Incidental Mutation 'R7196:Plekha5'
ID |
559919 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Plekha5
|
Ensembl Gene |
ENSMUSG00000030231 |
Gene Name |
pleckstrin homology domain containing, family A member 5 |
Synonyms |
2810431N21Rik, PEPP2 |
MMRRC Submission |
045275-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.163)
|
Stock # |
R7196 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
140369780-140542836 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 140489648 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Leucine
at position 236
(V236L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144832
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000087622]
[ENSMUST00000203012]
[ENSMUST00000203517]
[ENSMUST00000203774]
[ENSMUST00000204080]
[ENSMUST00000204145]
[ENSMUST00000204876]
[ENSMUST00000205026]
|
AlphaFold |
E9Q6H8 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000087622
AA Change: V351L
PolyPhen 2
Score 0.825 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000084904 Gene: ENSMUSG00000030231 AA Change: V351L
Domain | Start | End | E-Value | Type |
WW
|
12 |
44 |
1.51e-3 |
SMART |
WW
|
58 |
90 |
2.17e-4 |
SMART |
PH
|
171 |
271 |
1.85e-17 |
SMART |
Blast:PH
|
592 |
715 |
7e-39 |
BLAST |
coiled coil region
|
747 |
781 |
N/A |
INTRINSIC |
low complexity region
|
896 |
916 |
N/A |
INTRINSIC |
low complexity region
|
924 |
938 |
N/A |
INTRINSIC |
low complexity region
|
1206 |
1224 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1258 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000203012
|
SMART Domains |
Protein: ENSMUSP00000145499 Gene: ENSMUSG00000030231
Domain | Start | End | E-Value | Type |
Blast:PH
|
210 |
250 |
2e-8 |
BLAST |
coiled coil region
|
268 |
302 |
N/A |
INTRINSIC |
low complexity region
|
417 |
437 |
N/A |
INTRINSIC |
low complexity region
|
445 |
459 |
N/A |
INTRINSIC |
low complexity region
|
727 |
745 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000203517
AA Change: V345L
PolyPhen 2
Score 0.164 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000145478 Gene: ENSMUSG00000030231 AA Change: V345L
Domain | Start | End | E-Value | Type |
WW
|
12 |
44 |
9e-6 |
SMART |
WW
|
58 |
90 |
1.3e-6 |
SMART |
PH
|
171 |
271 |
8.6e-20 |
SMART |
Blast:PH
|
586 |
697 |
3e-15 |
BLAST |
coiled coil region
|
702 |
736 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000203774
AA Change: V236L
PolyPhen 2
Score 0.830 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000144832 Gene: ENSMUSG00000030231 AA Change: V236L
Domain | Start | End | E-Value | Type |
PH
|
62 |
162 |
8.6e-20 |
SMART |
Blast:PH
|
477 |
511 |
4e-8 |
BLAST |
low complexity region
|
512 |
521 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204080
|
SMART Domains |
Protein: ENSMUSP00000144872 Gene: ENSMUSG00000030231
Domain | Start | End | E-Value | Type |
Blast:PH
|
220 |
260 |
1e-8 |
BLAST |
coiled coil region
|
278 |
312 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204145
|
SMART Domains |
Protein: ENSMUSP00000145457 Gene: ENSMUSG00000030231
Domain | Start | End | E-Value | Type |
WW
|
12 |
44 |
9e-6 |
SMART |
WW
|
58 |
90 |
1.3e-6 |
SMART |
Blast:PH
|
114 |
151 |
6e-14 |
BLAST |
PDB:2DKP|A
|
163 |
196 |
1e-5 |
PDB |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000204876
AA Change: V242L
PolyPhen 2
Score 0.833 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000145336 Gene: ENSMUSG00000030231 AA Change: V242L
Domain | Start | End | E-Value | Type |
PH
|
62 |
162 |
8.6e-20 |
SMART |
Blast:PH
|
483 |
517 |
3e-8 |
BLAST |
low complexity region
|
518 |
527 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000205026
|
SMART Domains |
Protein: ENSMUSP00000144973 Gene: ENSMUSG00000030231
Domain | Start | End | E-Value | Type |
Blast:PH
|
165 |
205 |
1e-8 |
BLAST |
coiled coil region
|
223 |
257 |
N/A |
INTRINSIC |
low complexity region
|
619 |
637 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.5%
|
Validation Efficiency |
99% (94/95) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
AGCTTCCCTGCTT |
AGCTT |
9: 57,165,505 (GRCm39) |
|
probably null |
Het |
4921504E06Rik |
A |
C |
2: 19,498,806 (GRCm39) |
S396A |
probably benign |
Het |
Actr6 |
C |
A |
10: 89,550,784 (GRCm39) |
V337F |
possibly damaging |
Het |
Agtpbp1 |
T |
C |
13: 59,680,994 (GRCm39) |
T73A |
possibly damaging |
Het |
AI182371 |
A |
T |
2: 34,976,441 (GRCm39) |
|
probably null |
Het |
Apob |
A |
G |
12: 8,033,893 (GRCm39) |
E202G |
possibly damaging |
Het |
Asb4 |
A |
T |
6: 5,423,356 (GRCm39) |
M168L |
probably benign |
Het |
AU018091 |
T |
C |
7: 3,213,788 (GRCm39) |
Y152C |
probably damaging |
Het |
Casp3 |
G |
A |
8: 47,088,498 (GRCm39) |
G132R |
possibly damaging |
Het |
Cbfa2t3 |
C |
A |
8: 123,365,729 (GRCm39) |
A229S |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,143,759 (GRCm39) |
Y2949N |
probably damaging |
Het |
Ceacam3 |
T |
C |
7: 16,888,881 (GRCm39) |
Y217H |
|
Het |
Cldn5 |
A |
T |
16: 18,595,630 (GRCm39) |
|
probably benign |
Het |
Cltc |
T |
C |
11: 86,597,657 (GRCm39) |
D1093G |
probably damaging |
Het |
Cnn3 |
G |
A |
3: 121,248,437 (GRCm39) |
|
probably null |
Het |
Col4a2 |
A |
G |
8: 11,448,693 (GRCm39) |
Y71C |
probably damaging |
Het |
Csf1 |
T |
C |
3: 107,661,214 (GRCm39) |
D77G |
possibly damaging |
Het |
Cyp2j7 |
T |
A |
4: 96,103,651 (GRCm39) |
T295S |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,724,000 (GRCm39) |
M133K |
probably benign |
Het |
Dock5 |
G |
A |
14: 67,993,919 (GRCm39) |
P1852L |
probably damaging |
Het |
Dpysl3 |
T |
A |
18: 43,462,910 (GRCm39) |
D489V |
probably damaging |
Het |
Dsg4 |
T |
C |
18: 20,599,537 (GRCm39) |
Y718H |
probably damaging |
Het |
Dync2h1 |
G |
A |
9: 7,147,715 (GRCm39) |
Q972* |
probably null |
Het |
Epn1 |
G |
A |
7: 5,096,380 (GRCm39) |
D225N |
possibly damaging |
Het |
Esp4 |
A |
G |
17: 40,913,256 (GRCm39) |
E41G |
probably benign |
Het |
Fam171a2 |
T |
C |
11: 102,329,172 (GRCm39) |
D529G |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,691,301 (GRCm39) |
I694N |
probably damaging |
Het |
Fshr |
C |
T |
17: 89,292,897 (GRCm39) |
A594T |
probably damaging |
Het |
Galnt3 |
A |
G |
2: 65,921,268 (GRCm39) |
Y533H |
probably damaging |
Het |
Gja5 |
C |
A |
3: 96,958,422 (GRCm39) |
R160S |
probably damaging |
Het |
Gm12353 |
A |
T |
4: 19,608,938 (GRCm39) |
D7V |
unknown |
Het |
Gm17669 |
T |
C |
18: 67,695,572 (GRCm39) |
F39S |
probably damaging |
Het |
Gm7145 |
T |
A |
1: 117,913,791 (GRCm39) |
N224K |
possibly damaging |
Het |
Gpd1 |
G |
T |
15: 99,619,936 (GRCm39) |
G245C |
probably benign |
Het |
Gpr4 |
G |
A |
7: 18,957,089 (GRCm39) |
G337D |
probably benign |
Het |
Hgd |
G |
A |
16: 37,409,078 (GRCm39) |
C14Y |
probably benign |
Het |
Ibtk |
A |
T |
9: 85,625,709 (GRCm39) |
S14T |
probably damaging |
Het |
Ifi205 |
G |
T |
1: 173,854,109 (GRCm39) |
N181K |
probably damaging |
Het |
Inppl1 |
G |
A |
7: 101,477,993 (GRCm39) |
A673V |
probably benign |
Het |
Itgb3 |
C |
A |
11: 104,524,438 (GRCm39) |
Y191* |
probably null |
Het |
Jrkl |
G |
T |
9: 13,244,162 (GRCm39) |
P500T |
probably benign |
Het |
Kcnq1 |
G |
A |
7: 142,912,478 (GRCm39) |
V515I |
possibly damaging |
Het |
Kifc3 |
A |
G |
8: 95,833,239 (GRCm39) |
V453A |
probably benign |
Het |
Krt10 |
C |
T |
11: 99,278,371 (GRCm39) |
E263K |
probably damaging |
Het |
Lingo1 |
A |
T |
9: 56,527,903 (GRCm39) |
F235I |
probably damaging |
Het |
Lmo7 |
T |
A |
14: 102,133,936 (GRCm39) |
D660E |
possibly damaging |
Het |
Magi3 |
A |
C |
