Incidental Mutation 'R4712:Zfat'
ID |
353328 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfat
|
Ensembl Gene |
ENSMUSG00000022335 |
Gene Name |
zinc finger and AT hook domain containing |
Synonyms |
LOC380993, Zfp406, Zfat1 |
MMRRC Submission |
041981-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4712 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
15 |
Chromosomal Location |
67955613-68130705 bp(-) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
A to T
at 67982324 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125732
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000160248]
[ENSMUST00000162054]
[ENSMUST00000162054]
[ENSMUST00000162054]
[ENSMUST00000162054]
[ENSMUST00000162173]
|
AlphaFold |
Q7TS63 |
PDB Structure |
Solution structure of the 5th C2H2 zinc finger of mouse Zinc finger protein 406 [SOLUTION NMR]
Solution structure of the 8th C2H2 zinc finger of mouse Zinc finger protein 406 [SOLUTION NMR]
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000160248
AA Change: V1063E
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000125257 Gene: ENSMUSG00000022335 AA Change: V1063E
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
2.45e0 |
SMART |
ZnF_C2H2
|
116 |
136 |
1.53e2 |
SMART |
low complexity region
|
220 |
236 |
N/A |
INTRINSIC |
ZnF_C2H2
|
271 |
293 |
1.47e-3 |
SMART |
ZnF_C2H2
|
299 |
321 |
1.18e-2 |
SMART |
ZnF_C2H2
|
326 |
349 |
2.36e-2 |
SMART |
ZnF_C2H2
|
354 |
377 |
4.4e-2 |
SMART |
ZnF_C2H2
|
404 |
426 |
1.67e-2 |
SMART |
ZnF_C2H2
|
432 |
454 |
1.33e-1 |
SMART |
ZnF_C2H2
|
458 |
481 |
2.05e-2 |
SMART |
low complexity region
|
601 |
617 |
N/A |
INTRINSIC |
ZnF_C2H2
|
737 |
759 |
1.43e-1 |
SMART |
ZnF_C2H2
|
765 |
788 |
3.52e-1 |
SMART |
ZnF_C2H2
|
793 |
817 |
5.59e-4 |
SMART |
ZnF_C2H2
|
825 |
848 |
3.83e-2 |
SMART |
ZnF_C2H2
|
875 |
898 |
3.95e1 |
SMART |
ZnF_C2H2
|
904 |
926 |
6.88e-4 |
SMART |
ZnF_C2H2
|
932 |
954 |
8.94e-3 |
SMART |
ZnF_C2H2
|
961 |
983 |
2.27e-4 |
SMART |
ZnF_C2H2
|
989 |
1012 |
9.3e-1 |
SMART |
ZnF_C2H2
|
1036 |
1059 |
5.21e-4 |
SMART |
low complexity region
|
1073 |
1082 |
N/A |
INTRINSIC |
low complexity region
|
1139 |
1149 |
N/A |
INTRINSIC |
low complexity region
|
1218 |
1236 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000162054
|
SMART Domains |
Protein: ENSMUSP00000125732 Gene: ENSMUSG00000022335
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
2.45e0 |
SMART |
ZnF_C2H2
|
116 |
136 |
1.53e2 |
SMART |
low complexity region
|
213 |
229 |
N/A |
INTRINSIC |
ZnF_C2H2
|
264 |
286 |
1.47e-3 |
SMART |
ZnF_C2H2
|
292 |
314 |
1.18e-2 |
SMART |
ZnF_C2H2
|
319 |
342 |
2.36e-2 |
SMART |
ZnF_C2H2
|
347 |
370 |
4.4e-2 |
SMART |
ZnF_C2H2
|
397 |
419 |
1.67e-2 |
SMART |
ZnF_C2H2
|
425 |
447 |
1.33e-1 |
SMART |
ZnF_C2H2
|
451 |
474 |
2.05e-2 |
SMART |
low complexity region
|
594 |
610 |
N/A |
INTRINSIC |
ZnF_C2H2
|
730 |
752 |
1.43e-1 |
SMART |
ZnF_C2H2
|
758 |
781 |
3.52e-1 |
SMART |
ZnF_C2H2
|
786 |
810 |
5.59e-4 |
SMART |
ZnF_C2H2
|
818 |
841 |
3.83e-2 |
SMART |
ZnF_C2H2
|
868 |
891 |
3.95e1 |
SMART |
ZnF_C2H2
|
897 |
919 |
6.88e-4 |
SMART |
ZnF_C2H2
|
925 |
947 |
8.94e-3 |
SMART |
ZnF_C2H2
|
954 |
976 |
2.27e-4 |
SMART |
ZnF_C2H2
|
982 |
1005 |
9.3e-1 |
SMART |
ZnF_C2H2
|
1029 |
1052 |
5.21e-4 |
SMART |
low complexity region
|
1121 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1200 |
1218 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000162054
|
SMART Domains |
Protein: ENSMUSP00000125732 Gene: ENSMUSG00000022335
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
2.45e0 |
SMART |
ZnF_C2H2
|
116 |
136 |
1.53e2 |
SMART |
low complexity region
|
213 |
229 |
N/A |
INTRINSIC |
ZnF_C2H2
|
264 |
286 |
1.47e-3 |
SMART |
ZnF_C2H2
|
292 |
314 |
1.18e-2 |
SMART |
ZnF_C2H2
|
319 |
342 |
2.36e-2 |
SMART |
ZnF_C2H2
|
347 |
370 |
4.4e-2 |
SMART |
ZnF_C2H2
|
397 |
419 |
1.67e-2 |
SMART |
ZnF_C2H2
|
425 |
447 |
1.33e-1 |
SMART |
ZnF_C2H2
|
451 |
474 |
2.05e-2 |
SMART |
low complexity region
|
594 |
610 |
N/A |
INTRINSIC |
ZnF_C2H2
|
730 |
752 |
1.43e-1 |
SMART |
ZnF_C2H2
|
758 |
781 |
3.52e-1 |
SMART |
ZnF_C2H2
|
786 |
810 |
5.59e-4 |
SMART |
ZnF_C2H2
|
818 |
841 |
3.83e-2 |
SMART |
ZnF_C2H2
|
868 |
891 |
3.95e1 |
SMART |
ZnF_C2H2
|
897 |
919 |
6.88e-4 |
SMART |
ZnF_C2H2
|
925 |
947 |
8.94e-3 |
SMART |
ZnF_C2H2
|
954 |
976 |
2.27e-4 |
SMART |
ZnF_C2H2
|
982 |
1005 |
9.3e-1 |
SMART |
ZnF_C2H2
|
1029 |
1052 |
5.21e-4 |
SMART |
low complexity region
|
1121 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1200 |
1218 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000162054
|
SMART Domains |
Protein: ENSMUSP00000125732 Gene: ENSMUSG00000022335
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
2.45e0 |
SMART |
ZnF_C2H2
|
116 |
136 |
1.53e2 |
SMART |
low complexity region
|
213 |
229 |
N/A |
INTRINSIC |
ZnF_C2H2
|
264 |
286 |
1.47e-3 |
SMART |
ZnF_C2H2
|
292 |
314 |
1.18e-2 |
SMART |
ZnF_C2H2
|
319 |
342 |
2.36e-2 |
SMART |
ZnF_C2H2
|
347 |
370 |
4.4e-2 |
SMART |
ZnF_C2H2
|
397 |
419 |
1.67e-2 |
SMART |
ZnF_C2H2
|
425 |
447 |
1.33e-1 |
SMART |
ZnF_C2H2
|
451 |
474 |
2.05e-2 |
SMART |
low complexity region
|
594 |
610 |
N/A |
INTRINSIC |
ZnF_C2H2
|
730 |
752 |
1.43e-1 |
SMART |
ZnF_C2H2
|
758 |
781 |
3.52e-1 |
SMART |
ZnF_C2H2
|
786 |
810 |
5.59e-4 |
SMART |
ZnF_C2H2
|
818 |
841 |
3.83e-2 |
SMART |
ZnF_C2H2
|
868 |
891 |
3.95e1 |
SMART |
ZnF_C2H2
|
897 |
919 |
6.88e-4 |
SMART |
ZnF_C2H2
|
925 |
947 |
8.94e-3 |
SMART |
ZnF_C2H2
|
954 |
976 |
2.27e-4 |
SMART |
ZnF_C2H2
|
982 |
1005 |
9.3e-1 |
SMART |
ZnF_C2H2
|
1029 |
1052 |
5.21e-4 |
SMART |
low complexity region
|
1121 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1200 |
1218 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000162054
|
SMART Domains |
Protein: ENSMUSP00000125732 Gene: ENSMUSG00000022335
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
2.45e0 |
SMART |
ZnF_C2H2
|
116 |
136 |
1.53e2 |
SMART |
low complexity region
|
213 |
229 |
N/A |
INTRINSIC |
ZnF_C2H2
|
264 |
286 |
1.47e-3 |
SMART |
ZnF_C2H2
|
292 |
314 |
1.18e-2 |
SMART |
ZnF_C2H2
|
319 |
342 |
2.36e-2 |
SMART |
ZnF_C2H2
|
347 |
370 |
