Incidental Mutation 'IGL03101:Zfp943'
ID |
418720 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp943
|
Ensembl Gene |
ENSMUSG00000053347 |
Gene Name |
zinc finger prtoein 943 |
Synonyms |
4930432O21Rik |
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.250)
|
Stock # |
IGL03101
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
22181540-22213347 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 22211156 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 81
(S81P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000059554
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055349]
[ENSMUST00000153985]
[ENSMUST00000174015]
|
AlphaFold |
Q6NZP4 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000055349
AA Change: S81P
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000059554 Gene: ENSMUSG00000053347 AA Change: S81P
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
72 |
2.62e-18 |
SMART |
ZnF_C2H2
|
180 |
202 |
1.6e-4 |
SMART |
ZnF_C2H2
|
208 |
230 |
1.38e-3 |
SMART |
ZnF_C2H2
|
236 |
258 |
1.13e-4 |
SMART |
ZnF_C2H2
|
264 |
286 |
1.03e-2 |
SMART |
ZnF_C2H2
|
292 |
314 |
2.24e-3 |
SMART |
ZnF_C2H2
|
320 |
342 |
9.58e-3 |
SMART |
ZnF_C2H2
|
348 |
370 |
5.67e-5 |
SMART |
ZnF_C2H2
|
376 |
398 |
4.54e-4 |
SMART |
ZnF_C2H2
|
404 |
426 |
2.15e-5 |
SMART |
ZnF_C2H2
|
432 |
454 |
5.59e-4 |
SMART |
ZnF_C2H2
|
460 |
482 |
3.34e-2 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000153985
|
SMART Domains |
Protein: ENSMUSP00000115817 Gene: ENSMUSG00000053347
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
73 |
3.51e-19 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174015
|
SMART Domains |
Protein: ENSMUSP00000133735 Gene: ENSMUSG00000053347
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
60 |
3.79e-15 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA474408 |
A |
T |
7: 109,660,177 (GRCm39) |
|
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,207,732 (GRCm39) |
V23D |
probably damaging |
Het |
Adam8 |
G |
T |
7: 139,568,456 (GRCm39) |
N260K |
possibly damaging |
Het |
Ap3b1 |
A |
T |
13: 94,591,906 (GRCm39) |
I457L |
probably benign |
Het |
Apaf1 |
T |
C |
10: 90,867,421 (GRCm39) |
N808S |
possibly damaging |
Het |
Arhgef26 |
A |
G |
3: 62,327,082 (GRCm39) |
T532A |
possibly damaging |
Het |
Cfap65 |
G |
T |
1: 74,967,592 (GRCm39) |
T162N |
possibly damaging |
Het |
Clec12b |
A |
G |
6: 129,356,480 (GRCm39) |
|
probably null |
Het |
Creb3 |
T |
C |
4: 43,563,081 (GRCm39) |
V60A |
probably benign |
Het |
Cyp11b1 |
A |
G |
15: 74,707,703 (GRCm39) |
F469L |
probably benign |
Het |
Defb28 |
A |
T |
2: 152,362,047 (GRCm39) |
E69V |
possibly damaging |
Het |
Etnppl |
T |
C |
3: 130,415,967 (GRCm39) |
L118S |
probably damaging |
Het |
Fsip1 |
T |
C |
2: 118,072,144 (GRCm39) |
Y213C |
probably damaging |
Het |
Glb1l2 |
A |
G |
9: 26,676,421 (GRCm39) |
W480R |
probably damaging |
Het |
Herc1 |
A |
T |
9: 66,395,279 (GRCm39) |
M4205L |
probably benign |
Het |
Kif5a |
A |
T |
10: 127,071,478 (GRCm39) |
|
probably benign |
Het |
Lmbrd2 |
C |
T |
15: 9,186,695 (GRCm39) |
R557C |
probably damaging |
Het |
Map4k3 |
A |
G |
17: 80,963,284 (GRCm39) |
|
probably null |
Het |
Npc1 |
A |
G |
18: 12,331,596 (GRCm39) |
I858T |
probably benign |
Het |
Or7e173 |
T |
C |
9: 19,938,725 (GRCm39) |
T170A |
probably benign |
Het |
Pecam1 |
A |
G |
11: 106,588,177 (GRCm39) |
V92A |
probably damaging |
Het |
