Incidental Mutation 'IGL02692:Zfp957'
ID |
303783 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp957
|
Ensembl Gene |
ENSMUSG00000071262 |
Gene Name |
zinc finger protein 957 |
Synonyms |
AU017455 |
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.454)
|
Stock # |
IGL02692
|
Quality Score |
|
Status
|
|
Chromosome |
14 |
Chromosomal Location |
79449795-79484807 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 79450825 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Isoleucine
at position 325
(V325I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124930
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040802]
[ENSMUST00000161649]
|
AlphaFold |
Q3UT76 |
Predicted Effect |
unknown
Transcript: ENSMUST00000040802
AA Change: V325I
|
SMART Domains |
Protein: ENSMUSP00000039470 Gene: ENSMUSG00000071262 AA Change: V325I
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
19 |
N/A |
INTRINSIC |
low complexity region
|
29 |
53 |
N/A |
INTRINSIC |
low complexity region
|
147 |
161 |
N/A |
INTRINSIC |
low complexity region
|
220 |
231 |
N/A |
INTRINSIC |
AT_hook
|
255 |
267 |
4.76e0 |
SMART |
AT_hook
|
298 |
310 |
4.76e0 |
SMART |
AT_hook
|
348 |
360 |
2.48e0 |
SMART |
low complexity region
|
390 |
398 |
N/A |
INTRINSIC |
AT_hook
|
422 |
434 |
5.38e0 |
SMART |
PHD
|
507 |
554 |
1.18e-6 |
SMART |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000161649
AA Change: V325I
|
SMART Domains |
Protein: ENSMUSP00000124930 Gene: ENSMUSG00000071262 AA Change: V325I
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
19 |
N/A |
INTRINSIC |
low complexity region
|
29 |
53 |
N/A |
INTRINSIC |
low complexity region
|
147 |
161 |
N/A |
INTRINSIC |
low complexity region
|
220 |
231 |
N/A |
INTRINSIC |
AT_hook
|
255 |
267 |
4.76e0 |
SMART |
AT_hook
|
298 |
310 |
4.76e0 |
SMART |
AT_hook
|
348 |
360 |
2.48e0 |
SMART |
low complexity region
|
390 |
398 |
N/A |
INTRINSIC |
AT_hook
|
422 |
434 |
5.38e0 |
SMART |
PHD
|
507 |
554 |
1.18e-6 |
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 |
1700017N19Rik |
A |
C |
10: 100,439,410 (GRCm39) |
S72R |
probably benign |
Het |
4930544G11Rik |
T |
C |
6: 65,929,792 (GRCm39) |
V9A |
probably damaging |
Het |
Actl11 |
A |
G |
9: 107,806,507 (GRCm39) |
N277D |
probably benign |
Het |
Adam2 |
T |
A |
14: 66,311,536 (GRCm39) |
I57F |
probably damaging |
Het |
Adgrf1 |
T |
C |
17: 43,614,669 (GRCm39) |
F251S |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,509,089 (GRCm39) |
I64V |
probably benign |
Het |
Anapc4 |
T |
C |
5: 53,021,871 (GRCm39) |
V651A |
probably damaging |
Het |
Atl2 |
T |
C |
17: 80,172,482 (GRCm39) |
N163D |
probably benign |
Het |
B4galnt3 |
G |
A |
6: 120,187,272 (GRCm39) |
R708C |
probably damaging |
Het |
Capza2 |
C |
T |
6: 17,654,115 (GRCm39) |
Q56* |
probably null |
Het |
Cspg4 |
T |
A |
9: 56,794,738 (GRCm39) |
H824Q |
probably benign |
Het |
Dock7 |
G |
A |
4: 98,875,623 (GRCm39) |
P1106S |
probably damaging |
Het |
Fat4 |
A |
G |
3: 39,005,235 (GRCm39) |
Y1878C |
probably damaging |
Het |
Grk2 |
A |
T |
19: 4,340,716 (GRCm39) |
|
probably benign |
Het |
Lmbrd2 |
G |
A |
15: 9,149,155 (GRCm39) |
V13I |
possibly damaging |
Het |
Loxhd1 |
G |
T |
18: 77,444,609 (GRCm39) |
C336F |
probably damaging |
Het |
Morc1 |
T |
A |
16: 48,330,596 (GRCm39) |
