Incidental Mutation 'IGL02209:Zfp692'
ID |
284611 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp692
|
Ensembl Gene |
ENSMUSG00000037243 |
Gene Name |
zinc finger protein 692 |
Synonyms |
Zfp692-ps |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL02209
|
Quality Score |
|
Status
|
|
Chromosome |
11 |
Chromosomal Location |
58197895-58205453 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
C to T
at 58204824 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Stop codon
at position 395
(R395*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000126674
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049353]
[ENSMUST00000057836]
[ENSMUST00000064786]
[ENSMUST00000108829]
[ENSMUST00000153510]
[ENSMUST00000155662]
[ENSMUST00000186859]
|
AlphaFold |
Q3U381 |
Predicted Effect |
probably null
Transcript: ENSMUST00000049353
AA Change: R395*
|
SMART Domains |
Protein: ENSMUSP00000131896 Gene: ENSMUSG00000037243 AA Change: R395*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
23 |
N/A |
INTRINSIC |
low complexity region
|
94 |
110 |
N/A |
INTRINSIC |
low complexity region
|
159 |
175 |
N/A |
INTRINSIC |
low complexity region
|
193 |
204 |
N/A |
INTRINSIC |
low complexity region
|
215 |
232 |
N/A |
INTRINSIC |
ZnF_C2H2
|
327 |
352 |
4.11e-2 |
SMART |
ZnF_C2H2
|
358 |
382 |
2.05e-2 |
SMART |
ZnF_C2H2
|
388 |
410 |
1.69e-3 |
SMART |
ZnF_C2H2
|
416 |
438 |
1.69e-3 |
SMART |
ZnF_C2H2
|
447 |
470 |
6.23e-2 |
SMART |
low complexity region
|
502 |
520 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000057836
|
SMART Domains |
Protein: ENSMUSP00000060088 Gene: ENSMUSG00000049755
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
15 |
37 |
4.17e-3 |
SMART |
ZnF_C2H2
|
43 |
65 |
8.75e0 |
SMART |
ZnF_C2H2
|
71 |
93 |
1.18e-2 |
SMART |
ZnF_C2H2
|
100 |
123 |
1.76e-1 |
SMART |
ZnF_C2H2
|
129 |
151 |
1.59e1 |
SMART |
ZnF_C2H2
|
167 |
189 |
4.47e-3 |
SMART |
ZnF_C2H2
|
202 |
224 |
9.58e-3 |
SMART |
ZnF_C2H2
|
230 |
252 |
7.37e-4 |
SMART |
ZnF_C2H2
|
258 |
280 |
3.16e-3 |
SMART |
ZnF_C2H2
|
286 |
308 |
1.45e-2 |
SMART |
ZnF_C2H2
|
314 |
336 |
4.01e-5 |
SMART |
ZnF_C2H2
|
342 |
364 |
5.5e-3 |
SMART |
ZnF_C2H2
|
370 |
392 |
1.12e-3 |
SMART |
ZnF_C2H2
|
398 |
420 |
6.67e-2 |
SMART |
low complexity region
|
421 |
441 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000064786
|
SMART Domains |
Protein: ENSMUSP00000070567 Gene: ENSMUSG00000049755
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
15 |
37 |
4.17e-3 |
SMART |
ZnF_C2H2
|
43 |
65 |
8.75e0 |
SMART |
ZnF_C2H2
|
71 |
93 |
1.18e-2 |
SMART |
ZnF_C2H2
|
100 |
123 |
1.76e-1 |
SMART |
ZnF_C2H2
|
129 |
151 |
1.59e1 |
SMART |
ZnF_C2H2
|
167 |
189 |
4.47e-3 |
SMART |
ZnF_C2H2
|
202 |
224 |
9.58e-3 |
SMART |
ZnF_C2H2
|
230 |
252 |
7.37e-4 |
SMART |
ZnF_C2H2
|
258 |
280 |
3.16e-3 |
SMART |
ZnF_C2H2
|
286 |
308 |
1.45e-2 |
SMART |
ZnF_C2H2
|
314 |
336 |
4.01e-5 |
SMART |
ZnF_C2H2
|
342 |
364 |
5.5e-3 |
SMART |
ZnF_C2H2
|
370 |
392 |
1.12e-3 |
SMART |
ZnF_C2H2
|
398 |
420 |
6.67e-2 |
SMART |
low complexity region
|
421 |
441 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108829
|
SMART Domains |
Protein: ENSMUSP00000104457 Gene: ENSMUSG00000049755
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
15 |
37 |
4.17e-3 |
SMART |
ZnF_C2H2
|
43 |
65 |
8.75e0 |
SMART |
ZnF_C2H2
|
71 |
93 |
1.18e-2 |
SMART |
ZnF_C2H2
|
100 |
123 |
1.76e-1 |
SMART |
ZnF_C2H2
|
129 |
151 |
1.59e1 |
SMART |
ZnF_C2H2
|
167 |
189 |
4.47e-3 |
SMART |
ZnF_C2H2
|
202 |
224 |
9.58e-3 |
SMART |
ZnF_C2H2
|
230 |
252 |
7.37e-4 |
SMART |
ZnF_C2H2
|
258 |
280 |
3.16e-3 |
SMART |
ZnF_C2H2
|
286 |
308 |
1.45e-2 |
SMART |
ZnF_C2H2
|
314 |
336 |
4.01e-5 |
SMART |
ZnF_C2H2
|
342 |
364 |
5.5e-3 |
SMART |
