Incidental Mutation 'R5405:Cdc42bpa'
ID |
428653 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cdc42bpa
|
Ensembl Gene |
ENSMUSG00000026490 |
Gene Name |
CDC42 binding protein kinase alpha |
Synonyms |
DMPK-like, A930014J19Rik |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.834)
|
Stock # |
R5405 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
179788037-179993168 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 179966085 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 1136
(E1136G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148469
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076687]
[ENSMUST00000097450]
[ENSMUST00000097453]
[ENSMUST00000111117]
[ENSMUST00000135056]
[ENSMUST00000212756]
|
AlphaFold |
Q3UU96 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000076687
AA Change: E1026G
PolyPhen 2
Score 0.808 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000075980 Gene: ENSMUSG00000026490 AA Change: E1026G
Domain | Start | End | E-Value | Type |
S_TKc
|
77 |
343 |
1.06e-86 |
SMART |
S_TK_X
|
344 |
406 |
1.18e-15 |
SMART |
coiled coil region
|
435 |
588 |
N/A |
INTRINSIC |
coiled coil region
|
632 |
735 |
N/A |
INTRINSIC |
Pfam:DMPK_coil
|
800 |
860 |
2.7e-29 |
PFAM |
C1
|
919 |
968 |
4.09e-7 |
SMART |
PH
|
989 |
1109 |
6.02e-8 |
SMART |
CNH
|
1134 |
1411 |
3.37e-17 |
SMART |
low complexity region
|
1456 |
1468 |
N/A |
INTRINSIC |
PBD
|
1477 |
1512 |
2.05e-10 |
SMART |
low complexity region
|
1531 |
1546 |
N/A |
INTRINSIC |
low complexity region
|
1567 |
1580 |
N/A |
INTRINSIC |
low complexity region
|
1606 |
1620 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000097450
AA Change: E1107G
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000095059 Gene: ENSMUSG00000026490 AA Change: E1107G
Domain | Start | End | E-Value | Type |
S_TKc
|
77 |
343 |
1.06e-86 |
SMART |
S_TK_X
|
344 |
406 |
1.18e-15 |
SMART |
coiled coil region
|
435 |
669 |
N/A |
INTRINSIC |
coiled coil region
|
713 |
816 |
N/A |
INTRINSIC |
Pfam:DMPK_coil
|
881 |
941 |
2.2e-29 |
PFAM |
C1
|
1000 |
1049 |
4.09e-7 |
SMART |
PH
|
1070 |
1190 |
6.02e-8 |
SMART |
CNH
|
1215 |
1492 |
3.37e-17 |
SMART |
low complexity region
|
1537 |
1549 |
N/A |
INTRINSIC |
PBD
|
1558 |
1593 |
2.05e-10 |
SMART |
low complexity region
|
1612 |
1627 |
N/A |
INTRINSIC |
low complexity region
|
1648 |
1661 |
N/A |
INTRINSIC |
low complexity region
|
1687 |
1701 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000097453
AA Change: E1079G
PolyPhen 2
Score 0.910 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000095062 Gene: ENSMUSG00000026490 AA Change: E1079G
Domain | Start | End | E-Value | Type |
S_TKc
|
77 |
343 |
1.06e-86 |
SMART |
S_TK_X
|
344 |
406 |
1.18e-15 |
SMART |
coiled coil region
|
435 |
669 |
N/A |
INTRINSIC |
coiled coil region
|
713 |
816 |
N/A |
INTRINSIC |
Pfam:DMPK_coil
|
881 |
941 |
2.5e-29 |
PFAM |
C1
|
972 |
1021 |
4.09e-7 |
SMART |
PH
|
1042 |
1162 |
6.02e-8 |
SMART |
CNH
|
1187 |
1464 |
3.37e-17 |
SMART |
low complexity region
|
1509 |
1521 |
N/A |
INTRINSIC |
PBD
|
1530 |
1565 |
2.05e-10 |
SMART |
low complexity region
|
1584 |
1599 |
N/A |
INTRINSIC |
low complexity region
|
1620 |
1633 |
N/A |
INTRINSIC |
low complexity region
|
1659 |
1673 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000111117
AA Change: E1120G
PolyPhen 2
Score 0.910 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000106746 Gene: ENSMUSG00000026490 AA Change: E1120G
Domain | Start | End | E-Value | Type |
S_TKc
|
77 |
343 |
1.06e-86 |
SMART |
S_TK_X
|
344 |
406 |
1.18e-15 |
SMART |
low complexity region
|
484 |
499 |
N/A |
INTRINSIC |
Pfam:KELK
|
529 |
608 |
1.1e-32 |
PFAM |
coiled coil region
|
713 |
816 |
N/A |
