Incidental Mutation 'IGL02154:Armh4'
ID 282154
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Armh4
Ensembl Gene ENSMUSG00000036242
Gene Name armadillo-like helical domain containing 4
Synonyms 3632451O06Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02154
Quality Score
Status
Chromosome 14
Chromosomal Location 49919017-50020843 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 50010399 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 436 (T436I)
Ref Sequence ENSEMBL: ENSMUSP00000113609 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036972] [ENSMUST00000118129]
AlphaFold Q8BT18
Predicted Effect probably benign
Transcript: ENSMUST00000036972
AA Change: T436I

PolyPhen 2 Score 0.273 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000036220
Gene: ENSMUSG00000036242
AA Change: T436I

DomainStartEndE-ValueType
Pfam:DUF4696 48 609 3.8e-224 PFAM
transmembrane domain 714 736 N/A INTRINSIC
low complexity region 741 753 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000118129
AA Change: T436I

PolyPhen 2 Score 0.584 (Sensitivity: 0.88; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000113609
Gene: ENSMUSG00000036242
AA Change: T436I

DomainStartEndE-ValueType
coiled coil region 603 644 N/A INTRINSIC
transmembrane domain 714 736 N/A INTRINSIC
low complexity region 741 754 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Armc3 G A 2: 19,290,948 (GRCm39) probably null Het
AW551984 G A 9: 39,500,398 (GRCm39) R787C possibly damaging Het
Cadm1 A T 9: 47,725,201 (GRCm39) I321L probably benign Het
Cfap57 A G 4: 118,470,214 (GRCm39) L222P probably damaging Het
Cox20 A G 1: 178,150,119 (GRCm39) I98V probably benign Het
Dmrta1 A G 4: 89,580,150 (GRCm39) N370S probably benign Het
Dnah17 A G 11: 118,015,087 (GRCm39) F386L probably benign Het
Fam135b T C 15: 71,320,559 (GRCm39) I1323V probably benign Het
Fndc3b A G 3: 27,592,266 (GRCm39) S211P probably damaging Het
Galnt10 T G 11: 57,675,531 (GRCm39) L597V probably damaging Het
Gtf2e2 T C 8: 34,245,989 (GRCm39) probably null Het
Inpp4b T A 8: 82,696,130 (GRCm39) probably benign Het
Irag2 T G 6: 145,083,967 (GRCm39) M44R possibly damaging Het
Lacc1 A G 14: 77,270,727 (GRCm39) V269A probably benign Het
Mdn1 A G 4: 32,740,395 (GRCm39) D3750G probably benign Het
Mme A T 3: 63,250,976 (GRCm39) Q339L probably benign Het
Mmp3 A T 9: 7,453,662 (GRCm39) I428L probably benign Het
Myrf A T 19: 10,193,482 (GRCm39) I558N probably damaging Het
Or52e8 C T 7: 104,625,188 (GRCm39) M1I probably null Het
Phb1 A G 11: 95,565,997 (GRCm39) I94V possibly damaging Het
Prg4 T A 1: 150,330,613 (GRCm39) probably benign Het
Sirpb1a T C 3: 15,475,504 (GRCm39) T344A probably damaging Het
Skap2 T C 6: 51,989,308 (GRCm39) probably benign Het
Slc29a1 A G 17: 45,897,089 (GRCm39) I399T probably damaging Het
Sorl1 C T 9: 41,915,330 (GRCm39) V1300I probably benign Het
Tas2r117 T C 6: 132,780,678 (GRCm39) V272A probably benign Het
Tctn2 C A 5: 124,746,624 (GRCm39) noncoding transcript Het
Tmem51 T C 4: 141,759,089 (GRCm39) N220D probably damaging Het
Trak2 T C 1: 58,947,888 (GRCm39) D584G probably damaging Het
Vmn1r78 A G 7: 11,886,472 (GRCm39) I28V probably benign Het
Vmn2r95 A C 17: 18,672,248 (GRCm39) I662L probably benign Het
Vwa8 C A 14: 79,086,733 (GRCm39) R4S possibly damaging Het
Other mutations in Armh4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00470:Armh4 APN 14 50,010,460 (GRCm39) missense probably damaging 1.00
IGL00981:Armh4 APN 14 50,010,447 (GRCm39) missense probably damaging 1.00
IGL01447:Armh4 APN 14 50,005,923 (GRCm39) missense probably damaging 0.99
IGL01645:Armh4 APN 14 50,011,011 (GRCm39) missense probably damaging 1.00
IGL02135:Armh4 APN 14 50,011,386 (GRCm39) missense probably damaging 0.99
IGL02163:Armh4 APN 14 50,011,614 (GRCm39) missense possibly damaging 0.61
IGL03234:Armh4 APN 14 50,005,973 (GRCm39) missense probably damaging 1.00
P0014:Armh4 UTSW 14 49,989,116 (GRCm39) missense probably damaging 1.00
R0165:Armh4 UTSW 14 50,011,243 (GRCm39) missense probably benign
R0240:Armh4 UTSW 14 50,005,859 (GRCm39) splice site probably benign
R0553:Armh4 UTSW 14 49,920,143 (GRCm39) missense probably damaging 0.99
R0616:Armh4 UTSW 14 50,011,113 (GRCm39) missense possibly damaging 0.74
R0635:Armh4 UTSW 14 50,010,600 (GRCm39) missense probably benign 0.00
R1423:Armh4 UTSW 14 49,988,896 (GRCm39) missense probably damaging 1.00
R1547:Armh4 UTSW 14 50,010,953 (GRCm39) missense probably benign 0.01
R1642:Armh4 UTSW 14 50,005,867 (GRCm39) splice site probably null
R1657:Armh4 UTSW 14 50,011,017 (GRCm39) missense probably damaging 0.99
R1717:Armh4 UTSW 14 49,989,121 (GRCm39) missense probably damaging 0.99
R1875:Armh4 UTSW 14 49,919,815 (GRCm39) missense probably damaging 1.00
R1900:Armh4 UTSW 14 50,008,040 (GRCm39) missense probably damaging 1.00
R1916:Armh4 UTSW 14 50,005,932 (GRCm39) missense probably damaging 1.00
R1945:Armh4 UTSW 14 50,005,940 (GRCm39) missense probably damaging 1.00
R2102:Armh4 UTSW 14 50,011,459 (GRCm39) missense probably damaging 0.98
R2147:Armh4 UTSW 14 49,989,028 (GRCm39) missense probably benign 0.31
R2149:Armh4 UTSW 14 49,989,028 (GRCm39) missense probably benign 0.31
R3921:Armh4 UTSW 14 50,011,659 (GRCm39) missense probably benign 0.13
R4063:Armh4 UTSW 14 50,011,444 (GRCm39) missense probably benign 0.02
R4373:Armh4 UTSW 14 50,007,893 (GRCm39) missense probably damaging 1.00
R4374:Armh4 UTSW 14 50,007,893 (GRCm39) missense probably damaging 1.00
R4377:Armh4 UTSW 14 50,007,893 (GRCm39) missense probably damaging 1.00
R4589:Armh4 UTSW 14 50,011,039 (GRCm39) missense probably damaging 1.00
R4940:Armh4 UTSW 14 50,010,939 (GRCm39) missense probably benign 0.15
R4986:Armh4 UTSW 14 49,989,111 (GRCm39) missense probably damaging 0.97
R5047:Armh4 UTSW 14 50,007,895 (GRCm39) missense probably damaging 1.00
R5104:Armh4 UTSW 14 50,010,929 (GRCm39) missense possibly damaging 0.77
R5682:Armh4 UTSW 14 49,989,043 (GRCm39) missense probably damaging 1.00
R6357:Armh4 UTSW 14 50,010,769 (GRCm39) missense probably benign 0.10
R6478:Armh4 UTSW 14 50,010,789 (GRCm39) missense possibly damaging 0.61
R6673:Armh4 UTSW 14 50,008,049 (GRCm39) missense probably benign 0.00
R7035:Armh4 UTSW 14 50,010,507 (GRCm39) missense possibly damaging 0.77
R7054:Armh4 UTSW 14 50,011,155 (GRCm39) missense probably damaging 1.00
R7458:Armh4 UTSW 14 49,920,196 (GRCm39) missense probably damaging 1.00
R7536:Armh4 UTSW 14 50,011,703 (GRCm39) splice site probably null
R7944:Armh4 UTSW 14 50,010,670 (GRCm39) missense probably benign 0.25
R7945:Armh4 UTSW 14 50,010,670 (GRCm39) missense probably benign 0.25
R8049:Armh4 UTSW 14 50,010,993 (GRCm39) missense probably damaging 0.97
R8066:Armh4 UTSW 14 50,005,980 (GRCm39) missense possibly damaging 0.83
R8519:Armh4 UTSW 14 50,010,693 (GRCm39) missense probably damaging 1.00
R8765:Armh4 UTSW 14 49,920,100 (GRCm39) missense probably damaging 1.00
R8766:Armh4 UTSW 14 50,011,497 (GRCm39) missense probably damaging 1.00
R8833:Armh4 UTSW 14 50,011,318 (GRCm39) missense probably benign 0.17
R8936:Armh4 UTSW 14 50,008,024 (GRCm39) missense probably damaging 0.98
R9007:Armh4 UTSW 14 50,011,695 (GRCm39) missense probably damaging 0.99
R9122:Armh4 UTSW 14 50,011,459 (GRCm39) missense possibly damaging 0.64
R9406:Armh4 UTSW 14 50,010,945 (GRCm39) missense possibly damaging 0.93
R9741:Armh4 UTSW 14 50,008,081 (GRCm39) missense probably benign 0.06
X0026:Armh4 UTSW 14 49,920,193 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16