Incidental Mutation 'R7904:Zfp407'
| ID |
610199 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp407
|
| Ensembl Gene |
ENSMUSG00000048410 |
| Gene Name |
zinc finger protein 407 |
| Synonyms |
LOC381139, 6430585N13Rik, LOC240469 |
| MMRRC Submission |
045956-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7904 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
18 |
| Chromosomal Location |
84225826-84612815 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 84579381 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Glutamine
at position 577
(H577Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118361
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000125763]
|
| AlphaFold |
G3UVV3 |
| Predicted Effect |
not run
Transcript: ENSMUST00000125763
AA Change: H577Q
|
| SMART Domains |
Protein: ENSMUSP00000118361
Gene: ENSMUSG00000048410
AA Change: H577Q
| 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: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
| Validation Efficiency |
97% (72/74) |
| 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: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam8 |
G |
A |
7: 139,567,591 (GRCm39) |
T384I |
probably benign |
Het |
| Astn1 |
T |
C |
1: 158,424,886 (GRCm39) |
F691L |
probably benign |
Het |
| Azgp1 |
A |
G |
5: 137,985,869 (GRCm39) |
E164G |
probably damaging |
Het |
| Bdp1 |
A |
G |
13: 100,177,944 (GRCm39) |
V1975A |
probably benign |
Het |
| Cactin |
T |
C |
10: 81,161,699 (GRCm39) |
Y744H |
possibly damaging |
Het |
| Clstn1 |
T |
A |
4: 149,698,594 (GRCm39) |
I60N |
probably benign |
Het |
| Col16a1 |
T |
A |
4: 129,948,001 (GRCm39) |
C240* |
probably null |
Het |
| Col6a5 |
T |
C |
9: 105,805,720 (GRCm39) |
D1062G |
unknown |
Het |
| Csmd2 |
T |
C |
4: 128,313,346 (GRCm39) |
L1341P |
|
Het |
| Cyp51 |
A |
T |
5: 4,150,173 (GRCm39) |
F183L |
probably damaging |
Het |
| Dbnl |
T |
A |
11: 5,741,779 (GRCm39) |
|
probably null |
Het |
| Ddx60 |
G |
A |
8: 62,430,924 (GRCm39) |
V820I |
possibly damaging |
Het |
| Dnaaf9 |
A |
T |
2: 130,633,923 (GRCm39) |
|
probably null |
Het |
| Dnah11 |
T |
A |
12: 117,867,003 (GRCm39) |
D4046V |
possibly damaging |
Het |
| Dnah6 |
G |
A |
6: 73,112,450 (GRCm39) |
|
probably null |
Het |
| Dnttip1 |
A |
G |
2: 164,589,472 (GRCm39) |
Y89C |
probably benign |
Het |
| Efr3a |
T |
A |
15: 65,696,527 (GRCm39) |
V144E |
probably damaging |
Het |
| Epha8 |
T |
C |
4: 136,659,050 (GRCm39) |
Q868R |
possibly damaging |
Het |
| Ercc5 |
G |
T |
1: 44,214,998 (GRCm39) |
|
probably null |
Het |
| Fam118a |
A |
G |
15: 84,929,834 (GRCm39) |
S21G |
probably damaging |
Het |
| Fam171b |
T |
C |
2: 83,683,849 (GRCm39) |
I122T |
probably damaging |
Het |
| Fat4 |
T |
A |
3: 38,941,690 (GRCm39) |
S194R |
probably damaging |
Het |
| Fcho2 |
T |
A |
13: 98,932,871 (GRCm39) |
T44S |
possibly damaging |
Het |
| Gm21698 |
C |
A |
5: 26,189,256 (GRCm39) |
L232F |
probably benign |
Het |
| Gpr149 |
T |
A |
3: 62,502,356 (GRCm39) |
D500V |
probably benign |
Het |
| Gpx8 |
T |
A |
13: 113,182,035 (GRCm39) |
T133S |
probably benign |
Het |
| Hdlbp |
A |
T |
1: 93,351,092 (GRCm39) |
I542N |
probably damaging |
Het |
| Hid1 |
G |
A |
11: 115,246,187 (GRCm39) |
S361F |
probably damaging |
Het |
| Igdcc4 |
C |
A |
9: 65,041,801 (GRCm39) |
A1076E |
probably benign |
Het |
| Il4ra |
A |
G |
7: 125,164,845 (GRCm39) |
K7E |
probably benign |
Het |
| Inka2 |
T |
C |
3: 105,623,730 (GRCm39) |
C35R |
probably damaging |
Het |
| Itga9 |
G |
T |
9: 118,706,294 (GRCm39) |
