Incidental Mutation 'R5685:Zfp62'
ID |
443297 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp62
|
Ensembl Gene |
ENSMUSG00000046311 |
Gene Name |
zinc finger protein 62 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.140)
|
Stock # |
R5685 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
49094119-49109643 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 49107044 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Stop codon
at position 378
(C378*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000137583
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061757]
[ENSMUST00000109197]
[ENSMUST00000109198]
[ENSMUST00000133150]
[ENSMUST00000136539]
[ENSMUST00000136691]
[ENSMUST00000180016]
[ENSMUST00000150284]
[ENSMUST00000151228]
[ENSMUST00000137061]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000061757
AA Change: C378*
|
SMART Domains |
Protein: ENSMUSP00000056226 Gene: ENSMUSG00000046311 AA Change: C378*
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 null
Transcript: ENSMUST00000109197
AA Change: C378*
|
SMART Domains |
Protein: ENSMUSP00000104820 Gene: ENSMUSG00000046311 AA Change: C378*
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 null
Transcript: ENSMUST00000109198
AA Change: C378*
|
SMART Domains |
Protein: ENSMUSP00000104821 Gene: ENSMUSG00000046311 AA Change: C378*
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 null
Transcript: ENSMUST00000133150
|
Predicted Effect |
probably null
Transcript: ENSMUST00000136539
AA Change: C378*
|
SMART Domains |
Protein: ENSMUSP00000116045 Gene: ENSMUSG00000046311 AA Change: C378*
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 null
Transcript: ENSMUST00000136691
|
Predicted Effect |
probably null
Transcript: ENSMUST00000180016
AA Change: C378*
|
SMART Domains |
Protein: ENSMUSP00000137583 Gene: ENSMUSG00000046311 AA Change: C378*
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 null
Transcript: ENSMUST00000150284
|
Predicted Effect |
probably null
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 null
Transcript: ENSMUST00000137061
|
Coding Region Coverage |
- 1x: 99.6%
- 3x: 98.8%
- 10x: 97.0%
- 20x: 94.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028J19Rik |
T |
A |
7: 43,879,974 (GRCm39) |
|
probably benign |
Het |
Abcb5 |
A |
T |
12: 118,896,348 (GRCm39) |
|
probably null |
Het |
Abcg1 |
G |
T |
17: 31,317,260 (GRCm39) |
E191* |
probably null |
Het |
Als2 |
A |
G |
1: 59,218,250 (GRCm39) |
Y1263H |
possibly damaging |
Het |
Amer2 |
T |
A |
14: 60,617,026 (GRCm39) |
L281* |
probably null |
Het |
Anxa6 |
T |
C |
11: 54,887,196 (GRCm39) |
N361D |
probably benign |
Het |
Ap1g1 |
A |
T |
8: 110,564,415 (GRCm39) |
N320I |
probably damaging |
Het |
Aqr |
T |
C |
2: 113,986,746 (GRCm39) |
D208G |
possibly damaging |
Het |
Arnt2 |
T |
C |
7: 83,912,473 (GRCm39) |
T545A |
probably benign |
Het |
Aspm |
G |
A |
1: 139,415,026 (GRCm39) |
V2701I |
probably benign |
Het |
Atad2 |
A |
G |
15: 57,980,194 (GRCm39) |
V106A |
possibly damaging |
Het |
Bbs2 |
A |
C |
8: 94,814,061 (GRCm39) |
F186V |
probably damaging |
Het |
Catsperg2 |
G |
A |
7: 29,400,613 (GRCm39) |
P247L |
probably damaging |
Het |
Cfap57 |
G |
T |
4: 118,426,656 (GRCm39) |
Q1098K |
probably benign |
Het |
Cxcr6 |
A |
G |
9: 123,639,811 (GRCm39) |
T271A |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,374,091 (GRCm39) |
E579G |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,421,932 (GRCm39) |
T2111A |
probably damaging |
Het |
Galnt1 |
A |
T |
18: 24,397,586 (GRCm39) |
D229V |
possibly damaging |
Het |
Gbp2b |
A |
C |
3: 142,313,919 (GRCm39) |
M400L |
probably benign |
Het |
Gm1123 |
T |
A |
9: 98,891,486 (GRCm39) |
|
probably null |
Het |
Gtpbp6 |
T |
C |
5: 110,252,805 (GRCm39) |
H349R |
probably damaging |
Het |
Hyal5 |
A |
G |
6: 24,876,691 (GRCm39) |
K188R |
probably benign |
Het |
Insrr |
T |
C |
3: 87,707,803 (GRCm39) |
|
probably null |
Het |
Kcnn1 |
A |
T |
8: 71,305,374 (GRCm39) |
C322S |
probably damaging |
Het |
Kdelr1 |
GTCTA |
G |
7: 45,531,041 (GRCm39) |
|
probably null |
Het |
Kif23 |
T |
C |
9: 61,852,691 (GRCm39) |
T8A |
probably benign |
Het |
Lrrk2 |
A |
T |
15: 91,687,504 (GRCm39) |
R2198* |
probably null |
Het |
Mcl1 |
T |
G |
3: 95,567,109 (GRCm39) |
D177E |
possibly damaging |
Het |
Mrps11 |
A |
T |
7: 78,441,628 (GRCm39) |
T137S |
probably benign |
Het |
Mtbp |
A |
G |
15: 55,426,168 (GRCm39) |
Y90C |
probably damaging |
Het |
Nkpd1 |
C |
T |
7: 19,257,498 (GRCm39) |
Q276* |
probably null |
Het |
Nxt1 |
G |
T |
2: 148,517,673 (GRCm39) |
W138L |
possibly damaging |
Het |
Or5al1 |
T |
C |
2: 85,990,139 (GRCm39) |
T192A |
probably damaging |
Het |
Or5h17 |
T |
A |
16: 58,820,709 (GRCm39) |
F220L |
probably benign |
Het |
Or5t17 |
T |
A |
2: 86,832,621 (GRCm39) |
S103T |
probably benign |
Het |
Osbpl7 |
C |
A |
11: 96,951,103 (GRCm39) |
P478H |
probably damaging |
Het |
Phf8-ps |
T |
A |
17: 33,285,746 (GRCm39) |
H352L |
probably benign |
Het |
Pitpna |
T |
A |
11: 75,511,095 (GRCm39) |
F222I |
probably damaging |
Het |
Plekhh2 |
A |
T |
17: 84,877,310 (GRCm39) |
R552W |
probably damaging |
Het |
Plxnb2 |
C |
T |
15: 89,051,235 (GRCm39) |
R328H |
probably damaging |
Het |
Pmaip1 |
C |
T |
18: 66,594,055 (GRCm39) |
T65I |
probably benign |
Het |
Ppil4 |
T |
G |
10: 7,674,186 (GRCm39) |
I110S |
probably damaging |
Het |
Prpf38a |
A |
G |
4: 108,427,351 (GRCm39) |
|
probably null |
Het |
Psme4 |
G |
A |
11: 30,759,837 (GRCm39) |
G320D |
probably damaging |
Het |
Rab17 |
C |
A |
1: 90,886,679 (GRCm39) |
R191L |
probably benign |
Het |
Rhag |
A |
T |
17: 41,142,222 (GRCm39) |
M222L |
possibly damaging |
Het |
Rims2 |
A |
T |
15: 39,300,602 (GRCm39) |
H111L |
possibly damaging |
Het |
Setx |
T |
C |
2: 29,061,292 (GRCm39) |
Y2234H |
probably damaging |
Het |
Slc2a8 |
T |
C |
2: 32,871,801 (GRCm39) |
I51V |
possibly damaging |
Het |
Slc34a1 |
T |
C |
13: 55,549,085 (GRCm39) |
|
probably null |
Het |
Slf1 |
T |
C |
13: 77,231,598 (GRCm39) |
T594A |
possibly damaging |
Het |
Sox6 |
A |
T |
7: 115,178,392 (GRCm39) |
|
probably null |
Het |
Spata13 |
C |
T |
14: 60,928,652 (GRCm39) |
S70L |
probably benign |
Het |
Stard13 |
A |
G |
5: 150,986,592 (GRCm39) |
I188T |
possibly damaging |
Het |
Stard9 |
A |
G |
2: 120,535,803 (GRCm39) |
D4020G |
probably damaging |
Het |
Tdp1 |
A |
G |
12: 99,868,611 (GRCm39) |
K255R |
possibly damaging |
Het |
Tns2 |
G |
T |
15: 102,015,538 (GRCm39) |
A124S |
probably benign |
Het |
Top2b |
T |
A |
14: 16,413,666 (GRCm38) |
W1045R |
probably damaging |
Het |
Trav12-2 |
T |
C |
14: 53,854,122 (GRCm39) |
V32A |
probably damaging |
Het |
Vps13c |
G |
T |
9: 67,870,455 (GRCm39) |
R3198L |
possibly damaging |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zfp52 |
T |
A |
17: 21,782,013 (GRCm39) |
S620R |
probably benign |
Het |
Zfp638 |
C |
A |
6: 83,906,969 (GRCm39) |
P378H |
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 |
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'- CCTGAACGTTTTGCCACACA -3'
Sequencing Primer
(F):5'- GTGATACCTGTGGGAAAACCTTC -3'
(R):5'- ACATCACATACATAAGGTCTTTCTCC -3'
|
Posted On |
2016-11-09 |