Rbm43 |
A |
T |
2: 51,816,757 (GRCm39) |
I70N |
probably benign |
Het |
Rps6kb1 |
T |
C |
11: 86,393,708 (GRCm39) |
Y474C |
probably benign |
Het |
Slco2a1 |
G |
A |
9: 102,954,205 (GRCm39) |
G459R |
possibly damaging |
Het |
Snca |
T |
A |
6: 60,804,595 (GRCm39) |
|
probably benign |
Het |
Spata31f1e |
T |
C |
4: 42,793,424 (GRCm39) |
D236G |
possibly damaging |
Het |
Stap2 |
T |
A |
17: 56,309,029 (GRCm39) |
I113F |
probably damaging |
Het |
Tas2r140 |
T |
C |
6: 40,468,764 (GRCm39) |
M198T |
probably benign |
Het |
Trim9 |
T |
C |
12: 70,393,428 (GRCm39) |
E172G |
probably damaging |
Het |
Ttll7 |
T |
C |
3: 146,602,445 (GRCm39) |
V81A |
possibly damaging |
Het |
Vmn2r103 |
A |
G |
17: 19,993,782 (GRCm39) |
Y53C |
probably damaging |
Het |
Vmn2r22 |
C |
A |
6: 123,614,295 (GRCm39) |
A432S |
probably benign |
Het |
|
Other mutations in Zfp943 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0019:Zfp943
|
UTSW |
17 |
22,211,070 (GRCm39) |
intron |
probably benign |
|
R0827:Zfp943
|
UTSW |
17 |
22,211,071 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1824:Zfp943
|
UTSW |
17 |
22,211,361 (GRCm39) |
missense |
probably benign |
0.32 |
R1958:Zfp943
|
UTSW |
17 |
22,211,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R2174:Zfp943
|
UTSW |
17 |
22,211,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Zfp943
|
UTSW |
17 |
22,211,403 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4093:Zfp943
|
UTSW |
17 |
22,211,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4094:Zfp943
|
UTSW |
17 |
22,211,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Zfp943
|
UTSW |
17 |
22,212,104 (GRCm39) |
missense |
probably damaging |
0.98 |
R4677:Zfp943
|
UTSW |
17 |
22,212,176 (GRCm39) |
missense |
probably benign |
0.17 |
R4735:Zfp943
|
UTSW |
17 |
22,211,391 (GRCm39) |
missense |
probably benign |
0.03 |
R5201:Zfp943
|
UTSW |
17 |
22,211,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5492:Zfp943
|
UTSW |
17 |
22,212,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Zfp943
|
UTSW |
17 |
22,211,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Zfp943
|
UTSW |
17 |
22,212,357 (GRCm39) |
missense |
probably benign |
|
R6031:Zfp943
|
UTSW |
17 |
22,212,357 (GRCm39) |
missense |
probably benign |
|
R6667:Zfp943
|
UTSW |
17 |
22,211,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R6864:Zfp943
|
UTSW |
17 |
22,211,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R6976:Zfp943
|
UTSW |
17 |
22,209,922 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7837:Zfp943
|
UTSW |
17 |
22,211,346 (GRCm39) |
missense |
probably benign |
0.39 |
R7934:Zfp943
|
UTSW |
17 |
22,212,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R8302:Zfp943
|
UTSW |
17 |
22,211,091 (GRCm39) |
missense |
probably benign |
0.18 |
R8323:Zfp943
|
UTSW |
17 |
22,211,763 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9025:Zfp943
|
UTSW |
17 |
22,211,321 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9101:Zfp943
|
UTSW |
17 |
22,212,392 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9279:Zfp943
|
UTSW |
17 |
22,209,832 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9640:Zfp943
|
UTSW |
17 |
22,209,899 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Zfp943
|
UTSW |
17 |
22,211,946 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zfp943
|
UTSW |
17 |
22,207,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2016-08-02 |