Incidental Mutation 'IGL03019:Zfp354c'
ID |
407996 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp354c
|
Ensembl Gene |
ENSMUSG00000044807 |
Gene Name |
zinc finger protein 354C |
Synonyms |
5330421P20Rik, Kid3, AJ18 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.073)
|
Stock # |
IGL03019
|
Quality Score |
|
Status
|
|
Chromosome |
11 |
Chromosomal Location |
50701913-50718551 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 50708021 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Threonine
at position 60
(P60T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000104763
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000632]
[ENSMUST00000109135]
|
AlphaFold |
Q571J5 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000000632
AA Change: P60T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000000632 Gene: ENSMUSG00000044807 AA Change: P60T
Domain | Start | End | E-Value | Type |
KRAB
|
14 |
74 |
9.98e-33 |
SMART |
ZnF_C2H2
|
218 |
240 |
5.9e-3 |
SMART |
ZnF_C2H2
|
246 |
268 |
3.74e-5 |
SMART |
ZnF_C2H2
|
274 |
296 |
1.72e-4 |
SMART |
ZnF_C2H2
|
302 |
324 |
7.78e-3 |
SMART |
ZnF_C2H2
|
330 |
352 |
1.92e-2 |
SMART |
ZnF_C2H2
|
358 |
380 |
4.79e-3 |
SMART |
ZnF_C2H2
|
386 |
408 |
1.1e-2 |
SMART |
ZnF_C2H2
|
414 |
436 |
5.67e-5 |
SMART |
ZnF_C2H2
|
442 |
464 |
9.08e-4 |
SMART |
ZnF_C2H2
|
470 |
492 |
5.59e-4 |
SMART |
ZnF_C2H2
|
498 |
520 |
3.39e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109135
AA Change: P60T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000104763 Gene: ENSMUSG00000044807 AA Change: P60T
Domain | Start | End | E-Value | Type |
KRAB
|
14 |
74 |
9.98e-33 |
SMART |
ZnF_C2H2
|
218 |
240 |
5.9e-3 |
SMART |
ZnF_C2H2
|
246 |
268 |
3.74e-5 |
SMART |
ZnF_C2H2
|
274 |
296 |
1.72e-4 |
SMART |
ZnF_C2H2
|
302 |
324 |
7.78e-3 |
SMART |
ZnF_C2H2
|
330 |
352 |
1.92e-2 |
SMART |
ZnF_C2H2
|
358 |
380 |
4.79e-3 |
SMART |
ZnF_C2H2
|
386 |
408 |
1.1e-2 |
SMART |
ZnF_C2H2
|
414 |
436 |
5.67e-5 |
SMART |
ZnF_C2H2
|
442 |
464 |
9.08e-4 |
SMART |
ZnF_C2H2
|
470 |
492 |
5.59e-4 |
SMART |
ZnF_C2H2
|
498 |
520 |
3.39e-3 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139465
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 22 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr2 |
T |
A |
9: 121,738,248 (GRCm39) |
Y208N |
probably benign |
Het |
Agap2 |
T |
C |
10: 126,927,431 (GRCm39) |
|
probably benign |
Het |
Arhgap21 |
A |
T |
2: 20,865,874 (GRCm39) |
I914N |
probably damaging |
Het |
Brsk1 |
T |
C |
7: 4,713,496 (GRCm39) |
|
probably benign |
Het |
Cachd1 |
A |
T |
4: 100,809,282 (GRCm39) |
T256S |
probably damaging |
Het |
Ccdc171 |
G |
T |
4: 83,713,545 (GRCm39) |
G1195W |
probably damaging |
Het |
Cept1 |
A |
G |
3: 106,411,957 (GRCm39) |
M339T |
probably damaging |
Het |
Cir1 |
T |
C |
2: 73,116,692 (GRCm39) |
K223E |
unknown |
Het |
Cited2 |
A |
T |
10: 17,599,910 (GRCm39) |
M73L |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,347,421 (GRCm39) |
Y37H |
probably damaging |
Het |
Drosha |
T |
C |
15: 12,846,185 (GRCm39) |
L440P |
probably damaging |
Het |
Dsc1 |
G |
A |
18: 20,221,421 (GRCm39) |
P685S |
probably benign |
Het |
Epha1 |
T |
A |
6: 42,339,686 (GRCm39) |
D639V |
probably damaging |
Het |
Inka2 |
G |
T |
3: 105,623,687 (GRCm39) |
M1I |
probably null |
Het |
Izumo4 |
A |
G |
10: 80,539,680 (GRCm39) |
|
probably benign |
Het |
Kcnmb2 |
A |
T |
3: 32,252,299 (GRCm39) |
R167W |
probably damaging |
Het |
Lce1k |
A |
C |
3: 92,714,086 (GRCm39) |
C33G |
unknown |
Het |
Map7 |
C |
T |
10: 20,143,101 (GRCm39) |
P417S |
unknown |
Het |
Myo18b |
A |
G |
5: 112,840,263 (GRCm39) |
V2510A |
probably benign |
Het |
Rubcn |
A |
T |
16: 32,647,077 (GRCm39) |
V787D |
probably damaging |
Het |
Spen |
A |
T |
4: 141,206,227 (GRCm39) |
L800Q |
unknown |
Het |
Zfp276 |
C |
A |
8: 123,994,673 (GRCm39) |
T580N |
probably damaging |
Het |
|
Other mutations in Zfp354c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00923:Zfp354c
|
APN |
11 |
50,706,440 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01615:Zfp354c
|
APN |
11 |
50,708,732 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0546:Zfp354c
|
UTSW |
11 |
50,706,457 (GRCm39) |
missense |
probably benign |
0.12 |
R1370:Zfp354c
|
UTSW |
11 |
50,706,667 (GRCm39) |
missense |
probably benign |
|
R2109:Zfp354c
|
UTSW |
11 |
50,707,969 (GRCm39) |
missense |
probably benign |
0.01 |
R2850:Zfp354c
|
UTSW |
11 |
50,706,158 (GRCm39) |
nonsense |
probably null |
|
R4010:Zfp354c
|
UTSW |
11 |
50,705,771 (GRCm39) |
missense |
probably damaging |
0.98 |
R5034:Zfp354c
|
UTSW |
11 |
50,705,866 (GRCm39) |
missense |
probably benign |
0.14 |
R5430:Zfp354c
|
UTSW |
11 |
50,706,022 (GRCm39) |
missense |
probably benign |
0.02 |
R5439:Zfp354c
|
UTSW |
11 |
50,706,597 (GRCm39) |
missense |
probably benign |
0.01 |
R5905:Zfp354c
|
UTSW |
11 |
50,706,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:Zfp354c
|
UTSW |
11 |
50,705,798 (GRCm39) |
missense |
probably benign |
0.41 |
R6264:Zfp354c
|
UTSW |
11 |
50,706,274 (GRCm39) |
missense |
probably benign |
0.00 |
R6591:Zfp354c
|
UTSW |
11 |
50,705,602 (GRCm39) |
missense |
probably benign |
0.41 |
R6650:Zfp354c
|
UTSW |
11 |
50,705,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R6691:Zfp354c
|
UTSW |
11 |
50,705,602 (GRCm39) |
missense |
probably benign |
0.41 |
R7087:Zfp354c
|
UTSW |
11 |
50,706,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Zfp354c
|
UTSW |
11 |
50,705,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Zfp354c
|
UTSW |
11 |
50,706,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R7619:Zfp354c
|
UTSW |
11 |
50,708,635 (GRCm39) |
critical splice donor site |
probably null |
|
R7699:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7710:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7712:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7747:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7748:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7784:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7816:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7817:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7853:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7855:Zfp354c
|
UTSW |
11 |
50,706,067 (GRCm39) |
small deletion |
probably benign |
|
R7870:Zfp354c
|
UTSW |
11 |
50,706,065 (GRCm39) |
small deletion |
probably benign |
|
R8852:Zfp354c
|
UTSW |
11 |
50,706,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R8860:Zfp354c
|
UTSW |
11 |
50,706,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R8862:Zfp354c
|
UTSW |
11 |
50,708,718 (GRCm39) |
missense |
probably benign |
0.15 |
R9169:Zfp354c
|
UTSW |
11 |
50,706,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Zfp354c
|
UTSW |
11 |
50,706,666 (GRCm39) |
missense |
probably benign |
0.31 |
R9273:Zfp354c
|
UTSW |
11 |
50,706,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R9762:Zfp354c
|
UTSW |
11 |
50,706,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2016-08-02 |