4.4e-2 |
SMART |
ZnF_C2H2
|
397 |
419 |
1.67e-2 |
SMART |
ZnF_C2H2
|
425 |
447 |
1.33e-1 |
SMART |
ZnF_C2H2
|
451 |
474 |
2.05e-2 |
SMART |
low complexity region
|
594 |
610 |
N/A |
INTRINSIC |
ZnF_C2H2
|
730 |
752 |
1.43e-1 |
SMART |
ZnF_C2H2
|
758 |
781 |
3.52e-1 |
SMART |
ZnF_C2H2
|
786 |
810 |
5.59e-4 |
SMART |
ZnF_C2H2
|
818 |
841 |
3.83e-2 |
SMART |
ZnF_C2H2
|
868 |
891 |
3.95e1 |
SMART |
ZnF_C2H2
|
897 |
919 |
6.88e-4 |
SMART |
ZnF_C2H2
|
925 |
947 |
8.94e-3 |
SMART |
ZnF_C2H2
|
954 |
976 |
2.27e-4 |
SMART |
ZnF_C2H2
|
982 |
1005 |
9.3e-1 |
SMART |
ZnF_C2H2
|
1029 |
1052 |
5.21e-4 |
SMART |
low complexity region
|
1121 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1200 |
1218 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162173
AA Change: V1063E
PolyPhen 2
Score 0.100 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000124974 Gene: ENSMUSG00000022335 AA Change: V1063E
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
2.45e0 |
SMART |
ZnF_C2H2
|
116 |
136 |
1.53e2 |
SMART |
low complexity region
|
220 |
236 |
N/A |
INTRINSIC |
ZnF_C2H2
|
271 |
293 |
1.47e-3 |
SMART |
ZnF_C2H2
|
299 |
321 |
1.18e-2 |
SMART |
ZnF_C2H2
|
326 |
349 |
2.36e-2 |
SMART |
ZnF_C2H2
|
354 |
377 |
4.4e-2 |
SMART |
ZnF_C2H2
|
404 |
426 |
1.67e-2 |
SMART |
ZnF_C2H2
|
432 |
454 |
1.33e-1 |
SMART |
ZnF_C2H2
|
458 |
481 |
2.05e-2 |
SMART |
low complexity region
|
601 |
617 |
N/A |
INTRINSIC |
ZnF_C2H2
|
737 |
759 |
1.43e-1 |
SMART |
ZnF_C2H2
|
765 |
788 |
3.52e-1 |
SMART |
ZnF_C2H2
|
793 |
817 |
5.59e-4 |
SMART |
ZnF_C2H2
|
825 |
848 |
3.83e-2 |
SMART |
ZnF_C2H2
|
875 |
898 |
3.95e1 |
SMART |
ZnF_C2H2
|
904 |
926 |
6.88e-4 |
SMART |
ZnF_C2H2
|
932 |
954 |
8.94e-3 |
SMART |
ZnF_C2H2
|
961 |
983 |
2.27e-4 |
SMART |
ZnF_C2H2
|
989 |
1012 |
9.3e-1 |
SMART |
ZnF_C2H2
|
1036 |
1059 |
5.21e-4 |
SMART |
low complexity region
|
1133 |
1151 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.3600 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.3%
|
Validation Efficiency |
98% (54/55) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that likely binds DNA and functions as a transcriptional regulator involved in apoptosis and cell survival. This gene resides in a susceptibility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009] PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete embryonic lethality associated with failure to initiation of embryo turning, abnormal embryonic hematopoiesis, abnormal spongiotrophoblast layer morphology, abnormal visceral yolk sac blood island morphology and pale yolk sac. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4galt |
G |
T |
15: 83,111,810 (GRCm39) |
N324K |
probably damaging |
Het |
Ahcyl1 |
A |
G |
3: 107,574,547 (GRCm39) |
|
probably benign |
Het |
Atrnl1 |
T |
A |
19: 57,641,382 (GRCm39) |
N343K |
probably benign |
Het |
Batf2 |
C |
A |
19: 6,221,357 (GRCm39) |
Q56K |
probably benign |
Het |
Cfh |
A |
T |
1: 140,036,274 (GRCm39) |
V691D |
probably damaging |
Het |
Chst10 |
T |
C |
1: 38,904,922 (GRCm39) |
Y257C |
probably damaging |
