Incidental Mutation 'IGL02586:Armc1'
ID299568
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Armc1
Ensembl Gene ENSMUSG00000027599
Gene Namearmadillo repeat containing 1
Synonyms2310016N05Rik, C330014L16Rik, 2900046P06Rik, Arcp, 3110009G21Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.182) question?
Stock #IGL02586
Quality Score
Status
Chromosome3
Chromosomal Location19131402-19163065 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) G to T at 19134028 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000029125 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029125]
Predicted Effect probably benign
Transcript: ENSMUST00000029125
SMART Domains Protein: ENSMUSP00000029125
Gene: ENSMUSG00000027599

DomainStartEndE-ValueType
Pfam:Arm 27 68 1.1e-6 PFAM
SCOP:d1fvqa_ 142 203 6e-10 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik G A 3: 37,044,608 W4626* probably null Het
Abca13 A G 11: 9,293,983 I1949V possibly damaging Het
Anapc2 T A 2: 25,285,096 M742K probably benign Het
Arhgef12 T A 9: 43,005,904 K380* probably null Het
Diaph3 A T 14: 86,986,076 L323* probably null Het
Fbxo11 C T 17: 88,011,283 probably benign Het
Flywch1 C T 17: 23,755,702 A655T probably benign Het
Frmpd1 A G 4: 45,285,160 D1327G probably damaging Het
Ggact G A 14: 122,891,530 T91I possibly damaging Het
Gm10250 T A 15: 5,120,930 probably benign Het
Gsdmc4 T C 15: 63,893,792 S303G probably damaging Het
Helt T C 8: 46,293,239 E15G probably damaging Het
Kcnf1 T A 12: 17,176,143 S26C probably benign Het
Lilra6 T C 7: 3,908,820 T280A probably benign Het
Lipo3 A T 19: 33,582,139 D110E possibly damaging Het
Mepe C A 5: 104,337,450 T152N probably benign Het
Nr2f1 C A 13: 78,195,156 probably benign Het
Olfr807 A G 10: 129,754,655 I265T possibly damaging Het
Olfr994 T C 2: 85,430,466 D121G possibly damaging Het
Peg3 T C 7: 6,710,069 D718G probably benign Het
Phf2 A T 13: 48,813,858 probably benign Het
Pigc A T 1: 161,970,934 I162F probably benign Het
Raf1 A G 6: 115,620,306 L11P probably damaging Het
Rlf T C 4: 121,150,064 Y573C probably damaging Het
Rnf123 G A 9: 108,068,302 R390* probably null Het
Rnf149 T G 1: 39,565,215 Q189P probably benign Het
Slc11a1 T C 1: 74,385,132 probably benign Het
Slc22a12 C T 19: 6,540,457 M234I probably benign Het
Slc28a1 A T 7: 81,164,419 I455F probably benign Het
Slc35f5 T G 1: 125,584,536 L358V probably damaging Het
Slc47a1 A T 11: 61,344,321 V562D probably benign Het
Srrm1 G A 4: 135,325,104 P658L unknown Het
Ushbp1 T C 8: 71,388,750 probably benign Het
Vmn1r88 T A 7: 13,177,808 Y30* probably null Het
Vmn2r27 A T 6: 124,224,475 Y174* probably null Het
Wwox T C 8: 114,712,207 Y338H possibly damaging Het
Zfp518a G A 19: 40,914,617 G997R probably damaging Het
Zufsp A T 10: 33,935,265 probably benign Het
Other mutations in Armc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00837:Armc1 APN 3 19144420 missense probably benign 0.21
IGL01453:Armc1 APN 3 19144430 missense probably benign 0.03
IGL02012:Armc1 APN 3 19157537 missense possibly damaging 0.57
R0512:Armc1 UTSW 3 19149495 missense possibly damaging 0.87
R1694:Armc1 UTSW 3 19134886 missense possibly damaging 0.81
R1878:Armc1 UTSW 3 19157544 missense probably damaging 1.00
R1881:Armc1 UTSW 3 19134896 missense possibly damaging 0.76
R2191:Armc1 UTSW 3 19134061 missense probably damaging 1.00
R2264:Armc1 UTSW 3 19134869 missense probably damaging 1.00
R2403:Armc1 UTSW 3 19157676 start gained probably benign
R2969:Armc1 UTSW 3 19134860 missense probably benign
R3861:Armc1 UTSW 3 19135032 missense probably damaging 1.00
R4296:Armc1 UTSW 3 19149516 missense probably damaging 0.99
R6753:Armc1 UTSW 3 19144398 missense possibly damaging 0.86
R6891:Armc1 UTSW 3 19135041 missense probably damaging 1.00
R7837:Armc1 UTSW 3 19144469 missense probably benign 0.01
R7920:Armc1 UTSW 3 19144469 missense probably benign 0.01
Z1088:Armc1 UTSW 3 19149507 missense probably damaging 1.00
Z1177:Armc1 UTSW 3 19149574 missense probably benign 0.08
Posted On2015-04-16