Incidental Mutation 'IGL02958:Mplkipl1'
| ID |
365231 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Mplkipl1
|
| Ensembl Gene |
ENSMUSG00000094649 |
| Gene Name |
M-phase specific PLK1 intereacting protein like 1 |
| Synonyms |
Gm7102 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.214)
|
| Stock # |
IGL02958
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
19 |
| Chromosomal Location |
61163124-61164747 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 61164118 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Lysine
at position 106
(Q106K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000137574
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000180168]
|
| AlphaFold |
J3QQ10 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000180168
AA Change: Q106K
PolyPhen 2
Score 0.833 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000137574
Gene: ENSMUSG00000094649
AA Change: Q106K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:MPLKIP
|
31 |
170 |
8.9e-27 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aars2 |
G |
T |
17: 45,829,098 (GRCm39) |
V755L |
probably benign |
Het |
| Abhd15 |
T |
C |
11: 77,406,791 (GRCm39) |
V256A |
possibly damaging |
Het |
| Agtr1b |
A |
T |
3: 20,370,258 (GRCm39) |
V116E |
possibly damaging |
Het |
| Ahi1 |
A |
T |
10: 20,839,698 (GRCm39) |
D203V |
probably damaging |
Het |
| Aplp2 |
G |
T |
9: 31,075,972 (GRCm39) |
|
probably benign |
Het |
| Arid4a |
T |
C |
12: 71,144,337 (GRCm39) |
S1249P |
probably benign |
Het |
| Asz1 |
T |
A |
6: 18,073,813 (GRCm39) |
K298M |
possibly damaging |
Het |
| C4bp |
A |
G |
1: 130,564,532 (GRCm39) |
I384T |
probably damaging |
Het |
| Cacna1e |
C |
A |
1: 154,341,487 (GRCm39) |
A1236S |
probably damaging |
Het |
| Cdh13 |
T |
C |
8: 120,039,460 (GRCm39) |
I634T |
possibly damaging |
Het |
| Cemip |
A |
T |
7: 83,624,263 (GRCm39) |
F524L |
probably damaging |
Het |
| Dnah7c |
G |
A |
1: 46,696,271 (GRCm39) |
R2051H |
probably damaging |
Het |
| Dnajc17 |
T |
C |
2: 119,016,243 (GRCm39) |
K77E |
probably benign |
Het |
| Efhc2 |
C |
T |
X: 17,027,485 (GRCm39) |
|
probably benign |
Het |
| Ergic2 |
A |
T |
6: 148,083,441 (GRCm39) |
*50K |
probably null |
Het |
| Fam83g |
C |
T |
11: 61,598,548 (GRCm39) |
P812S |
probably damaging |
Het |
| Flg2 |
C |
T |
3: 93,110,920 (GRCm39) |
R983W |
unknown |
Het |
| Itih3 |
T |
C |
14: 30,635,139 (GRCm39) |
T73A |
probably benign |
Het |
| Kcnj1 |
A |
G |
9: 32,307,851 (GRCm39) |
S72G |
probably damaging |
Het |
| Kcnn4 |
T |
C |
7: 24,074,170 (GRCm39) |
V78A |
probably benign |
Het |
| Lrp1b |
T |
A |
2: 41,192,928 (GRCm39) |
D1353V |
probably damaging |
Het |
| Lrrc2 |
T |
A |
9: 110,791,741 (GRCm39) |
|
probably null |
Het |
| Ndufs8 |
T |
C |
19: 3,961,232 (GRCm39) |
E45G |
probably benign |
Het |
| Nell1 |
G |
A |
7: 49,870,085 (GRCm39) |
|
probably null |
Het |
| Nxt1 |
A |
G |
2: 148,517,692 (GRCm39) |
|
probably benign |
Het |
| Or2y17 |
A |
G |
11: 49,232,127 (GRCm39) |
Y256C |
probably benign |
Het |
| Or5al5 |
T |
A |
2: 85,961,351 (GRCm39) |
I219F |
probably benign |
Het |
| Pdzd8 |
A |
T |
19: 59,288,804 (GRCm39) |
C865* |
probably null |
Het |
| Pop1 |
G |
T |
15: 34,530,509 (GRCm39) |
C969F |
probably damaging |
Het |
| Rc3h2 |
A |
C |
2: 37,304,712 (GRCm39) |
I16S |
probably damaging |
Het |
| Shank1 |
T |
C |
7: 44,003,897 (GRCm39) |
V1863A |
possibly damaging |
Het |
| Slc15a4 |
A |
T |
5: 127,681,729 (GRCm39) |
L296Q |
possibly damaging |
Het |
| Spmip1 |
G |
A |
6: 29,471,625 (GRCm39) |
G34R |
probably damaging |
Het |
| Ssr4 |
T |
C |
X: 72,830,856 (GRCm39) |
|
probably benign |
Het |
| Supt20 |
T |
A |
3: 54,621,144 (GRCm39) |
|
probably benign |
Het |
| Ttc8 |
A |
T |
12: 98,930,803 (GRCm39) |
K282N |
probably benign |
Het |
| Usp40 |
A |
T |
1: 87,906,207 (GRCm39) |
V676E |
probably damaging |
Het |
| Vmn1r43 |
T |
C |
6: 89,847,031 (GRCm39) |
I152V |
probably benign |
Het |
| Vmn2r61 |
A |
T |
7: 41,949,361 (GRCm39) |
I594F |
probably benign |
Het |
| Vps53 |
A |
C |
11: 76,008,537 (GRCm39) |
I261S |
probably damaging |
Het |
| Wdr19 |
T |
A |
5: 65,370,150 (GRCm39) |
|
probably null |
Het |
| Zc3hav1 |
T |
A |
6: 38,309,919 (GRCm39) |
D301V |
probably damaging |
Het |
|
| Other mutations in Mplkipl1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01718:Mplkipl1
|
APN |
19 |
61,164,199 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0427:Mplkipl1
|
UTSW |
19 |
61,163,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1886:Mplkipl1
|
UTSW |
19 |
61,164,136 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4576:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4578:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4615:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4616:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4617:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4621:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4622:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4623:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4826:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4827:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4829:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4830:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4870:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4871:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R4951:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5112:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5301:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5317:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5335:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5397:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5399:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5591:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5592:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5594:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5616:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5884:Mplkipl1
|
UTSW |
19 |
61,164,364 (GRCm39) |
missense |
unknown |
|
|
R5919:Mplkipl1
|
UTSW |
19 |
61,163,907 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7003:Mplkipl1
|
UTSW |
19 |
61,164,319 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7112:Mplkipl1
|
UTSW |
19 |
61,163,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7266:Mplkipl1
|
UTSW |
19 |
61,163,973 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R8489:Mplkipl1
|
UTSW |
19 |
61,164,085 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8979:Mplkipl1
|
UTSW |
19 |
61,164,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Mplkipl1
|
UTSW |
19 |
61,164,188 (GRCm39) |
frame shift |
probably null |
|
|
| Posted On |
2015-12-18 |
Incidental Mutation