F355L |
probably null |
Het |
Mov10 |
C |
A |
3: 104,708,119 (GRCm39) |
E503* |
probably null |
Het |
Nt5dc3 |
T |
A |
10: 86,640,642 (GRCm39) |
|
probably null |
Het |
Or2w3b |
A |
G |
11: 58,623,343 (GRCm39) |
V216A |
probably benign |
Het |
Phf20 |
T |
A |
2: 156,140,498 (GRCm39) |
M724K |
probably damaging |
Het |
Pla2g2e |
G |
T |
4: 138,609,870 (GRCm39) |
|
probably benign |
Het |
Polq |
T |
A |
16: 36,880,989 (GRCm39) |
V772E |
probably damaging |
Het |
Rhoh |
A |
G |
5: 66,050,143 (GRCm39) |
R138G |
probably benign |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Septin7 |
A |
G |
9: 25,207,786 (GRCm39) |
|
probably benign |
Het |
Serpina9 |
A |
C |
12: 103,974,665 (GRCm39) |
F163V |
probably damaging |
Het |
Slc2a13 |
A |
T |
15: 91,205,861 (GRCm39) |
F442Y |
probably benign |
Het |
Slc34a1 |
G |
A |
13: 55,551,049 (GRCm39) |
|
probably benign |
Het |
Slc6a11 |
T |
C |
6: 114,139,100 (GRCm39) |
F236S |
probably damaging |
Het |
Usp1 |
A |
G |
4: 98,817,197 (GRCm39) |
K130E |
probably benign |
Het |
Zfp386 |
A |
G |
12: 116,022,855 (GRCm39) |
E156G |
probably damaging |
Het |
|
Other mutations in Zfp957 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00672:Zfp957
|
APN |
14 |
79,450,838 (GRCm39) |
missense |
unknown |
|
IGL01646:Zfp957
|
APN |
14 |
79,451,331 (GRCm39) |
missense |
probably benign |
0.00 |
R0632:Zfp957
|
UTSW |
14 |
79,450,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Zfp957
|
UTSW |
14 |
79,450,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:Zfp957
|
UTSW |
14 |
79,451,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Zfp957
|
UTSW |
14 |
79,451,053 (GRCm39) |
missense |
probably benign |
0.06 |
R2411:Zfp957
|
UTSW |
14 |
79,451,782 (GRCm39) |
missense |
unknown |
|
R2517:Zfp957
|
UTSW |
14 |
79,451,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R3195:Zfp957
|
UTSW |
14 |
79,450,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Zfp957
|
UTSW |
14 |
79,451,796 (GRCm39) |
start codon destroyed |
probably null |
|
R4881:Zfp957
|
UTSW |
14 |
79,450,849 (GRCm39) |
missense |
unknown |
|
R5138:Zfp957
|
UTSW |
14 |
79,450,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Zfp957
|
UTSW |
14 |
79,450,828 (GRCm39) |
missense |
unknown |
|
R5531:Zfp957
|
UTSW |
14 |
79,450,622 (GRCm39) |
missense |
unknown |
|
R5547:Zfp957
|
UTSW |
14 |
79,451,406 (GRCm39) |
missense |
probably benign |
0.03 |
R5677:Zfp957
|
UTSW |
14 |
79,450,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5968:Zfp957
|
UTSW |
14 |
79,451,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6897:Zfp957
|
UTSW |
14 |
79,451,344 (GRCm39) |
missense |
probably damaging |
0.98 |
R6994:Zfp957
|
UTSW |
14 |
79,451,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R7105:Zfp957
|
UTSW |
14 |
79,450,402 (GRCm39) |
missense |
probably benign |
0.09 |
R7214:Zfp957
|
UTSW |
14 |
79,450,750 (GRCm39) |
missense |
unknown |
|
R7264:Zfp957
|
UTSW |
14 |
79,451,080 (GRCm39) |
missense |
probably damaging |
0.98 |
R8407:Zfp957
|
UTSW |
14 |
79,451,352 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8549:Zfp957
|
UTSW |
14 |
79,451,346 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zfp957
|
UTSW |
14 |
79,451,578 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
Posted On |
2015-04-16 |