Incidental Mutation 'R1644:Zfp62'
| ID |
173760 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp62
|
| Ensembl Gene |
ENSMUSG00000046311 |
| Gene Name |
zinc finger protein 62 |
| Synonyms |
|
| MMRRC Submission |
039680-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.176)
|
| Stock # |
R1644 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 49106596 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 229
(I229T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000116045
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061757]
[ENSMUST00000109197]
[ENSMUST00000109198]
[ENSMUST00000133150]
[ENSMUST00000136539]
[ENSMUST00000136691]
[ENSMUST00000180016]
[ENSMUST00000151228]
[ENSMUST00000137061]
[ENSMUST00000150284]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000061757
AA Change: I229T
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000056226
Gene: ENSMUSG00000046311
AA Change: I229T
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
124 |
146 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
152 |
174 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
180 |
202 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
208 |
230 |
2.71e-2 |
SMART |
|
ZnF_C2H2
|
236 |
258 |
7.37e-4 |
SMART |
|
ZnF_C2H2
|
264 |
286 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
292 |
314 |
4.11e-2 |
SMART |
|
ZnF_C2H2
|
320 |
342 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
348 |
370 |
4.54e-4 |
SMART |
|
ZnF_C2H2
|
376 |
398 |
4.47e-3 |
SMART |
|
ZnF_C2H2
|
404 |
426 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
432 |
454 |
2.43e-4 |
SMART |
|
ZnF_C2H2
|
460 |
482 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
488 |
510 |
2.79e-4 |
SMART |
|
ZnF_C2H2
|
516 |
538 |
5.9e-3 |
SMART |
|
ZnF_C2H2
|
544 |
566 |
3.39e-3 |
SMART |
|
ZnF_C2H2
|
572 |
594 |
3.89e-3 |
SMART |
|
ZnF_C2H2
|
600 |
622 |
5.5e-3 |
SMART |
|
ZnF_C2H2
|
628 |
650 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
656 |
678 |
3.63e-3 |
SMART |
|
ZnF_C2H2
|
684 |
706 |
7.9e-4 |
SMART |
|
ZnF_C2H2
|
712 |
734 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
740 |
762 |
1.98e-4 |
SMART |
|
ZnF_C2H2
|
768 |
790 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
796 |
817 |
1.16e1 |
SMART |
|
ZnF_C2H2
|
823 |
845 |
5.99e-4 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000109197
AA Change: I229T
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000104820
Gene: ENSMUSG00000046311
AA Change: I229T
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
124 |
146 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
152 |
174 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
180 |
202 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
208 |
230 |
2.71e-2 |
SMART |
|
ZnF_C2H2
|
236 |
258 |
7.37e-4 |
SMART |
|
ZnF_C2H2
|
264 |
286 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
292 |
314 |
4.11e-2 |
SMART |
|
ZnF_C2H2
|
320 |
342 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
348 |
370 |
4.54e-4 |
SMART |
|
ZnF_C2H2
|
376 |
398 |
4.47e-3 |
SMART |
|
ZnF_C2H2
|
404 |
426 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
432 |
454 |
2.43e-4 |
SMART |
|
ZnF_C2H2
|
460 |
482 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
488 |
510 |
2.79e-4 |
SMART |
|
ZnF_C2H2
|
516 |
538 |
5.9e-3 |
SMART |
|
ZnF_C2H2
|
544 |
566 |
3.39e-3 |
SMART |
|
ZnF_C2H2
|
572 |
594 |
3.89e-3 |
SMART |
|
ZnF_C2H2
|
600 |
622 |
5.5e-3 |
SMART |
|
ZnF_C2H2
|
628 |
650 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
