Incidental Mutation 'R7487:Plekha5'
ID |
580246 |
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 |
045561-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.163)
|
Stock # |
R7487 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
140369780-140542836 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 140516059 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Lysine
at position 771
(Q771K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000084904
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000087622]
[ENSMUST00000203012]
[ENSMUST00000203517]
[ENSMUST00000204080]
[ENSMUST00000204145]
[ENSMUST00000205026]
[ENSMUST00000213444]
|
AlphaFold |
E9Q6H8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000087622
AA Change: Q771K
PolyPhen 2
Score 0.250 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000084904 Gene: ENSMUSG00000030231 AA Change: Q771K
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 |
possibly damaging
Transcript: ENSMUST00000203012
AA Change: Q292K
PolyPhen 2
Score 0.805 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000145499 Gene: ENSMUSG00000030231 AA Change: Q292K
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: Q726K
PolyPhen 2
Score 0.347 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000145478 Gene: ENSMUSG00000030231 AA Change: Q726K
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 |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000204080
AA Change: Q302K
PolyPhen 2
Score 0.271 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000144872 Gene: ENSMUSG00000030231 AA Change: Q302K
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 |
probably damaging
Transcript: ENSMUST00000205026
AA Change: Q247K
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000144973 Gene: ENSMUSG00000030231 AA Change: Q247K
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 |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000213444
AA Change: Q98K
PolyPhen 2
Score 0.961 (Sensitivity: 0.78; Specificity: 0.95)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
Validation Efficiency |
100% (89/89) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,772,629 (GRCm39) |
D606V |
probably damaging |
Het |
1700009N14Rik |
T |
A |
4: 39,450,929 (GRCm39) |
V45E |
probably damaging |
Het |
2510009E07Rik |
C |
T |
16: 21,472,479 (GRCm39) |
V74M |
probably damaging |
Het |
Abca2 |
C |
T |
2: 25,327,915 (GRCm39) |
T739M |
probably benign |
Het |
Abra |
T |
C |
15: 41,732,949 (GRCm39) |
E39G |
probably damaging |
Het |
Adam34 |
A |
T |
8: 44,104,191 (GRCm39) |
C485S |
probably damaging |
Het |
Add2 |
G |
T |
6: 86,070,432 (GRCm39) |
V175F |
possibly damaging |
Het |
Alk |
T |
A |
17: 72,256,893 (GRCm39) |
K655N |
probably benign |
Het |
Ap3m1 |
A |
G |
14: 21,088,107 (GRCm39) |
V317A |
probably benign |
Het |
Astn1 |
A |
G |
1: 158,438,352 (GRCm39) |
|
probably null |
Het |
Atm |
A |
T |
9: 53,435,654 (GRCm39) |
Y219N |
probably benign |
Het |
Cep128 |
C |
T |
12: 90,966,404 (GRCm39) |
A1068T |
probably benign |
Het |
Cep20 |
T |
C |
16: 14,128,968 (GRCm39) |
D85G |
probably benign |
Het |
Cnksr3 |
T |
C |
10: 7,085,097 (GRCm39) |
Q250R |
probably benign |
Het |
Cst7 |
A |
G |
2: 150,419,624 (GRCm39) |
T97A |
probably benign |
Het |
Ctps1 |
G |
A |
4: 120,415,997 (GRCm39) |
L209F |
probably damaging |
Het |
Cyp2d10 |
A |
T |
15: 82,288,793 (GRCm39) |
F230I |
probably benign |
Het |
Daam2 |
T |
C |
17: 49,793,510 (GRCm39) |
N336D |
probably benign |
Het |
Dchs2 |
T |
C |
3: 83,263,613 (GRCm39) |
S3294P |
probably damaging |
Het |
Dhx36 |
G |
T |
3: 62,391,623 (GRCm39) |
N574K |
possibly damaging |
Het |
Dock10 |
G |
T |
1: 80,562,765 (GRCm39) |
Q533K |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,132,041 (GRCm39) |
S1589P |
probably benign |
Het |
Enpp3 |
T |
A |
10: 24,681,821 (GRCm39) |
Y295F |
probably benign |
Het |
Esrrg |
T |
A |
1: 187,878,620 (GRCm39) |
Y234N |
probably benign |
Het |
Fadd |
A |
C |
7: 144,134,462 (GRCm39) |
V141G |
probably damaging |
Het |
Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
Fam170b |
T |
A |
14: 32,557,776 (GRCm39) |
C204S |
probably damaging |
Het |
Fam186a |
T |
A |
15: 99,840,017 (GRCm39) |
I2076F |
possibly damaging |
Het |
Fdxacb1 |
G |
A |
9: 50,681,519 (GRCm39) |
V147I |
possibly damaging |
Het |
Frem2 |
C |
A |
3: 53,561,970 (GRCm39) |
V846F |
probably benign |
Het |
Fry |
G |
A |
5: 150,338,039 (GRCm39) |
S1449N |
possibly damaging |
Het |
Gucy1b2 |
A |
G |
14: 62,685,672 (GRCm39) |
F98L |
probably damaging |
Het |
Hps1 |
T |
C |
19: 42,744,700 (GRCm39) |
Y658C |
probably damaging |
Het |
Igkv3-9 |
T |
A |
6: 70,565,506 (GRCm39) |
L35Q |
probably damaging |
Het |
Irx2 |
A |
G |
13: 72,778,739 (GRCm39) |
Y101C |
probably damaging |
Het |
Kcnj11 |
G |
T |
7: 45,748,265 (GRCm39) |
R353S |
probably benign |
Het |
Kyat3 |
C |
T |
3: 142,431,955 (GRCm39) |
Q228* |
probably null |
Het |
Lama3 |
T |
A |
18: 12,552,294 (GRCm39) |
D415E |
probably benign |
Het |
Lcn3 |
G |
A |
2: 25,656,174 (GRCm39) |
|
probably null |
Het |
Lin7b |
T |
C |
7: 45,019,364 (GRCm39) |
E68G |
possibly damaging |
Het |
Lmbr1 |
T |
A |
5: 29,459,262 (GRCm39) |
K379M |
probably benign |
Het |
Lrig1 |
A |
G |
6: 94,583,099 (GRCm39) |
S1006P |
probably benign |
Het |
Lrrc37a |
T |
G |
11: 103,389,045 (GRCm39) |
T2127P |
unknown |
Het |
Map4 |
A |
G |
9: 109,856,783 (GRCm39) |
D151G |
probably damaging |
Het |
Marchf1 |
A |
T |
8: 66,908,726 (GRCm39) |
T149S |
probably benign |
Het |
Msh4 |
A |
T |
3: 153,569,147 (GRCm39) |
F809I |
probably damaging |
Het |
Muc16 |
G |
A |
9: 18,496,095 (GRCm39) |
P6699S |
possibly damaging |
Het |
Mxi1 |
A |
T |
19: 53,360,088 (GRCm39) |
D270V |
probably damaging |
Het |
Myh6 |
A |
T |
14: 55,190,953 (GRCm39) |
C907* |
probably null |
Het |
Myo18b |
T |
C |
5: 112,982,299 (GRCm39) |
R1145G |
possibly damaging |
Het |
Nkx2-6 |
A |
C |
14: 69,409,389 (GRCm39) |
N47H |
probably benign |
Het |
Nol7 |
G |
A |
13: 43,552,076 (GRCm39) |
A66T |
probably damaging |
Het |
Ntrk3 |
T |
C |
7: 77,900,461 (GRCm39) |
N626S |
probably damaging |
Het |
Nwd1 |
A |
G |
8: 73,393,266 (GRCm39) |
Y77C |
unknown |
Het |
Or12d17 |
G |
T |
17: 37,777,457 (GRCm39) |
R120L |
probably damaging |
Het |
Or12k5 |
A |
C |
2: 36,894,786 (GRCm39) |
V280G |
probably damaging |
Het |
Or8c14-ps1 |
A |
G |
9: 38,101,356 (GRCm39) |
S112G |
probably damaging |
Het |
Or8j3b |
A |
T |
2: 86,205,475 (GRCm39) |
Y94N |
probably damaging |
Het |
Or9s23 |
G |
A |
1: 92,501,517 (GRCm39) |
G208D |
possibly damaging |
Het |
Otop3 |
A |
G |
11: 115,235,826 (GRCm39) |
D486G |
probably benign |
Het |
Pak1ip1 |
A |
G |
13: 41,162,731 (GRCm39) |
K178R |
probably benign |
Het |
Pcsk1 |
G |
A |
13: 75,259,002 (GRCm39) |
G259S |
probably benign |
Het |
Pde6a |
A |
G |
18: 61,383,031 (GRCm39) |
D338G |
probably damaging |
Het |
Pias4 |
A |
T |
10: 80,999,806 (GRCm39) |
D82E |
probably benign |
Het |
Plekhh3 |
C |
A |
11: 101,056,405 (GRCm39) |
A397S |
possibly damaging |
Het |
Prg4 |
G |
T |
1: 150,331,656 (GRCm39) |
T339N |
unknown |
Het |
Prss22 |
A |
T |
17: 24,216,971 (GRCm39) |
I3N |
probably damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,118,424 (GRCm39) |
I522V |
probably damaging |
Het |
Rspo2 |
T |
C |
15: 42,941,510 (GRCm39) |
T138A |
probably benign |
Het |
Rtcb |
C |
T |
10: 85,789,333 (GRCm39) |
G70S |
probably benign |
Het |
Selenov |
A |
T |
7: 27,989,803 (GRCm39) |
S234T |
probably damaging |
Het |
Shtn1 |
T |
C |
19: 58,992,292 (GRCm39) |
T429A |
probably damaging |
Het |
Slc4a3 |
G |
T |
1: 75,530,021 (GRCm39) |
R622L |
probably benign |
Het |
Smc2 |
T |
C |
4: 52,478,448 (GRCm39) |
I1015T |
probably damaging |
Het |
Spata9 |
G |
T |
13: 76,115,959 (GRCm39) |
V3F |
possibly damaging |
Het |
Tlr4 |
T |
C |
4: 66,842,659 (GRCm39) |
I105T |
probably benign |
Het |
Trav6d-4 |
A |
T |
14: 52,991,096 (GRCm39) |
Y47F |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,657,377 (GRCm39) |
I12450N |
unknown |
Het |
Umad1 |
G |
T |
6: 8,270,560 (GRCm39) |
A21S |
probably damaging |
Het |
Unc5a |
G |
A |
13: 55,144,362 (GRCm39) |
R229H |
probably benign |
Het |
Vmn1r216 |
A |
T |
13: 23,284,030 (GRCm39) |
M238L |
probably damaging |
Het |
Vps16 |
T |
A |
2: 130,280,977 (GRCm39) |
C255* |
probably null |
Het |
Wdr89 |
A |
G |
12: 75,679,388 (GRCm39) |
F289L |
probably benign |
Het |
Zfp180 |
A |
T |
7: 23,805,525 (GRCm39) |
H648L |
probably damaging |
Het |
Zfp735 |
A |
G |
11: 73,581,154 (GRCm39) |
K64E |
possibly damaging |
Het |
Zfp990 |
G |
A |
4: 145,264,157 (GRCm39) |
C385Y |
probably damaging |
Het |
Zswim3 |
G |
T |
2: 164,662,135 (GRCm39) |
S205I |
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 |
R7196:Plekha5
|
UTSW |
6 |
140,489,648 (GRCm39) |
missense |
possibly damaging |
0.83 |
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'- CAGGATAAAGTGGTCCGAGC -3'
(R):5'- ACCATTGACCAAGTGGCCAAG -3'
Sequencing Primer
(F):5'- TAAAGTGGTCCGAGCGCTGG -3'
(R):5'- GAAAGGTTCTCACTAAGTTGCG -3'
|
Posted On |
2019-10-07 |