Incidental Mutation 'IGL02566:Map10'
ID |
298835 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Map10
|
Ensembl Gene |
ENSMUSG00000050930 |
Gene Name |
microtubule-associated protein 10 |
Synonyms |
4933403G14Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.089)
|
Stock # |
IGL02566
|
Quality Score |
|
Status
|
|
Chromosome |
8 |
Chromosomal Location |
126396557-126400098 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 126398494 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Serine
at position 629
(N629S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000061679
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053078]
|
AlphaFold |
Q8BJS7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000053078
AA Change: N629S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000061679 Gene: ENSMUSG00000050930 AA Change: N629S
Domain | Start | End | E-Value | Type |
low complexity region
|
38 |
54 |
N/A |
INTRINSIC |
low complexity region
|
68 |
91 |
N/A |
INTRINSIC |
Pfam:HPHLAWLY
|
243 |
535 |
1.4e-130 |
PFAM |
Pfam:HPHLAWLY
|
527 |
890 |
9.1e-133 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arl4d |
A |
G |
11: 101,557,980 (GRCm39) |
S169G |
probably damaging |
Het |
Bbx |
A |
T |
16: 50,043,603 (GRCm39) |
|
probably benign |
Het |
Blm |
A |
T |
7: 80,123,944 (GRCm39) |
M959K |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cyb5d1 |
T |
C |
11: 69,284,594 (GRCm39) |
N186S |
probably benign |
Het |
Elk3 |
A |
G |
10: 93,101,325 (GRCm39) |
L142P |
probably damaging |
Het |
Gk5 |
G |
A |
9: 96,011,099 (GRCm39) |
D70N |
possibly damaging |
Het |
Gpr84 |
T |
C |
15: 103,217,150 (GRCm39) |
D309G |
probably benign |
Het |
Greb1l |
T |
C |
18: 10,503,299 (GRCm39) |
V450A |
probably damaging |
Het |
Gucy1b1 |
A |
G |
3: 81,965,636 (GRCm39) |
F70S |
probably damaging |
Het |
Jmjd4 |
T |
A |
11: 59,345,880 (GRCm39) |
M320K |
probably damaging |
Het |
Nmd3 |
G |
T |
3: 69,647,247 (GRCm39) |
|
probably benign |
Het |
Obscn |
G |
T |
11: 58,958,973 (GRCm39) |
T3359K |
probably damaging |
Het |
Or2t1 |
C |
A |
14: 14,328,138 (GRCm38) |
T9K |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,389,450 (GRCm39) |
|
probably null |
Het |
Plcb1 |
T |
C |
2: 135,314,183 (GRCm39) |
F1212L |
probably benign |
Het |
Rabep1 |
A |
G |
11: 70,808,540 (GRCm39) |
S459G |
probably damaging |
Het |
Septin4 |
T |
G |
11: 87,458,468 (GRCm39) |
S281A |
probably benign |
Het |
Slc26a1 |
A |
G |
5: 108,821,665 (GRCm39) |
S75P |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Sult1d1 |
A |
T |
5: 87,712,670 (GRCm39) |
L58Q |
probably damaging |
Het |
Tnrc18 |
A |
T |
5: 142,758,068 (GRCm39) |
|
probably benign |
Het |
Vps35l |
C |
T |
7: 118,352,055 (GRCm39) |
A154V |
probably benign |
Het |
Zfp442 |
T |
C |
2: 150,251,711 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Map10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00813:Map10
|
APN |
8 |
126,398,671 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01567:Map10
|
APN |
8 |
126,398,232 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03088:Map10
|
APN |
8 |
126,397,809 (GRCm39) |
missense |
probably benign |
0.14 |
debauched
|
UTSW |
8 |
126,397,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R1083:Map10
|
UTSW |
8 |
126,397,178 (GRCm39) |
nonsense |
probably null |
|
R1543:Map10
|
UTSW |
8 |
126,397,611 (GRCm39) |
missense |
probably benign |
0.00 |
R3155:Map10
|
UTSW |
8 |
126,398,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4076:Map10
|
UTSW |
8 |
126,398,584 (GRCm39) |
missense |
probably benign |
0.23 |
R4559:Map10
|
UTSW |
8 |
126,398,553 (GRCm39) |
missense |
probably benign |
|
R4856:Map10
|
UTSW |
8 |
126,397,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Map10
|
UTSW |
8 |
126,397,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R5412:Map10
|
UTSW |
8 |
126,397,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Map10
|
UTSW |
8 |
126,399,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Map10
|
UTSW |
8 |
126,399,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R6150:Map10
|
UTSW |
8 |
126,398,328 (GRCm39) |
missense |
probably damaging |
0.96 |
R6351:Map10
|
UTSW |
8 |
126,397,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6466:Map10
|
UTSW |
8 |
126,399,123 (GRCm39) |
nonsense |
probably null |
|
R6544:Map10
|
UTSW |
8 |
126,398,113 (GRCm39) |
missense |
probably benign |
0.00 |
R6557:Map10
|
UTSW |
8 |
126,396,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R6821:Map10
|
UTSW |
8 |
126,397,138 (GRCm39) |
missense |
probably benign |
0.01 |
R7096:Map10
|
UTSW |
8 |
126,398,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R7128:Map10
|
UTSW |
8 |
126,398,592 (GRCm39) |
missense |
probably benign |
|
R7177:Map10
|
UTSW |
8 |
126,398,584 (GRCm39) |
missense |
probably benign |
0.23 |
R7237:Map10
|
UTSW |
8 |
126,397,963 (GRCm39) |
missense |
probably benign |
0.03 |
R7814:Map10
|
UTSW |
8 |
126,398,350 (GRCm39) |
missense |
probably benign |
0.14 |
R7819:Map10
|
UTSW |
8 |
126,397,260 (GRCm39) |
frame shift |
probably null |
|
R8202:Map10
|
UTSW |
8 |
126,397,647 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8812:Map10
|
UTSW |
8 |
126,396,664 (GRCm39) |
missense |
probably damaging |
0.99 |
R8859:Map10
|
UTSW |
8 |
126,397,291 (GRCm39) |
missense |
probably benign |
0.04 |
R8947:Map10
|
UTSW |
8 |
126,397,839 (GRCm39) |
missense |
probably benign |
0.06 |
R9178:Map10
|
UTSW |
8 |
126,397,649 (GRCm39) |
missense |
probably damaging |
0.98 |
R9698:Map10
|
UTSW |
8 |
126,398,723 (GRCm39) |
missense |
probably benign |
0.16 |
Z1088:Map10
|
UTSW |
8 |
126,398,670 (GRCm39) |
frame shift |
probably null |
|
Z1177:Map10
|
UTSW |
8 |
126,396,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-04-16 |