656 |
678 |
3.63e-3 |
SMART |
|
ZnF_C2H2
|
684 |
706 |
7.9e-4 |
SMART |
|
ZnF_C2H2
|
712 |
734 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
740 |
762 |
1.98e-4 |
SMART |
|
ZnF_C2H2
|
768 |
790 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
796 |
817 |
1.16e1 |
SMART |
|
ZnF_C2H2
|
823 |
845 |
5.99e-4 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000109198
AA Change: I229T
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000104821
Gene: ENSMUSG00000046311
AA Change: I229T
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
124 |
146 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
152 |
174 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
180 |
202 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
208 |
230 |
2.71e-2 |
SMART |
|
ZnF_C2H2
|
236 |
258 |
7.37e-4 |
SMART |
|
ZnF_C2H2
|
264 |
286 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
292 |
314 |
4.11e-2 |
SMART |
|
ZnF_C2H2
|
320 |
342 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
348 |
370 |
4.54e-4 |
SMART |
|
ZnF_C2H2
|
376 |
398 |
4.47e-3 |
SMART |
|
ZnF_C2H2
|
404 |
426 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
432 |
454 |
2.43e-4 |
SMART |
|
ZnF_C2H2
|
460 |
482 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
488 |
510 |
2.79e-4 |
SMART |
|
ZnF_C2H2
|
516 |
538 |
5.9e-3 |
SMART |
|
ZnF_C2H2
|
544 |
566 |
3.39e-3 |
SMART |
|
ZnF_C2H2
|
572 |
594 |
3.89e-3 |
SMART |
|
ZnF_C2H2
|
600 |
622 |
5.5e-3 |
SMART |
|
ZnF_C2H2
|
628 |
650 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
656 |
678 |
3.63e-3 |
SMART |
|
ZnF_C2H2
|
684 |
706 |
7.9e-4 |
SMART |
|
ZnF_C2H2
|
712 |
734 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
740 |
762 |
1.98e-4 |
SMART |
|
ZnF_C2H2
|
768 |
790 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
796 |
817 |
1.16e1 |
SMART |
|
ZnF_C2H2
|
823 |
845 |
5.99e-4 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128932
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000133150
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000136539
AA Change: I229T
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000116045
Gene: ENSMUSG00000046311
AA Change: I229T
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
124 |
146 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
152 |
174 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
180 |
202 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
208 |
230 |
2.71e-2 |
SMART |
|
ZnF_C2H2
|
236 |
258 |
7.37e-4 |
SMART |
|
ZnF_C2H2
|
264 |
286 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
292 |
314 |
4.11e-2 |
SMART |
|
ZnF_C2H2
|
320 |
342 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
348 |
370 |
4.54e-4 |
SMART |
|
ZnF_C2H2
|
376 |
398 |
4.47e-3 |
SMART |
|
ZnF_C2H2
|
404 |
426 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
432 |
454 |
2.43e-4 |
SMART |
|
ZnF_C2H2
|
460 |
482 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
488 |
510 |
2.79e-4 |
SMART |
|
ZnF_C2H2
|
516 |
538 |
5.9e-3 |
SMART |
|
ZnF_C2H2
|
544 |
566 |
3.39e-3 |
SMART |
|
ZnF_C2H2
|
572 |
594 |
3.89e-3 |
SMART |
|
ZnF_C2H2
|
600 |
622 |
5.5e-3 |
SMART |
|
ZnF_C2H2
|
628 |
650 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
656 |
678 |
3.63e-3 |
SMART |
|
ZnF_C2H2
|
684 |
706 |
7.9e-4 |
SMART |
|
ZnF_C2H2
|
712 |
734 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
740 |
762 |
1.98e-4 |
SMART |
|
ZnF_C2H2
|
768 |
790 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
796 |
817 |
1.16e1 |
SMART |
|
ZnF_C2H2
