Incidental Mutation 'R1698:Zfp407'
| ID |
192457 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp407
|
| Ensembl Gene |
ENSMUSG00000048410 |
| Gene Name |
zinc finger protein 407 |
| Synonyms |
LOC381139, 6430585N13Rik, LOC240469 |
| MMRRC Submission |
039731-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1698 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
18 |
| Chromosomal Location |
84225826-84612815 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 84580282 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 277
(T277I)
|
| 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: T277I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000118361
Gene: ENSMUSG00000048410
AA Change: T277I
| 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 |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156181
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182297
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.6%
|
| Validation Efficiency |
|
| 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: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2m |
A |
C |
6: 121,622,117 (GRCm39) |
E340A |
possibly damaging |
Het |
| Abca13 |
A |
G |
11: 9,264,507 (GRCm39) |
D2963G |
probably benign |
Het |
| Actn3 |
T |
C |
19: 4,912,235 (GRCm39) |
D783G |
possibly damaging |
Het |
| Adamtsl2 |
A |
G |
2: 26,993,139 (GRCm39) |
E723G |
possibly damaging |
Het |
| Agrn |
G |
T |
4: 156,251,015 (GRCm39) |
Q1931K |
probably benign |
Het |
| Ankrd27 |
G |
A |
7: 35,313,946 (GRCm39) |
A426T |
probably benign |
Het |
| Atg9b |
C |
A |
5: 24,593,186 (GRCm39) |
G406C |
probably damaging |
Het |
| C1ra |
A |
T |
6: 124,499,725 (GRCm39) |
Q637L |
probably benign |
Het |
| Cdhr2 |
A |
T |
13: 54,867,394 (GRCm39) |
M438L |
probably benign |
Het |
| Cep350 |
T |
C |
1: 155,829,104 (GRCm39) |
I267V |
possibly damaging |
Het |
| Chrna5 |
A |
G |
9: 54,911,926 (GRCm39) |
Y138C |
probably damaging |
Het |
| Chst3 |
T |
A |
10: 60,021,525 (GRCm39) |
M441L |
probably benign |
Het |
| Cmya5 |
G |
A |
13: 93,200,027 (GRCm39) |
P3434S |
probably benign |
Het |
| Cog2 |
T |
A |
8: 125,252,422 (GRCm39) |
L42Q |
probably damaging |
Het |
| Cpq |
A |
T |
15: 33,250,272 (GRCm39) |
I210F |
probably benign |
Het |
| Crnn |
C |
A |
3: 93,055,765 (GRCm39) |
Q184K |
probably damaging |
Het |
| Csnka2ip |
A |
T |
16: 64,298,422 (GRCm39) |
Y647* |
probably null |
Het |
| D5Ertd579e |
C |
T |
5: 36,761,874 (GRCm39) |
R1331H |
probably benign |
Het |
| Dennd5a |
C |
T |
7: 109,516,587 (GRCm39) |
|
probably null |
Het |
| Dync1h1 |
A |
G |
12: 110,593,426 (GRCm39) |
Q1231R |
possibly damaging |
Het |
| Erbin |
T |
A |
13: 103,970,239 (GRCm39) |
I1126F |
possibly damaging |
Het |
| Fastkd1 |
T |
C |
2: 69,532,813 (GRCm39) |
D518G |
probably benign |
Het |
| Gcc1 |
A |
G |
6: 28,421,110 (GRCm39) |
L69P |
possibly damaging |
Het |
| Gkn1 |
T |
C |
6: 87,324,151 (GRCm39) |
Y119C |
probably damaging |
Het |
| Gmpr |
T |
G |
13: 45,670,520 (GRCm39) |
W81G |
probably benign |
Het |
| Gyg1 |
T |
A |
3: 20,192,215 (GRCm39) |
I236F |
probably benign |
Het |
| Hcrtr2 |
T |
C |
9: 76,153,735 (GRCm39) |
Y219C |
probably damaging |
Het |
| Hmcn1 |
G |
A |
1: 150,441,120 (GRCm39) |
Q5379* |
probably null |
Het |
| Kank1 |
T |
C |
19: 25,388,681 (GRCm39) |
C785R |
probably benign |
Het |
| Lrp1b |
A |
T |
2: 40,741,818 (GRCm39) |
C3036* |
probably null |
Het |
| Mdga2 |
T |
C |
12: 66,736,109 (GRCm39) |
D373G |
probably damaging |
Het |
| Mgat2 |
A |
T |
12: 69,232,493 (GRCm39) |
I356F |
probably benign |
Het |
| Miga2 |
A |
G |
2: 30,268,009 (GRCm39) |
D346G |
probably damaging |
Het |
| Mprip |
T |
A |
11: 59,651,084 (GRCm39) |
L1596Q |
possibly damaging |
Het |
| Mroh2b |
G |
A |
15: 4,943,622 (GRCm39) |
R386Q |
probably benign |
Het |
| Mst1r |
T |
A |
9: 107,797,179 (GRCm39) |
