Incidental Mutation 'R6306:Zfp644'
| ID |
509648 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zfp644
|
| Ensembl Gene |
ENSMUSG00000049606 |
| Gene Name |
zinc finger protein 644 |
| Synonyms |
BM-005, Zep-2, D5Ertd689e, 1110068L01Rik |
| MMRRC Submission |
044468-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.299)
|
| Stock # |
R6306 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
5 |
| Chromosomal Location |
106764605-106844696 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 106785990 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Aspartic acid
at position 186
(N186D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118856
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045466]
[ENSMUST00000112695]
[ENSMUST00000112696]
[ENSMUST00000112698]
[ENSMUST00000122980]
[ENSMUST00000124263]
[ENSMUST00000127434]
[ENSMUST00000137285]
[ENSMUST00000155495]
[ENSMUST00000135108]
|
| AlphaFold |
E9QA22 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000045466
AA Change: N186D
PolyPhen 2
Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000038047
Gene: ENSMUSG00000049606
AA Change: N186D
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
411 |
433 |
1.89e-1 |
SMART |
|
ZnF_C2H2
|
449 |
471 |
6.52e-5 |
SMART |
|
ZnF_C2H2
|
497 |
519 |
1.99e0 |
SMART |
|
ZnF_C2H2
|
526 |
549 |
6.4e0 |
SMART |
|
ZnF_C2H2
|
587 |
610 |
3.72e0 |
SMART |
|
low complexity region
|
668 |
676 |
N/A |
INTRINSIC |
|
low complexity region
|
771 |
788 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
928 |
950 |
1.07e0 |
SMART |
|
ZnF_C2H2
|
1003 |
1025 |
1.43e-1 |
SMART |
|
low complexity region
|
1199 |
1212 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1226 |
1252 |
5.4e1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000112695
|
| SMART Domains |
Protein: ENSMUSP00000108315
Gene: ENSMUSG00000049606
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
12 |
25 |
N/A |
INTRINSIC |
|
Blast:ZnF_C2H2
|
39 |
65 |
2e-14 |
BLAST |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000112696
AA Change: N186D
PolyPhen 2
Score 0.525 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000108316
Gene: ENSMUSG00000049606
AA Change: N186D
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
411 |
433 |
1.89e-1 |
SMART |
|
ZnF_C2H2
|
449 |
471 |
6.52e-5 |
SMART |
|
ZnF_C2H2
|
497 |
519 |
1.99e0 |
SMART |
|
ZnF_C2H2
|
526 |
549 |
6.4e0 |
SMART |
|
ZnF_C2H2
|
587 |
610 |
3.72e0 |
SMART |
|
low complexity region
|
668 |
676 |
N/A |
INTRINSIC |
|
low complexity region
|
767 |
783 |
N/A |
INTRINSIC |
|
low complexity region
|
802 |
819 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
959 |
981 |
1.07e0 |
SMART |
|
ZnF_C2H2
|
1034 |
1056 |
1.43e-1 |
SMART |
|
low complexity region
|
1230 |
1243 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1257 |
1283 |
5.4e1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000112698
AA Change: N186D
PolyPhen 2
Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000108318
Gene: ENSMUSG00000049606
AA Change: N186D
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
411 |
433 |
1.89e-1 |
SMART |
|
ZnF_C2H2
|
449 |
471 |
6.52e-5 |
SMART |
|
ZnF_C2H2
|
497 |
519 |
1.99e0 |
SMART |
|
ZnF_C2H2
|
526 |
549 |
6.4e0 |
SMART |
|
ZnF_C2H2
|
587 |
610 |
3.72e0 |
SMART |
|
low complexity region
|
668 |
676 |
N/A |
INTRINSIC |
|
low complexity region
|
771 |
788 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
928 |
950 |
1.07e0 |
SMART |
|
ZnF_C2H2
|
1003 |
1025 |
1.43e-1 |
SMART |
|
low complexity region
|
1199 |
1212 |
N/A |
INTRINSIC |
|
ZnF_C2H2
|
1226 |
1252 |