Het |
Dlg5 |
A |
T |
14: 24,228,051 (GRCm39) |
L290Q |
possibly damaging |
Het |
Dnah2 |
T |
A |
11: 69,407,416 (GRCm39) |
T456S |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,001,995 (GRCm39) |
|
probably null |
Het |
Efhb |
T |
C |
17: 53,758,697 (GRCm39) |
K313R |
probably damaging |
Het |
Eprs1 |
T |
A |
1: 185,160,305 (GRCm39) |
N1500K |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,183,236 (GRCm39) |
T1748A |
probably benign |
Het |
Gfra2 |
T |
A |
14: 71,163,377 (GRCm39) |
L87H |
probably damaging |
Het |
Gfral |
T |
A |
9: 76,100,727 (GRCm39) |
Y237F |
possibly damaging |
Het |
Gpr137b |
T |
C |
13: 13,533,974 (GRCm39) |
N361D |
probably benign |
Het |
Gsdmc |
G |
T |
15: 63,651,386 (GRCm39) |
T272N |
probably benign |
Het |
Hspe1 |
T |
A |
1: 55,128,269 (GRCm39) |
S21R |
probably benign |
Het |
Kctd16 |
G |
T |
18: 40,390,233 (GRCm39) |
|
probably benign |
Het |
Kif21a |
A |
T |
15: 90,868,958 (GRCm39) |
I483N |
probably damaging |
Het |
Kif4-ps |
T |
C |
12: 101,112,534 (GRCm39) |
|
noncoding transcript |
Het |
Lpp |
T |
C |
16: 24,580,407 (GRCm39) |
V166A |
possibly damaging |
Het |
Lrp2 |
A |
C |
2: 69,336,895 (GRCm39) |
D1292E |
probably damaging |
Het |
Manba |
T |
C |
3: 135,250,575 (GRCm39) |
Y401H |
probably damaging |
Het |
Msh2 |
T |
G |
17: 87,985,813 (GRCm39) |
|
probably benign |
Het |
Myef2 |
A |
T |
2: 124,930,757 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
T |
A |
11: 62,235,660 (GRCm39) |
Q598L |
probably damaging |
Het |
Obox3 |
A |
G |
7: 15,360,764 (GRCm39) |
V125A |
probably benign |
Het |
Or1n1 |
A |
T |
2: 36,750,381 (GRCm39) |
|
probably null |
Het |
Or2b4 |
T |
A |
17: 38,116,591 (GRCm39) |
L185* |
probably null |
Het |
Or9k7 |
G |
A |
10: 130,046,291 (GRCm39) |
T236I |
possibly damaging |
Het |
Pcdh9 |
C |
A |
14: 94,126,067 (GRCm39) |
L34F |
probably damaging |
Het |
Pcdha3 |
A |
T |
18: 37,079,560 (GRCm39) |
I101F |
probably damaging |
Het |
Pced1b |
A |
G |
15: 97,282,675 (GRCm39) |
E238G |
probably benign |
Het |
Pla2r1 |
A |
T |
2: 60,258,994 (GRCm39) |
N1131K |
probably damaging |
Het |
Prmt1 |
A |
T |
7: 44,631,060 (GRCm39) |
S99R |
probably damaging |
Het |
Qng1 |
G |
A |
13: 58,529,617 (GRCm39) |
R332C |
probably benign |
Het |
Rbp3 |
T |
C |
14: 33,682,615 (GRCm39) |
S1116P |
probably damaging |
Het |
Rhobtb2 |
T |
C |
14: 70,037,160 (GRCm39) |
D88G |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,379,394 (GRCm39) |
E432G |
probably benign |
Het |
Sh3rf1 |
A |
G |
8: 61,814,793 (GRCm39) |
T451A |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Siva1 |
T |
A |
12: 112,613,336 (GRCm39) |
D61E |
probably benign |
Het |
Skor1 |
A |
C |
9: 63,046,855 (GRCm39) |
|
probably null |
Het |
Slc20a1 |
A |
G |
2: 129,041,611 (GRCm39) |
|
probably benign |
Het |
Slc2a7 |
A |
G |
4: 150,252,926 (GRCm39) |
E522G |
probably benign |
Het |
Tmprss7 |
A |
T |
16: 45,511,123 (GRCm39) |
I85N |
probably damaging |
Het |
Tpx2 |
T |
A |
2: 152,726,958 (GRCm39) |
D408E |
probably damaging |
Het |
Ulk4 |
A |
T |
9: 121,073,436 (GRCm39) |