S1349R |
probably benign |
Het |
| Mtmr3 |
C |
T |
11: 4,442,825 (GRCm39) |
R403H |
possibly damaging |
Het |
| Mycbpap |
G |
A |
11: 94,398,969 (GRCm39) |
Q460* |
probably null |
Het |
| Myo9a |
T |
C |
9: 59,775,464 (GRCm39) |
V1025A |
probably benign |
Het |
| Ncapd2 |
C |
T |
6: 125,145,553 (GRCm39) |
E1365K |
probably null |
Het |
| Nkiras2 |
C |
A |
11: 100,515,989 (GRCm39) |
D105E |
probably damaging |
Het |
| Nolc1 |
T |
G |
19: 46,069,870 (GRCm39) |
|
probably null |
Het |
| Nos1 |
T |
C |
5: 118,005,297 (GRCm39) |
F6L |
probably benign |
Het |
| Or10j3 |
A |
T |
1: 173,030,938 (GRCm39) |
N5I |
probably damaging |
Het |
| Or12e1 |
G |
T |
2: 87,022,081 (GRCm39) |
V17L |
probably benign |
Het |
| Or2t46 |
T |
C |
11: 58,472,077 (GRCm39) |
Y136H |
probably damaging |
Het |
| Or2w1b |
C |
T |
13: 21,300,735 (GRCm39) |
T291I |
probably benign |
Het |
| Or4f54 |
T |
A |
2: 111,122,905 (GRCm39) |
C97* |
probably null |
Het |
| Or8b46 |
T |
A |
9: 38,450,552 (GRCm39) |
Y120* |
probably null |
Het |
| Pfkm |
A |
G |
15: 98,026,199 (GRCm39) |
E598G |
possibly damaging |
Het |
| Phf2 |
A |
T |
13: 48,961,106 (GRCm39) |
D861E |
unknown |
Het |
| Polr2a |
A |
G |
11: 69,630,703 (GRCm39) |
|
probably null |
Het |
| Popdc2 |
G |
A |
16: 38,189,853 (GRCm39) |
V167M |
probably damaging |
Het |
| Ptpn22 |
T |
C |
3: 103,793,114 (GRCm39) |
S422P |
probably benign |
Het |
| Rasa2 |
T |
C |
9: 96,450,428 (GRCm39) |
K490R |
possibly damaging |
Het |
| Rbfox3 |
T |
A |
11: 118,386,047 (GRCm39) |
D286V |
probably damaging |
Het |
| Rdh13 |
A |
G |
7: 4,430,790 (GRCm39) |
W223R |
probably damaging |
Het |
| Riok3 |
T |
C |
18: 12,261,986 (GRCm39) |
S7P |
probably benign |
Het |
| Rnaseh2b |
A |
G |
14: 62,591,081 (GRCm39) |
E144G |
probably benign |
Het |
| Rnf20 |
C |
T |
4: 49,651,498 (GRCm39) |
Q655* |
probably null |
Het |
| Rpap2 |
T |
C |
5: 107,751,416 (GRCm39) |
Y8H |
probably damaging |
Het |
| Slc5a10 |
T |
C |
11: 61,600,428 (GRCm39) |
Y181C |
probably benign |
Het |
| Snd1 |
G |
T |
6: 28,888,252 (GRCm39) |
G896* |
probably null |
Het |
| Spast |
C |
T |
17: 74,663,155 (GRCm39) |
Q158* |
probably null |
Het |
| Tas2r104 |
G |
A |
6: 131,662,547 (GRCm39) |
S54F |
probably damaging |
Het |
| Tcaf2 |
C |
T |
6: 42,604,951 (GRCm39) |
W611* |
probably null |
Het |
| Thoc2l |
C |
T |
5: 104,668,376 (GRCm39) |
A966V |
probably benign |
Het |
| Timp4 |
G |
A |
6: 115,227,364 (GRCm39) |
|
probably null |
Het |
| Tmem45a |
G |
A |
16: 56,643,933 (GRCm39) |
S72L |
probably benign |
Het |
| Tnrc18 |
T |
C |
5: 142,774,458 (GRCm39) |
T124A |
possibly damaging |
Het |
| Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
| Ttn |
T |
C |
2: 76,773,259 (GRCm39) |
D2381G |
probably damaging |
Het |
| Uevld |
T |
C |
7: 46,605,372 (GRCm39) |
T41A |
possibly damaging |
Het |
| Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
| Unc5d |
T |
C |
8: 29,186,506 (GRCm39) |
E527G |
probably damaging |
Het |
| Vmn2r125 |
C |
T |
4: 156,703,333 (GRCm39) |
T237I |
probably benign |
Het |
| Vmn2r63 |
A |
C |
7: 42,583,038 (GRCm39) |
I59S |
probably benign |
Het |
| Vps72 |
G |
A |
3: 95,026,006 (GRCm39) |
S106N |
probably benign |
Het |
| Zan |
A |
C |
5: 137,407,931 (GRCm39) |
|
probably benign |
Het |
| Zbtb38 |
T |
C |
9: 96,567,515 (GRCm39) |
K1190E |
probably benign |
Het |
| Zc3h6 |
T |
C |
2: 128,859,278 (GRCm39) |
V1103A |
probably benign |
Het |
| Zfp804b |
A |
G |
5: 6,819,509 (GRCm39) |
S1149P |
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 |
|
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 |
|
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'- AGGAGGTTTCGCTCAGATCTTGGC -3'
(R):5'- GCTTTGGAAAAGCATGTGGAGTGTC -3'
Sequencing Primer
(F):5'- GTACTGATACTGACATGCGCC -3'
(R):5'- TGCCACTGTAGCCACAGAG -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation