Incidental Mutation 'R4486:Armc10'
ID 331606
Institutional Source Beutler Lab
Gene Symbol Armc10
Ensembl Gene ENSMUSG00000038525
Gene Name armadillo repeat containing 10
Synonyms 2810037C14Rik
MMRRC Submission 041742-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.096) question?
Stock # R4486 (G1)
Quality Score 225
Status Validated
Chromosome 5
Chromosomal Location 21851004-21867697 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 21858432 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Arginine at position 159 (Q159R)
Ref Sequence ENSEMBL: ENSMUSP00000093149 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072896] [ENSMUST00000095495] [ENSMUST00000148873]
AlphaFold Q9D0L7
Predicted Effect probably damaging
Transcript: ENSMUST00000072896
AA Change: Q159R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000072669
Gene: ENSMUSG00000038525
AA Change: Q159R

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
Pfam:Arm_2 48 300 2e-104 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000095495
AA Change: Q159R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000093149
Gene: ENSMUSG00000038525
AA Change: Q159R

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
Pfam:Arm_2 48 234 6.5e-86 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139521
Predicted Effect noncoding transcript
Transcript: ENSMUST00000146599
SMART Domains Protein: ENSMUSP00000120368
Gene: ENSMUSG00000038525

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
low complexity region 64 84 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000148873
AA Change: Q145R

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000120269
Gene: ENSMUSG00000038525
AA Change: Q145R

DomainStartEndE-ValueType
transmembrane domain 7 29 N/A INTRINSIC
Pfam:Arm_2 38 286 4.7e-113 PFAM
Meta Mutation Damage Score 0.6855 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.7%
Validation Efficiency 94% (45/48)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that contains an armadillo repeat and transmembrane domain. The encoded protein decreases the transcriptional activity of the tumor suppressor protein p53 through direct interaction with the DNA-binding domain of p53, and may play a role in cell growth and survival. Upregulation of this gene may play a role in hepatocellular carcinoma. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 3. [provided by RefSeq, Sep 2011]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcd2 A G 15: 91,062,486 (GRCm39) V484A probably damaging Het
Adam22 A T 5: 8,230,227 (GRCm39) probably benign Het
Adamts18 G T 8: 114,439,825 (GRCm39) P923T probably benign Het
Ank3 C T 10: 69,837,804 (GRCm39) T1604I possibly damaging Het
Arnt2 T A 7: 83,924,553 (GRCm39) T425S probably benign Het
B4galt3 A G 1: 171,099,343 (GRCm39) T36A possibly damaging Het
Bbx A G 16: 50,020,777 (GRCm39) V799A probably damaging Het
Bud23 T C 5: 135,092,779 (GRCm39) probably null Het
Cnga2 T A X: 71,049,733 (GRCm39) F133I possibly damaging Het
Crispld1 A G 1: 17,823,102 (GRCm39) T390A probably benign Het
Cyp4f39 T A 17: 32,702,428 (GRCm39) D308E probably damaging Het
Dnah6 A G 6: 73,015,729 (GRCm39) V3584A probably damaging Het
Ecpas A G 4: 58,820,086 (GRCm39) probably benign Het
Frk T C 10: 34,484,377 (GRCm39) I450T probably benign Het
Grm6 T C 11: 50,750,816 (GRCm39) S660P probably damaging Het
Hao2 T A 3: 98,789,341 (GRCm39) I116F probably damaging Het
Hyi G A 4: 118,219,674 (GRCm39) G237D probably damaging Het
Jrkl T C 9: 13,245,376 (GRCm39) N95S probably benign Het
Kifbp A G 10: 62,398,806 (GRCm39) probably benign Het
Nanog T C 6: 122,689,676 (GRCm39) probably null Het
Ngf G A 3: 102,428,015 (GRCm39) D255N probably damaging Het
Nlrp4e A G 7: 23,020,652 (GRCm39) I380V probably benign Het
Or52e7 T C 7: 104,684,510 (GRCm39) F35S probably benign Het
Or6c76b T C 10: 129,692,567 (GRCm39) F60S probably damaging Het
Pcdha3 T C 18: 37,080,404 (GRCm39) V382A probably damaging Het
Pla2g4c T A 7: 13,071,676 (GRCm39) N165K probably benign Het
Rexo5 T C 7: 119,424,800 (GRCm39) I362T probably benign Het
Rpl7a-ps3 G A 15: 36,308,429 (GRCm39) noncoding transcript Het
Rpusd2 T C 2: 118,865,705 (GRCm39) V134A probably damaging Het
Serpina1c T A 12: 103,863,259 (GRCm39) probably null Het
Slc6a19 A T 13: 73,829,836 (GRCm39) I606N probably damaging Het
Smchd1 T C 17: 71,714,230 (GRCm39) T878A probably benign Het
Tas2r143 A G 6: 42,377,628 (GRCm39) M153V probably benign Het
Thrb G T 14: 17,925,640 (GRCm38) M1I probably null Het
Trbc2 A G 6: 41,523,814 (GRCm39) probably benign Het
Trim37 T A 11: 87,087,651 (GRCm39) S587R probably benign Het
Ulbp1 T A 10: 7,397,397 (GRCm39) H151L probably benign Het
Vmn2r54 A T 7: 12,366,199 (GRCm39) L245* probably null Het
Vmn2r78 A C 7: 86,569,959 (GRCm39) probably null Het
Xlr5b T C X: 72,201,504 (GRCm39) probably null Het
Xrcc4 A C 13: 90,140,707 (GRCm39) S167R possibly damaging Het
Zfp994 C T 17: 22,420,541 (GRCm39) C136Y probably damaging Het
Other mutations in Armc10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00838:Armc10 APN 5 21,866,579 (GRCm39) missense probably damaging 1.00
IGL01647:Armc10 APN 5 21,851,091 (GRCm39) utr 5 prime probably benign
IGL02296:Armc10 APN 5 21,865,631 (GRCm39) missense probably benign 0.00
R0220:Armc10 UTSW 5 21,866,582 (GRCm39) missense probably benign 0.05
R0308:Armc10 UTSW 5 21,852,295 (GRCm39) intron probably benign
R1757:Armc10 UTSW 5 21,858,455 (GRCm39) missense probably damaging 1.00
R4332:Armc10 UTSW 5 21,866,579 (GRCm39) missense probably damaging 1.00
R4656:Armc10 UTSW 5 21,866,548 (GRCm39) missense probably benign 0.11
R4741:Armc10 UTSW 5 21,856,834 (GRCm39) missense probably damaging 1.00
R4906:Armc10 UTSW 5 21,866,522 (GRCm39) missense probably damaging 1.00
R5273:Armc10 UTSW 5 21,858,426 (GRCm39) missense possibly damaging 0.89
R5988:Armc10 UTSW 5 21,865,581 (GRCm39) missense probably damaging 1.00
R7088:Armc10 UTSW 5 21,858,390 (GRCm39) missense probably damaging 0.96
R7212:Armc10 UTSW 5 21,865,581 (GRCm39) missense probably damaging 1.00
R8063:Armc10 UTSW 5 21,853,768 (GRCm39) critical splice donor site probably null
R8715:Armc10 UTSW 5 21,858,516 (GRCm39) missense possibly damaging 0.49
Predicted Primers PCR Primer
(F):5'- ATGCCAGGTTATTAGCAAAGGC -3'
(R):5'- ATCTCAGGAAGTGTGCTGCC -3'

Sequencing Primer
(F):5'- GACACAAGTGCCATCTTTTCTGAAG -3'
(R):5'- TGCCCAGCTCTTCAGGAC -3'
Posted On 2015-07-21