Incidental Mutation 'R5806:Zfp407'
| ID |
448551 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp407
|
| Ensembl Gene |
ENSMUSG00000048410 |
| Gene Name |
zinc finger protein 407 |
| Synonyms |
LOC381139, 6430585N13Rik, LOC240469 |
| MMRRC Submission |
043392-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R5806 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
18 |
| Chromosomal Location |
84225826-84612815 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 84576739 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Aspartic acid
at position 1458
(G1458D)
|
| 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: G1458D
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000118361
Gene: ENSMUSG00000048410
AA Change: G1458D
| 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: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.5%
|
| 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: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A930011G23Rik |
A |
G |
5: 99,388,731 (GRCm39) |
M216T |
probably benign |
Het |
| Abhd4 |
A |
G |
14: 54,499,147 (GRCm39) |
N36D |
probably benign |
Het |
| Ankra2 |
T |
C |
13: 98,405,005 (GRCm39) |
|
probably null |
Het |
| Btd |
A |
G |
14: 31,389,469 (GRCm39) |
T397A |
probably benign |
Het |
| Ccbe1 |
T |
A |
18: 66,209,426 (GRCm39) |
K205* |
probably null |
Het |
| Clspn |
A |
G |
4: 126,479,899 (GRCm39) |
K1081E |
probably damaging |
Het |
| Cmya5 |
A |
G |
13: 93,230,445 (GRCm39) |
S1548P |
possibly damaging |
Het |
| Coq8b |
T |
A |
7: 26,950,050 (GRCm39) |
Y376* |
probably null |
Het |
| Cpxm1 |
C |
A |
2: 130,239,393 (GRCm39) |
A12S |
probably damaging |
Het |
| Cttn |
T |
C |
7: 144,015,005 (GRCm39) |
T68A |
probably damaging |
Het |
| Cyp2a12 |
T |
A |
7: 26,728,504 (GRCm39) |
|
probably null |
Het |
| Ddx46 |
A |
G |
13: 55,811,150 (GRCm39) |
Q582R |
possibly damaging |
Het |
| Ddx55 |
A |
G |
5: 124,697,262 (GRCm39) |
E208G |
probably damaging |
Het |
| Dnaaf4 |
T |
C |
9: 72,869,336 (GRCm39) |
L182P |
probably benign |
Het |
| Dync1h1 |
A |
T |
12: 110,618,087 (GRCm39) |
T3209S |
probably damaging |
Het |
| Ep400 |
A |
T |
5: 110,903,420 (GRCm39) |
L393* |
probably null |
Het |
| Ern1 |
G |
C |
11: 106,289,531 (GRCm39) |
S924C |
probably damaging |
Het |
| Fanci |
T |
C |
7: 79,098,596 (GRCm39) |
I1249T |
probably damaging |
Het |
| Fgfbp3 |
T |
G |
19: 36,895,949 (GRCm39) |
D223A |
probably damaging |
Het |
| Frmd6 |
T |
C |
12: 70,936,794 (GRCm39) |
L313P |
probably damaging |
Het |
| Galnt17 |
A |
G |
5: 130,906,657 (GRCm39) |
Y504H |
probably damaging |
Het |
| Gjb5 |
A |
G |
4: 127,249,718 (GRCm39) |
I142T |
probably benign |
Het |
| Gvin1 |
T |
C |
7: 105,757,413 (GRCm39) |
D2352G |
probably benign |
Het |
| H2-M2 |
G |
A |
17: 37,792,617 (GRCm39) |
T218I |
probably damaging |
Het |
| Hal |
A |
G |
10: 93,326,846 (GRCm39) |
T161A |
probably damaging |
Het |
| Helb |
G |
A |
10: 119,928,424 (GRCm39) |
R806C |
probably damaging |
Het |
| Ift80 |
T |
A |
3: 68,857,809 (GRCm39) |
I279F |
probably benign |
Het |
| Itln1 |
A |
T |
1: 171,358,720 (GRCm39) |
I149N |
possibly damaging |
Het |
| Kcnt2 |
A |
C |
1: 140,437,234 (GRCm39) |
T556P |
probably damaging |
Het |
| Klk1b22 |
A |
T |
7: 43,765,301 (GRCm39) |
E84D |
possibly damaging |
Het |
| Krt78 |
A |
G |
15: 101,858,937 (GRCm39) |
L305P |
probably damaging |
Het |
| Lzts2 |
T |
C |
19: 45,014,806 (GRCm39) |
|
probably benign |
Het |
| Macf1 |
A |
G |
4: 123,265,680 (GRCm39) |
L6843P |
probably damaging |
Het |
