Incidental Mutation 'IGL02049:Armh1'
ID |
185031 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Armh1
|
Ensembl Gene |
ENSMUSG00000060268 |
Gene Name |
armadillo-like helical domain containing 1 |
Synonyms |
LOC381544, LOC381543, Ncrna00082, Gm1661 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.093)
|
Stock # |
IGL02049
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
117070531-117109322 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 117094860 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Lysine
at position 60
(I60K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000128613
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000077500]
[ENSMUST00000165128]
|
AlphaFold |
E9Q963 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000077500
AA Change: I60K
PolyPhen 2
Score 0.128 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000076706 Gene: ENSMUSG00000060268 AA Change: I60K
Domain | Start | End | E-Value | Type |
SCOP:d1qbkb_
|
156 |
272 |
3e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165128
AA Change: I60K
PolyPhen 2
Score 0.369 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000128613 Gene: ENSMUSG00000060268 AA Change: I60K
Domain | Start | End | E-Value | Type |
low complexity region
|
162 |
176 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
A |
2: 35,254,801 (GRCm39) |
R27S |
probably benign |
Het |
4930596D02Rik |
C |
A |
14: 35,533,535 (GRCm39) |
V78L |
probably benign |
Het |
Abca3 |
T |
A |
17: 24,595,704 (GRCm39) |
C352* |
probably null |
Het |
Acat3 |
T |
A |
17: 13,144,207 (GRCm39) |
Y324F |
probably benign |
Het |
Adamts8 |
T |
C |
9: 30,862,650 (GRCm39) |
V285A |
probably damaging |
Het |
Anpep |
A |
G |
7: 79,484,929 (GRCm39) |
I652T |
probably damaging |
Het |
Arhgef6 |
T |
A |
X: 56,321,271 (GRCm39) |
Q320L |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,854,642 (GRCm39) |
V145A |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,580,880 (GRCm39) |
T1674A |
probably benign |
Het |
Capn2 |
A |
T |
1: 182,301,519 (GRCm39) |
|
probably benign |
Het |
Cfd |
A |
G |
10: 79,726,776 (GRCm39) |
Y6C |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,183,113 (GRCm39) |
K157R |
possibly damaging |
Het |
Csmd3 |
T |
A |
15: 47,864,870 (GRCm39) |
R786S |
possibly damaging |
Het |
Dna2 |
A |
T |
10: 62,792,815 (GRCm39) |
I277L |
probably damaging |
Het |
Gm5168 |
A |
T |
X: 25,999,005 (GRCm39) |
D50E |
probably damaging |
Het |
Grik4 |
T |
A |
9: 42,455,049 (GRCm39) |
|
probably benign |
Het |
Ift56 |
A |
G |
6: 38,402,067 (GRCm39) |
T520A |
probably benign |
Het |
Iqgap2 |
A |
G |
13: 95,811,913 (GRCm39) |
|
probably benign |
Het |
Klk10 |
A |
T |
7: 43,433,882 (GRCm39) |
|
probably benign |
Het |
Kng1 |
A |
G |
16: 22,892,187 (GRCm39) |
Y250C |
probably damaging |
Het |
Las1l |
A |
T |
X: 94,981,059 (GRCm39) |
M690K |
probably benign |
Het |
Mug1 |
T |
A |
6: 121,848,295 (GRCm39) |
M673K |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,654,070 (GRCm39) |
H1245R |
probably benign |
Het |
Oprk1 |
C |
T |
1: 5,669,067 (GRCm39) |
T171I |
probably damaging |
Het |
Pgm5 |
A |
T |
19: 24,801,782 (GRCm39) |
S149T |
probably benign |
Het |
Pla2g4a |
T |
C |
1: 149,736,847 (GRCm39) |
N424S |
probably benign |
Het |
Plec |
A |
T |
15: 76,063,149 (GRCm39) |
L2334Q |
probably damaging |
Het |
Pus7l |
G |
A |
15: 94,438,059 (GRCm39) |
S262F |
probably damaging |
Het |
Rps24 |
C |
A |
14: 24,541,823 (GRCm39) |
D3E |
probably benign |
Het |
Rxfp1 |
T |
C |
3: 79,557,799 (GRCm39) |
N560D |
probably damaging |
Het |
Sema3c |
C |
T |
5: 17,926,923 (GRCm39) |
|
probably benign |
Het |
Slc47a2 |
A |
G |
11: 61,233,365 (GRCm39) |
F55S |
probably damaging |
Het |
Slco1a6 |
A |
G |
6: 142,047,309 (GRCm39) |
|
probably benign |
Het |
Taf4b |
A |
T |
18: 14,963,196 (GRCm39) |
E645D |
probably benign |
Het |
Tmem161a |
T |
A |
8: 70,631,624 (GRCm39) |
V158E |
probably damaging |
Het |
Trav13-2 |
A |
G |
14: 53,872,604 (GRCm39) |
S27G |
possibly damaging |
Het |
Trav13-2 |
G |
T |
14: 53,872,603 (GRCm39) |
Q26H |
probably damaging |
Het |
Trav13-2 |
A |
T |
14: 53,872,602 (GRCm39) |
Q26L |
possibly damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,691,608 (GRCm39) |
H305L |
probably benign |
Het |
Zfp263 |
A |
G |
16: 3,562,482 (GRCm39) |
I82V |
probably damaging |
Het |
|
Other mutations in Armh1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0350:Armh1
|
UTSW |
4 |
117,072,753 (GRCm39) |
nonsense |
probably null |
|
R0584:Armh1
|
UTSW |
4 |
117,087,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R1570:Armh1
|
UTSW |
4 |
117,087,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4335:Armh1
|
UTSW |
4 |
117,071,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Armh1
|
UTSW |
4 |
117,094,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R5939:Armh1
|
UTSW |
4 |
117,087,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Armh1
|
UTSW |
4 |
117,088,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R6815:Armh1
|
UTSW |
4 |
117,087,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R7526:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7529:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7630:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7632:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7659:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7660:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7662:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7663:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7665:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7666:Armh1
|
UTSW |
4 |
117,070,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7713:Armh1
|
UTSW |
4 |
117,071,425 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8030:Armh1
|
UTSW |
4 |
117,087,184 (GRCm39) |
missense |
probably benign |
0.31 |
R8433:Armh1
|
UTSW |
4 |
117,085,535 (GRCm39) |
missense |
probably benign |
0.43 |
R8693:Armh1
|
UTSW |
4 |
117,088,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R8756:Armh1
|
UTSW |
4 |
117,094,861 (GRCm39) |
missense |
probably benign |
|
R8832:Armh1
|
UTSW |
4 |
117,094,867 (GRCm39) |
missense |
probably damaging |
0.97 |
R8957:Armh1
|
UTSW |
4 |
117,087,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Armh1
|
UTSW |
4 |
117,094,855 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Armh1
|
UTSW |
4 |
117,070,992 (GRCm39) |
missense |
probably benign |
|
|
Posted On |
2014-05-07 |