I551N |
probably benign |
Het |
Zfp101 |
C |
A |
17: 33,613,457 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00542:Zfat
|
APN |
15 |
68,042,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00862:Zfat
|
APN |
15 |
68,130,512 (GRCm39) |
splice site |
probably null |
|
IGL01021:Zfat
|
APN |
15 |
68,042,015 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01152:Zfat
|
APN |
15 |
67,982,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01733:Zfat
|
APN |
15 |
68,052,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01873:Zfat
|
APN |
15 |
68,096,744 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01990:Zfat
|
APN |
15 |
68,096,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Zfat
|
APN |
15 |
68,052,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Zfat
|
APN |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Zfat
|
APN |
15 |
68,052,963 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03201:Zfat
|
APN |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R0145:Zfat
|
UTSW |
15 |
68,058,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0408:Zfat
|
UTSW |
15 |
68,052,141 (GRCm39) |
missense |
probably benign |
0.10 |
R0633:Zfat
|
UTSW |
15 |
68,052,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Zfat
|
UTSW |
15 |
68,084,432 (GRCm39) |
splice site |
probably benign |
|
R1508:Zfat
|
UTSW |
15 |
68,050,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Zfat
|
UTSW |
15 |
68,084,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1641:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.19 |
R1889:Zfat
|
UTSW |
15 |
67,973,388 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Zfat
|
UTSW |
15 |
68,018,392 (GRCm39) |
missense |
probably benign |
0.32 |
R2030:Zfat
|
UTSW |
15 |
67,990,783 (GRCm39) |
critical splice donor site |
probably null |
|
R2202:Zfat
|
UTSW |
15 |
68,051,709 (GRCm39) |
missense |
probably benign |
0.36 |
R2340:Zfat
|
UTSW |
15 |
67,973,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R3440:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R3442:Zfat
|
UTSW |
15 |
67,973,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R4406:Zfat
|
UTSW |
15 |
68,052,040 (GRCm39) |
missense |
probably benign |
0.00 |
R4649:Zfat
|
UTSW |
15 |
68,056,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Zfat
|
UTSW |
15 |
68,052,131 (GRCm39) |
missense |
probably benign |
|
R4745:Zfat
|
UTSW |
15 |
68,052,223 (GRCm39) |
missense |
probably benign |
0.09 |
R4862:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.02 |
R5015:Zfat
|
UTSW |
15 |
68,050,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Zfat
|
UTSW |
15 |
68,052,079 (GRCm39) |
missense |
probably benign |
|
R5208:Zfat
|
UTSW |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Zfat
|
UTSW |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Zfat
|
UTSW |
15 |
67,982,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Zfat
|
UTSW |
15 |
68,052,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Zfat
|
UTSW |
15 |
67,990,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Zfat
|
UTSW |
15 |
68,051,806 (GRCm39) |
missense |
probably benign |
|
R6046:Zfat
|
UTSW |
15 |
68,052,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R6315:Zfat
|
UTSW |
15 |
67,956,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Zfat
|
UTSW |
15 |
68,052,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Zfat
|
UTSW |
15 |
68,037,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6789:Zfat
|
UTSW |
15 |
67,956,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Zfat
|
UTSW |
15 |
68,052,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Zfat
|
UTSW |
15 |
68,052,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Zfat
|
UTSW |
15 |
68,052,211 (GRCm39) |
missense |
probably benign |
|
R7065:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Zfat
|
UTSW |
15 |
68,050,631 (GRCm39) |
missense |
probably benign |
0.12 |
R7208:Zfat
|
UTSW |
15 |
68,051,856 (GRCm39) |
missense |
probably benign |
0.39 |
R7330:Zfat
|
UTSW |
15 |
68,084,600 (GRCm39) |
missense |
probably benign |
0.00 |
R7345:Zfat
|
UTSW |
15 |
67,976,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Zfat
|
UTSW |
15 |
68,056,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Zfat
|
UTSW |
15 |
68,050,715 (GRCm39) |
nonsense |
probably null |
|
R7672:Zfat
|
UTSW |
15 |
68,130,535 (GRCm39) |
start codon destroyed |
probably null |
0.39 |
R7676:Zfat
|
UTSW |
15 |
68,096,693 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7701:Zfat
|
UTSW |
15 |
68,052,757 (GRCm39) |
nonsense |
probably null |
|
R7825:Zfat
|
UTSW |
15 |
68,051,769 (GRCm39) |
missense |
probably benign |
0.01 |
R8152:Zfat
|
UTSW |
15 |
67,973,355 (GRCm39) |
missense |
probably benign |
0.23 |
R8404:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8405:Zfat
|
UTSW |
15 |
68,018,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8502:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Zfat
|
UTSW |
15 |
68,037,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Zfat
|
UTSW |
15 |
67,956,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8887:Zfat
|
UTSW |
15 |
68,056,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Zfat
|
UTSW |
15 |
68,052,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Zfat
|
UTSW |
15 |
67,956,404 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9117:Zfat
|
UTSW |
15 |
68,058,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R9137:Zfat
|
UTSW |
15 |
68,051,794 (GRCm39) |
missense |
probably benign |
0.00 |
R9310:Zfat
|
UTSW |
15 |
67,956,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R9482:Zfat
|
UTSW |
15 |
68,084,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9611:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9630:Zfat
|
UTSW |
15 |
67,990,793 (GRCm39) |
missense |
probably benign |
0.37 |
Z1088:Zfat
|
UTSW |
15 |
68,058,950 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- ATGATCTGAAATGGCTGCCG -3'
(R):5'- GGCTGCTGTTGTATTCCAATAC -3'
Sequencing Primer
(F):5'- AAATGGCTGCCGAGGATTTCC -3'
(R):5'- GCTGCTGTTGTATTCCAATACTAAGG -3'
|
Posted On |
2015-10-21 |