592,537 C174* probably null Het
Met T G 6: 17,558,835 V1154G probably damaging Het
Mindy3 A G 2: 12,419,189 S22P probably benign Het
Mroh2b G A 15: 4,917,131 R471Q probably damaging Het
Nfe2l3 T C 6: 51,458,272 L604P probably damaging Het
Olfr1044 A T 2: 86,171,220 I199N possibly damaging Het
Olfr1145 A G 2: 87,810,339 Q173R probably damaging Het
Olfr186 T A 16: 59,027,019 Q296L possibly damaging Het
Olfr294 A G 7: 86,616,561 F28S possibly damaging Het
Olfr824 A C 10: 130,126,586 I157S probably damaging Het
Olfr918 C T 9: 38,672,623 V274I probably benign Het
Pcdha9 T A 18: 36,999,796 Y639* probably null Het
Pom121l2 A T 13: 21,983,529 I657L probably damaging Het
Prr14l T A 5: 32,829,623 T843S possibly damaging Het
Rln1 A T 19: 29,332,099 N93K probably damaging Het
Rpl3l A T 17: 24,732,427 M101L probably benign Het
Rtkn A G 6: 83,152,177 Y551C probably benign Het
Scarf1 T A 11: 75,514,416 probably null Het
Serpinb1b T A 13: 33,091,639 probably null Het
Sgsm1 A T 5: 113,274,335 C484* probably null Het
Slc22a19 T A 19: 7,673,303 K547* probably null Het
Slc22a19 T C 19: 7,693,818 T177A probably benign Het
Slc6a5 A C 7: 49,941,866 K526N probably benign Het
Sqle G A 15: 59,330,754 R519Q probably benign Het
Stard9 T C 2: 120,688,146 I517T probably benign Het
Taf15 A T 11: 83,505,023 D518V unknown Het
Tdgf1 C T 9: 110,945,949 probably benign Het
Tenm4 A G 7: 96,895,985 M2440V possibly damaging Het
Tm6sf1 A G 7: 81,868,710 M122V possibly damaging Het
Tmprss9 T A 10: 80,892,219 S548T possibly damaging Het
Trim62 A T 4: 128,883,678 probably benign Het
Ugt2b34 C T 5: 86,891,282 V507M possibly damaging Het
Usp16 T A 16: 87,476,805 M423K probably benign Het
Vmn1r199 T A 13: 22,382,736 S67T probably benign Het
Vmn1r62 A T 7: 5,675,601 M94L probably benign Het
Wnk4 G T 11: 101,264,354 E364* probably null Het
Xpo1 T A 11: 23,282,584 I368N probably damaging Het
Zfp366 A G 13: 99,246,296 T656A probably benign Het
Zfp934 T C 13: 62,518,524 M113V probably benign Het
Zkscan2 A G 7: 123,498,771 V134A probably damaging Het
Other mutations in Rundc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00769:Rundc1 APN 11 101434274 missense probably damaging 1.00
IGL01068:Rundc1 APN 11 101434142 missense probably damaging 0.96
IGL02112:Rundc1 APN 11 101433599 missense probably benign 0.01
R0379:Rundc1 UTSW 11 101425147 missense probably benign 0.01
R1847:Rundc1 UTSW 11 101433681 missense probably benign
R1959:Rundc1 UTSW 11 101431496 missense probably damaging 1.00
R2185:Rundc1 UTSW 11 101425331 missense probably benign 0.34
R2225:Rundc1 UTSW 11 101431344 splice site probably benign
R2323:Rundc1 UTSW 11 101425275 missense probably damaging 0.98
R3791:Rundc1 UTSW 11 101434201 missense probably damaging 0.96
R4599:Rundc1 UTSW 11 101433926 missense probably damaging 1.00
R4660:Rundc1 UTSW 11 101434004 missense possibly damaging 0.89
R4871:Rundc1 UTSW 11 101434048 missense probably benign 0.18
R5054:Rundc1 UTSW 11 101425141 missense probably benign 0.00
R5058:Rundc1 UTSW 11 101425537 missense probably benign
R6349:Rundc1 UTSW 11 101434162 missense probably benign 0.07
R6965:Rundc1 UTSW 11 101433911 missense possibly damaging 0.96
R7240:Rundc1 UTSW 11 101431548 critical splice donor site probably null
R7286:Rundc1 UTSW 11 101429587 missense probably benign 0.00
R8243:Rundc1 UTSW 11 101425558 missense probably benign 0.00
R8322:Rundc1 UTSW 11 101432166 missense probably benign 0.01
R8401:Rundc1 UTSW 11 101433557 missense probably damaging 0.99
Z1176:Rundc1 UTSW 11 101432122 missense probably benign 0.00
Z1176:Rundc1 UTSW 11 101433734 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GATAAGCCAGTCCAGTTGCATCC -3'
(R):5'- AGGTTGGCCGAAGTGATGAC -3'

Sequencing Primer
(F):5'- AGTTGCATCCTGGCCTTCATATG -3'
(R):5'- ATGTCTCAAGGCTAGCTGC -3'
Posted On2019-10-24