Incidental Mutation 'R2507:Armcx4'
ID 251423
Institutional Source Beutler Lab
Gene Symbol Armcx4
Ensembl Gene ENSMUSG00000049804
Gene Name armadillo repeat containing, X-linked 4
Synonyms
MMRRC Submission 040413-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.109) question?
Stock # R2507 (G1)
Quality Score 222
Status Not validated
Chromosome X
Chromosomal Location 133587268-133597506 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 133596128 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 2012 (V2012G)
Ref Sequence ENSEMBL: ENSMUSP00000132914 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000124226]
AlphaFold E9PWM3
Predicted Effect possibly damaging
Transcript: ENSMUST00000124226
AA Change: V2012G

PolyPhen 2 Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000132914
Gene: ENSMUSG00000049804
AA Change: V2012G

DomainStartEndE-ValueType
low complexity region 75 85 N/A INTRINSIC
low complexity region 107 121 N/A INTRINSIC
low complexity region 155 166 N/A INTRINSIC
internal_repeat_3 167 357 5.37e-6 PROSPERO
internal_repeat_1 211 401 2.32e-9 PROSPERO
internal_repeat_2 277 414 9.67e-8 PROSPERO
low complexity region 416 437 N/A INTRINSIC
low complexity region 501 525 N/A INTRINSIC
low complexity region 539 554 N/A INTRINSIC
internal_repeat_2 560 697 9.67e-8 PROSPERO
internal_repeat_1 574 764 2.32e-9 PROSPERO
internal_repeat_3 616 790 5.37e-6 PROSPERO
low complexity region 792 805 N/A INTRINSIC
low complexity region 828 838 N/A INTRINSIC
low complexity region 1217 1234 N/A INTRINSIC
low complexity region 1465 1482 N/A INTRINSIC
low complexity region 1620 1637 N/A INTRINSIC
low complexity region 1680 1736 N/A INTRINSIC
low complexity region 1754 1770 N/A INTRINSIC
low complexity region 1792 1829 N/A INTRINSIC
low complexity region 1850 1871 N/A INTRINSIC
low complexity region 1946 1959 N/A INTRINSIC
Pfam:Arm_2 2094 2350 2.6e-89 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the armadillo repeat-containing family of proteins, which interact with other proteins in a variety of cellular processes. The function of this family member is currently unknown. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700020N01Rik A G 10: 21,497,681 (GRCm39) probably benign Het
4930535I16Rik G A 4: 123,811,740 (GRCm39) probably benign Het
Akr1b1 C T 6: 34,286,999 (GRCm39) E186K probably damaging Het
Apc A T 18: 34,449,590 (GRCm39) N2128I possibly damaging Het
Api5 T C 2: 94,260,162 (GRCm39) I31M probably damaging Het
Aurka T C 2: 172,212,365 (GRCm39) E4G probably benign Het
B4galt5 T A 2: 167,148,558 (GRCm39) M187L probably benign Het
Bsn T C 9: 107,993,313 (GRCm39) D813G probably damaging Het
Bub1 A T 2: 127,643,343 (GRCm39) D1000E probably benign Het
Cacna1f T G X: 7,492,687 (GRCm39) probably null Het
Cdh6 A G 15: 13,041,447 (GRCm39) I539T probably benign Het
Cdhr3 T C 12: 33,088,914 (GRCm39) D756G probably benign Het
Cenph A T 13: 100,907,744 (GRCm39) D85E probably benign Het
Chd9 C T 8: 91,760,615 (GRCm39) P2120L probably benign Het
Clec2h A G 6: 128,650,945 (GRCm39) N75S probably benign Het
Cnga1 C T 5: 72,776,404 (GRCm39) V20I possibly damaging Het
Cox4i1 T A 8: 121,400,029 (GRCm39) V51E possibly damaging Het
Cpne3 A T 4: 19,553,871 (GRCm39) N53K probably damaging Het
Cpt1b A G 15: 89,303,301 (GRCm39) F585L probably benign Het
Daam1 G A 12: 72,021,997 (GRCm39) D732N probably damaging Het
Dner A T 1: 84,560,801 (GRCm39) C115S probably damaging Het
Dop1a T A 9: 86,395,170 (GRCm39) F759Y probably damaging Het
Dst T C 1: 34,050,990 (GRCm39) Y29H probably damaging Het
Dst T C 1: 34,227,498 (GRCm39) V1875A possibly damaging Het
Duox1 A G 2: 122,163,619 (GRCm39) D817G probably benign Het
Emc2 A T 15: 43,375,094 (GRCm39) probably null Het
Erich3 A T 3: 154,404,296 (GRCm39) E51V probably null Het
Exoc2 A G 13: 31,066,348 (GRCm39) Y443H possibly damaging Het
Fbf1 T C 11: 116,046,252 (GRCm39) R200G probably benign Het
Fdxr G A 11: 115,162,806 (GRCm39) T100I probably damaging Het
Galnt11 C G 5: 25,452,610 (GRCm39) P41A probably damaging Het
Galnt4 A G 10: 98,945,148 (GRCm39) K291R possibly damaging Het
Gm12695 T A 4: 96,642,426 (GRCm39) E301V probably damaging Het
Gopc C T 10: 52,229,422 (GRCm39) probably null Het
Gria1 A T 11: 57,180,146 (GRCm39) T699S probably null Het
Gsr T G 8: 34,170,316 (GRCm39) D200E probably benign Het
Ikzf2 G A 1: 69,578,447 (GRCm39) A282V probably benign Het
Irak2 T C 6: 113,624,639 (GRCm39) I45T probably damaging Het
Irx1 T C 13: 72,107,939 (GRCm39) K248E probably damaging Het
Kcns3 A C 12: 11,142,087 (GRCm39) V204G possibly damaging Het
Lmo1 C A 7: 108,739,848 (GRCm39) M91I probably damaging Het
Map3k21 A G 8: 126,666,677 (GRCm39) D623G possibly damaging Het
Map4 A G 9: 109,866,551 (GRCm39) probably benign Het
Mark3 T A 12: 111,593,676 (GRCm39) V236E probably damaging Het
Med23 A G 10: 24,786,711 (GRCm39) D939G probably damaging Het
Mrgpra9 A G 7: 46,885,242 (GRCm39) C142R possibly damaging Het
N4bp2 T A 5: 65,947,404 (GRCm39) D11E probably benign Het
Ntng2 T C 2: 29,097,531 (GRCm39) N310S probably damaging Het
Or10ak7 T C 4: 118,791,122 (GRCm39) M308V probably benign Het
Or6b3 A G 1: 92,439,100 (GRCm39) S217P probably damaging Het
Pcolce A G 5: 137,605,313 (GRCm39) V260A possibly damaging Het
Pds5b C A 5: 150,679,893 (GRCm39) T533K possibly damaging Het
Pecr A G 1: 72,301,135 (GRCm39) Y268H probably benign Het
Phax T A 18: 56,719,956 (GRCm39) F299Y probably damaging Het
Phip T C 9: 82,797,392 (GRCm39) H537R possibly damaging Het
Pramel32 T A 4: 88,547,448 (GRCm39) K161N possibly damaging Het
Prpf39 T A 12: 65,104,589 (GRCm39) F551L probably benign Het
Ptch1 T G 13: 63,672,773 (GRCm39) E944A probably benign Het
Ralgapa1 G A 12: 55,764,986 (GRCm39) P889S probably damaging Het
Rpap1 A G 2: 119,610,535 (GRCm39) probably null Het
Rufy3 T C 5: 88,797,757 (GRCm39) S645P probably damaging Het
Samd1 CGAGGAGGAGGAGGAGGAGGA CGAGGAGGAGGAGGAGGA 8: 84,725,625 (GRCm39) probably benign Het
Spata7 G T 12: 98,624,709 (GRCm39) A172S probably benign Het
Stk35 A G 2: 129,643,435 (GRCm39) T140A probably damaging Het
Thop1 T G 10: 80,906,098 (GRCm39) M1R probably null Het
Tlr1 T C 5: 65,082,639 (GRCm39) Y646C probably damaging Het
Tpp2 A G 1: 44,040,609 (GRCm39) Y290C probably benign Het
Tpr A G 1: 150,268,695 (GRCm39) M1V probably null Het
Trim6 T C 7: 103,877,392 (GRCm39) F161L probably damaging Het
Ubash3b T C 9: 41,068,650 (GRCm39) K25E possibly damaging Het
Unc45b G A 11: 82,830,963 (GRCm39) probably null Het
Unc80 A G 1: 66,651,266 (GRCm39) N1537S possibly damaging Het
Usb1 T C 8: 96,069,752 (GRCm39) F100S probably damaging Het
Vmn1r17 C A 6: 57,338,244 (GRCm39) L40F probably damaging Het
Vmn1r233 A T 17: 21,214,110 (GRCm39) M280K probably benign Het
Zfp37 A T 4: 62,109,493 (GRCm39) C524S probably damaging Het
Zfp426 T C 9: 20,381,727 (GRCm39) K420R probably benign Het
Other mutations in Armcx4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02366:Armcx4 APN X 133,592,261 (GRCm39) missense possibly damaging 0.72
R0627:Armcx4 UTSW X 133,596,572 (GRCm39) missense possibly damaging 0.71
R3411:Armcx4 UTSW X 133,591,774 (GRCm39) missense probably benign 0.18
X0013:Armcx4 UTSW X 133,595,056 (GRCm39) missense possibly damaging 0.53
Z1176:Armcx4 UTSW X 133,594,840 (GRCm39) missense possibly damaging 0.53
Z1176:Armcx4 UTSW X 133,593,791 (GRCm39) missense not run
Z1177:Armcx4 UTSW X 133,593,791 (GRCm39) missense not run
Predicted Primers PCR Primer
(F):5'- TGAACTAAGTAGAGAATCCAGCCC -3'
(R):5'- GACTTGCCTTCTGAAGCCATC -3'

Sequencing Primer
(F):5'- CAGCCCTGGTATTGAAGAGATTAGTC -3'
(R):5'- GCCATCTTCACCTGGAAAGCTTG -3'
Posted On 2014-12-04