|
probably null |
Het |
| Kif5c |
T |
C |
2: 49,591,095 (GRCm39) |
S316P |
probably damaging |
Het |
| Kmt5c |
A |
T |
7: 4,749,158 (GRCm39) |
T264S |
probably damaging |
Het |
| Litafd |
A |
G |
16: 8,501,681 (GRCm39) |
H61R |
|
Het |
| Lrrc18 |
A |
G |
14: 32,731,052 (GRCm39) |
N197S |
probably benign |
Het |
| Mcoln1 |
C |
A |
8: 3,558,356 (GRCm39) |
D203E |
probably benign |
Het |
| Mitf |
T |
C |
6: 97,990,671 (GRCm39) |
V358A |
probably damaging |
Het |
| Mki67 |
A |
T |
7: 135,294,816 (GRCm39) |
L3161Q |
possibly damaging |
Het |
| Mmp20 |
T |
A |
9: 7,644,076 (GRCm39) |
F255I |
possibly damaging |
Het |
| Muc16 |
T |
C |
9: 18,566,946 (GRCm39) |
T1858A |
unknown |
Het |
| Mug1 |
G |
A |
6: 121,828,424 (GRCm39) |
V279I |
probably benign |
Het |
| Or6c68 |
T |
C |
10: 129,157,665 (GRCm39) |
Y58H |
probably damaging |
Het |
| Otulin |
G |
T |
15: 27,630,580 (GRCm39) |
A39E |
probably benign |
Het |
| Pcdh17 |
A |
T |
14: 84,685,924 (GRCm39) |
D797V |
possibly damaging |
Het |
| Pdlim5 |
G |
A |
3: 142,018,154 (GRCm39) |
S147L |
probably damaging |
Het |
| Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
| Ppp2r1a |
T |
G |
17: 21,182,003 (GRCm39) |
|
probably null |
Het |
| Ranbp6 |
T |
C |
19: 29,789,813 (GRCm39) |
I180V |
probably benign |
Het |
| Rbm27 |
G |
T |
18: 42,465,921 (GRCm39) |
R869L |
probably damaging |
Het |
| Rtn4r |
A |
G |
16: 17,969,349 (GRCm39) |
D259G |
probably benign |
Het |
| Ryr3 |
T |
C |
2: 112,611,369 (GRCm39) |
E2271G |
probably damaging |
Het |
| Sbk1 |
A |
G |
7: 125,891,208 (GRCm39) |
Y214C |
probably damaging |
Het |
| Scg3 |
C |
T |
9: 75,551,149 (GRCm39) |
E459K |
probably damaging |
Het |
| Scin |
T |
G |
12: 40,126,999 (GRCm39) |
E449D |
probably damaging |
Het |
| Sel1l3 |
T |
C |
5: 53,297,166 (GRCm39) |
K760R |
probably benign |
Het |
| Sh3pxd2a |
A |
G |
19: 47,308,753 (GRCm39) |
L145S |
possibly damaging |
Het |
| Sh3yl1 |
A |
G |
12: 30,991,995 (GRCm39) |
D188G |
probably benign |
Het |
| Slc38a1 |
A |
T |
15: 96,521,921 (GRCm39) |
L13Q |
possibly damaging |
Het |
| Smyd4 |
T |
C |
11: 75,240,613 (GRCm39) |
I36T |
possibly damaging |
Het |
| Spata31f1a |
A |
G |
4: 42,850,765 (GRCm39) |
S464P |
possibly damaging |
Het |
| Stab2 |
A |
T |
10: 86,790,056 (GRCm39) |
L570* |
probably null |
Het |
| Tg |
G |
T |
15: 66,577,128 (GRCm39) |
A1484S |
probably benign |
Het |
| Tm7sf2 |
A |
T |
19: 6,118,942 (GRCm39) |
N677K |
probably damaging |
Het |
| Tmem235 |
T |
G |
11: 117,751,717 (GRCm39) |
L47R |
probably damaging |
Het |
| Tmem87a |
A |
G |
2: 120,210,198 (GRCm39) |
S252P |
probably damaging |
Het |
| Unc13b |
A |
G |
4: 43,217,075 (GRCm39) |
D458G |
probably benign |
Het |
| Wfdc1 |
A |
G |
8: 120,406,770 (GRCm39) |
|
probably null |
Het |
| Wnt16 |
A |
G |
6: 22,297,989 (GRCm39) |
Y285C |
probably damaging |
Het |
| Wwc2 |
A |
T |
8: 48,309,270 (GRCm39) |
N837K |
unknown |
Het |
| Xdh |
A |
G |
17: 74,229,467 (GRCm39) |
F329L |
probably benign |
Het |
| Yaf2 |
G |
T |
15: 93,183,466 (GRCm39) |
H115N |
probably benign |
Het |
| Zbtb16 |
G |
T |
9: 48,744,272 (GRCm39) |
N13K |
probably damaging |
Het |
| Zfhx3 |
A |
T |
8: 109,677,695 (GRCm39) |
D2915V |
probably damaging |
Het |
| Zfp236 |
A |
T |
18: 82,627,507 (GRCm39) |
V1564E |
possibly 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 |
|
R7038:Zfp407
|
UTSW |
18 |
84,579,982 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
|
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 |
|
| Posted On |
2019-12-20 |
Incidental Mutation