5.4e1 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000122980
AA Change: N186D
PolyPhen 2
Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124263
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125895
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127434
AA Change: N186D
PolyPhen 2
Score 0.039 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000122421
Gene: ENSMUSG00000049606
AA Change: N186D
| Domain | Start | End | E-Value | Type |
|---|
|
ZnF_C2H2
|
411 |
433 |
1.89e-1 |
SMART |
|
ZnF_C2H2
|
449 |
471 |
6.52e-5 |
SMART |
|
ZnF_C2H2
|
497 |
519 |
1.99e0 |
SMART |
|
ZnF_C2H2
|
526 |
549 |
6.4e0 |
SMART |
|
ZnF_C2H2
|
587 |
610 |
3.72e0 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000137285
AA Change: N186D
PolyPhen 2
Score 0.211 (Sensitivity: 0.92; Specificity: 0.88)
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149128
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000155495
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135108
|
| Meta Mutation Damage Score |
0.1209 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.4%
|
| Validation Efficiency |
100% (88/88) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a zinc finger transcription factor that may play a role in eye development. Defects in this gene have been associated with high myopia. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
PHENOTYPE: Mice homozygous for an ENU-induced allele exhibit normal blood lymphocyte populations. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts7 |
G |
A |
9: 90,060,331 (GRCm39) |
|
probably null |
Het |
| Adora2a |
T |
A |
10: 75,169,238 (GRCm39) |
V234E |
probably damaging |
Het |
| Alpk1 |
T |
C |
3: 127,479,965 (GRCm39) |
D188G |
probably damaging |
Het |
| Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
| Ankrd17 |
A |
G |
5: 90,392,013 (GRCm39) |
F1886L |
probably benign |
Het |
| Anks1 |
T |
G |
17: 28,269,613 (GRCm39) |
L769R |
probably damaging |
Het |
| Apol10a |
A |
G |
15: 77,373,161 (GRCm39) |
I266V |
probably benign |
Het |
| Arhgef28 |
T |
C |
13: 98,121,896 (GRCm39) |
Y556C |
probably damaging |
Het |
| Brd8 |
T |
A |
18: 34,744,304 (GRCm39) |
T175S |
probably damaging |
Het |
| Camsap2 |
C |
T |
1: 136,208,937 (GRCm39) |
V852I |
probably benign |
Het |
| Cd55b |
G |
T |
1: 130,341,803 (GRCm39) |
P278Q |
probably damaging |
Het |
| Cep290 |
T |
A |
10: 100,367,028 (GRCm39) |
S1126R |
possibly damaging |
Het |
| Cfh |
C |
T |
1: 140,030,155 (GRCm39) |
C906Y |
probably damaging |
Het |
| Chst13 |
C |
A |
6: 90,286,260 (GRCm39) |
R234L |
probably damaging |
Het |
| Clcn7 |
T |
C |
17: 25,376,502 (GRCm39) |
F611L |
probably benign |
Het |
| Cntnap1 |
A |
G |
11: 101,075,441 (GRCm39) |
D873G |
probably damaging |
Het |
| Cntnap5b |
T |
C |
1: 100,091,871 (GRCm39) |
I518T |
probably damaging |
Het |
| Col28a1 |
T |
C |
6: 8,014,969 (GRCm39) |
E812G |
probably damaging |
Het |
| Cpa1 |
T |
C |
6: 30,640,953 (GRCm39) |
I148T |
probably damaging |
Het |
| Cyp11a1 |
A |
G |
9: 57,932,383 (GRCm39) |
N232S |
probably benign |
Het |
| Dhrs13 |
A |
G |
11: 77,923,519 (GRCm39) |
D79G |
probably damaging |
Het |
| Disp1 |
T |
C |
1: 182,868,712 (GRCm39) |
E1236G |
possibly damaging |
Het |
| Dnah1 |
A |
C |
14: 31,026,544 (GRCm39) |
L778R |
probably damaging |
Het |
| Dnah14 |
CTGTG |
CTG |
1: 181,412,589 (GRCm39) |
|
probably null |
Het |
| Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
| Dock9 |
A |
T |
14: 121,799,492 (GRCm39) |
I1729N |
probably damaging |
Het |
| Dysf |
T |
C |
6: 84,114,248 (GRCm39) |
V1192A |
possibly damaging |
Het |
| Enpp2 |
A |
G |
