Incidental Mutation 'IGL03234:Armh4'
ID 414009
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 # IGL03234
Quality Score
Status
Chromosome 14
Chromosomal Location 49919017-50020843 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 50005973 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 574 (E574G)
Ref Sequence ENSEMBL: ENSMUSP00000036220 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036972] [ENSMUST00000118129]
AlphaFold Q8BT18
Predicted Effect probably damaging
Transcript: ENSMUST00000036972
AA Change: E574G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000036220
Gene: ENSMUSG00000036242
AA Change: E574G

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 probably benign
Transcript: ENSMUST00000118129
AA Change: E574G

PolyPhen 2 Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000113609
Gene: ENSMUSG00000036242
AA Change: E574G

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: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anxa1 A G 19: 20,354,965 (GRCm39) probably benign Het
Aox3 A G 1: 58,191,845 (GRCm39) I466V probably benign Het
Arid4a A G 12: 71,091,834 (GRCm39) K207E probably benign Het
Cftr T C 6: 18,225,987 (GRCm39) F312L probably damaging Het
Cwf19l1 A G 19: 44,115,809 (GRCm39) Y207H probably damaging Het
Dnttip2 A G 3: 122,076,087 (GRCm39) D673G probably damaging Het
Fut2 C T 7: 45,300,193 (GRCm39) G193E possibly damaging Het
Herc2 T C 7: 55,753,610 (GRCm39) S670P probably damaging Het
Mdn1 C T 4: 32,732,842 (GRCm39) P3081S probably benign Het
Mtrex T C 13: 113,017,509 (GRCm39) probably benign Het
N4bp2l2 G A 5: 150,574,191 (GRCm39) Q75* probably null Het
Naip5 A T 13: 100,349,135 (GRCm39) S1398T probably damaging Het
Nav2 T C 7: 49,111,756 (GRCm39) V754A possibly damaging Het
Nox4 T C 7: 86,966,521 (GRCm39) probably null Het
Pramel25 A G 4: 143,521,506 (GRCm39) E374G probably benign Het
Prox1 T C 1: 189,893,833 (GRCm39) Y204C probably damaging Het
Slitrk5 A G 14: 111,916,717 (GRCm39) S114G probably benign Het
Sprtn G A 8: 125,629,888 (GRCm39) V394M possibly damaging Het
Tars3 T A 7: 65,302,026 (GRCm39) H183Q probably benign Het
Thsd7a A G 6: 12,343,177 (GRCm39) C1147R probably damaging Het
Uba7 G A 9: 107,853,599 (GRCm39) R143Q probably damaging Het
Zp1 A G 19: 10,892,187 (GRCm39) probably benign 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
IGL02154:Armh4 APN 14 50,010,399 (GRCm39) missense possibly damaging 0.58
IGL02163:Armh4 APN 14 50,011,614 (GRCm39) missense possibly damaging 0.61
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 2016-08-02