Incidental Mutation 'R7175:Zfp62'
| ID |
558560 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp62
|
| Ensembl Gene |
ENSMUSG00000046311 |
| Gene Name |
zinc finger protein 62 |
| Synonyms |
|
| MMRRC Submission |
045231-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.176)
|
| Stock # |
R7175 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 49107580 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Leucine
at position 557
(S557L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000056226
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061757]
[ENSMUST00000109197]
[ENSMUST00000109198]
[ENSMUST00000133150]
[ENSMUST00000136539]
[ENSMUST00000136691]
[ENSMUST00000137061]
[ENSMUST00000150284]
[ENSMUST00000151228]
[ENSMUST00000180016]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000061757
AA Change: S557L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000056226
Gene: ENSMUSG00000046311
AA Change: S557L
| 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: S557L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000104820
Gene: ENSMUSG00000046311
AA Change: S557L
| 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: S557L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000104821
Gene: ENSMUSG00000046311
AA Change: S557L
| 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: ENSMUST00000133150
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000136539
AA Change: S557L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000116045
Gene: ENSMUSG00000046311
AA Change: S557L
| 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 benign
Transcript: ENSMUST00000137061
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000150284
|
| 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 damaging
Transcript: ENSMUST00000180016
AA Change: S557L
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000137583
Gene: ENSMUSG00000046311
AA Change: S557L
| 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 |
|
| Meta Mutation Damage Score |
0.2265 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
100% (63/63) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 63 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb5 |
G |
A |
12: 118,831,611 (GRCm39) |
T1247I |
probably benign |
Het |
| Afdn |
T |
C |
17: 14,108,869 (GRCm39) |
L1479P |
probably damaging |
Het |
| Alox12e |
T |
C |
11: 70,210,534 (GRCm39) |
R363G |
probably damaging |
Het |
| Ank2 |
A |
T |
3: 126,740,590 (GRCm39) |
S1765T |
unknown |
Het |
| Anks6 |
T |
C |
4: 47,046,268 (GRCm39) |
|
probably null |
Het |
| Apob |
A |
C |
12: 8,057,034 (GRCm39) |
I1839L |
probably benign |
Het |
| Bdp1 |
C |
A |
13: 100,186,478 (GRCm39) |
R1658I |
probably damaging |
Het |
| Ccs |
T |
A |
19: 4,883,390 (GRCm39) |
D136V |
probably damaging |
Het |
| Cd200 |
T |
C |
16: 45,220,578 (GRCm39) |
|
probably null |
Het |
| Cirbp |
T |
C |
10: 80,006,297 (GRCm39) |
S130P |
probably benign |
Het |
| Cpb1 |
A |
G |
3: 20,317,927 (GRCm39) |
I199T |
probably benign |
Het |
| Csn3 |
C |
T |
5: 88,077,586 (GRCm39) |
R31C |
probably damaging |
Het |
| Dcaf1 |
A |
T |
9: 106,735,775 (GRCm39) |
I908F |
probably benign |
Het |
| Dhcr7 |
C |
T |
7: 143,399,227 (GRCm39) |
T199I |
probably damaging |
Het |
| Dnah9 |
T |
A |
11: 66,024,463 (GRCm39) |
Q277L |
probably benign |
Het |
| Echdc2 |
C |
A |
4: 108,031,366 (GRCm39) |
P237T |
probably damaging |
Het |
| Efcab3 |
T |
C |
11: 104,838,237 (GRCm39) |
V3625A |
unknown |
Het |
| Eif4g3 |
A |
G |
4: 137,853,526 (GRCm39) |
N364S |
probably damaging |
Het |
| Eml6 |
T |
A |
11: 29,734,231 (GRCm39) |
I1170L |
probably benign |
Het |
| Epha3 |
C |
T |
16: 63,403,863 (GRCm39) |
R746Q |
probably damaging |
Het |
| Exosc5 |
G |
A |
7: 25,363,794 (GRCm39) |
C102Y |
probably damaging |
Het |
| Fam91a1 |
A |
T |
15: 58,302,527 (GRCm39) |
Y289F |
probably benign |
Het |
| Fbxo38 |
A |
C |
18: 62,648,544 (GRCm39) |
F665V |
probably benign |
Het |
| Fcrl5 |
T |
C |
3: 87,353,645 (GRCm39) |
V330A |
probably benign |
Het |
| Fer |
T |
A |
17: 64,231,090 (GRCm39) |
D280E |
probably benign |
Het |
| Gpr158 |
A |
G |
2: 21,373,113 (GRCm39) |
H16R |
probably benign |
Het |
| Gzmg |
C |
T |
14: 56,396,979 (GRCm39) |
M1I |
probably null |
Het |
| Hectd4 |
C |
T |
5: 121,411,692 (GRCm39) |
A456V |
possibly damaging |
Het |
| Hk2 |
T |
A |
6: 82,711,830 (GRCm39) |
Q613L |
probably benign |
Het |
| Inhca |
A |
G |
9: 103,128,988 (GRCm39) |
|
probably null |
Het |
| Itsn1 |
T |
C |
16: 91,664,938 (GRCm39) |
F1121L |
unknown |
Het |
| Lztr1 |
G |
T |
16: 17,340,895 (GRCm39) |
C557F |
possibly damaging |
Het |
| Mdn1 |
A |
G |
4: 32,694,634 (GRCm39) |
Y1119C |
probably damaging |
Het |
| Nfkb1 |
A |
T |
3: 135,319,751 (GRCm39) |
L248Q |
probably damaging |
Het |
| Or1a1 |
T |
A |
11: 74,087,004 (GRCm39) |
L225* |
probably null |
Het |
| Or1p1b |
T |
C |
11: 74,130,803 (GRCm39) |
F138L |
probably benign |
Het |
| Or2g7 |
T |
A |
17: 38,378,370 (GRCm39) |
S103T |
probably damaging |
Het |
| Or52e19 |
T |
C |
7: 102,959,054 (GRCm39) |
V42A |
probably benign |
Het |
| Otulinl |
A |
C |
15: 27,658,374 (GRCm39) |
D165E |
probably damaging |
Het |
| Pate1 |
T |
G |
9: 35,596,408 (GRCm39) |
D119A |
probably damaging |
Het |
| Pcdhgc4 |
T |
C |
18: 37,949,424 (GRCm39) |
V280A |
possibly damaging |
Het |
| Pik3ap1 |
T |
C |
19: 41,275,929 (GRCm39) |
D717G |
probably damaging |
Het |
| Prdm13 |
A |
T |
4: 21,679,473 (GRCm39) |
L339Q |
unknown |
Het |
| Rasgrf1 |
T |
A |
9: 89,862,802 (GRCm39) |
N519K |
probably benign |
Het |
| Rergl |
A |
G |
6: 139,473,533 (GRCm39) |
V39A |
probably benign |
Het |
| Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
| Sema4b |
T |
A |
7: 79,848,402 (GRCm39) |
M1K |
probably null |
Het |
| Slc20a1 |
T |
G |
2: 129,052,662 (GRCm39) |
L648R |
probably damaging |
Het |
| Spata31h1 |
T |
A |
10: 82,122,583 (GRCm39) |
S3476C |
probably damaging |
Het |
| Speg |
A |
G |
1: 75,399,134 (GRCm39) |
T2194A |
probably benign |
Het |
| Spns1 |
T |
C |
7: 125,972,961 (GRCm39) |
D215G |
probably damaging |
Het |
| Tle4 |
A |
T |
19: 14,429,071 (GRCm39) |
V717E |
probably damaging |
Het |
| Trim50 |
T |
A |
5: 135,382,151 (GRCm39) |
M1K |
probably null |
Het |
| Trpa1 |
A |
G |
1: 14,963,431 (GRCm39) |
V597A |
possibly damaging |
Het |
| Usp13 |
C |
T |
3: 32,971,757 (GRCm39) |
Q746* |
probably null |
Het |
| Vmn1r35 |
A |
T |
6: 66,655,906 (GRCm39) |
W255R |
probably benign |
Het |
| Vps35 |
A |
T |
8: 85,990,189 (GRCm39) |
|
probably null |
Het |
| Vps54 |
T |
C |
11: 21,265,028 (GRCm39) |
|
probably null |
Het |
| Zfp318 |
T |
A |
17: 46,697,774 (GRCm39) |
L210Q |
probably damaging |
Het |
| Zfp319 |
C |
A |
8: 96,055,410 (GRCm39) |
K264N |
probably damaging |
Het |
| Zgrf1 |
T |
C |
3: 127,357,239 (GRCm39) |
S822P |
probably damaging |
Het |
| Zxdc |
A |
G |
6: 90,346,645 (GRCm39) |
D2G |
possibly damaging |
Het |
| Zzef1 |
T |
C |
11: 72,742,727 (GRCm39) |
I769T |
possibly damaging |
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 |
|
R1644:Zfp62
|
UTSW |
11 |
49,106,596 (GRCm39) |
missense |
probably damaging |
0.99 |
|
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 |
|
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'- GGAAGGCCTATATCTCACGCTC -3'
(R):5'- TATAGGACGTCTTGCCAGGGTG -3'
Sequencing Primer
(F):5'- GCCCTATAAATGCAGCTATTGTGAG -3'
(R):5'- TTCCACATATGTCACACTCATAGGG -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation