Incidental Mutation 'R3177:Zfp423'
ID |
476049 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp423
|
Ensembl Gene |
ENSMUSG00000045333 |
Gene Name |
zinc finger protein 423 |
Synonyms |
Roaz, Zfp104, Ebfaz, ataxia1 |
MMRRC Submission |
040615-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.838)
|
Stock # |
R3177 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
88388438-88686223 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 88508959 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Histidine
at position 462
(Y462H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000105282
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000052250]
[ENSMUST00000109655]
[ENSMUST00000165770]
[ENSMUST00000174249]
[ENSMUST00000174764]
|
AlphaFold |
Q80TS5 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000052250
AA Change: Y441H
PolyPhen 2
Score 0.951 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000052379 Gene: ENSMUSG00000045333 AA Change: Y441H
Domain | Start | End | E-Value | Type |
low complexity region
|
39 |
51 |
N/A |
INTRINSIC |
ZnF_C2H2
|
54 |
75 |
5.07e0 |
SMART |
low complexity region
|
107 |
123 |
N/A |
INTRINSIC |
ZnF_C2H2
|
125 |
147 |
1.28e-3 |
SMART |
ZnF_C2H2
|
153 |
175 |
1.64e-1 |
SMART |
ZnF_C2H2
|
181 |
203 |
2.05e-2 |
SMART |
ZnF_C2H2
|
209 |
231 |
3.21e-4 |
SMART |
ZnF_C2H2
|
250 |
273 |
5.42e-2 |
SMART |
ZnF_C2H2
|
282 |
305 |
1.76e-1 |
SMART |
ZnF_C2H2
|
310 |
332 |
8.67e-1 |
SMART |
low complexity region
|
350 |
364 |
N/A |
INTRINSIC |
ZnF_C2H2
|
396 |
420 |
1.16e-1 |
SMART |
ZnF_C2H2
|
428 |
451 |
3.52e-1 |
SMART |
ZnF_C2H2
|
467 |
490 |
7.9e-4 |
SMART |
low complexity region
|
492 |
503 |
N/A |
INTRINSIC |
ZnF_C2H2
|
504 |
527 |
2.53e-2 |
SMART |
ZnF_C2H2
|
550 |
575 |
3.99e0 |
SMART |
low complexity region
|
591 |
602 |
N/A |
INTRINSIC |
ZnF_C2H2
|
619 |
641 |
3.16e-3 |
SMART |
ZnF_C2H2
|
649 |
671 |
5.81e-2 |
SMART |
ZnF_C2H2
|
679 |
702 |
4.87e-4 |
SMART |
ZnF_C2H2
|
707 |
730 |
7.26e-3 |
SMART |
ZnF_C2H2
|
737 |
760 |
4.79e-3 |
SMART |
ZnF_C2H2
|
768 |
790 |
1.36e-2 |
SMART |
ZnF_C2H2
|
794 |
817 |
4.72e-2 |
SMART |
ZnF_C2H2
|
873 |
896 |
4.12e0 |
SMART |
ZnF_C2H2
|
917 |
939 |
5.59e-4 |
SMART |
ZnF_C2H2
|
946 |
968 |
6.42e-4 |
SMART |
ZnF_C2H2
|
975 |
997 |
4.94e0 |
SMART |
ZnF_C2H2
|
1007 |
1029 |
4.99e1 |
SMART |
Pfam:zf-C2H2_6
|
1050 |
1068 |
1.6e-1 |
PFAM |
ZnF_C2H2
|
1107 |
1130 |
1.12e-3 |
SMART |
ZnF_C2H2
|
1155 |
1177 |
1.45e-2 |
SMART |
ZnF_C2H2
|
1185 |
1207 |
5.72e-1 |
SMART |
ZnF_C2H2
|
1216 |
1239 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1246 |
1269 |
4.05e-1 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109655
AA Change: Y462H
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000105282 Gene: ENSMUSG00000045333 AA Change: Y462H
Domain | Start | End | E-Value | Type |
low complexity region
|
60 |
72 |
N/A |
INTRINSIC |
ZnF_C2H2
|
75 |
96 |
5.07e0 |
SMART |
low complexity region
|
128 |
144 |
N/A |
INTRINSIC |
ZnF_C2H2
|
146 |
168 |
1.28e-3 |
SMART |
ZnF_C2H2
|
174 |
196 |
1.64e-1 |
SMART |
ZnF_C2H2
|
202 |
224 |
2.05e-2 |
SMART |
ZnF_C2H2
|
230 |
252 |
3.21e-4 |
SMART |
ZnF_C2H2
|
271 |
294 |
5.42e-2 |
SMART |
ZnF_C2H2
|
303 |
326 |
1.76e-1 |
SMART |
ZnF_C2H2
|
331 |
353 |
8.67e-1 |
SMART |
low complexity region
|
371 |
385 |
N/A |
INTRINSIC |
ZnF_C2H2
|
417 |
441 |
1.16e-1 |
SMART |
ZnF_C2H2
|
449 |
472 |
3.52e-1 |
SMART |
ZnF_C2H2
|
488 |
511 |
7.9e-4 |
SMART |
low complexity region
|
513 |
524 |
N/A |
INTRINSIC |
ZnF_C2H2
|
525 |
548 |
2.53e-2 |
SMART |
ZnF_C2H2
|
571 |
596 |
3.99e0 |
SMART |
low complexity region
|
612 |
623 |
N/A |
INTRINSIC |
ZnF_C2H2
|
640 |
662 |
3.16e-3 |
SMART |
ZnF_C2H2
|
670 |
692 |
5.81e-2 |
SMART |
ZnF_C2H2
|
700 |
723 |
4.87e-4 |
SMART |
ZnF_C2H2
|
728 |
751 |
7.26e-3 |
SMART |
ZnF_C2H2
|
758 |
781 |
4.79e-3 |
SMART |
ZnF_C2H2
|
789 |
811 |
1.36e-2 |
SMART |
ZnF_C2H2
|
815 |
838 |
4.72e-2 |
SMART |
ZnF_C2H2
|
894 |
917 |
4.12e0 |
SMART |
ZnF_C2H2
|
938 |
960 |
5.59e-4 |
SMART |
ZnF_C2H2
|
967 |
989 |
6.42e-4 |
SMART |
ZnF_C2H2
|
996 |
1018 |
4.94e0 |
SMART |
ZnF_C2H2
|
1028 |
1050 |
4.99e1 |
SMART |
ZnF_C2H2
|
1128 |
1151 |
1.12e-3 |
SMART |
ZnF_C2H2
|
1176 |
1198 |
1.45e-2 |
SMART |
ZnF_C2H2
|
1206 |
1228 |
5.72e-1 |
SMART |
ZnF_C2H2
|
1237 |
1260 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1267 |
1290 |
4.05e-1 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000165770
AA Change: Y337H
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000129724 Gene: ENSMUSG00000045333 AA Change: Y337H
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
19 |
N/A |
INTRINSIC |
ZnF_C2H2
|
21 |
43 |
1.28e-3 |
SMART |
ZnF_C2H2
|
49 |
71 |
1.64e-1 |
SMART |
ZnF_C2H2
|
77 |
99 |
2.05e-2 |
SMART |
ZnF_C2H2
|
105 |
127 |
3.21e-4 |
SMART |
ZnF_C2H2
|
146 |
169 |
5.42e-2 |
SMART |
ZnF_C2H2
|
178 |
201 |
1.76e-1 |
SMART |
ZnF_C2H2
|
206 |
228 |
8.67e-1 |
SMART |
low complexity region
|
246 |
260 |
N/A |
INTRINSIC |
ZnF_C2H2
|
292 |
316 |
1.16e-1 |
SMART |
ZnF_C2H2
|
324 |
347 |
3.52e-1 |
SMART |
ZnF_C2H2
|
363 |
386 |
7.9e-4 |
SMART |
low complexity region
|
388 |
399 |
N/A |
INTRINSIC |
ZnF_C2H2
|
400 |
423 |
2.53e-2 |
SMART |
ZnF_C2H2
|
446 |
471 |
3.99e0 |
SMART |
low complexity region
|
487 |
498 |
N/A |
INTRINSIC |
ZnF_C2H2
|
515 |
537 |
3.16e-3 |
SMART |
ZnF_C2H2
|
545 |
567 |
5.81e-2 |
SMART |
ZnF_C2H2
|
575 |
598 |
4.87e-4 |
SMART |
ZnF_C2H2
|
603 |
626 |
7.26e-3 |
SMART |
ZnF_C2H2
|
633 |
656 |
4.79e-3 |
SMART |
ZnF_C2H2
|
664 |
686 |
1.36e-2 |
SMART |
ZnF_C2H2
|
690 |
713 |
4.72e-2 |
SMART |
ZnF_C2H2
|
769 |
792 |
4.12e0 |
SMART |
ZnF_C2H2
|
813 |
835 |
5.59e-4 |
SMART |
ZnF_C2H2
|
842 |
864 |
6.42e-4 |
SMART |
ZnF_C2H2
|
871 |
893 |
4.94e0 |
SMART |
ZnF_C2H2
|
903 |
925 |
4.99e1 |
SMART |
Pfam:zf-C2H2_6
|
946 |
964 |
2.5e-1 |
PFAM |
ZnF_C2H2
|
1003 |
1026 |
1.12e-3 |
SMART |
ZnF_C2H2
|
1051 |
1073 |
1.45e-2 |
SMART |
ZnF_C2H2
|
1081 |
1103 |
5.72e-1 |
SMART |
ZnF_C2H2
|
1112 |
1135 |
1.18e-2 |
SMART |
ZnF_C2H2
|
1142 |
1165 |
4.05e-1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173092
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173725
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174249
|
SMART Domains |
Protein: ENSMUSP00000134103 Gene: ENSMUSG00000045333
Domain | Start | End | E-Value | Type |
low complexity region
|
60 |
76 |
N/A |
INTRINSIC |
ZnF_C2H2
|
78 |
100 |
1.28e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174764
|
SMART Domains |
Protein: ENSMUSP00000134575 Gene: ENSMUSG00000045333
Domain | Start | End | E-Value | Type |
low complexity region
|
63 |
75 |
N/A |
INTRINSIC |
ZnF_C2H2
|
78 |
99 |
5.07e0 |
SMART |
low complexity region
|
131 |
147 |
N/A |
INTRINSIC |
ZnF_C2H2
|
149 |
171 |
1.28e-3 |
SMART |
ZnF_C2H2
|
177 |
199 |
1.64e-1 |
SMART |
ZnF_C2H2
|
205 |
227 |
2.05e-2 |
SMART |
Pfam:zf-C2H2_6
|
232 |
244 |
2.5e-1 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.4%
|
Validation Efficiency |
100% (21/21) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a nuclear protein that belongs to the family of Kruppel-like C2H2 zinc finger proteins. It functions as a DNA-binding transcription factor by using distinct zinc fingers in different signaling pathways. Thus, it is thought that this gene may have multiple roles in signal transduction during development. Mutations in this gene are associated with nephronophthisis-14 and Joubert syndrome-19. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2012] PHENOTYPE: Mutations in this gene lead to postnatal lethality, abnormal gait, ataxia, reduced body size, loss of the corpus callosum, reduction of the hippocampus, olfactory bulb defects, and variable malformation of the cerebellum, including vermis agenesis, due to reduced proliferation of neural precursors. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
T |
C |
2: 151,314,020 (GRCm39) |
R553G |
possibly damaging |
Het |
Adarb2 |
A |
G |
13: 8,802,663 (GRCm39) |
N646S |
probably damaging |
Het |
Adcy8 |
C |
T |
15: 64,571,008 (GRCm39) |
G1242S |
probably benign |
Het |
Ano9 |
T |
A |
7: 140,684,037 (GRCm39) |
T543S |
probably damaging |
Het |
Btnl10 |
A |
G |
11: 58,813,216 (GRCm39) |
K282E |
probably benign |
Het |
Btnl9 |
T |
C |
11: 49,060,503 (GRCm39) |
D330G |
probably damaging |
Het |
Ccdc178 |
G |
T |
18: 22,200,709 (GRCm39) |
A416E |
possibly damaging |
Het |
Cdx2 |
A |
T |
5: 147,240,002 (GRCm39) |
S225T |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,617,120 (GRCm39) |
I843M |
probably benign |
Het |
Cntn4 |
G |
A |
6: 106,414,925 (GRCm39) |
|
probably null |
Het |
Cyb561 |
T |
C |
11: 105,826,613 (GRCm39) |
|
probably benign |
Het |
Cyp4f18 |
T |
C |
8: 72,747,044 (GRCm39) |
D317G |
possibly damaging |
Het |
Dennd4a |
G |
T |
9: 64,796,275 (GRCm39) |
R767L |
probably damaging |
Het |
Dgkb |
G |
A |
12: 38,134,216 (GRCm39) |
V41M |
probably damaging |
Het |
Duox1 |
T |
C |
2: 122,170,597 (GRCm39) |
Y1206H |
probably damaging |
Het |
Dync1i1 |
T |
C |
6: 5,972,211 (GRCm39) |
|
probably null |
Het |
Fbxw2 |
T |
C |
2: 34,712,762 (GRCm39) |
T100A |
probably benign |
Het |
Fcgbp |
C |
A |
7: 27,791,086 (GRCm39) |
H782Q |
probably damaging |
Het |
Flg2 |
A |
T |
3: 93,122,195 (GRCm39) |
Q1455L |
unknown |
Het |
Frrs1 |
T |
C |
3: 116,692,873 (GRCm39) |
F49S |
probably damaging |
Het |
Gli3 |
A |
T |
13: 15,900,567 (GRCm39) |
Q1318L |
probably benign |
Het |
Gm5581 |
C |
G |
6: 131,143,928 (GRCm39) |
|
noncoding transcript |
Het |
Gm5592 |
A |
G |
7: 40,937,804 (GRCm39) |
E362G |
probably benign |
Het |
Gm7104 |
A |
T |
12: 88,252,498 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch2l |
A |
G |
12: 86,291,089 (GRCm39) |
T91A |
possibly damaging |
Het |
Hacd4 |
T |
C |
4: 88,355,747 (GRCm39) |
H46R |
probably damaging |
Het |
Hao2 |
T |
C |
3: 98,787,644 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,803,176 (GRCm39) |
V2175A |
probably benign |
Het |
Hey1 |
T |
C |
3: 8,729,951 (GRCm39) |
S169G |
probably benign |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hlf |
T |
C |
11: 90,236,661 (GRCm39) |
K199E |
probably damaging |
Het |
Hpgd |
C |
A |
8: 56,751,448 (GRCm39) |
A92E |
probably damaging |
Het |
Hsp90aa1 |
T |
A |
12: 110,662,114 (GRCm39) |
M1L |
possibly damaging |
Het |
Hsp90aa1 |
C |
A |
12: 110,662,115 (GRCm39) |
|
probably null |
Het |
Itgad |
C |
A |
7: 127,790,153 (GRCm39) |
H651N |
possibly damaging |
Het |
Itgav |
A |
G |
2: 83,606,886 (GRCm39) |
D409G |
probably damaging |
Het |
Kif2a |
A |
G |
13: 107,113,264 (GRCm39) |
I455T |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lamc3 |
G |
T |
2: 31,798,637 (GRCm39) |
G448C |
probably damaging |
Het |
Ltbp1 |
G |
A |
17: 75,583,475 (GRCm39) |
G425D |
possibly damaging |
Het |
Ltbp1 |
T |
A |
17: 75,666,273 (GRCm39) |
|
probably null |
Het |
Mag |
C |
T |
7: 30,601,073 (GRCm39) |
|
probably null |
Het |
Mdh1b |
G |
A |
1: 63,750,690 (GRCm39) |
T426M |
possibly damaging |
Het |
Nr1h4 |
G |
A |
10: 89,314,650 (GRCm39) |
T282I |
possibly damaging |
Het |
Nsf |
C |
T |
11: 103,821,578 (GRCm39) |
E26K |
possibly damaging |
Het |
Or4c1 |
C |
T |
2: 89,133,562 (GRCm39) |
V125M |
possibly damaging |
Het |
Or52k2 |
T |
C |
7: 102,253,783 (GRCm39) |
V74A |
possibly damaging |
Het |
Or9s27 |
A |
G |
1: 92,516,535 (GRCm39) |
N161S |
probably benign |
Het |
Padi6 |
A |
G |
4: 140,462,700 (GRCm39) |
L307P |
probably damaging |
Het |
Parp9 |
T |
C |
16: 35,768,578 (GRCm39) |
S20P |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,101,703 (GRCm39) |
F963L |
probably damaging |
Het |
Pwp1 |
C |
T |
10: 85,717,943 (GRCm39) |
L294F |
probably benign |
Het |
Radil |
A |
G |
5: 142,492,611 (GRCm39) |
L339P |
probably damaging |
Het |
Raver1 |
G |
A |
9: 20,990,573 (GRCm39) |
P316S |
possibly damaging |
Het |
Rell1 |
A |
G |
5: 64,084,330 (GRCm39) |
|
probably null |
Het |
Rxrg |
A |
G |
1: 167,463,269 (GRCm39) |
D257G |
possibly damaging |
Het |
Sema4c |
C |
T |
1: 36,588,960 (GRCm39) |
R722H |
possibly damaging |
Het |
Sgk1 |
C |
T |
10: 21,872,500 (GRCm39) |
R171W |
probably damaging |
Het |
Spata7 |
A |
G |
12: 98,603,857 (GRCm39) |
N75D |
possibly damaging |
Het |
Ttc23l |
A |
G |
15: 10,547,318 (GRCm39) |
F99L |
possibly damaging |
Het |
Unc13a |
A |
C |
8: 72,082,339 (GRCm39) |
C1642G |
probably benign |
Het |
Usp36 |
C |
T |
11: 118,167,585 (GRCm39) |
|
probably null |
Het |
Wrn |
A |
G |
8: 33,807,582 (GRCm39) |
M292T |
probably damaging |
Het |
Zscan5b |
T |
A |
7: 6,234,345 (GRCm39) |
Y124N |
possibly damaging |
Het |
Zswim9 |
T |
C |
7: 13,011,196 (GRCm39) |
T51A |
possibly damaging |
Het |
|
Other mutations in Zfp423 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Zfp423
|
APN |
8 |
88,508,239 (GRCm39) |
splice site |
probably null |
|
IGL01359:Zfp423
|
APN |
8 |
88,507,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01780:Zfp423
|
APN |
8 |
88,508,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Zfp423
|
APN |
8 |
88,509,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02301:Zfp423
|
APN |
8 |
88,508,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02320:Zfp423
|
APN |
8 |
88,508,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02804:Zfp423
|
APN |
8 |
88,509,285 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03090:Zfp423