15: 54,762,742 (GRCm39) |
S169P |
probably damaging |
Het |
| Fam114a2 |
T |
G |
11: 57,404,972 (GRCm39) |
R43S |
probably damaging |
Het |
| Fam13a |
T |
C |
6: 58,917,239 (GRCm39) |
T546A |
probably benign |
Het |
| Fos |
A |
T |
12: 85,522,460 (GRCm39) |
D163V |
probably damaging |
Het |
| Fras1 |
T |
C |
5: 96,912,805 (GRCm39) |
Y3370H |
probably damaging |
Het |
| Fshr |
T |
C |
17: 89,507,961 (GRCm39) |
N27S |
probably null |
Het |
| Galnt6 |
A |
G |
15: 100,591,305 (GRCm39) |
S600P |
possibly damaging |
Het |
| Gars1 |
T |
A |
6: 55,032,809 (GRCm39) |
N260K |
probably damaging |
Het |
| Gpr158 |
C |
G |
2: 21,820,422 (GRCm39) |
P640A |
possibly damaging |
Het |
| Grep1 |
T |
C |
17: 23,925,124 (GRCm39) |
N495S |
possibly damaging |
Het |
| Grik3 |
A |
G |
4: 125,526,205 (GRCm39) |
D146G |
probably benign |
Het |
| Hdac4 |
T |
C |
1: 91,923,896 (GRCm39) |
T205A |
probably benign |
Het |
| Kcnq3 |
T |
C |
15: 65,876,643 (GRCm39) |
D500G |
probably benign |
Het |
| Kmt5c |
A |
G |
7: 4,749,480 (GRCm39) |
K333E |
probably benign |
Het |
| Krt81 |
A |
G |
15: 101,357,404 (GRCm39) |
S443P |
probably benign |
Het |
| M6pr |
T |
C |
6: 122,292,121 (GRCm39) |
|
probably null |
Het |
| Mccc2 |
T |
A |
13: 100,130,085 (GRCm39) |
I91L |
probably benign |
Het |
| Nip7 |
A |
G |
8: 107,785,055 (GRCm39) |
D110G |
probably damaging |
Het |
| Nol8 |
T |
A |
13: 49,829,829 (GRCm39) |
F1093I |
probably damaging |
Het |
| Nrxn1 |
T |
C |
17: 90,872,874 (GRCm39) |
T1027A |
possibly damaging |
Het |
| Ofcc1 |
T |
A |
13: 40,302,052 (GRCm39) |
M495L |
probably benign |
Het |
| Or13p10 |
A |
T |
4: 118,523,490 (GRCm39) |
M259L |
probably benign |
Het |
| Or7e178 |
A |
G |
9: 20,225,742 (GRCm39) |
M158T |
probably benign |
Het |
| Pafah1b2 |
A |
T |
9: 45,886,425 (GRCm39) |
V81D |
probably damaging |
Het |
| Pcdhga4 |
A |
T |
18: 37,818,966 (GRCm39) |
S172C |
probably damaging |
Het |
| Pds5a |
A |
G |
5: 65,813,639 (GRCm39) |
V282A |
probably damaging |
Het |
| Plat |
A |
G |
8: 23,262,282 (GRCm39) |
D102G |
possibly damaging |
Het |
| Plce1 |
C |
A |
19: 38,757,909 (GRCm39) |
Q1961K |
probably damaging |
Het |
| Plppr3 |
T |
A |
10: 79,697,566 (GRCm39) |
K444* |
probably null |
Het |
| Plscr3 |
A |
G |
11: 69,738,472 (GRCm39) |
|
probably null |
Het |
| Prtg |
A |
T |
9: 72,813,468 (GRCm39) |
T943S |
probably benign |
Het |
| Racgap1 |
A |
G |
15: 99,521,834 (GRCm39) |
F519L |
probably benign |
Het |
| Rbms2 |
A |
T |
10: 127,987,050 (GRCm39) |
|
probably null |
Het |
| Rfx7 |
A |
G |
9: 72,524,237 (GRCm39) |
T476A |
possibly damaging |
Het |
| Rnf150 |
T |
A |
8: 83,810,131 (GRCm39) |
L421Q |
possibly damaging |
Het |
| Sema3b |
A |
G |
9: 107,478,119 (GRCm39) |
L422P |
possibly damaging |
Het |
| Shank2 |
G |
A |
7: 143,963,417 (GRCm39) |
A921T |
probably benign |
Het |
| Skint3 |
A |
T |
4: 112,113,072 (GRCm39) |
E227D |
probably damaging |
Het |
| Slc25a19 |
G |
A |
11: 115,508,386 (GRCm39) |
R201C |
possibly damaging |
Het |
| Slc38a10 |
G |
T |
11: 120,038,645 (GRCm39) |
A40D |
probably damaging |
Het |
| Slc5a4b |
T |
C |
10: 75,917,185 (GRCm39) |
T284A |
probably benign |
Het |
| Smc1b |
A |
T |
15: 85,011,824 (GRCm39) |
F154I |
probably benign |
Het |
| Spry2 |
A |
T |
14: 106,130,418 (GRCm39) |
M256K |
possibly damaging |
Het |
| Stkld1 |
C |
T |
2: 26,833,899 (GRCm39) |
P129S |
probably damaging |
Het |
| Syce2 |
T |
C |
8: 85,599,371 (GRCm39) |
L13S |
possibly damaging |
Het |
| Tbc1d15 |
C |
A |
10: 115,069,148 (GRCm39) |
V74L |
possibly damaging |
Het |
| Tecpr2 |
T |
A |
12: 110,911,185 (GRCm39) |
V1074D |
probably damaging |
