Incidental Mutation 'R5739:Zfp407'
| ID |
444726 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp407
|
| Ensembl Gene |
ENSMUSG00000048410 |
| Gene Name |
zinc finger protein 407 |
| Synonyms |
LOC381139, 6430585N13Rik, LOC240469 |
| MMRRC Submission |
043351-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R5739 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
18 |
| Chromosomal Location |
84225826-84612815 bp(-) (GRCm39) |
| Type of Mutation |
makesense |
| DNA Base Change (assembly) |
T to C
at 84226867 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Stop codon to Tryptophan
at position 2247
(*2247W)
|
| 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 null
Transcript: ENSMUST00000125763
AA Change: *2247W
|
| SMART Domains |
Protein: ENSMUSP00000118361
Gene: ENSMUSG00000048410
AA Change: *2247W
| 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 |
|
| Meta Mutation Damage Score |
0.8543 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 95.0%
|
| Validation Efficiency |
100% (82/82) |
| 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: 79 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4931429L15Rik |
A |
T |
9: 46,220,717 (GRCm39) |
S50T |
probably benign |
Het |
| A930011G23Rik |
A |
G |
5: 99,369,289 (GRCm39) |
L529P |
probably damaging |
Het |
| Acer2 |
A |
T |
4: 86,818,792 (GRCm39) |
N147Y |
probably damaging |
Het |
| Adamtsl1 |
A |
G |
4: 86,150,901 (GRCm39) |
E353G |
probably damaging |
Het |
| Alg6 |
T |
C |
4: 99,632,737 (GRCm39) |
F60L |
probably benign |
Het |
| Ano6 |
A |
T |
15: 95,811,260 (GRCm39) |
D120V |
probably damaging |
Het |
| Armc3 |
A |
G |
2: 19,258,728 (GRCm39) |
D265G |
possibly damaging |
Het |
| Aurkc |
A |
T |
7: 7,005,859 (GRCm39) |
Y249F |
probably benign |
Het |
| Bmal1 |
G |
A |
7: 112,884,238 (GRCm39) |
R92Q |
probably damaging |
Het |
| Cacna2d2 |
A |
G |
9: 107,389,528 (GRCm39) |
I274V |
probably benign |
Het |
| Camk2n2 |
C |
A |
16: 20,439,830 (GRCm39) |
G39C |
probably damaging |
Het |
| Ccdc39 |
A |
G |
3: 33,880,710 (GRCm39) |
L419P |
possibly damaging |
Het |
| Cdh23 |
T |
C |
10: 60,141,388 (GRCm39) |
M3117V |
probably damaging |
Het |
| Celsr3 |
A |
G |
9: 108,704,357 (GRCm39) |
E280G |
probably benign |
Het |
| Cherp |
TGCTGGTGGTGGGG |
TG |
8: 73,221,659 (GRCm39) |
|
probably benign |
Het |
| Clcn6 |
A |
G |
4: 148,098,646 (GRCm39) |
V494A |
probably damaging |
Het |
| Col19a1 |
C |
T |
1: 24,376,996 (GRCm39) |
G450S |
probably damaging |
Het |
| Crb2 |
T |
G |
2: 37,683,666 (GRCm39) |
V1056G |
probably damaging |
Het |
| Crtac1 |
A |
G |
19: 42,290,612 (GRCm39) |
F363S |
probably damaging |
Het |
| Dipk2a |
A |
T |
9: 94,402,594 (GRCm39) |
V356E |
possibly damaging |
Het |
| Dnaaf2 |
T |
C |
12: 69,243,715 (GRCm39) |
S449G |
probably benign |
Het |
| Dnah7b |
A |
T |
1: 46,273,152 (GRCm39) |
I2427F |
probably damaging |
Het |
| Dnah8 |
T |
A |
17: 30,937,981 (GRCm39) |
D1619E |
probably benign |
Het |
| Dock3 |
A |
T |
9: 106,850,995 (GRCm39) |
S836T |
possibly damaging |
Het |
| Donson |
A |
T |
16: 91,478,117 (GRCm39) |
|
probably null |
Het |
| Drc3 |
G |
A |
11: 60,265,956 (GRCm39) |
R215H |
possibly damaging |
Het |
| Entpd2 |
T |
C |
2: 25,289,504 (GRCm39) |
S329P |
possibly damaging |
Het |
| Eya2 |
T |
C |
2: 165,603,857 (GRCm39) |
S332P |
probably damaging |
Het |
| Fam83f |
T |
A |
15: 80,576,206 (GRCm39) |
Y286N |
probably damaging |
Het |
| Fat4 |
T |
C |
3: 39,037,283 (GRCm39) |
V3645A |
probably benign |
Het |
| G2e3 |
T |
C |
12: 51,419,287 (GRCm39) |
F668L |
possibly damaging |
Het |
| Gm14403 |
T |
A |
2: 177,201,040 (GRCm39) |
C329S |
probably damaging |
Het |
| Hmcn1 |
G |
A |
1: 150,684,448 (GRCm39) |
T374I |
probably benign |
Het |
| Hmcn1 |
A |
T |
1: 150,634,225 (GRCm39) |
|
probably null |
Het |
| Hrnr |
T |
C |
3: 93,230,436 (GRCm39) |
S225P |
unknown |
Het |
| Ifi202b |
C |
T |
1: 173,798,918 (GRCm39) |
|
probably null |
Het |
| Il10ra |
A |
T |
9: 45,167,368 (GRCm39) |
D394E |
possibly damaging |
Het |
| Itga2b |
A |
T |
11: 102,356,735 (GRCm39) |
D275E |
probably benign |
Het |
| Jaml |
A |
T |
9: 45,000,026 (GRCm39) |
D108V |
probably damaging |
Het |
| Kir3dl1 |
G |
A |
X: 135,427,231 (GRCm39) |
D56N |
probably damaging |
Het |
| Lrrtm1 |
T |
C |
6: 77,221,872 (GRCm39) |
V443A |
probably damaging |
Het |
| Mkln1 |
T |
A |
6: 31,473,637 (GRCm39) |
S126R |
probably benign |
Het |
| Myo19 |
T |
C |
11: 84,788,450 (GRCm39) |
I354T |
probably damaging |
Het |
| Nucb1 |
A |
T |
7: 45,151,084 (GRCm39) |
L99Q |
probably damaging |
Het |
| Or4f59 |
A |
G |
2: 111,873,128 (GRCm39) |
F83S |
probably damaging |
Het |
| Pask |
A |
G |
1: 93,249,778 (GRCm39) |
S541P |
probably benign |
Het |
| Pdpr |
A |
T |
8: 111,861,252 (GRCm39) |
I749F |
possibly damaging |
Het |
| Pgap6 |
T |
A |
17: 26,339,425 (GRCm39) |
F580I |
probably damaging |
Het |
| Phyhipl |
T |
C |
10: 70,395,399 (GRCm39) |
D269G |
possibly damaging |
Het |
| Pkdcc |
A |
G |
17: 83,523,223 (GRCm39) |
D110G |
probably benign |
Het |
| Ppox |
A |
G |
1: 171,107,570 (GRCm39) |
L115P |
probably damaging |
Het |
| Ppp1r12c |
A |
G |
7: 4,500,281 (GRCm39) |
L94P |
probably damaging |
Het |
| Ppp6r2 |
T |
A |
15: 89,143,276 (GRCm39) |
M141K |
probably benign |
Het |
| Prl3d1 |
A |
T |
13: 27,283,995 (GRCm39) |
H188L |
probably benign |
Het |
| Psmb3 |
T |
A |
11: 97,604,296 (GRCm39) |
|
probably benign |
Het |
| Pxdn |
T |
A |
12: 30,032,333 (GRCm39) |
S150T |
probably benign |
Het |
| Ripor3 |
T |
C |
2: 167,823,203 (GRCm39) |
T903A |
probably damaging |
Het |
| Rnase4 |
T |
C |
14: 51,342,306 (GRCm39) |
L10S |
probably benign |
Het |
| Rnf224 |
T |
C |
2: 25,126,012 (GRCm39) |
T114A |
probably benign |
Het |
| Rp1l1 |
A |
T |
14: 64,269,619 (GRCm39) |
E1735V |
probably benign |
Het |
| Rrp1b |
T |
A |
17: 32,264,950 (GRCm39) |
Y60N |
probably damaging |
Het |
| Rsbn1l |
A |
T |
5: 21,110,814 (GRCm39) |
V508E |
probably damaging |
Het |
| Rubcnl |
T |
C |
14: 75,278,381 (GRCm39) |
|
probably null |
Het |
| Rxfp4 |
A |
G |
3: 88,559,209 (GRCm39) |
|
probably benign |
Het |
| Sdccag8 |
A |
G |
1: 176,653,797 (GRCm39) |
T85A |
probably benign |
Het |
| Slc46a1 |
A |
T |
11: 78,357,975 (GRCm39) |
I343F |
possibly damaging |
Het |
| Ssh2 |
A |
G |
11: 77,340,639 (GRCm39) |
D597G |
probably damaging |
Het |
| Syne2 |
T |
A |
12: 76,044,239 (GRCm39) |
V3942E |
possibly damaging |
Het |
| Timd4 |
T |
C |
11: 46,708,573 (GRCm39) |
S200P |
probably benign |
Het |
| Tmc5 |
G |
A |
7: 118,265,834 (GRCm39) |
|
probably null |
Het |
| Trbv16 |
A |
G |
6: 41,129,013 (GRCm39) |
T66A |
probably benign |
Het |
| Ttc3 |
A |
T |
16: 94,240,183 (GRCm39) |
K1103* |
probably null |
Het |
| Ttc7b |
A |
G |
12: 100,350,492 (GRCm39) |
V458A |
probably damaging |
Het |
| Ubxn10 |
A |
G |
4: 138,448,134 (GRCm39) |
S181P |
probably benign |
Het |
| Vmn2r11 |
A |
G |
5: 109,207,114 (GRCm39) |
|
probably null |
Het |
| Vmn2r26 |
A |
T |
6: 124,002,925 (GRCm39) |
N112Y |
probably benign |
Het |
| Vmn2r5 |
T |
C |
3: 64,411,497 (GRCm39) |
D357G |
probably damaging |
Het |
| Zc3h10 |
T |
C |
10: 128,380,670 (GRCm39) |
N229S |
probably benign |
Het |
| Zfyve1 |
C |
A |
12: 83,621,910 (GRCm39) |
V162L |
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 |
|
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 |
|
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'- TGCTCCCCACAATGGTACTC -3'
(R):5'- CCAGCTCTCCAGAGATTCTG -3'
Sequencing Primer
(F):5'- CCACAATGGTACTCGAGGG -3'
(R):5'- TCTCCAGAGATTCTGCAGGCTG -3'
|
| Posted On |
2016-11-21 |
Incidental Mutation