Incidental Mutation 'R7038:Zfp407'
ID |
546900 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp407
|
Ensembl Gene |
ENSMUSG00000048410 |
Gene Name |
zinc finger protein 407 |
Synonyms |
LOC381139, 6430585N13Rik, LOC240469 |
MMRRC Submission |
045138-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7038 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
18 |
Chromosomal Location |
84225826-84612815 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 84579982 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 377
(V377A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118361
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000125763]
|
AlphaFold |
G3UVV3 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000125450
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000125763
AA Change: V377A
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000118361 Gene: ENSMUSG00000048410 AA Change: V377A
Domain | Start | End | E-Value | Type |
low complexity region
|
20 |
37 |
N/A |
INTRINSIC |
ZnF_C2H2
|
178 |
200 |
8.67e-1 |
SMART |
ZnF_U1
|
233 |
267 |
6.79e-1 |
SMART |
ZnF_C2H2
|
236 |
260 |
4.65e-1 |
SMART |
ZnF_C2H2
|
522 |
545 |
7.05e-1 |
SMART |
ZnF_U1
|
548 |
582 |
1.54e1 |
SMART |
ZnF_C2H2
|
551 |
575 |
1.01e-1 |
SMART |
ZnF_C2H2
|
582 |
605 |
1.41e0 |
SMART |
ZnF_U1
|
606 |
639 |
2.22e0 |
SMART |
ZnF_C2H2
|
609 |
632 |
1.01e2 |
SMART |
ZnF_C2H2
|
695 |
718 |
6.23e-2 |
SMART |
ZnF_U1
|
721 |
755 |
2.96e0 |
SMART |
ZnF_C2H2
|
724 |
748 |
7.11e0 |
SMART |
ZnF_C2H2
|
840 |
863 |
7.55e-1 |
SMART |
ZnF_U1
|
866 |
900 |
3.81e-1 |
SMART |
ZnF_C2H2
|
869 |
893 |
1.07e0 |
SMART |
ZnF_C2H2
|
1009 |
1032 |
6.13e-1 |
SMART |
ZnF_U1
|
1035 |
1069 |
2.22e0 |
SMART |
ZnF_C2H2
|
1038 |
1062 |
5.62e0 |
SMART |
low complexity region
|
1223 |
1234 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1405 |
1428 |
5.92e0 |
SMART |
ZnF_U1
|
1432 |
1466 |
2.35e0 |
SMART |
ZnF_C2H2
|
1435 |
1459 |
1.76e-1 |
SMART |
ZnF_C2H2
|
1477 |
1500 |
5.42e-2 |
SMART |
ZnF_C2H2
|
1528 |
1552 |
1.68e1 |
SMART |
ZnF_C2H2
|
1558 |
1580 |
1.43e-1 |
SMART |
ZnF_C2H2
|
1586 |
1609 |
9.58e-3 |
SMART |
ZnF_C2H2
|
1619 |
1641 |
2.61e-4 |
SMART |
ZnF_C2H2
|
1647 |
1671 |
1.04e-3 |
SMART |
ZnF_C2H2
|
1677 |
1699 |
9.44e-2 |
SMART |
ZnF_C2H2
|
1705 |
1727 |
1.82e-3 |
SMART |
ZnF_C2H2
|
1733 |
1758 |
4.65e-1 |
SMART |
ZnF_C2H2
|
1764 |
1787 |
1.26e-2 |
SMART |
low complexity region
|
1876 |
1887 |
N/A |
INTRINSIC |
low complexity region
|
2017 |
2032 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
99% (101/102) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a zinc finger protein whose exact function is not known. It may be involved in transcriptional regulation. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
C |
1: 156,468,979 (GRCm39) |
S748P |
possibly damaging |
Het |
Alppl2 |
T |
C |
1: 87,016,833 (GRCm39) |
D104G |
probably damaging |
Het |
Als2 |
C |
A |
1: 59,206,673 (GRCm39) |
W1590L |
possibly damaging |
Het |
Aopep |
G |
T |
13: 63,338,339 (GRCm39) |
V571F |
possibly damaging |
Het |
Aplf |
C |
T |
6: 87,630,805 (GRCm39) |
W210* |
probably null |
Het |
Ash1l |
A |
T |
3: 88,889,978 (GRCm39) |
H619L |
probably benign |
Het |
Baiap3 |
G |
A |
17: 25,462,814 (GRCm39) |
R1075C |
probably benign |
Het |
Bpifb1 |
G |
T |
2: 154,044,589 (GRCm39) |
V19F |
probably damaging |
Het |
Capn1 |
A |
T |
19: 6,064,349 (GRCm39) |
L50Q |
probably benign |
Het |
Carmil1 |
A |
G |
13: 24,323,318 (GRCm39) |
S245P |
probably damaging |
Het |
Cavin4 |
A |
G |
4: 48,672,479 (GRCm39) |
H308R |
probably benign |
Het |
Cd4 |
C |
T |
6: 124,847,217 (GRCm39) |
V316M |
probably damaging |
Het |
Cdcp1 |
T |
C |
9: 123,002,662 (GRCm39) |
Y803C |
probably damaging |
Het |
Cep295nl |
A |
G |
11: 118,223,815 (GRCm39) |
I343T |
probably benign |
Het |
Cgn |
T |
G |
3: 94,670,392 (GRCm39) |
T1021P |
possibly damaging |
Het |
Cilk1 |
C |
T |
9: 78,016,484 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,822,937 (GRCm39) |
V140A |
unknown |
Het |
Cops8 |
T |
C |
1: 90,531,320 (GRCm39) |
|
probably benign |
Het |
Crhbp |
A |
G |
13: 95,580,699 (GRCm39) |
Y54H |
probably damaging |
Het |
Cyp2c29 |
G |
A |
19: 39,275,571 (GRCm39) |
V4I |
probably benign |
Het |
Cyp2j6 |
T |
A |
4: 96,423,708 (GRCm39) |
Y220F |
probably benign |
Het |
D130043K22Rik |
A |
G |
13: 25,077,391 (GRCm39) |
D1008G |
probably damaging |
Het |
Ddx47 |
T |
A |
6: 135,000,336 (GRCm39) |
V444E |
possibly damaging |
Het |
Dnttip2 |
T |
A |
3: 122,070,181 (GRCm39) |
C465* |
probably null |
Het |
Dst |
C |
A |
1: 34,221,879 (GRCm39) |
S2561* |
probably null |
Het |
Dstyk |
T |
C |
1: 132,381,847 (GRCm39) |
S534P |
probably benign |
Het |
Eif4e |
A |
G |
3: 138,232,943 (GRCm39) |
|
probably benign |
Het |
Eipr1 |
C |
T |
12: 28,801,817 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
T |
A |
1: 63,771,032 (GRCm39) |
D129E |
possibly damaging |
Het |
Fndc3b |
C |
T |
3: 27,555,618 (GRCm39) |
G312D |
probably benign |
Het |
Gab2 |
T |
A |
7: 96,952,290 (GRCm39) |
I562N |
probably damaging |
Het |
Gata5 |
C |
A |
2: 179,975,685 (GRCm39) |
D160Y |
possibly damaging |
Het |
Gcn1 |
G |
A |
5: 115,749,203 (GRCm39) |
V1912I |
probably damaging |
Het |
Gdf5 |
C |
A |
2: 155,786,655 (GRCm39) |
Q107H |
probably damaging |
Het |
Gdpd1 |
A |
G |
11: 86,926,118 (GRCm39) |
Y276H |
probably damaging |
Het |
Gins1 |
A |
G |
2: 150,759,791 (GRCm39) |
Y81C |
probably damaging |
Het |
Gm28360 |
T |
C |
1: 117,781,329 (GRCm39) |
C107R |
probably damaging |
Het |
Hadha |
T |
C |
5: 30,324,998 (GRCm39) |
|
probably null |
Het |
Hcn4 |
A |
T |
9: 58,730,867 (GRCm39) |
I25F |
unknown |
Het |
Hectd4 |
A |
G |
5: 121,437,660 (GRCm39) |
Y1095C |
possibly damaging |
Het |
Hsp90b1 |
A |
T |
10: 86,531,730 (GRCm39) |
L73Q |
probably damaging |
Het |
Hspa12a |
A |
G |
19: 58,793,132 (GRCm39) |
V351A |
probably damaging |
Het |
Htr1b |
T |
A |
9: 81,514,296 (GRCm39) |
M104L |
probably benign |
Het |
Igf2r |
T |
C |
17: 12,917,212 (GRCm39) |
T1563A |
probably benign |
Het |
Kif13a |
C |
T |
13: 46,905,931 (GRCm39) |
V671M |
possibly damaging |
Het |
Liph |
A |
T |
16: 21,795,009 (GRCm39) |
V201E |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,221,759 (GRCm39) |
D196G |
probably damaging |
Het |
Med15 |
C |
T |
16: 17,470,591 (GRCm39) |
D589N |
possibly damaging |
Het |
Mknk1 |
A |
G |
4: 115,714,307 (GRCm39) |
D26G |
probably damaging |
Het |
Mpi |
T |
C |
9: 57,452,500 (GRCm39) |
D344G |
probably damaging |
Het |
Mrc2 |
A |
G |
11: 105,223,062 (GRCm39) |
E435G |
possibly damaging |
Het |
Mrps5 |
A |
G |
2: 127,442,786 (GRCm39) |
E285G |
probably damaging |
Het |
Ms4a20 |
A |
T |
19: 11,087,675 (GRCm39) |
F85L |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,531,764 (GRCm39) |
M6197L |
probably damaging |
Het |
Myo3b |
A |
T |
2: 69,925,552 (GRCm39) |
E34D |
probably benign |
Het |
Nsd3 |
T |
C |
8: 26,131,279 (GRCm39) |
S215P |
probably damaging |
Het |
Nsmce2 |
T |
A |
15: 59,368,679 (GRCm39) |
|
probably benign |
Het |
Ntan1 |
T |
C |
16: 13,644,774 (GRCm39) |
S37P |
probably benign |
Het |
Nup210l |
T |
A |
3: 90,067,254 (GRCm39) |
Y765N |
probably damaging |
Het |
Or10q12 |
A |
T |
19: 13,745,715 (GRCm39) |
D3V |
probably benign |
Het |
Or2aa1 |
T |
C |
11: 59,480,408 (GRCm39) |
Y169C |
possibly damaging |
Het |
Or4s2b |
A |
T |
2: 88,509,085 (GRCm39) |
R288S |
probably damaging |
Het |
Or7g30 |
A |
C |
9: 19,352,888 (GRCm39) |
L226F |
possibly damaging |
Het |
Pald1 |
T |
C |
10: 61,175,078 (GRCm39) |
H724R |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,475,257 (GRCm39) |
D131V |
possibly damaging |
Het |
Pds5b |
G |
T |
5: 150,724,225 (GRCm39) |
R1269S |
probably benign |
Het |
Pikfyve |
T |
C |
1: 65,273,520 (GRCm39) |
V645A |
probably damaging |
Het |
Plag1 |
G |
T |
4: 3,904,676 (GRCm39) |
H172N |
probably damaging |
Het |
Plch2 |
G |
C |
4: 155,074,489 (GRCm39) |
|
probably null |
Het |
Plxnb1 |
T |
A |
9: 108,929,453 (GRCm39) |
V103E |
probably damaging |
Het |
Prpf8 |
T |
A |
11: 75,386,984 (GRCm39) |
M1143K |
probably benign |
Het |
Ptpn18 |
T |
A |
1: 34,498,906 (GRCm39) |
M1K |
probably null |
Het |
Rasgrf2 |
G |
A |
13: 92,130,952 (GRCm39) |
T703I |
possibly damaging |
Het |
Rassf6 |
A |
T |
5: 90,757,584 (GRCm39) |
H125Q |
probably benign |
Het |
Sdad1 |
A |
G |
5: 92,446,049 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
T |
A |
4: 124,622,219 (GRCm39) |
F426L |
probably benign |
Het |
Sgsm3 |
T |
C |
15: 80,892,576 (GRCm39) |
F6L |
possibly damaging |
Het |
Slc14a2 |
A |
T |
18: 78,202,252 (GRCm39) |
I626N |
probably damaging |
Het |
Slc17a8 |
T |
C |
10: 89,436,083 (GRCm39) |
N165S |
probably benign |
Het |
Slc41a1 |
C |
A |
1: 131,769,795 (GRCm39) |
A305D |
possibly damaging |
Het |
Smyd4 |
C |
A |
11: 75,281,340 (GRCm39) |
P271Q |
probably damaging |
Het |
Spag17 |
C |
A |
3: 99,891,925 (GRCm39) |
H260N |
probably benign |
Het |
Spata2 |
A |
T |
2: 167,327,283 (GRCm39) |
V38E |
possibly damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Syt14 |
T |
A |
1: 192,665,966 (GRCm39) |
|
probably benign |
Het |
Tbx21 |
A |
G |
11: 96,990,597 (GRCm39) |
S329P |
probably damaging |
Het |
Tex2 |
A |
T |
11: 106,402,726 (GRCm39) |
|
probably null |
Het |
Tmem62 |
A |
G |
2: 120,824,058 (GRCm39) |
I244M |
possibly damaging |
Het |
Tnks |