3: 103,956,484 (GRCm39) |
C661W |
probably benign |
Het |
Mmp1a |
C |
T |
9: 7,476,018 (GRCm39) |
Q428* |
probably null |
Het |
Msrb1 |
A |
T |
17: 24,958,556 (GRCm39) |
T47S |
probably benign |
Het |
Naip6 |
A |
T |
13: 100,436,666 (GRCm39) |
I619K |
probably benign |
Het |
Ndfip2 |
T |
C |
14: 105,535,472 (GRCm39) |
S253P |
probably damaging |
Het |
Nebl |
A |
T |
2: 17,457,329 (GRCm39) |
V77E |
probably damaging |
Het |
Nit1 |
T |
C |
1: 171,172,003 (GRCm39) |
E65G |
probably benign |
Het |
Ntn4 |
C |
T |
10: 93,569,576 (GRCm39) |
H430Y |
probably benign |
Het |
Nxpe5 |
A |
T |
5: 138,237,586 (GRCm39) |
I49F |
probably benign |
Het |
Or10a2 |
A |
G |
7: 106,673,935 (GRCm39) |
N300S |
probably benign |
Het |
Or10c1 |
A |
G |
17: 37,522,084 (GRCm39) |
I220T |
probably damaging |
Het |
Or14c46 |
A |
T |
7: 85,918,649 (GRCm39) |
M116K |
probably damaging |
Het |
Or1e23 |
A |
G |
11: 73,407,957 (GRCm39) |
Y23H |
probably benign |
Het |
Or1m1 |
A |
T |
9: 18,666,886 (GRCm39) |
L15* |
probably null |
Het |
Or4k49 |
T |
G |
2: 111,495,042 (GRCm39) |
L157W |
probably damaging |
Het |
Or52s6 |
A |
T |
7: 103,092,204 (GRCm39) |
M42K |
probably benign |
Het |
Or7e178 |
A |
G |
9: 20,225,494 (GRCm39) |
Y241H |
probably benign |
Het |
Oxct2a |
T |
A |
4: 123,217,165 (GRCm39) |
N72I |
probably damaging |
Het |
Pappa |
G |
A |
4: 65,242,128 (GRCm39) |
|
probably null |
Het |
Pcnx1 |
G |
A |
12: 82,042,312 (GRCm39) |
R34H |
possibly damaging |
Het |
Prdm1 |
A |
G |
10: 44,332,988 (GRCm39) |
S44P |
probably benign |
Het |
Prss46 |
T |
A |
9: 110,680,533 (GRCm39) |
L226Q |
probably benign |
Het |
Prss47 |
C |
A |
13: 65,192,640 (GRCm39) |
W380C |
probably benign |
Het |
Ptch2 |
T |
G |
4: 116,971,946 (GRCm39) |
V1156G |
probably benign |
Het |
Rab3gap2 |
T |
C |
1: 185,013,864 (GRCm39) |
F1190S |
probably damaging |
Het |
Raver2 |
T |
G |
4: 100,960,056 (GRCm39) |
Y179D |
probably damaging |
Het |
Rgl2 |
C |
T |
17: 34,152,403 (GRCm39) |
R367W |
probably damaging |
Het |
Ripor2 |
T |
G |
13: 24,888,808 (GRCm39) |
I629S |
possibly damaging |
Het |
Robo4 |
T |
A |
9: 37,314,001 (GRCm39) |
M84K |
possibly damaging |
Het |
Rps6ka5 |
A |
T |
12: 100,562,123 (GRCm39) |
S252T |
possibly damaging |
Het |
Rtl1 |
C |
T |
12: 109,559,221 (GRCm39) |
V873M |
possibly damaging |
Het |
Sla |
T |
A |
15: 66,703,420 (GRCm39) |
R4W |
probably benign |
Het |
Smco1 |
A |
G |
16: 32,092,620 (GRCm39) |
D97G |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,676,753 (GRCm39) |
T414A |
probably benign |
Het |
Syt14 |
A |
G |
1: 192,717,936 (GRCm39) |
I3T |
probably benign |
Het |
Tnpo2 |
G |
A |
8: 85,773,766 (GRCm39) |
V303M |
possibly damaging |
Het |
Tstd2 |
A |
C |
4: 46,119,955 (GRCm39) |
S332R |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,582,386 (GRCm39) |
A22836S |
possibly damaging |
Het |
Ufl1 |
A |
G |
4: 25,250,669 (GRCm39) |
V728A |
probably benign |
Het |
Usp33 |
A |
T |
3: 152,089,828 (GRCm39) |
K789N |
possibly damaging |
Het |
Usp54 |
T |
A |
14: 20,638,438 (GRCm39) |
Q214L |
probably damaging |
Het |
Vmn2r7 |
T |
G |
3: 64,623,198 (GRCm39) |
N374T |
probably benign |
Het |
Zbtb7a |
T |
A |
10: 80,980,434 (GRCm39) |
N209K |
probably damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,306,207 (GRCm39) |
V615A |
probably benign |
Het |
Zdhhc20 |
A |
G |
14: 58,111,348 (GRCm39) |
|
probably null |
Het |
Zfp90 |
G |
T |
8: 107,151,780 (GRCm39) |
V498L |
probably damaging |
Het |
|
Other mutations in Plekha5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00577:Plekha5
|
APN |
6 |
140,515,822 (GRCm39) |
splice site |
probably benign |
|
IGL00908:Plekha5
|
APN |
6 |
140,496,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01346:Plekha5
|
APN |
6 |
140,480,292 (GRCm39) |
splice site |
probably benign |
|
IGL01380:Plekha5
|
APN |
6 |
140,516,042 (GRCm39) |
splice site |
probably benign |
|
IGL01406:Plekha5
|
APN |
6 |
140,518,676 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01408:Plekha5
|
APN |
6 |
140,516,042 (GRCm39) |
splice site |
probably benign |
|
IGL01688:Plekha5
|
APN |
6 |
140,515,115 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01719:Plekha5
|
APN |
6 |
140,515,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01926:Plekha5
|
APN |
6 |
140,471,642 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01936:Plekha5
|
APN |
6 |
140,470,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02326:Plekha5
|
APN |
6 |
140,529,576 (GRCm39) |
nonsense |
probably null |
|
IGL02544:Plekha5
|
APN |
6 |
140,535,454 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02573:Plekha5
|
APN |
6 |
140,527,742 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02704:Plekha5
|
APN |
6 |
140,489,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02959:Plekha5
|
APN |
6 |
140,489,904 (GRCm39) |
missense |
probably damaging |
1.00 |
Doubletime
|
UTSW |
6 |
140,471,655 (GRCm39) |
nonsense |
probably null |
|
R0067:Plekha5
|
UTSW |
6 |
140,470,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Plekha5
|
UTSW |
6 |
140,470,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:Plekha5
|
UTSW |
6 |
140,474,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:Plekha5
|
UTSW |
6 |
140,474,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0105:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0107:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0359:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0360:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0362:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0363:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0364:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0365:Plekha5
|
UTSW |
6 |
140,537,473 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0833:Plekha5
|
UTSW |
6 |
140,535,360 (GRCm39) |
splice site |
probably benign |
|
R0835:Plekha5
|
UTSW |
6 |
140,514,576 (GRCm39) |
nonsense |
probably null |
|
R0836:Plekha5
|
UTSW |
6 |
140,535,360 (GRCm39) |
splice site |
probably benign |
|
R0944:Plekha5
|
UTSW |
6 |
140,515,922 (GRCm39) |
splice site |
probably benign |
|
R2015:Plekha5
|
UTSW |
6 |
140,480,290 (GRCm39) |
critical splice donor site |
probably null |
|
R2043:Plekha5
|
UTSW |
6 |
140,498,530 (GRCm39) |
splice site |
probably benign |
|
R2086:Plekha5
|
UTSW |
6 |
140,516,044 (GRCm39) |
splice site |
probably null |
|
R2102:Plekha5
|
UTSW |
6 |
140,518,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Plekha5
|
UTSW |
6 |
140,369,942 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2135:Plekha5
|
UTSW |
6 |
140,526,225 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2150:Plekha5
|
UTSW |
6 |
140,516,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Plekha5
|
UTSW |
6 |
140,471,587 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2414:Plekha5
|
UTSW |
6 |
140,496,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R2915:Plekha5
|
UTSW |
6 |
140,534,925 (GRCm39) |
missense |
probably damaging |
0.96 |
R3120:Plekha5
|
UTSW |
6 |
140,537,367 (GRCm39) |
missense |
probably benign |
0.00 |
R3924:Plekha5
|
UTSW |
6 |
140,516,105 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4049:Plekha5
|
UTSW |
6 |
140,529,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R4056:Plekha5
|
UTSW |
6 |
140,534,958 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4077:Plekha5
|
UTSW |
6 |
140,501,647 (GRCm39) |
splice site |
probably null |
|
R4320:Plekha5
|
UTSW |
6 |
140,489,543 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4343:Plekha5
|
UTSW |
6 |
140,501,780 (GRCm39) |
missense |
probably damaging |
0.99 |
R4359:Plekha5
|
UTSW |
6 |
140,537,414 (GRCm39) |
missense |
probably benign |
0.07 |
R4377:Plekha5
|
UTSW |
6 |
140,525,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R4480:Plekha5
|
UTSW |
6 |
140,472,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R4533:Plekha5
|
UTSW |
6 |
140,516,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Plekha5
|
UTSW |
6 |
140,496,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R4672:Plekha5
|
UTSW |
6 |
140,470,655 (GRCm39) |
missense |
probably damaging |
0.98 |
R4871:Plekha5
|
UTSW |
6 |
140,471,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4903:Plekha5
|
UTSW |
6 |
140,532,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Plekha5
|
UTSW |
6 |
140,525,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Plekha5
|
UTSW |
6 |
140,372,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R5376:Plekha5
|
UTSW |
6 |
140,496,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R5445:Plekha5
|
UTSW |
6 |
140,498,459 (GRCm39) |
nonsense |
probably null |
|
R5753:Plekha5
|
UTSW |
6 |
140,482,730 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5836:Plekha5
|
UTSW |
6 |
140,372,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R5972:Plekha5
|
UTSW |
6 |
140,518,639 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6196:Plekha5
|
UTSW |
6 |
140,525,179 (GRCm39) |
missense |
probably benign |
0.28 |
R6254:Plekha5
|
UTSW |
6 |
140,532,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R6501:Plekha5
|
UTSW |
6 |
140,471,655 (GRCm39) |
nonsense |
probably null |
|
R6620:Plekha5
|
UTSW |
6 |
140,518,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6663:Plekha5
|
UTSW |
6 |
140,523,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Plekha5
|
UTSW |
6 |
140,471,584 (GRCm39) |
missense |
probably benign |
0.16 |
R6992:Plekha5
|
UTSW |
6 |
140,489,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R7487:Plekha5
|
UTSW |
6 |
140,516,059 (GRCm39) |
missense |
probably benign |
0.25 |
R7493:Plekha5
|
UTSW |
6 |
140,526,161 (GRCm39) |
missense |
probably benign |
0.02 |
R7557:Plekha5
|
UTSW |
6 |
140,372,271 (GRCm39) |
missense |
probably damaging |
0.96 |
R7743:Plekha5
|
UTSW |
6 |
140,501,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Plekha5
|
UTSW |
6 |
140,534,950 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7808:Plekha5
|
UTSW |
6 |
140,529,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R7910:Plekha5
|
UTSW |
6 |
140,472,184 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7944:Plekha5
|
UTSW |
6 |
140,526,201 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7945:Plekha5
|
UTSW |
6 |
140,526,201 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7992:Plekha5
|
UTSW |
6 |
140,472,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Plekha5
|
UTSW |
6 |
140,496,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R9024:Plekha5
|
UTSW |
6 |
140,370,176 (GRCm39) |
missense |
probably benign |
0.10 |
R9135:Plekha5
|
UTSW |
6 |
140,480,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Plekha5
|
UTSW |
6 |
140,501,733 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9241:Plekha5
|
UTSW |
6 |
140,525,204 (GRCm39) |
critical splice donor site |
probably null |
|
R9447:Plekha5
|
UTSW |
6 |
140,525,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R9625:Plekha5
|
UTSW |
6 |
140,372,253 (GRCm39) |
missense |
probably benign |
0.24 |
X0027:Plekha5
|
UTSW |
6 |
140,370,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TCTGCTTTCAGAGTGGACAAG -3'
(R):5'- TTCTCTGAATGACTCGGTCG -3'
Sequencing Primer
(F):5'- CTGCTTTCAGAGTGGACAAGATTAC -3'
(R):5'- TGAATGACTCGGTCGGCCTC -3'
|
Posted On |
2019-06-26 |