|
823 |
845 |
5.99e-4 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136691
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000180016
AA Change: I229T
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000137583
Gene: ENSMUSG00000046311
AA Change: I229T
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
124 |
146 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
152 |
174 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
180 |
202 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
208 |
230 |
2.71e-2 |
SMART |
|
ZnF_C2H2
|
236 |
258 |
7.37e-4 |
SMART |
|
ZnF_C2H2
|
264 |
286 |
2.27e-4 |
SMART |
|
ZnF_C2H2
|
292 |
314 |
4.11e-2 |
SMART |
|
ZnF_C2H2
|
320 |
342 |
1.03e-2 |
SMART |
|
ZnF_C2H2
|
348 |
370 |
4.54e-4 |
SMART |
|
ZnF_C2H2
|
376 |
398 |
4.47e-3 |
SMART |
|
ZnF_C2H2
|
404 |
426 |
4.4e-2 |
SMART |
|
ZnF_C2H2
|
432 |
454 |
2.43e-4 |
SMART |
|
ZnF_C2H2
|
460 |
482 |
1.38e-3 |
SMART |
|
ZnF_C2H2
|
488 |
510 |
2.79e-4 |
SMART |
|
ZnF_C2H2
|
516 |
538 |
5.9e-3 |
SMART |
|
ZnF_C2H2
|
544 |
566 |
3.39e-3 |
SMART |
|
ZnF_C2H2
|
572 |
594 |
3.89e-3 |
SMART |
|
ZnF_C2H2
|
600 |
622 |
5.5e-3 |
SMART |
|
ZnF_C2H2
|
628 |
650 |
2.75e-3 |
SMART |
|
ZnF_C2H2
|
656 |
678 |
3.63e-3 |
SMART |
|
ZnF_C2H2
|
684 |
706 |
7.9e-4 |
SMART |
|
ZnF_C2H2
|
712 |
734 |
8.34e-3 |
SMART |
|
ZnF_C2H2
|
740 |
762 |
1.98e-4 |
SMART |
|
ZnF_C2H2
|
768 |
790 |
1.53e-1 |
SMART |
|
ZnF_C2H2
|
796 |
817 |
1.16e1 |
SMART |
|
ZnF_C2H2
|
823 |
845 |
5.99e-4 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000157023
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000151228
|
| SMART Domains |
Protein: ENSMUSP00000117774
Gene: ENSMUSG00000046311
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
124 |
146 |
7.26e-3 |
SMART |
|
ZnF_C2H2
|
152 |
174 |
7.26e-3 |
SMART |
|
Pfam:zf-C2H2_6
|
179 |
195 |
2.3e-3 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000137061
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000150284
|
| Meta Mutation Damage Score |
0.2553 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 96.0%
- 20x: 91.6%
|
| Validation Efficiency |
98% (62/63) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 57 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A830018L16Rik |
C |
T |
1: 11,484,814 (GRCm39) |
R8* |
probably null |
Het |
| Acacb |
A |
T |
5: 114,333,346 (GRCm39) |
H490L |
probably damaging |
Het |
| Ace |
C |
A |
11: 105,875,932 (GRCm39) |
H417N |
probably damaging |
Het |
| Adamtsl3 |
A |
G |
7: 82,099,298 (GRCm39) |
N151D |
possibly damaging |
Het |
| Agap1 |
A |
G |
1: 89,591,452 (GRCm39) |
N114S |
probably damaging |
Het |
| Arap3 |
A |
T |
18: 38,117,298 (GRCm39) |
V926D |
probably damaging |
Het |
| Arhgap12 |
A |
T |
18: 6,112,340 (GRCm39) |
I8N |
probably benign |
Het |
| Arhgef17 |
A |
T |
7: 100,578,711 (GRCm39) |
F746I |
probably damaging |
Het |
| Atp6v0a1 |
T |
C |
11: 100,929,612 (GRCm39) |
S471P |
possibly damaging |
Het |
| Bdp1 |
A |
G |
13: 100,197,448 (GRCm39) |
V979A |
probably benign |
Het |
| Ccdc88c |
C |
A |
12: 100,879,733 (GRCm39) |
R1789L |
probably damaging |
Het |
| Cckar |
A |
T |
5: 53,857,215 (GRCm39) |
N327K |
probably benign |
Het |
| Cfap65 |
T |
C |
1: 74,956,334 (GRCm39) |
T1082A |
probably damaging |
Het |
| Clcn7 |
T |
A |
17: 25,378,672 (GRCm39) |
I719N |
probably damaging |
Het |
| Col27a1 |
C |
G |
4: 63,246,868 (GRCm39) |
|
probably benign |
Het |
| Cspp1 |
C |
T |
1: 10,196,663 (GRCm39) |
T179I |
probably damaging |
Het |
| Dnah1 |
C |
T |
14: 31,024,249 (GRCm39) |
|
probably benign |
Het |
| Dnah6 |
A |
G |
6: 73,132,279 (GRCm39) |
V1141A |
probably benign |
Het |
| Dusp4 |
A |
G |
8: 35,285,633 (GRCm39) |
Y298C |
probably damaging |
Het |
| Efhc1 |
C |
A |
1: 21,037,625 (GRCm39) |
Y267* |
probably null |
Het |
| Eif2s1 |
T |
A |
12: 78,913,295 (GRCm39) |
|
probably null |
Het |
| Epo |
A |
G |
5: 137,481,417 (GRCm39) |
V169A |
possibly damaging |
Het |
| Esr1 |
A |
T |
10: 4,951,380 (GRCm39) |
Y586F |
probably benign |
Het |
| Fat2 |
T |
C |
11: 55,178,609 (GRCm39) |
T1484A |
possibly damaging |
Het |
| Fat2 |
T |
C |
11: 55,187,007 (GRCm39) |
T1280A |
possibly damaging |
Het |
| Gm5828 |
T |
C |
1: 16,839,485 (GRCm39) |
|
noncoding transcript |
Het |
| Idh3b |
T |
C |
2: 130,123,430 (GRCm39) |
I187V |
possibly damaging |
Het |
| Kif13a |
A |
C |
13: 46,947,398 (GRCm39) |
V862G |
probably benign |
Het |
| Kndc1 |
A |
G |
7: 139,510,669 (GRCm39) |
D1327G |
probably damaging |
Het |
| Mfsd9 |
T |
A |
1: 40,812,958 (GRCm39) |
R452S |
probably benign |
Het |
| Myh15 |
C |
T |
16: 48,952,566 (GRCm39) |
R879C |
probably benign |
Het |
| Naip2 |
T |
C |
13: 100,319,437 (GRCm39) |
R260G |
possibly damaging |
Het |
| Npat |
T |
G |
9: 53,481,472 (GRCm39) |
L1060R |
probably damaging |
Het |
| Or2aj4 |
T |
A |
16: 19,385,156 (GRCm39) |
H159L |
probably benign |
Het |
| Or4c126 |
A |
T |
2: 89,824,297 (GRCm39) |
T187S |
possibly damaging |
Het |
| Or4c15 |
A |
T |
2: 88,759,731 (GRCm39) |
D309E |
probably benign |
Het |
| Or52n2b |
A |
C |
7: 104,566,015 (GRCm39) |
F163V |
probably benign |
Het |
| Or6f2 |
T |
C |
7: 139,756,561 (GRCm39) |
V176A |
probably benign |
Het |
| Pld5 |
T |
C |
1: 175,803,192 (GRCm39) |
T296A |
possibly damaging |
Het |
| Polq |
C |
T |
16: 36,880,626 (GRCm39) |
A651V |
probably damaging |
Het |
| Polr3a |
G |
A |
14: 24,520,692 (GRCm39) |
P607S |
probably damaging |
Het |
| Ranbp9 |
G |
A |
13: 43,566,015 (GRCm39) |
R424C |
probably damaging |
Het |
| Rsl1 |
G |
A |
13: 67,325,229 (GRCm39) |
|
probably benign |
Het |
| Sema4c |
A |
G |
1: 36,589,885 (GRCm39) |
S490P |
probably damaging |
Het |
| Setd3 |
A |
T |
12: 108,079,603 (GRCm39) |
L300Q |
possibly damaging |
Het |
| Slc15a3 |
T |
C |
19: 10,834,595 (GRCm39) |
I492T |
possibly damaging |
Het |
| Stag1 |
T |
C |
9: 100,762,953 (GRCm39) |
|
probably benign |
Het |
| Tgm4 |
A |
G |
9: 122,880,481 (GRCm39) |
Y294C |
probably damaging |
Het |
| Tm9sf1 |
A |
G |
14: 55,878,757 (GRCm39) |
S212P |
probably benign |
Het |
| Tmcc1 |
A |
G |
6: 116,110,826 (GRCm39) |
S156P |
probably damaging |
Het |
| Vmn1r184 |
A |
C |
7: 25,966,670 (GRCm39) |
M139L |
probably benign |
Het |
| Vmn1r209 |
A |
C |
13: 22,990,652 (GRCm39) |
F13V |
possibly damaging |
Het |
| Xkr5 |
T |
C |
8: 18,984,141 (GRCm39) |
E467G |
probably benign |
Het |
| Zdbf2 |
C |
T |
1: 63,348,131 (GRCm39) |
S2170L |
possibly damaging |
Het |
| Zfp277 |
G |
T |
12: 40,379,609 (GRCm39) |
|
probably null |
Het |
| Zfp810 |
A |
G |
9: 22,190,324 (GRCm39) |
S195P |
possibly damaging |
Het |
| Zfp94 |
G |
A |
7: 24,010,927 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Zfp62 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL03342:Zfp62
|
APN |
11 |
49,106,298 (GRCm39) |
nonsense |
probably null |
|
|
R0416:Zfp62
|
UTSW |
11 |
49,106,503 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0540:Zfp62
|
UTSW |
11 |
49,106,227 (GRCm39) |
missense |
probably benign |
|
|
R0607:Zfp62
|
UTSW |
11 |
49,106,227 (GRCm39) |
missense |
probably benign |
|
|
R1119:Zfp62
|
UTSW |
11 |
49,107,517 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1230:Zfp62
|
UTSW |
11 |
49,105,926 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1710:Zfp62
|
UTSW |
11 |
49,108,510 (GRCm39) |
missense |
probably benign |
|
|
R1840:Zfp62
|
UTSW |
11 |
49,107,215 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1908:Zfp62
|
UTSW |
11 |
49,107,047 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3878:Zfp62
|
UTSW |
11 |
49,105,960 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4571:Zfp62
|
UTSW |
11 |
49,106,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4571:Zfp62
|
UTSW |
11 |
49,106,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4580:Zfp62
|
UTSW |
11 |
49,107,099 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4631:Zfp62
|
UTSW |
11 |
49,108,632 (GRCm39) |
makesense |
probably null |
|
|
R5022:Zfp62
|
UTSW |
11 |
49,106,556 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5023:Zfp62
|
UTSW |
11 |
49,106,556 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5289:Zfp62
|
UTSW |
11 |
49,107,975 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5362:Zfp62
|
UTSW |
11 |
49,107,439 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5685:Zfp62
|
UTSW |
11 |
49,107,044 (GRCm39) |
nonsense |
probably null |
|
|
R6420:Zfp62
|
UTSW |
11 |
49,107,340 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6764:Zfp62
|
UTSW |
11 |
49,105,996 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7000:Zfp62
|
UTSW |
11 |
49,107,206 (GRCm39) |
nonsense |
probably null |
|
|
R7016:Zfp62
|
UTSW |
11 |
49,106,764 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7175:Zfp62
|
UTSW |
11 |
49,107,580 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7670:Zfp62
|
UTSW |
11 |
49,105,903 (GRCm39) |
start gained |
probably benign |
|
|
R7675:Zfp62
|
UTSW |
11 |
49,106,847 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R7686:Zfp62
|
UTSW |
11 |
49,107,985 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7801:Zfp62
|
UTSW |
11 |
49,108,155 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8190:Zfp62
|
UTSW |
11 |
49,106,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8390:Zfp62
|
UTSW |
11 |
49,106,019 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8401:Zfp62
|
UTSW |
11 |
49,108,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8479:Zfp62
|
UTSW |
11 |
49,107,319 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8735:Zfp62
|
UTSW |
11 |
49,108,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8809:Zfp62
|
UTSW |
11 |
49,107,238 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8972:Zfp62
|
UTSW |
11 |
49,106,892 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9220:Zfp62
|
UTSW |
11 |
49,106,075 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9261:Zfp62
|
UTSW |
11 |
49,108,350 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9484:Zfp62
|
UTSW |
11 |
49,108,108 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9599:Zfp62
|
UTSW |
11 |
49,106,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9640:Zfp62
|
UTSW |
11 |
49,106,458 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9781:Zfp62
|
UTSW |
11 |
49,106,297 (GRCm39) |
nonsense |
probably null |
|
|
X0011:Zfp62
|
UTSW |
11 |
49,106,425 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTACGAGTGTGATGACTGTAGGGG -3'
(R):5'- TCCGATGAACTTTGAGACCTGAATTGTT -3'
Sequencing Primer
(F):5'- agtccacaagcgcatcc -3'
(R):5'- tcccacattcatcacattcataag -3'
|
| Posted On |
2014-04-24 |
Incidental Mutation