A |
T |
8: 35,318,790 (GRCm39) |
N830K |
probably damaging |
Het |
Tox2 |
A |
G |
2: 163,156,264 (GRCm39) |
E145G |
probably damaging |
Het |
Tpcn1 |
T |
C |
5: 120,723,342 (GRCm39) |
D7G |
probably damaging |
Het |
Ttc28 |
T |
A |
5: 111,414,445 (GRCm39) |
M1320K |
probably benign |
Het |
Tubgcp5 |
T |
G |
7: 55,455,114 (GRCm39) |
V270G |
probably damaging |
Het |
Unc5a |
A |
G |
13: 55,152,297 (GRCm39) |
R62G |
probably damaging |
Het |
Unc5d |
A |
G |
8: 29,205,749 (GRCm39) |
|
probably null |
Het |
Utrn |
T |
C |
10: 12,558,082 (GRCm39) |
H1459R |
probably damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,725,263 (GRCm39) |
L64Q |
possibly damaging |
Het |
Wdr55 |
T |
G |
18: 36,893,473 (GRCm39) |
L45R |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,816,357 (GRCm39) |
Y306H |
probably damaging |
Het |
Zfp398 |
G |
T |
6: 47,843,243 (GRCm39) |
D300Y |
probably damaging |
Het |
Zfp457 |
G |
A |
13: 67,441,997 (GRCm39) |
H97Y |
probably benign |
Het |
Zfp467 |
T |
C |
6: 48,415,072 (GRCm39) |
T527A |
probably damaging |
Het |
|
Other mutations in Zfp407 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Zfp407
|
APN |
18 |
84,579,877 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02105:Zfp407
|
APN |
18 |
84,580,845 (GRCm39) |
nonsense |
probably null |
|
IGL02110:Zfp407
|
APN |
18 |
84,577,165 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02343:Zfp407
|
APN |
18 |
84,227,849 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02456:Zfp407
|
APN |
18 |
84,576,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02705:Zfp407
|
APN |
18 |
84,577,156 (GRCm39) |
nonsense |
probably null |
|
IGL02946:Zfp407
|
APN |
18 |
84,578,834 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03069:Zfp407
|
APN |
18 |
84,369,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03145:Zfp407
|
APN |
18 |
84,227,846 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03403:Zfp407
|
APN |
18 |
84,578,922 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Zfp407
|
UTSW |
18 |
84,228,080 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4362001:Zfp407
|
UTSW |
18 |
84,579,393 (GRCm39) |
missense |
possibly damaging |
0.87 |
PIT4520001:Zfp407
|
UTSW |
18 |
84,450,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R0087:Zfp407
|
UTSW |
18 |
84,578,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Zfp407
|
UTSW |
18 |
84,576,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Zfp407
|
UTSW |
18 |
84,580,692 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0766:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R0787:Zfp407
|
UTSW |
18 |
84,227,471 (GRCm39) |
missense |
probably benign |
0.00 |
R0787:Zfp407
|
UTSW |
18 |
84,227,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R1065:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1086:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1165:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1186:Zfp407
|
UTSW |
18 |
84,227,573 (GRCm39) |
missense |
probably benign |
0.39 |
R1203:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1312:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1345:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1385:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1421:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1430:Zfp407
|
UTSW |
18 |
84,227,580 (GRCm39) |
missense |
probably benign |
0.18 |
R1436:Zfp407
|
UTSW |
18 |
84,361,196 (GRCm39) |
splice site |
probably benign |
|
R1498:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1526:Zfp407
|
UTSW |
18 |
84,579,158 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1579:Zfp407
|
UTSW |
18 |
84,227,763 (GRCm39) |
missense |
probably benign |
0.00 |
R1594:Zfp407
|
UTSW |
18 |
84,227,456 (GRCm39) |
missense |
probably benign |
0.01 |
R1628:Zfp407
|
UTSW |
18 |
84,372,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R1698:Zfp407
|
UTSW |
18 |
84,580,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Zfp407
|
UTSW |
18 |
84,577,461 (GRCm39) |
missense |
probably benign |
0.01 |
R1984:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1985:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R1986:Zfp407
|
UTSW |
18 |
84,577,898 (GRCm39) |
missense |
probably benign |
0.14 |
R2151:Zfp407
|
UTSW |
18 |
84,227,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2152:Zfp407
|
UTSW |
18 |
84,227,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2154:Zfp407
|
UTSW |
18 |
84,227,774 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2259:Zfp407
|
UTSW |
18 |
84,227,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2353:Zfp407
|
UTSW |
18 |
84,578,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2845:Zfp407
|
UTSW |
18 |
84,576,522 (GRCm39) |
nonsense |
probably null |
|
R3407:Zfp407
|
UTSW |
18 |
84,576,997 (GRCm39) |
missense |
probably benign |
0.08 |
R3432:Zfp407
|
UTSW |
18 |
84,226,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Zfp407
|
UTSW |
18 |
84,578,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R4026:Zfp407
|
UTSW |
18 |
84,577,721 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4107:Zfp407
|
UTSW |
18 |
84,361,132 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4398:Zfp407
|
UTSW |
18 |
84,580,856 (GRCm39) |
nonsense |
probably null |
|
R4447:Zfp407
|
UTSW |
18 |
84,580,819 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4752:Zfp407
|
UTSW |
18 |
84,581,039 (GRCm39) |
missense |
probably benign |
0.01 |
R4881:Zfp407
|
UTSW |
18 |
84,577,828 (GRCm39) |
missense |
probably benign |
0.27 |
R4936:Zfp407
|
UTSW |
18 |
84,577,589 (GRCm39) |
missense |
probably benign |
0.00 |
R5194:Zfp407
|
UTSW |
18 |
84,579,434 (GRCm39) |
missense |
probably benign |
0.05 |
R5243:Zfp407
|
UTSW |
18 |
84,579,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5258:Zfp407
|
UTSW |
18 |
84,334,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R5591:Zfp407
|
UTSW |
18 |
84,579,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R5633:Zfp407
|
UTSW |
18 |
84,579,169 (GRCm39) |
missense |
probably benign |
0.35 |
R5739:Zfp407
|
UTSW |
18 |
84,226,867 (GRCm39) |
makesense |
probably null |
|
R5806:Zfp407
|
UTSW |
18 |
84,576,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R5820:Zfp407
|
UTSW |
18 |
84,578,649 (GRCm39) |
missense |
probably benign |
0.01 |
R6187:Zfp407
|
UTSW |
18 |
84,577,134 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6512:Zfp407
|
UTSW |
18 |
84,578,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R6521:Zfp407
|
UTSW |
18 |
84,450,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6748:Zfp407
|
UTSW |
18 |
84,226,955 (GRCm39) |
missense |
probably damaging |
0.98 |
R6882:Zfp407
|
UTSW |
18 |
84,361,194 (GRCm39) |
splice site |
probably null |
|
R6899:Zfp407
|
UTSW |
18 |
84,579,559 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7076:Zfp407
|
UTSW |
18 |
84,576,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Zfp407
|
UTSW |
18 |
84,577,167 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7397:Zfp407
|
UTSW |
18 |
84,579,944 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7402:Zfp407
|
UTSW |
18 |
84,579,661 (GRCm39) |
missense |
probably benign |
0.02 |
R7783:Zfp407
|
UTSW |
18 |
84,228,047 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7800:Zfp407
|
UTSW |
18 |
84,578,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R7904:Zfp407
|
UTSW |
18 |
84,579,381 (GRCm39) |
missense |
not run |
|
R7942:Zfp407
|
UTSW |
18 |
84,577,754 (GRCm39) |
missense |
probably benign |
0.02 |
R7955:Zfp407
|
UTSW |
18 |
84,577,416 (GRCm39) |
missense |
probably benign |
0.02 |
R7988:Zfp407
|
UTSW |
18 |
84,577,525 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8125:Zfp407
|
UTSW |
18 |
84,579,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Zfp407
|
UTSW |
18 |
84,578,269 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8364:Zfp407
|
UTSW |
18 |
84,570,993 (GRCm39) |
critical splice donor site |
probably null |
|
R8443:Zfp407
|
UTSW |
18 |
84,227,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R8487:Zfp407
|
UTSW |
18 |
84,580,895 (GRCm39) |
nonsense |
probably null |
|
R8497:Zfp407
|
UTSW |
18 |
84,578,021 (GRCm39) |
missense |
probably damaging |
0.98 |
R8808:Zfp407
|
UTSW |
18 |
84,361,185 (GRCm39) |
missense |
probably benign |
0.17 |
R8848:Zfp407
|
UTSW |
18 |
84,578,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Zfp407
|
UTSW |
18 |
84,578,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R8962:Zfp407
|
UTSW |
18 |
84,577,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R9087:Zfp407
|
UTSW |
18 |
84,227,982 (GRCm39) |
missense |
probably damaging |
0.96 |
R9452:Zfp407
|
UTSW |
18 |
84,580,579 (GRCm39) |
missense |
probably benign |
0.02 |
R9691:Zfp407
|
UTSW |
18 |
84,578,312 (GRCm39) |
missense |
probably benign |
0.03 |
R9766:Zfp407
|
UTSW |
18 |
84,577,574 (GRCm39) |
missense |
probably benign |
0.06 |
RF003:Zfp407
|
UTSW |
18 |
84,227,688 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Zfp407
|
UTSW |
18 |
84,228,079 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Predicted Primers |
PCR Primer
(F):5'- CTTTGCCTGGCCCTTTAAAG -3'
(R):5'- TCTAAACCAATAGCAAAGACTGGG -3'
Sequencing Primer
(F):5'- AGTAAAAGTGCCACTTCGTCTGC -3'
(R):5'- TTCAAGAGTAGTGCCGAGTACTG -3'
|
Posted On |
2019-05-13 |