Incidental Mutation 'R4571:Zfp62'
ID |
342149 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp62
|
Ensembl Gene |
ENSMUSG00000046311 |
Gene Name |
zinc finger protein 62 |
Synonyms |
|
MMRRC Submission |
041795-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.176)
|
Stock # |
R4571 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 49106569 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Isoleucine
at position 220
(S220I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000116045
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061757]
[ENSMUST00000109197]
[ENSMUST00000109198]
[ENSMUST00000133150]
[ENSMUST00000136539]
[ENSMUST00000180016]
[ENSMUST00000150284]
[ENSMUST00000136691]
[ENSMUST00000137061]
[ENSMUST00000151228]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000061757
AA Change: S220I
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000056226 Gene: ENSMUSG00000046311 AA Change: S220I
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: S220I
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000104820 Gene: ENSMUSG00000046311 AA Change: S220I
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: S220I
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000104821 Gene: ENSMUSG00000046311 AA Change: S220I
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: S220I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000116045 Gene: ENSMUSG00000046311 AA Change: S220I
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: S220I
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000137583 Gene: ENSMUSG00000046311 AA Change: S220I
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: ENSMUST00000150284
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136691
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000137061
|
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 |
|
Meta Mutation Damage Score |
0.3261 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.3%
|
Validation Efficiency |
100% (69/69) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
T |
11: 109,920,884 (GRCm39) |
C1497S |
probably damaging |
Het |
Acoxl |
G |
T |
2: 127,719,727 (GRCm39) |
G163W |
probably damaging |
Het |
Apbb1 |
T |
A |
7: 105,222,969 (GRCm39) |
N214I |
probably damaging |
Het |
Apol7b |
T |
C |
15: 77,307,734 (GRCm39) |
K254E |
probably benign |
Het |
Arl4d |
T |
A |
11: 101,557,969 (GRCm39) |
V165E |
possibly damaging |
Het |
Brca1 |
C |
A |
11: 101,408,192 (GRCm39) |
R1377L |
probably benign |
Het |
Btf3 |
A |
G |
13: 98,449,792 (GRCm39) |
F65L |
probably benign |
Het |
C2 |
T |
C |
17: 35,082,635 (GRCm39) |
N495D |
probably benign |
Het |
Cacna1c |
T |
C |
6: 118,607,341 (GRCm39) |
T1188A |
probably benign |
Het |
Chd7 |
C |
A |
4: 8,866,217 (GRCm39) |
D796E |
probably benign |
Het |
Clasp2 |
G |
T |
9: 113,676,789 (GRCm39) |
L173F |
probably damaging |
Het |
Clec4g |
A |
T |
8: 3,768,766 (GRCm39) |
|
probably null |
Het |
Col9a3 |
T |
C |
2: 180,258,159 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
T |
A |
4: 128,373,888 (GRCm39) |
|
probably null |
Het |
Ddx11 |
T |
C |
17: 66,437,768 (GRCm39) |
C165R |
probably benign |
Het |
Dnah7c |
A |
C |
1: 46,572,376 (GRCm39) |
M950L |
probably damaging |
Het |
Dusp23 |
A |
C |
1: 172,460,181 (GRCm39) |
|
probably null |
Het |
Ebag9 |
A |
T |
15: 44,500,158 (GRCm39) |
|
probably null |
Het |
Edn3 |
G |
A |
2: 174,623,697 (GRCm39) |
A211T |
probably benign |
Het |
Eif3e |
G |
A |
15: 43,129,558 (GRCm39) |
T190I |
possibly damaging |
Het |
Fam76a |
T |
C |
4: 132,648,208 (GRCm39) |
H3R |
possibly damaging |
Het |
Gabbr1 |
G |
T |
17: 37,365,128 (GRCm39) |
E138* |
probably null |
Het |
Galc |
T |
C |
12: 98,188,876 (GRCm39) |
T412A |
probably benign |
Het |
Gimap3 |
T |
C |
6: 48,742,654 (GRCm39) |
D92G |
possibly damaging |
Het |
Gin1 |
T |
C |
1: 97,712,801 (GRCm39) |
Y285H |
probably damaging |
Het |
Gm4868 |
A |
G |
5: 125,925,782 (GRCm39) |
|
noncoding transcript |
Het |
Gm7052 |
T |
A |
17: 22,259,405 (GRCm39) |
|
probably benign |
Het |
Gpcpd1 |
T |
A |
2: 132,392,270 (GRCm39) |
E226D |
probably benign |
Het |
Hoxb4 |
T |
C |
11: 96,209,992 (GRCm39) |
S133P |
possibly damaging |
Het |
Hrg |
C |
T |
16: 22,779,972 (GRCm39) |
|
probably benign |
Het |
Insrr |
A |
G |
3: 87,708,194 (GRCm39) |
K212R |
probably benign |
Het |
Ipp |
A |
G |
4: 116,387,655 (GRCm39) |
D411G |
probably damaging |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kcnq3 |
A |
G |
15: 65,902,461 (GRCm39) |
F172L |
probably damaging |
Het |
Kdm5d |
T |
C |
Y: 927,110 (GRCm39) |
F616S |
probably damaging |
Het |
Lars1 |
T |
C |
18: 42,361,295 (GRCm39) |
|
probably null |
Het |
Lmo7 |
G |
T |
14: 102,125,030 (GRCm39) |
Q496H |
probably damaging |
Het |
Map3k9 |
C |
A |
12: 81,780,865 (GRCm39) |
A432S |
probably benign |
Het |
Nop2 |
T |
G |
6: 125,117,844 (GRCm39) |
|
probably null |
Het |
Nup50l |
T |
A |
6: 96,141,862 (GRCm39) |
N394I |
probably damaging |
Het |
Or10ag53 |
C |
A |
2: 87,082,802 (GRCm39) |
Q174K |
possibly damaging |
Het |
Or2h2 |
T |
C |
17: 37,396,471 (GRCm39) |
I195M |
probably damaging |
Het |
Or5m11b |
A |
T |
2: 85,806,175 (GRCm39) |
E196V |
probably damaging |
Het |
Or6k2 |
A |
T |
1: 173,986,494 (GRCm39) |
N52Y |
possibly damaging |
Het |
Pan2 |
A |
G |
10: 128,144,512 (GRCm39) |
T187A |
probably benign |
Het |
Pcmtd2 |
A |
G |
2: 181,484,217 (GRCm39) |
E9G |
possibly damaging |
Het |
Pik3cb |
T |
A |
9: 98,972,310 (GRCm39) |
I283F |
possibly damaging |
Het |
Pkhd1 |
G |
A |
1: 20,683,633 (GRCm39) |
T40I |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,493,296 (GRCm39) |
V1857A |
possibly damaging |
Het |
Polg |
T |
C |
7: 79,110,127 (GRCm39) |
S334G |
probably damaging |
Het |
Rem2 |
T |
C |
14: 54,715,116 (GRCm39) |
S98P |
probably damaging |
Het |
Rpl5-ps2 |
G |
T |
2: 154,546,156 (GRCm39) |
|
noncoding transcript |
Het |
Slc6a18 |
A |
T |
13: 73,814,489 (GRCm39) |
N468K |
possibly damaging |
Het |
Slco4a1 |
A |
T |
2: 180,106,171 (GRCm39) |
T118S |
probably benign |
Het |
Smg1 |
A |
T |
7: 117,738,688 (GRCm39) |
N3520K |
possibly damaging |
Het |
Tapbp |
C |
A |
17: 34,145,427 (GRCm39) |
D415E |
probably damaging |
Het |
Topaz1 |
A |
G |
9: 122,576,501 (GRCm39) |
T31A |
probably benign |
Het |
Trpv6 |
C |
T |
6: 41,598,678 (GRCm39) |
R649H |
probably damaging |
Het |
Vmn1r188 |
A |
G |
13: 22,272,688 (GRCm39) |
Y214C |
probably benign |
Het |
Vps8 |
T |
A |
16: 21,254,525 (GRCm39) |
I59N |
probably damaging |
Het |
Wnt9a |
T |
C |
11: 59,222,163 (GRCm39) |
C354R |
probably damaging |
Het |
Zcchc2 |
A |
G |
1: 105,958,987 (GRCm39) |
T1153A |
possibly damaging |
Het |
Zfp30 |
A |
G |
7: 29,492,627 (GRCm39) |
R294G |
probably damaging |
Het |
Zfp558 |
A |
T |
9: 18,367,799 (GRCm39) |
C330S |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,505,757 (GRCm39) |
S423P |
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 |
49,106,568 (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'- GGGGACTTTTCGGAGTAGCTC -3'
(R):5'- AGCGTGAGATATAGGCCTTCC -3'
Sequencing Primer
(F):5'- GAGTAGCTCCAGTCTTCGAGTC -3'
(R):5'- ATGCACTATAAGGCCTGAGCTGTTC -3'
|
Posted On |
2015-09-24 |