Incidental Mutation 'R2403:Armc1'
ID 248801
Institutional Source Beutler Lab
Gene Symbol Armc1
Ensembl Gene ENSMUSG00000027599
Gene Name armadillo repeat containing 1
Synonyms Arcp, 2310016N05Rik, 2900046P06Rik, C330014L16Rik, 3110009G21Rik
MMRRC Submission 040369-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.178) question?
Stock # R2403 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 19185566-19217229 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to C at 19211840 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000029125 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029125]
AlphaFold Q9D7A8
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
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 93.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 A G 3: 121,964,592 (GRCm39) E925G probably damaging Het
Abca9 T G 11: 110,006,280 (GRCm39) Q1275P probably benign Het
Adgrl1 T A 8: 84,657,870 (GRCm39) M492K probably benign Het
Ankrd50 T A 3: 38,537,234 (GRCm39) K3* probably null Het
Arl5b T C 2: 15,079,848 (GRCm39) S140P probably damaging Het
Ascc1 T C 10: 59,840,663 (GRCm39) I8T probably benign Het
Bche A G 3: 73,608,805 (GRCm39) V207A probably damaging Het
Cacna2d3 A G 14: 28,627,259 (GRCm39) L1080P probably benign Het
Ceacam3 C A 7: 16,895,779 (GRCm39) A583D probably damaging Het
Cep290 C T 10: 100,373,299 (GRCm39) A1193V probably benign Het
Clcn1 T C 6: 42,290,046 (GRCm39) I827T probably damaging Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Col28a1 T C 6: 8,175,641 (GRCm39) D69G possibly damaging Het
Cts3 A G 13: 61,712,806 (GRCm39) W305R probably damaging Het
Dmwd T C 7: 18,815,084 (GRCm39) I578T possibly damaging Het
Dnmt3a G A 12: 3,949,883 (GRCm39) V559M probably damaging Het
Dysf T C 6: 84,016,549 (GRCm39) V70A possibly damaging Het
Eml6 A G 11: 29,752,434 (GRCm39) V993A probably benign Het
Etl4 T A 2: 20,812,117 (GRCm39) L1768* probably null Het
F11 A G 8: 45,701,675 (GRCm39) S353P probably damaging Het
Fat3 T G 9: 15,881,167 (GRCm39) D3235A probably damaging Het
Fbxo36 T A 1: 84,877,823 (GRCm39) F162I probably damaging Het
Fgfrl1 T C 5: 108,852,897 (GRCm39) W200R probably damaging Het
Fsip2 T C 2: 82,811,064 (GRCm39) M2461T possibly damaging Het
Fut1 A G 7: 45,268,643 (GRCm39) Y144C probably benign Het
Gprin3 G A 6: 59,331,134 (GRCm39) A391V probably benign Het
H2-Q4 A G 17: 35,598,973 (GRCm39) E81G probably damaging Het
Hacd3 A G 9: 64,908,311 (GRCm39) S162P probably damaging Het
Itga1 A T 13: 115,114,150 (GRCm39) H918Q probably benign Het
Lrp5 C A 19: 3,647,430 (GRCm39) D1271Y probably damaging Het
Lsm8 C T 6: 18,849,643 (GRCm39) T17I probably benign Het
Mup4 T A 4: 59,958,145 (GRCm39) D141V probably damaging Het
Nckap5 G A 1: 125,955,146 (GRCm39) H405Y probably benign Het
Obscn T C 11: 59,022,472 (GRCm39) R758G possibly damaging Het
Or12k8 T C 2: 36,974,986 (GRCm39) Y258C probably benign Het
Ostf1 T C 19: 18,562,026 (GRCm39) K190R probably benign Het
Pnldc1 A T 17: 13,118,777 (GRCm39) V197E probably damaging Het
Ptprc A G 1: 138,016,270 (GRCm39) S531P probably damaging Het
Ryr3 C T 2: 112,516,973 (GRCm39) E3318K probably damaging Het
Scamp2 T C 9: 57,484,995 (GRCm39) V67A possibly damaging Het
Serpina3g C A 12: 104,207,421 (GRCm39) L195M probably damaging Het
Siglec1 G T 2: 130,916,395 (GRCm39) T1185N possibly damaging Het
Sycp2 G A 2: 178,045,528 (GRCm39) Q31* probably null Het
Tmprss15 T G 16: 78,854,578 (GRCm39) T277P probably damaging Het
Trim34b C T 7: 103,978,876 (GRCm39) S41L probably benign Het
Ttn T C 2: 76,557,705 (GRCm39) T21507A possibly damaging Het
Umad1 T C 6: 8,427,161 (GRCm39) V138A possibly damaging Het
Zfp523 A G 17: 28,414,183 (GRCm39) I72M probably damaging Het
Zfp655 C T 5: 145,181,356 (GRCm39) R405C probably benign Het
Zfp715 G A 7: 42,948,692 (GRCm39) R423C possibly damaging Het
Other mutations in Armc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00837:Armc1 APN 3 19,198,584 (GRCm39) missense probably benign 0.21
IGL01453:Armc1 APN 3 19,198,594 (GRCm39) missense probably benign 0.03
IGL02012:Armc1 APN 3 19,211,701 (GRCm39) missense possibly damaging 0.57
IGL02586:Armc1 APN 3 19,188,192 (GRCm39) utr 3 prime probably benign
R0512:Armc1 UTSW 3 19,203,659 (GRCm39) missense possibly damaging 0.87
R1694:Armc1 UTSW 3 19,189,050 (GRCm39) missense possibly damaging 0.81
R1878:Armc1 UTSW 3 19,211,708 (GRCm39) missense probably damaging 1.00
R1881:Armc1 UTSW 3 19,189,060 (GRCm39) missense possibly damaging 0.76
R2191:Armc1 UTSW 3 19,188,225 (GRCm39) missense probably damaging 1.00
R2264:Armc1 UTSW 3 19,189,033 (GRCm39) missense probably damaging 1.00
R2969:Armc1 UTSW 3 19,189,024 (GRCm39) missense probably benign
R3861:Armc1 UTSW 3 19,189,196 (GRCm39) missense probably damaging 1.00
R4296:Armc1 UTSW 3 19,203,680 (GRCm39) missense probably damaging 0.99
R6753:Armc1 UTSW 3 19,198,562 (GRCm39) missense possibly damaging 0.86
R6891:Armc1 UTSW 3 19,189,205 (GRCm39) missense probably damaging 1.00
R7837:Armc1 UTSW 3 19,198,633 (GRCm39) missense probably benign 0.01
R8373:Armc1 UTSW 3 19,203,731 (GRCm39) missense probably damaging 1.00
R8743:Armc1 UTSW 3 19,211,700 (GRCm39) missense probably benign 0.19
Z1088:Armc1 UTSW 3 19,203,671 (GRCm39) missense probably damaging 1.00
Z1177:Armc1 UTSW 3 19,203,738 (GRCm39) missense probably benign 0.08
Predicted Primers PCR Primer
(F):5'- GCAACTTACAAGCAAAGCTGAG -3'
(R):5'- GCTTTTGAGAATCAGAGGCAGG -3'

Sequencing Primer
(F):5'- CTTACAAGCAAAGCTGAGTGAAC -3'
(R):5'- GGGGATAATACACGGACAGCATC -3'
Posted On 2014-11-11