Incidental Mutation 'R6420:Zfp62'
ID |
518156 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp62
|
Ensembl Gene |
ENSMUSG00000046311 |
Gene Name |
zinc finger protein 62 |
Synonyms |
|
MMRRC Submission |
044562-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.176)
|
Stock # |
R6420 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 49107340 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Isoleucine
at position 477
(N477I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000116045
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061757]
[ENSMUST00000109197]
[ENSMUST00000109198]
[ENSMUST00000133150]
[ENSMUST00000136539]
[ENSMUST00000180016]
[ENSMUST00000151228]
[ENSMUST00000136691]
[ENSMUST00000150284]
[ENSMUST00000137061]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000061757
AA Change: N477I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000056226 Gene: ENSMUSG00000046311 AA Change: N477I
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: N477I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000104820 Gene: ENSMUSG00000046311 AA Change: N477I
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: N477I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000104821 Gene: ENSMUSG00000046311 AA Change: N477I
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: N477I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000116045 Gene: ENSMUSG00000046311 AA Change: N477I
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: ENSMUST00000180016
AA Change: N477I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000137583 Gene: ENSMUSG00000046311 AA Change: N477I
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: 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: ENSMUST00000136691
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150284
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000157023
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000137061
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.4%
- 20x: 95.5%
|
Validation Efficiency |
100% (38/38) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A530064D06Rik |
A |
T |
17: 48,473,566 (GRCm39) |
I117N |
probably damaging |
Het |
Abca15 |
A |
G |
7: 119,996,351 (GRCm39) |
K1426E |
possibly damaging |
Het |
Arhgef17 |
A |
G |
7: 100,579,269 (GRCm39) |
S560P |
probably damaging |
Het |
Asb13 |
G |
A |
13: 3,693,574 (GRCm39) |
V111I |
probably damaging |
Het |
Dhx16 |
A |
G |
17: 36,193,906 (GRCm39) |
E367G |
possibly damaging |
Het |
Epc2 |
T |
C |
2: 49,341,912 (GRCm39) |
V32A |
probably damaging |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Hdlbp |
T |
C |
1: 93,358,726 (GRCm39) |
E275G |
probably damaging |
Het |
Kdm7a |
T |
C |
6: 39,142,102 (GRCm39) |
D392G |
probably damaging |
Het |
Lgmn |
T |
A |
12: 102,389,978 (GRCm39) |
R4* |
probably null |
Het |
Lrrk2 |
C |
T |
15: 91,696,549 (GRCm39) |
R2446C |
probably benign |
Het |
Map3k10 |
A |
G |
7: 27,362,709 (GRCm39) |
F459S |
probably damaging |
Het |
Mup1 |
C |
G |
4: 60,457,758 (GRCm39) |
E31Q |
possibly damaging |
Het |
Nckap1l |
G |
C |
15: 103,399,893 (GRCm39) |
G1025A |
possibly damaging |
Het |
Or4d10 |
T |
G |
19: 12,051,324 (GRCm39) |
K224T |
probably benign |
Het |
Or5b24 |
A |
C |
19: 12,912,584 (GRCm39) |
T161P |
probably damaging |
Het |
Or8b39 |
T |
A |
9: 37,996,890 (GRCm39) |
S253T |
probably benign |
Het |
Or8b41 |
T |
G |
9: 38,054,611 (GRCm39) |
L55R |
probably damaging |
Het |
Or8k38 |
A |
T |
2: 86,488,510 (GRCm39) |
C97* |
probably null |
Het |
Pik3r5 |
G |
A |
11: 68,366,250 (GRCm39) |
W42* |
probably null |
Het |
Pkd1l2 |
C |
T |
8: 117,740,638 (GRCm39) |
C2153Y |
probably damaging |
Het |
Rad1 |
T |
C |
15: 10,488,098 (GRCm39) |
V74A |
probably benign |
Het |
Scara3 |
C |
T |
14: 66,175,701 (GRCm39) |
G22D |
possibly damaging |
Het |
Scn1a |
A |
G |
2: 66,103,542 (GRCm39) |
I1906T |
probably damaging |
Het |
Sema5b |
T |
A |
16: 35,483,516 (GRCm39) |
D1051E |
probably benign |
Het |
Slc16a12 |
T |
C |
19: 34,650,097 (GRCm39) |
|
probably null |
Het |
Slc25a23 |
T |
C |
17: 57,359,780 (GRCm39) |
I324V |
probably damaging |
Het |
Sord |
A |
T |
2: 122,094,602 (GRCm39) |
K330M |
possibly damaging |
Het |
Spag9 |
T |
C |
11: 93,977,128 (GRCm39) |
V78A |
probably damaging |
Het |
St3gal1 |
A |
G |
15: 66,983,195 (GRCm39) |
V187A |
possibly damaging |
Het |
Tnrc6a |
A |
G |
7: 122,770,297 (GRCm39) |
T696A |
probably benign |
Het |
Ttn |
A |
G |
2: 76,542,619 (GRCm39) |
Y33456H |
possibly damaging |
Het |
Unc45a |
C |
G |
7: 79,989,400 (GRCm39) |
E23Q |
probably benign |
Het |
Urb2 |
C |
T |
8: 124,773,938 (GRCm39) |
R1490W |
probably damaging |
Het |
Zfp846 |
T |
C |
9: 20,505,007 (GRCm39) |
L289P |
probably damaging |
Het |
Zfp959 |
G |
A |
17: 56,205,094 (GRCm39) |
G377D |
probably damaging |
Het |
Zswim3 |
G |
A |
2: 164,662,653 (GRCm39) |
V378M |
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 |
|
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'- CAGCATAAGACCATTCATACTGG -3'
(R):5'- TGTATAGGACGTCTTGCCAGGG -3'
Sequencing Primer
(F):5'- ACTGGAGAAAGACCTTATGTATGTG -3'
(R):5'- GTGATGAAGGCTTTCTCACAC -3'
|
Posted On |
2018-05-24 |