| Magi2 |
C |
A |
5: 20,856,202 (GRCm39) |
H841Q |
probably benign |
Het |
| Mdm1 |
A |
T |
10: 118,002,563 (GRCm39) |
H628L |
probably benign |
Het |
| Med23 |
A |
G |
10: 24,783,119 (GRCm39) |
D734G |
probably damaging |
Het |
| Mfsd13a |
T |
C |
19: 46,354,849 (GRCm39) |
W9R |
probably benign |
Het |
| Mki67 |
T |
C |
7: 135,306,334 (GRCm39) |
H576R |
probably damaging |
Het |
| Muc5b |
A |
G |
7: 141,416,572 (GRCm39) |
T3173A |
possibly damaging |
Het |
| Mx1 |
A |
T |
16: 97,255,351 (GRCm39) |
V234E |
possibly damaging |
Het |
| Myh2 |
T |
C |
11: 67,072,141 (GRCm39) |
L623P |
probably damaging |
Het |
| Naip1 |
C |
T |
13: 100,581,243 (GRCm39) |
M1I |
probably null |
Het |
| Ncapd2 |
A |
T |
6: 125,158,117 (GRCm39) |
V337E |
probably damaging |
Het |
| Nit2 |
G |
A |
16: 56,982,056 (GRCm39) |
T64M |
possibly damaging |
Het |
| Or1e34 |
A |
T |
11: 73,778,373 (GRCm39) |
M275K |
probably damaging |
Het |
| Or4c103 |
T |
C |
2: 88,513,495 (GRCm39) |
N194D |
probably damaging |
Het |
| Or6e1 |
A |
T |
14: 54,520,264 (GRCm39) |
F29L |
probably benign |
Het |
| Otub2 |
A |
G |
12: 103,369,656 (GRCm39) |
E245G |
probably benign |
Het |
| Pde8b |
T |
C |
13: 95,178,548 (GRCm39) |
K524R |
probably damaging |
Het |
| Pih1d2 |
C |
T |
9: 50,529,750 (GRCm39) |
|
probably benign |
Het |
| Pik3cg |
T |
A |
12: 32,254,952 (GRCm39) |
D345V |
possibly damaging |
Het |
| Plekhg4 |
A |
T |
8: 106,105,542 (GRCm39) |
Q669L |
possibly damaging |
Het |
| Prlr |
A |
T |
15: 10,319,290 (GRCm39) |
Y73F |
probably damaging |
Het |
| Ptk6 |
T |
C |
2: 180,841,523 (GRCm39) |
I129V |
possibly damaging |
Het |
| Ranbp3 |
A |
T |
17: 57,017,717 (GRCm39) |
T458S |
probably benign |
Het |
| Ren1 |
T |
A |
1: 133,283,249 (GRCm39) |
Y128* |
probably null |
Het |
| Rimkla |
A |
T |
4: 119,325,663 (GRCm39) |
S249T |
probably damaging |
Het |
| Rnf222 |
T |
C |
11: 68,783,789 (GRCm39) |
S119P |
possibly damaging |
Het |
| Rrbp1 |
T |
A |
2: 143,805,251 (GRCm39) |
E1007V |
probably benign |
Het |
| Septin11 |
G |
A |
5: 93,315,437 (GRCm39) |
E389K |
probably benign |
Het |
| Setbp1 |
A |
G |
18: 78,899,697 (GRCm39) |
|
probably null |
Het |
| Slc25a54 |
T |
C |
3: 108,987,894 (GRCm39) |
S12P |
probably benign |
Het |
| Slc26a5 |
A |
C |
5: 22,028,561 (GRCm39) |
F336V |
probably damaging |
Het |
| Slc5a6 |
T |
C |
5: 31,198,114 (GRCm39) |
T254A |
probably damaging |
Het |
| Smcr8 |
G |
T |
11: 60,671,208 (GRCm39) |
|
probably null |
Het |
| Srcap |
A |
T |
7: 127,158,335 (GRCm39) |
|
probably benign |
Het |
| Srrt |
A |
T |
5: 137,296,179 (GRCm39) |
I509N |
probably damaging |
Het |
| Tcf25 |
T |
A |
8: 124,108,243 (GRCm39) |
H99Q |
probably benign |
Het |
| Tmem40 |
A |
G |
6: 115,713,373 (GRCm39) |
V76A |
probably benign |
Het |
| Tnni3k |
A |
T |
3: 154,533,248 (GRCm39) |
S740T |
possibly damaging |
Het |
| Top3a |
A |
G |
11: 60,667,746 (GRCm39) |
|
probably null |
Het |
| Tpd52l2 |
C |
A |
2: 181,144,680 (GRCm39) |
T109K |
probably damaging |
Het |
| Tsnaxip1 |
C |
A |
8: 106,564,128 (GRCm39) |
D109E |
possibly damaging |
Het |
| Uty |
G |
T |
Y: 1,170,921 (GRCm39) |
D313E |
probably damaging |
Het |
| Zfp143 |
A |
T |
7: 109,685,442 (GRCm39) |
K423* |
probably null |
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 |
|
|
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'- GCTCGGTGTCTTCCACTATG -3'
(R):5'- TGAAAGACTGTGCTCAGGGG -3'
Sequencing Primer
(F):5'- ATGTACTTGTTTACCTCCCGCAG -3'
(R):5'- CTGTGCTCAGGGGTTGAAGAAG -3'
|
| Posted On |
2016-12-15 |
Incidental Mutation