Incidental Mutation 'R7016:Zfp62'
| ID |
545325 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp62
|
| Ensembl Gene |
ENSMUSG00000046311 |
| Gene Name |
zinc finger protein 62 |
| Synonyms |
|
| MMRRC Submission |
045117-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.176)
|
| Stock # |
R7016 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 49106764 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Serine
at position 285
(I285S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000137583
(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: I285S
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000056226
Gene: ENSMUSG00000046311
AA Change: I285S
| 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: I285S
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000104820
Gene: ENSMUSG00000046311
AA Change: I285S
| 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: I285S
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000104821
Gene: ENSMUSG00000046311
AA Change: I285S
| 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: I285S
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000116045
Gene: ENSMUSG00000046311
AA Change: I285S
| 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: I285S
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000137583
Gene: ENSMUSG00000046311
AA Change: I285S
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.2%
|
| Validation Efficiency |
98% (63/64) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 65 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcb4 |
T |
A |
5: 8,986,843 (GRCm39) |
V754D |
probably benign |
Het |
| Actn1 |
T |
A |
12: 80,219,742 (GRCm39) |
M710L |
possibly damaging |
Het |
| Adam1a |
A |
G |
5: 121,659,101 (GRCm39) |
F64S |
probably benign |
Het |
| Aip |
G |
T |
19: 4,171,402 (GRCm39) |
D11E |
probably benign |
Het |
| Ak7 |
T |
A |
12: 105,747,938 (GRCm39) |
Y714* |
probably null |
Het |
| Amhr2 |
A |
G |
15: 102,362,799 (GRCm39) |
E522G |
possibly damaging |
Het |
| Amotl1 |
A |
G |
9: 14,504,995 (GRCm39) |
L108P |
probably damaging |
Het |
| Arhgef17 |
A |
G |
7: 100,528,184 (GRCm39) |
S677P |
probably benign |
Het |
| Asph |
T |
C |
4: 9,630,604 (GRCm39) |
|
probably null |
Het |
| Atp11b |
T |
C |
3: 35,895,185 (GRCm39) |
S908P |
probably benign |
Het |
| Atp13a3 |
C |
A |
16: 30,157,308 (GRCm39) |
V903L |
possibly damaging |
Het |
| Bcam |
G |
A |
7: 19,492,368 (GRCm39) |
R576* |
probably null |
Het |
| Btbd2 |
A |
G |
10: 80,484,449 (GRCm39) |
S141P |
probably damaging |
Het |
| Cacna1b |
T |
C |
2: 24,652,860 (GRCm39) |
N67S |
possibly damaging |
Het |
| Cc2d2b |
A |
G |
19: 40,784,248 (GRCm39) |
T872A |
possibly damaging |
Het |
| Ccdc24 |
T |
A |
4: 117,728,313 (GRCm39) |
I144F |
probably null |
Het |
| Cep44 |
A |
T |
8: 56,997,234 (GRCm39) |
F101L |
possibly damaging |
Het |
| Cfap410 |
T |
A |
10: 77,818,790 (GRCm39) |
C154S |
probably benign |
Het |
| Cimap1d |
T |
C |
10: 79,475,790 (GRCm39) |
Y258C |
probably damaging |
Het |
| Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
| Dnajc21 |
G |
T |
15: 10,461,493 (GRCm39) |
Y152* |
probably null |
Het |
| Edem2 |
A |
G |
2: 155,557,992 (GRCm39) |
F214L |
possibly damaging |
Het |
| Fam118b |
G |
A |
9: 35,135,014 (GRCm39) |
R198W |
probably damaging |
Het |
| Fgb |
A |
G |
3: 82,953,371 (GRCm39) |
V133A |
probably benign |
Het |
| Fsip2 |
A |
G |
2: 82,820,979 (GRCm39) |
T5571A |
probably benign |
Het |
| Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
| Hjurp |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT |
C |
1: 88,193,999 (GRCm39) |
|
probably benign |
Het |
| Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
| Hnf4a |
T |
A |
2: 163,406,193 (GRCm39) |
Y277N |
probably damaging |
Het |
| Htatip2 |
A |
G |
7: 49,420,583 (GRCm39) |
D143G |
possibly damaging |
Het |
| Itgae |
A |
G |
11: 73,010,342 (GRCm39) |
N611D |
probably damaging |
Het |
| Ksr1 |
A |
T |
11: 78,918,362 (GRCm39) |
N515K |
probably damaging |
Het |
| Lrp1 |
C |
A |
10: 127,395,836 (GRCm39) |
|
probably null |
Het |
| Map3k20 |
T |
A |
2: 72,208,979 (GRCm39) |
V195D |
probably damaging |
Het |
| Meox2 |
A |
G |
12: 37,159,223 (GRCm39) |
S132G |
probably benign |
Het |
| Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
| Nell2 |
T |
A |
15: 95,127,032 (GRCm39) |
N781I |
possibly damaging |
Het |
| Or12d16-ps1 |
G |
A |
17: 37,706,094 (GRCm39) |
G221D |
possibly damaging |
Het |
| Or13a22 |
A |
G |
7: 140,073,153 (GRCm39) |
T201A |
probably benign |
Het |
| Or51m1 |
A |
G |
7: 103,578,737 (GRCm39) |
I236V |
probably benign |
Het |
| Or5e1 |
A |
G |
7: 108,354,918 (GRCm39) |
N285S |
probably damaging |
Het |
| Otoa |
A |
T |
7: 120,746,989 (GRCm39) |
Q918L |
probably damaging |
Het |
| Palld |
T |
G |
8: 61,969,032 (GRCm39) |
K1022T |
probably damaging |
Het |
| Parp8 |
A |
T |
13: 117,031,627 (GRCm39) |
S362T |
probably damaging |
Het |
| Phrf1 |
A |
G |
7: 140,817,476 (GRCm39) |
E95G |
probably damaging |
Het |
| Pls1 |
A |
T |
9: 95,668,994 (GRCm39) |
F76I |
probably damaging |
Het |
| Pnp |
T |
A |
14: 51,187,706 (GRCm39) |
|
probably null |
Het |
| Ptdss1 |
A |
C |
13: 67,120,685 (GRCm39) |
M294L |
probably benign |
Het |
| Rictor |
T |
A |
15: 6,804,361 (GRCm39) |
|
probably null |
Het |
| Rilp |
A |
G |
11: 75,401,745 (GRCm39) |
E175G |
probably damaging |
Het |
| Serpina16 |
T |
A |
12: 103,641,630 (GRCm39) |
T32S |
probably benign |
Het |
| Sim1 |
C |
T |
10: 50,860,346 (GRCm39) |
S736L |
probably benign |
Het |
| Smarcc2 |
T |
G |
10: 128,321,198 (GRCm39) |
|
probably null |
Het |
| Smtn |
A |
G |
11: 3,480,368 (GRCm39) |
|
probably null |
Het |
| Sspo |
T |
A |
6: 48,426,098 (GRCm39) |
W98R |
probably damaging |
Het |
| St8sia3 |
A |
T |
18: 64,402,654 (GRCm39) |
I98F |
probably benign |
Het |
| Taf10 |
A |
T |
7: 105,393,205 (GRCm39) |
|
probably null |
Het |
| Tasor2 |
A |
T |
13: 3,626,857 (GRCm39) |
V1031E |
possibly damaging |
Het |
| Tbc1d4 |
T |
A |
14: 101,724,877 (GRCm39) |
N580I |
probably damaging |
Het |
| Trim12c |
A |
T |
7: 103,997,413 (GRCm39) |
C48S |
|
Het |
| Tsc22d1 |
C |
A |
14: 76,654,982 (GRCm39) |
T405K |
probably damaging |
Het |
| Tubgcp5 |
A |
G |
7: 55,443,977 (GRCm39) |
D2G |
possibly damaging |
Het |
| Wwc2 |
T |
C |
8: 48,300,583 (GRCm39) |
E960G |
unknown |
Het |
| Yme1l1 |
T |
A |
2: 23,076,367 (GRCm39) |
|
probably null |
Het |
| Zbtb2 |
G |
C |
10: 4,318,646 (GRCm39) |
P460R |
probably 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 |
|
|
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'- GGGACTTTTCGGAGTAGCTC -3'
(R):5'- TGGTCTTATGCTGAAGAAGAAGTG -3'
Sequencing Primer
(F):5'- GTTCTGTTCTGGACCAGCATAAAAGG -3'
(R):5'- ATGCACTATAAGGCCTGAGCTGTTC -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation