Incidental Mutation 'R9640:Zfp62'
| ID |
725934 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp62
|
| Ensembl Gene |
ENSMUSG00000046311 |
| Gene Name |
zinc finger protein 62 |
| Synonyms |
|
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.176)
|
| Stock # |
R9640 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 49106458 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 183
(D183G)
|
| 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 benign
Transcript: ENSMUST00000061757
AA Change: D183G
PolyPhen 2
Score 0.206 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000056226
Gene: ENSMUSG00000046311
AA Change: D183G
| 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: ENSMUST00000109197
AA Change: D183G
PolyPhen 2
Score 0.206 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104820
Gene: ENSMUSG00000046311
AA Change: D183G
| 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: ENSMUST00000109198
AA Change: D183G
PolyPhen 2
Score 0.206 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104821
Gene: ENSMUSG00000046311
AA Change: D183G
| 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 benign
Transcript: ENSMUST00000136539
AA Change: D183G
PolyPhen 2
Score 0.206 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000116045
Gene: ENSMUSG00000046311
AA Change: D183G
| 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
AA Change: D183G
PolyPhen 2
Score 0.206 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000117774
Gene: ENSMUSG00000046311
AA Change: D183G
| 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: ENSMUST00000180016
AA Change: D183G
PolyPhen 2
Score 0.206 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000137583
Gene: ENSMUSG00000046311
AA Change: D183G
| 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: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A630010A05Rik |
T |
C |
16: 14,436,589 (GRCm39) |
V214A |
|
Het |
| A830018L16Rik |
A |
G |
1: 12,021,200 (GRCm39) |
K403R |
probably damaging |
Het |
| Aadacl4fm4 |
T |
A |
4: 144,412,809 (GRCm39) |
R44W |
possibly damaging |
Het |
| Abhd17c |
A |
T |
7: 83,800,814 (GRCm39) |
L80Q |
probably damaging |
Het |
| Adam30 |
T |
A |
3: 98,069,620 (GRCm39) |
D484E |
probably damaging |
Het |
| Aspm |
T |
A |
1: 139,408,010 (GRCm39) |
V2299E |
possibly damaging |
Het |
| Atp6v1c1 |
C |
T |
15: 38,689,381 (GRCm39) |
R281W |
probably damaging |
Het |
| Bclaf1 |
T |
C |
10: 20,201,553 (GRCm39) |
|
probably null |
Het |
| Ccdc50 |
T |
C |
16: 27,225,461 (GRCm39) |
V58A |
probably damaging |
Het |
| Cep162 |
A |
G |
9: 87,126,352 (GRCm39) |
S187P |
probably benign |
Het |
| Clip4 |
C |
T |
17: 72,163,264 (GRCm39) |
T612M |
possibly damaging |
Het |
| Corin |
C |
T |
5: 72,592,597 (GRCm39) |
V267I |
probably benign |
Het |
| Cyp2c37 |
T |
A |
19: 40,000,180 (GRCm39) |
I434K |
probably benign |
Het |
| Ddx43 |
T |
G |
9: 78,303,389 (GRCm39) |
D76E |
probably benign |
Het |
| Dusp5 |
A |
G |
19: 53,526,051 (GRCm39) |
E231G |
probably damaging |
Het |
| Fam114a1 |
G |
A |
5: 65,166,394 (GRCm39) |
V242I |
probably damaging |
Het |
| Frem1 |
T |
A |
4: 82,831,896 (GRCm39) |
R1973S |
probably benign |
Het |
| Gas2l3 |
A |
T |
10: 89,266,774 (GRCm39) |
D55E |
probably damaging |
Het |
| Grwd1 |
T |
C |
7: 45,477,303 (GRCm39) |
I195V |
probably benign |
Het |
| H2-M1 |
G |
T |
17: 36,983,031 (GRCm39) |
T20K |
probably benign |
Het |
| H2-Q2 |
T |
G |
17: 35,562,206 (GRCm39) |
L151R |
probably damaging |
Het |
| Hbegf |
T |
C |
18: 36,640,643 (GRCm39) |
Y138C |
probably damaging |
Het |
| Hectd1 |
C |
A |
12: 51,795,197 (GRCm39) |
E2411* |
probably null |
Het |
| Igkv11-125 |
T |
A |
6: 67,890,783 (GRCm39) |
S34T |
possibly damaging |
Het |
| Jam2 |
A |
T |
16: 84,609,960 (GRCm39) |
T191S |
probably benign |
Het |
| Kcnh8 |
T |
C |
17: 53,185,089 (GRCm39) |
I457T |
probably damaging |
Het |
| Khk |
A |
G |
5: 31,079,303 (GRCm39) |
D15G |
probably damaging |
Het |
| Lrba |
T |
A |
3: 86,526,875 (GRCm39) |
Y2244* |
probably null |
Het |
| Lrp1b |
T |
C |
2: 41,078,929 (GRCm39) |
N1841S |
|
Het |
| Lrp4 |
A |
G |
2: 91,316,296 (GRCm39) |
T805A |
probably benign |
Het |
| Lrp6 |
C |
T |
6: 134,441,414 (GRCm39) |
R1184Q |
probably damaging |
Het |
| Map3k1 |
A |
T |
13: 111,900,699 (GRCm39) |
L442* |
probably null |
Het |
| Mapk8ip3 |
T |
C |
17: 25,155,647 (GRCm39) |
N61S |
possibly damaging |
Het |
| Matcap2 |
A |
T |
9: 22,351,228 (GRCm39) |
I457L |
possibly damaging |
Het |
| Mdn1 |
T |
A |
4: 32,754,539 (GRCm39) |
V4685E |
probably damaging |
Het |
| Mib2 |
T |
C |
4: 155,745,325 (GRCm39) |
E134G |
possibly damaging |
Het |
| Mtss2 |
T |
C |
8: 111,464,575 (GRCm39) |
V403A |
probably benign |
Het |
| Ndst4 |
C |
A |
3: 125,232,196 (GRCm39) |
T255K |
probably damaging |
Het |
| Or1i2 |
G |
C |
10: 78,448,311 (GRCm39) |
L55V |
probably damaging |
Het |
| Or2l13 |
A |
T |
16: 19,305,761 (GRCm39) |
M58L |
probably damaging |
Het |
| Or5ae2 |
G |
A |
7: 84,506,114 (GRCm39) |
C181Y |
probably damaging |
Het |
| Or8g20 |
A |
G |
9: 39,396,396 (GRCm39) |
L51P |
probably damaging |
Het |
| Pak1 |
T |
A |
7: 97,515,355 (GRCm39) |
D126E |
probably benign |
Het |
| Rgl1 |
T |
C |
1: 152,397,142 (GRCm39) |
T675A |
probably damaging |
Het |
| Rgs1 |
T |
C |
1: 144,121,116 (GRCm39) |
D185G |
probably damaging |
Het |
| Rnase2a |
G |
A |
14: 51,493,117 (GRCm39) |
R83C |
probably damaging |
Het |
| Sfmbt2 |
A |
G |
2: 10,583,994 (GRCm39) |
T784A |
probably damaging |
Het |
| Slc6a21 |
A |
T |
7: 44,937,189 (GRCm39) |
T272S |
|
Het |
| Sorcs2 |
G |
T |
5: 36,222,765 (GRCm39) |
S330* |
probably null |
Het |
| Spdef |
G |
T |
17: 27,936,183 (GRCm39) |
H253Q |
|
Het |
| Tas2r144 |
A |
G |
6: 42,192,428 (GRCm39) |
E56G |
probably benign |
Het |
| Trim66 |
A |
G |
7: 109,074,825 (GRCm39) |
C479R |
probably damaging |
Het |
| Ttc36 |
A |
T |
9: 44,714,034 (GRCm39) |
L28Q |
probably benign |
Het |
| Ugt1a5 |
T |
C |
1: 88,094,098 (GRCm39) |
S109P |
possibly damaging |
Het |
| Vamp5 |
G |
A |
6: 72,347,276 (GRCm39) |
|
probably benign |
Het |
| Wwox |
A |
G |
8: 115,166,540 (GRCm39) |
D10G |
possibly damaging |
Het |
| Zfp40 |
T |
C |
17: 23,394,493 (GRCm39) |
Y698C |
probably damaging |
Het |
| Zfp932 |
T |
C |
5: 110,157,064 (GRCm39) |
V254A |
probably benign |
Het |
| Zfp943 |
T |
A |
17: 22,209,899 (GRCm39) |
L57H |
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 |
|
|
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 |
|
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'- AACATTAATGGAAACGTACACCCTG -3'
(R):5'- ACTCACCACATTCATAGGGC -3'
Sequencing Primer
(F):5'- ACACCCTGCTCATATTGCTGATAAG -3'
(R):5'- CATAGGGCTTCTCTCCGGTG -3'
|
| Posted On |
2022-09-12 |
Incidental Mutation