|
APN |
8 |
88,508,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03198:Zfp423
|
APN |
8 |
88,508,304 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03383:Zfp423
|
APN |
8 |
88,586,080 (GRCm39) |
nonsense |
probably null |
|
swell
|
UTSW |
8 |
88,413,187 (GRCm39) |
splice site |
probably null |
|
Temptation
|
UTSW |
8 |
88,508,381 (GRCm39) |
missense |
probably benign |
0.25 |
trials
|
UTSW |
8 |
88,507,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Zfp423
|
UTSW |
8 |
88,508,887 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0142:Zfp423
|
UTSW |
8 |
88,506,968 (GRCm39) |
nonsense |
probably null |
|
R0256:Zfp423
|
UTSW |
8 |
88,500,262 (GRCm39) |
nonsense |
probably null |
|
R0538:Zfp423
|
UTSW |
8 |
88,508,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R0542:Zfp423
|
UTSW |
8 |
88,507,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Zfp423
|
UTSW |
8 |
88,508,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R1179:Zfp423
|
UTSW |
8 |
88,414,700 (GRCm39) |
missense |
probably damaging |
0.97 |
R1417:Zfp423
|
UTSW |
8 |
88,500,284 (GRCm39) |
splice site |
probably null |
|
R1429:Zfp423
|
UTSW |
8 |
88,413,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R1570:Zfp423
|
UTSW |
8 |
88,509,186 (GRCm39) |
missense |
probably benign |
0.37 |
R2013:Zfp423
|
UTSW |
8 |
88,509,025 (GRCm39) |
missense |
probably benign |
0.43 |
R2043:Zfp423
|
UTSW |
8 |
88,509,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Zfp423
|
UTSW |
8 |
88,507,986 (GRCm39) |
missense |
probably benign |
0.04 |
R2108:Zfp423
|
UTSW |
8 |
88,507,806 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2358:Zfp423
|
UTSW |
8 |
88,507,179 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3277:Zfp423
|
UTSW |
8 |
88,508,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R3738:Zfp423
|
UTSW |
8 |
88,507,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3739:Zfp423
|
UTSW |
8 |
88,507,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Zfp423
|
UTSW |
8 |
88,507,140 (GRCm39) |
missense |
probably benign |
0.03 |
R4034:Zfp423
|
UTSW |
8 |
88,507,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Zfp423
|
UTSW |
8 |
88,509,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Zfp423
|
UTSW |
8 |
88,414,709 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4700:Zfp423
|
UTSW |
8 |
88,508,338 (GRCm39) |
splice site |
probably null |
|
R4753:Zfp423
|
UTSW |
8 |
88,508,074 (GRCm39) |
missense |
probably benign |
0.00 |
R4818:Zfp423
|
UTSW |
8 |
88,631,128 (GRCm39) |
missense |
probably benign |
0.00 |
R5026:Zfp423
|
UTSW |
8 |
88,507,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R5190:Zfp423
|
UTSW |
8 |
88,509,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5243:Zfp423
|
UTSW |
8 |
88,500,275 (GRCm39) |
missense |
probably benign |
0.03 |
R5284:Zfp423
|
UTSW |
8 |
88,508,305 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5586:Zfp423
|
UTSW |
8 |
88,585,968 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5601:Zfp423
|
UTSW |
8 |
88,508,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Zfp423
|
UTSW |
8 |
88,508,955 (GRCm39) |
missense |
probably damaging |
0.99 |
R5717:Zfp423
|
UTSW |
8 |
88,413,187 (GRCm39) |
splice site |
probably null |
|
R5801:Zfp423
|
UTSW |
8 |
88,585,990 (GRCm39) |
missense |
probably damaging |
0.99 |
R5917:Zfp423
|
UTSW |
8 |
88,508,860 (GRCm39) |
nonsense |
probably null |
|
R5985:Zfp423
|
UTSW |
8 |
88,508,774 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6111:Zfp423
|
UTSW |
8 |
88,509,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R6306:Zfp423
|
UTSW |
8 |
88,508,662 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6770:Zfp423
|
UTSW |
8 |
88,508,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R6970:Zfp423
|
UTSW |
8 |
88,530,407 (GRCm39) |
missense |
probably benign |
0.00 |
R7029:Zfp423
|
UTSW |
8 |
88,414,694 (GRCm39) |
missense |
probably damaging |
0.99 |
R7060:Zfp423
|
UTSW |
8 |
88,509,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7074:Zfp423
|
UTSW |
8 |
88,509,060 (GRCm39) |
missense |
probably benign |
0.00 |
R7121:Zfp423
|
UTSW |
8 |
88,507,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Zfp423
|
UTSW |
8 |
88,631,155 (GRCm39) |
missense |
probably benign |
0.07 |
R7359:Zfp423
|
UTSW |
8 |
88,508,871 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7426:Zfp423
|
UTSW |
8 |
88,507,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R7540:Zfp423
|
UTSW |
8 |
88,414,695 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7640:Zfp423
|
UTSW |
8 |
88,507,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Zfp423
|
UTSW |
8 |
88,507,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R7938:Zfp423
|
UTSW |
8 |
88,622,304 (GRCm39) |
missense |
unknown |
|
R7986:Zfp423
|
UTSW |
8 |
88,506,978 (GRCm39) |
missense |
probably benign |
0.04 |
R8347:Zfp423
|
UTSW |
8 |
88,509,784 (GRCm39) |
missense |
probably damaging |
0.99 |
R8356:Zfp423
|
UTSW |
8 |
88,509,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Zfp423
|
UTSW |
8 |
88,509,338 (GRCm39) |
missense |
probably benign |
0.04 |
R8710:Zfp423
|
UTSW |
8 |
88,507,549 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8794:Zfp423
|
UTSW |
8 |
88,507,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8832:Zfp423
|
UTSW |
8 |
88,507,827 (GRCm39) |
missense |
probably damaging |
0.98 |
R9018:Zfp423
|
UTSW |
8 |
88,508,381 (GRCm39) |
missense |
probably benign |
0.25 |
R9182:Zfp423
|
UTSW |
8 |
88,508,742 (GRCm39) |
missense |
probably damaging |
0.99 |
R9309:Zfp423
|
UTSW |
8 |
88,509,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R9312:Zfp423
|
UTSW |
8 |
88,508,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9453:Zfp423
|
UTSW |
8 |
88,508,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9469:Zfp423
|
UTSW |
8 |
88,509,519 (GRCm39) |
missense |
probably damaging |
0.99 |
R9480:Zfp423
|
UTSW |
8 |
88,631,115 (GRCm39) |
critical splice donor site |
probably null |
|
R9483:Zfp423
|
UTSW |
8 |
88,507,725 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9510:Zfp423
|
UTSW |
8 |
88,510,041 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9521:Zfp423
|
UTSW |
8 |
88,509,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Zfp423
|
UTSW |
8 |
88,414,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R9789:Zfp423
|
UTSW |
8 |
88,506,877 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Zfp423
|
UTSW |
8 |
88,586,048 (GRCm39) |
missense |
possibly damaging |
0.49 |
Z1177:Zfp423
|
UTSW |
8 |
88,507,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
|
Posted On |
2017-05-11 |