ZnF_C2H2
|
370 |
392 |
1.12e-3 |
SMART |
ZnF_C2H2
|
398 |
420 |
6.67e-2 |
SMART |
low complexity region
|
421 |
441 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000153510
AA Change: R395*
|
SMART Domains |
Protein: ENSMUSP00000126674 Gene: ENSMUSG00000037243 AA Change: R395*
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
23 |
N/A |
INTRINSIC |
low complexity region
|
94 |
110 |
N/A |
INTRINSIC |
low complexity region
|
159 |
175 |
N/A |
INTRINSIC |
low complexity region
|
193 |
204 |
N/A |
INTRINSIC |
low complexity region
|
215 |
232 |
N/A |
INTRINSIC |
ZnF_C2H2
|
327 |
352 |
4.11e-2 |
SMART |
ZnF_C2H2
|
358 |
382 |
2.05e-2 |
SMART |
ZnF_C2H2
|
388 |
410 |
1.69e-3 |
SMART |
ZnF_C2H2
|
416 |
438 |
1.69e-3 |
SMART |
ZnF_C2H2
|
447 |
470 |
6.23e-2 |
SMART |
low complexity region
|
502 |
520 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000155662
|
SMART Domains |
Protein: ENSMUSP00000114561 Gene: ENSMUSG00000049755
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
15 |
37 |
4.17e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000186859
|
SMART Domains |
Protein: ENSMUSP00000140236 Gene: ENSMUSG00000049755
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
15 |
37 |
1.8e-5 |
SMART |
ZnF_C2H2
|
43 |
65 |
3.6e-2 |
SMART |
ZnF_C2H2
|
71 |
90 |
6.1e-1 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
C |
T |
17: 36,274,901 (GRCm39) |
R82Q |
probably damaging |
Het |
Acmsd |
A |
G |
1: 127,687,492 (GRCm39) |
Y258C |
probably damaging |
Het |
Anapc5 |
A |
G |
5: 122,938,676 (GRCm39) |
I366T |
possibly damaging |
Het |
Crkl |
C |
T |
16: 17,287,098 (GRCm39) |
T218I |
probably benign |
Het |
Egf |
A |
T |
3: 129,500,956 (GRCm39) |
I213K |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,360,491 (GRCm39) |
T33A |
probably benign |
Het |
Garnl3 |
T |
C |
2: 32,975,942 (GRCm39) |
D93G |
probably damaging |
Het |
Hook3 |
C |
T |
8: 26,560,293 (GRCm39) |
D311N |
probably damaging |
Het |
Iglv3 |
T |
C |
16: 19,060,420 (GRCm39) |
T4A |
probably benign |
Het |
Kctd17 |
A |
G |
15: 78,319,792 (GRCm39) |
N70S |
probably damaging |
Het |
Kmt2d |
T |
C |
15: 98,752,448 (GRCm39) |
|
probably benign |
Het |
Lrif1 |
A |
C |
3: 106,639,045 (GRCm39) |
L18F |
probably damaging |
Het |
Mfsd1 |
A |
G |
3: 67,505,465 (GRCm39) |
|
probably benign |
Het |
Msh4 |
A |
G |
3: 153,594,499 (GRCm39) |
Y101H |
probably damaging |
Het |
Mycbpap |
G |
A |
11: 94,400,708 (GRCm39) |
|
probably benign |
Het |
Myt1 |
A |
G |
2: 181,439,027 (GRCm39) |
D183G |
probably benign |
Het |
Nppc |
T |
C |
1: 86,597,387 (GRCm39) |
*127W |
probably null |
Het |
Or10al3 |
G |
A |
17: 38,011,883 (GRCm39) |
M107I |
probably damaging |
Het |
Or1ak2 |
C |
T |
2: 36,827,517 (GRCm39) |
P129S |
probably damaging |
Het |
Or2n1e |
A |
G |
17: 38,586,123 (GRCm39) |
I154V |
probably benign |
Het |
Or51i2 |
T |
G |
7: 103,689,663 (GRCm39) |
L220R |
probably damaging |
Het |
Or8b3b |
T |
C |
9: 38,584,342 (GRCm39) |
K146E |
possibly damaging |
Het |
Pde5a |
A |
G |
3: 122,618,664 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
T |
C |
8: 110,365,296 (GRCm39) |
V1139A |
probably damaging |
Het |
Pwwp2b |
G |
A |
7: 138,835,021 (GRCm39) |
R154Q |
probably damaging |
Het |
Satb2 |
C |
T |
1: 56,910,677 (GRCm39) |
V264I |
probably damaging |
Het |
Slc6a2 |
T |
A |
8: 93,720,688 (GRCm39) |
F435Y |
probably benign |
Het |
Stmn2 |
T |
C |
3: 8,625,321 (GRCm39) |
|
probably benign |
Het |
Synj1 |
A |
G |
16: 90,784,307 (GRCm39) |
I277T |
probably damaging |
Het |
Trio |
C |
T |
15: 27,744,139 (GRCm39) |
A2598T |
probably damaging |
Het |
Tshz2 |
G |
A |
2: 169,726,684 (GRCm39) |
V427M |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,559,039 (GRCm39) |
S1405P |
probably damaging |
Het |
Vmn1r173 |
G |
A |
7: 23,402,586 (GRCm39) |
V274I |
probably benign |
Het |
Vmn2r116 |
T |
C |
17: 23,607,761 (GRCm39) |
F443S |
probably damaging |
Het |
Vps13d |
C |
A |
4: 144,882,671 (GRCm39) |
R974L |
probably damaging |
Het |
Wapl |
T |
A |
14: 34,399,218 (GRCm39) |
S96T |
possibly damaging |
Het |
Zfp516 |
A |
G |
18: 83,012,622 (GRCm39) |
D1125G |
probably benign |
Het |
|
Other mutations in Zfp692 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00978:Zfp692
|
APN |
11 |
58,200,824 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00978:Zfp692
|
APN |
11 |
58,204,855 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01667:Zfp692
|
APN |
11 |
58,202,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02873:Zfp692
|
APN |
11 |
58,199,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Zfp692
|
UTSW |
11 |
58,201,229 (GRCm39) |
splice site |
probably benign |
|
R0267:Zfp692
|
UTSW |
11 |
58,205,140 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0506:Zfp692
|
UTSW |
11 |
58,199,881 (GRCm39) |
nonsense |
probably null |
|
R0554:Zfp692
|
UTSW |
11 |
58,205,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R0628:Zfp692
|
UTSW |
11 |
58,200,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R0712:Zfp692
|
UTSW |
11 |
58,205,140 (GRCm39) |
missense |
probably benign |
0.00 |
R1112:Zfp692
|
UTSW |
11 |
58,202,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Zfp692
|
UTSW |
11 |
58,204,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Zfp692
|
UTSW |
11 |
58,201,002 (GRCm39) |
splice site |
probably benign |
|
R1853:Zfp692
|
UTSW |
11 |
58,200,805 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3551:Zfp692
|
UTSW |
11 |
58,200,254 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3552:Zfp692
|
UTSW |
11 |
58,200,254 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4281:Zfp692
|
UTSW |
11 |
58,205,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Zfp692
|
UTSW |
11 |
58,200,997 (GRCm39) |
missense |
probably null |
0.12 |
R5150:Zfp692
|
UTSW |
11 |
58,198,413 (GRCm39) |
start codon destroyed |
probably null |
0.77 |
R7035:Zfp692
|
UTSW |
11 |
58,200,268 (GRCm39) |
critical splice donor site |
probably null |
|
R7343:Zfp692
|
UTSW |
11 |
58,202,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Zfp692
|
UTSW |
11 |
58,205,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Zfp692
|
UTSW |
11 |
58,198,560 (GRCm39) |
missense |
probably damaging |
0.96 |
R8163:Zfp692
|
UTSW |
11 |
58,201,199 (GRCm39) |
splice site |
probably null |
|
R9043:Zfp692
|
UTSW |
11 |
58,198,550 (GRCm39) |
missense |
probably damaging |
0.98 |
R9487:Zfp692
|
UTSW |
11 |
58,199,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Zfp692
|
UTSW |
11 |
58,199,638 (GRCm39) |
missense |
probably benign |
0.14 |
Z1186:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1186:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
Z1187:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1187:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
Z1188:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1188:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
Z1189:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1189:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
Z1190:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1190:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
Z1191:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1191:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
Z1192:Zfp692
|
UTSW |
11 |
58,200,844 (GRCm39) |
missense |
probably benign |
|
Z1192:Zfp692
|
UTSW |
11 |
58,199,859 (GRCm39) |
missense |
probably benign |
0.02 |
|
Posted On |
2015-04-16 |