Het |
| Tex36 |
G |
A |
7: 133,197,054 (GRCm39) |
T21I |
probably benign |
Het |
| Ttn |
T |
G |
2: 76,554,454 (GRCm39) |
D30787A |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,622,264 (GRCm39) |
Q13710L |
probably benign |
Het |
| Usp34 |
T |
C |
11: 23,362,260 (GRCm39) |
F1569L |
possibly damaging |
Het |
| Vat1l |
C |
T |
8: 115,098,391 (GRCm39) |
A387V |
probably damaging |
Het |
| Vil1 |
G |
A |
1: 74,460,470 (GRCm39) |
G209D |
possibly damaging |
Het |
| Vmn1r113 |
G |
T |
7: 20,521,792 (GRCm39) |
D195Y |
probably damaging |
Het |
| Vmn2r69 |
A |
C |
7: 85,064,799 (GRCm39) |
I29R |
probably benign |
Het |
| Vti1b |
G |
A |
12: 79,207,323 (GRCm39) |
Q76* |
probably null |
Het |
| Zfp423 |
C |
A |
8: 88,508,662 (GRCm39) |
V540F |
possibly damaging |
Het |
| Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
| Zfp787 |
G |
A |
7: 6,135,360 (GRCm39) |
A297V |
probably damaging |
Het |
| Zfp827 |
G |
T |
8: 79,787,324 (GRCm39) |
Q163H |
probably damaging |
Het |
| Zfp955b |
T |
A |
17: 33,522,160 (GRCm39) |
V543E |
probably benign |
Het |
|
| Other mutations in Zfp644 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00963:Zfp644
|
APN |
5 |
106,786,503 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01654:Zfp644
|
APN |
5 |
106,783,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01967:Zfp644
|
APN |
5 |
106,786,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02132:Zfp644
|
APN |
5 |
106,783,760 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL02164:Zfp644
|
APN |
5 |
106,785,965 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02303:Zfp644
|
APN |
5 |
106,785,180 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03091:Zfp644
|
APN |
5 |
106,784,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03102:Zfp644
|
APN |
5 |
106,785,134 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03298:Zfp644
|
APN |
5 |
106,782,967 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
PIT4466001:Zfp644
|
UTSW |
5 |
106,784,343 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0012:Zfp644
|
UTSW |
5 |
106,782,909 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0012:Zfp644
|
UTSW |
5 |
106,782,909 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0038:Zfp644
|
UTSW |
5 |
106,782,909 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0038:Zfp644
|
UTSW |
5 |
106,782,909 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0058:Zfp644
|
UTSW |
5 |
106,784,869 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0058:Zfp644
|
UTSW |
5 |
106,784,869 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0178:Zfp644
|
UTSW |
5 |
106,784,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0497:Zfp644
|
UTSW |
5 |
106,786,199 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1302:Zfp644
|
UTSW |
5 |
106,782,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1337:Zfp644
|
UTSW |
5 |
106,785,420 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1400:Zfp644
|
UTSW |
5 |
106,785,336 (GRCm39) |
splice site |
probably null |
|
|
R1597:Zfp644
|
UTSW |
5 |
106,786,199 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1911:Zfp644
|
UTSW |
5 |
106,783,137 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2021:Zfp644
|
UTSW |
5 |
106,783,548 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R2196:Zfp644
|
UTSW |
5 |
106,786,469 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
|
R2256:Zfp644
|
UTSW |
5 |
106,783,711 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2311:Zfp644
|
UTSW |
5 |
106,782,822 (GRCm39) |
missense |
probably benign |
0.21 |
|
R2420:Zfp644
|
UTSW |
5 |
106,785,110 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2421:Zfp644
|
UTSW |
5 |
106,785,110 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2422:Zfp644
|
UTSW |
5 |
106,785,110 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3752:Zfp644
|
UTSW |
5 |
106,784,249 (GRCm39) |
missense |
probably benign |
|
|
R4207:Zfp644
|
UTSW |
5 |
106,766,142 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4285:Zfp644
|
UTSW |
5 |
106,782,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4874:Zfp644
|
UTSW |
5 |
106,783,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4961:Zfp644
|
UTSW |
5 |
106,766,081 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4984:Zfp644
|
UTSW |
5 |
106,784,783 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R5007:Zfp644
|
UTSW |
5 |
106,783,867 (GRCm39) |
missense |
probably benign |
|
|
R5358:Zfp644
|
UTSW |
5 |
106,783,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5382:Zfp644
|
UTSW |
5 |
106,782,735 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R5416:Zfp644
|
UTSW |
5 |
106,766,294 (GRCm39) |
splice site |
silent |
|
|
R5641:Zfp644
|
UTSW |
5 |
106,767,461 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5656:Zfp644
|
UTSW |
5 |
106,785,848 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5732:Zfp644
|
UTSW |
5 |
106,784,989 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6039:Zfp644
|
UTSW |
5 |
106,783,291 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6039:Zfp644
|
UTSW |
5 |
106,783,291 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6317:Zfp644
|
UTSW |
5 |
106,783,711 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6354:Zfp644
|
UTSW |
5 |
106,784,619 (GRCm39) |
missense |
probably benign |
0.23 |
|
R6886:Zfp644
|
UTSW |
5 |
106,785,777 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7223:Zfp644
|
UTSW |
5 |
106,785,448 (GRCm39) |
nonsense |
probably null |
|
|
R7326:Zfp644
|
UTSW |
5 |
106,786,143 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7450:Zfp644
|
UTSW |
5 |
106,786,392 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8095:Zfp644
|
UTSW |
5 |
106,766,280 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8710:Zfp644
|
UTSW |
5 |
106,782,997 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8822:Zfp644
|
UTSW |
5 |
106,783,087 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8936:Zfp644
|
UTSW |
5 |
106,783,503 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8975:Zfp644
|
UTSW |
5 |
106,785,467 (GRCm39) |
missense |
probably benign |
|
|
R9056:Zfp644
|
UTSW |
5 |
106,783,944 (GRCm39) |
nonsense |
probably null |
|
|
R9192:Zfp644
|
UTSW |
5 |
106,785,829 (GRCm39) |
missense |
probably benign |
|
|
R9250:Zfp644
|
UTSW |
5 |
106,784,699 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9287:Zfp644
|
UTSW |
5 |
106,785,774 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9313:Zfp644
|
UTSW |
5 |
106,784,324 (GRCm39) |
missense |
probably benign |
0.25 |
|
R9600:Zfp644
|
UTSW |
5 |
106,783,909 (GRCm39) |
missense |
probably benign |
|
|
R9766:Zfp644
|
UTSW |
5 |
106,784,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9789:Zfp644
|
UTSW |
5 |
106,786,131 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
X0011:Zfp644
|
UTSW |
5 |
106,766,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Zfp644
|
UTSW |
5 |
106,783,610 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTGAGGAAATCACTGCTAACGC -3'
(R):5'- GCTGTTGTTAATGGACCAGTC -3'
Sequencing Primer
(F):5'- TAACGCGCTGACACAGTCG -3'
(R):5'- TGTTAATGGACCAGTCTCATGC -3'
|
| Posted On |
2018-04-02 |
Incidental Mutation