INTRINSIC |
Pfam:DMPK_coil
|
881 |
941 |
2.6e-29 |
PFAM |
C1
|
1013 |
1062 |
4.09e-7 |
SMART |
PH
|
1083 |
1203 |
6.02e-8 |
SMART |
CNH
|
1228 |
1505 |
3.37e-17 |
SMART |
low complexity region
|
1550 |
1562 |
N/A |
INTRINSIC |
PBD
|
1571 |
1606 |
2.05e-10 |
SMART |
low complexity region
|
1625 |
1640 |
N/A |
INTRINSIC |
low complexity region
|
1661 |
1674 |
N/A |
INTRINSIC |
low complexity region
|
1700 |
1714 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000133890
AA Change: E435G
|
SMART Domains |
Protein: ENSMUSP00000116337 Gene: ENSMUSG00000026490 AA Change: E435G
Domain | Start | End | E-Value | Type |
coiled coil region
|
6 |
109 |
N/A |
INTRINSIC |
Pfam:DMPK_coil
|
175 |
235 |
1.4e-29 |
PFAM |
C1
|
329 |
378 |
4.09e-7 |
SMART |
PH
|
399 |
519 |
6.02e-8 |
SMART |
CNH
|
544 |
821 |
3.37e-17 |
SMART |
low complexity region
|
866 |
878 |
N/A |
INTRINSIC |
PBD
|
887 |
922 |
2.05e-10 |
SMART |
low complexity region
|
941 |
956 |
N/A |
INTRINSIC |
low complexity region
|
977 |
990 |
N/A |
INTRINSIC |
low complexity region
|
1016 |
1030 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000135056
AA Change: E336G
PolyPhen 2
Score 0.164 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000114333 Gene: ENSMUSG00000026490 AA Change: E336G
Domain | Start | End | E-Value | Type |
Pfam:DMPK_coil
|
59 |
119 |
9e-30 |
PFAM |
low complexity region
|
148 |
156 |
N/A |
INTRINSIC |
C1
|
229 |
278 |
4.09e-7 |
SMART |
PH
|
299 |
419 |
6.02e-8 |
SMART |
CNH
|
444 |
721 |
3.37e-17 |
SMART |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000143176
AA Change: E309G
|
SMART Domains |
Protein: ENSMUSP00000115261 Gene: ENSMUSG00000026490 AA Change: E309G
Domain | Start | End | E-Value | Type |
Pfam:DMPK_coil
|
84 |
144 |
1.3e-29 |
PFAM |
C1
|
203 |
252 |
4.09e-7 |
SMART |
PH
|
273 |
393 |
6.02e-8 |
SMART |
CNH
|
418 |
695 |
3.37e-17 |
SMART |
low complexity region
|
740 |
752 |
N/A |
INTRINSIC |
PBD
|
761 |
796 |
1.02e-5 |
SMART |
PBD
|
802 |
839 |
2.21e-1 |
SMART |
low complexity region
|
877 |
892 |
N/A |
INTRINSIC |
low complexity region
|
913 |
926 |
N/A |
INTRINSIC |
low complexity region
|
952 |
966 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145274
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212756
AA Change: E1136G
PolyPhen 2
Score 0.950 (Sensitivity: 0.79; Specificity: 0.95)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000145181
|
SMART Domains |
Protein: ENSMUSP00000118039 Gene: ENSMUSG00000026490
Domain | Start | End | E-Value | Type |
Pfam:DMPK_coil
|
30 |
90 |
1e-30 |
PFAM |
low complexity region
|
119 |
127 |
N/A |
INTRINSIC |
SCOP:d1faq__
|
163 |
185 |
2e-4 |
SMART |
Blast:C1
|
165 |
185 |
1e-7 |
BLAST |
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.1%
|
Validation Efficiency |
|
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 member of the Serine/Threonine protein kinase family. This kinase contains multiple functional domains. Its kinase domain is highly similar to that of the myotonic dystrophy protein kinase (DMPK). This kinase also contains a Rac interactive binding (CRIB) domain, and has been shown to bind CDC42. It may function as a CDC42 downstream effector mediating CDC42 induced peripheral actin formation, and promoting cytoskeletal reorganization. Multiple alternatively spliced transcript variants have been described, and the full-length nature of two of them has been reported. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Add2 |
A |
T |
6: 86,078,179 (GRCm39) |
T298S |
probably benign |
Het |
Atad2b |
G |
A |
12: 4,990,098 (GRCm39) |
R141Q |
possibly damaging |
Het |
B3glct |
A |
G |
5: 149,632,818 (GRCm39) |
Q56R |
probably damaging |
Het |
Ceacam1 |
A |
T |
7: 25,163,290 (GRCm39) |
N314K |
probably benign |
Het |
Ces1g |
A |
T |
8: 94,032,496 (GRCm39) |
I488N |
probably benign |
Het |
Chd6 |
C |
T |
2: 160,807,310 (GRCm39) |
R1968K |
probably benign |
Het |
Cyp27b1 |
C |
T |
10: 126,886,255 (GRCm39) |
T312I |
possibly damaging |
Het |
Cyp39a1 |
C |
T |
17: 43,987,831 (GRCm39) |
A99V |
probably damaging |
Het |
Dipk1a |
C |
T |
5: 108,057,827 (GRCm39) |
V199I |
probably benign |
Het |
Dnaaf9 |
A |
G |
2: 130,554,380 (GRCm39) |
S890P |
probably damaging |
Het |
Efcab3 |
A |
T |
11: 104,612,018 (GRCm39) |
D620V |
probably benign |
Het |
Elapor1 |
A |
T |
3: 108,375,102 (GRCm39) |
C588* |
probably null |
Het |
Erc1 |
A |
T |
6: 119,801,905 (GRCm39) |
S37R |
probably damaging |
Het |
Gm10801 |
TC |
TCGAC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Gm14443 |
T |
C |
2: 175,013,644 (GRCm39) |
I43V |
possibly damaging |
Het |
Ins2 |
C |
T |
7: 142,233,134 (GRCm39) |
R46H |
probably damaging |
Het |
Krt77 |
T |
C |
15: 101,769,523 (GRCm39) |
I413V |
probably damaging |
Het |
Lpin3 |
A |
G |
2: 160,745,849 (GRCm39) |
D660G |
probably damaging |
Het |
Mpp3 |
T |
C |
11: 101,901,047 (GRCm39) |
Q318R |
probably benign |
Het |
Mpzl2 |
T |
C |
9: 44,958,503 (GRCm39) |
S80P |
probably damaging |
Het |
Mrpl2 |
T |
C |
17: 46,960,036 (GRCm39) |
|
probably null |
Het |
Mrpl48 |
T |
C |
7: 100,209,000 (GRCm39) |
Y108C |
probably damaging |
Het |
Ndufaf7 |
C |
A |
17: 79,246,044 (GRCm39) |
F92L |
probably damaging |
Het |
Or14c43 |
T |
C |
7: 86,115,383 (GRCm39) |
Y255H |
probably damaging |
Het |
Or6c8 |
T |
A |
10: 128,915,265 (GRCm39) |
D189V |
probably damaging |
Het |
Rec114 |
T |
C |
9: 58,567,624 (GRCm39) |
S121G |
probably benign |
Het |
Rnase10 |
A |
T |
14: 51,247,317 (GRCm39) |
I195F |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rreb1 |
A |
G |
13: 38,133,087 (GRCm39) |
E1754G |
probably damaging |
Het |
Sec31a |
G |
T |
5: 100,531,657 (GRCm39) |
C238* |
probably null |
Het |
Slc12a6 |
T |
C |
2: 112,169,724 (GRCm39) |
V337A |
probably damaging |
Het |
Slc25a37 |
A |
G |
14: 69,482,344 (GRCm39) |
V319A |
possibly damaging |
Het |
Slc26a10 |
T |
C |
10: 127,010,864 (GRCm39) |
Y456C |
probably benign |
Het |
Slc27a3 |
G |
A |
3: 90,294,382 (GRCm39) |
T463I |
probably benign |
Het |
Slc66a3 |
A |
G |
12: 17,043,315 (GRCm39) |
|
probably benign |
Het |
Stard9 |
T |
A |
2: 120,524,149 (GRCm39) |
D781E |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,057,208 (GRCm39) |
|
probably benign |
Het |
Tmem229b-ps |
T |
C |
10: 53,351,325 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Vmn2r71 |
A |
G |
7: 85,268,622 (GRCm39) |
D275G |
probably benign |
Het |
Wdr1 |
T |
C |
5: 38,692,543 (GRCm39) |
T121A |
probably benign |
Het |
Zdhhc19 |
C |
T |
16: 32,325,869 (GRCm39) |
R240C |
possibly damaging |
Het |
|
Other mutations in Cdc42bpa |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Cdc42bpa
|
APN |
1 |
179,933,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00807:Cdc42bpa
|
APN |
1 |
179,969,018 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00972:Cdc42bpa
|
APN |
1 |
179,902,249 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01084:Cdc42bpa
|
APN |
1 |
179,969,839 (GRCm39) |
splice site |
probably benign |
|
IGL01149:Cdc42bpa
|
APN |
1 |
179,902,137 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01377:Cdc42bpa
|
APN |
1 |
179,892,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01541:Cdc42bpa
|
APN |
1 |
179,978,723 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01657:Cdc42bpa
|
APN |
1 |
179,939,431 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01720:Cdc42bpa
|
APN |
1 |
179,938,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02227:Cdc42bpa
|
APN |
1 |
179,921,989 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02234:Cdc42bpa
|
APN |
1 |
179,978,756 (GRCm39) |
nonsense |
probably null |
|
IGL02253:Cdc42bpa
|
APN |
1 |
179,859,161 (GRCm39) |
splice site |
probably benign |
|
IGL02587:Cdc42bpa
|
APN |
1 |
179,921,510 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02671:Cdc42bpa
|
APN |
1 |
179,889,387 (GRCm39) |
missense |
probably benign |
|
IGL02746:Cdc42bpa
|
APN |
1 |
179,939,312 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02756:Cdc42bpa
|
APN |
1 |
179,936,824 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02994:Cdc42bpa
|
APN |
1 |
179,827,002 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03073:Cdc42bpa
|
APN |
1 |
179,921,941 (GRCm39) |
splice site |
probably benign |
|
IGL03295:Cdc42bpa
|
APN |
1 |
179,977,769 (GRCm39) |
missense |
probably benign |
0.00 |
P0022:Cdc42bpa
|
UTSW |
1 |
179,788,841 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4142001:Cdc42bpa
|
UTSW |
1 |
179,859,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Cdc42bpa
|
UTSW |
1 |
179,788,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Cdc42bpa
|
UTSW |
1 |
179,983,347 (GRCm39) |
intron |
probably benign |
|
R0472:Cdc42bpa
|
UTSW |
1 |
179,867,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Cdc42bpa
|
UTSW |
1 |
179,928,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0609:Cdc42bpa
|
UTSW |
1 |
179,867,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Cdc42bpa
|
UTSW |
1 |
179,972,400 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0738:Cdc42bpa
|
UTSW |
1 |
179,827,027 (GRCm39) |
splice site |
probably benign |
|
R1547:Cdc42bpa
|
UTSW |
1 |
179,902,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R1553:Cdc42bpa
|
UTSW |
1 |
179,921,540 (GRCm39) |
missense |
probably benign |
0.01 |
R1601:Cdc42bpa
|
UTSW |
1 |
179,892,566 (GRCm39) |
nonsense |
probably null |
|
R1709:Cdc42bpa
|
UTSW |
1 |
179,894,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Cdc42bpa
|
UTSW |
1 |
179,974,533 (GRCm39) |
missense |
probably benign |
0.39 |
R2279:Cdc42bpa
|
UTSW |
1 |
179,864,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R2357:Cdc42bpa
|
UTSW |
1 |
179,894,792 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2373:Cdc42bpa
|
UTSW |
1 |
179,939,349 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2570:Cdc42bpa
|
UTSW |
1 |
179,977,742 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3709:Cdc42bpa
|
UTSW |
1 |
179,892,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:Cdc42bpa
|
UTSW |
1 |
179,892,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Cdc42bpa
|
UTSW |
1 |
179,972,451 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3854:Cdc42bpa
|
UTSW |
1 |
179,983,543 (GRCm39) |
intron |
probably benign |
|
R3855:Cdc42bpa
|
UTSW |
1 |
179,983,543 (GRCm39) |
intron |
probably benign |
|
R3917:Cdc42bpa
|
UTSW |
1 |
179,933,719 (GRCm39) |
critical splice donor site |
probably null |
|
R4604:Cdc42bpa
|
UTSW |
1 |
179,936,759 (GRCm39) |
missense |
probably benign |
0.00 |
R4622:Cdc42bpa
|
UTSW |
1 |
179,902,223 (GRCm39) |
missense |
probably damaging |
0.98 |
R4664:Cdc42bpa
|
UTSW |
1 |
179,972,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R4665:Cdc42bpa
|
UTSW |
1 |
179,972,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R4887:Cdc42bpa
|
UTSW |
1 |
179,972,200 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4989:Cdc42bpa
|
UTSW |
1 |
179,965,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R5033:Cdc42bpa
|
UTSW |
1 |
179,892,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R5050:Cdc42bpa
|
UTSW |
1 |
179,900,018 (GRCm39) |
nonsense |
probably null |
|
R5077:Cdc42bpa
|
UTSW |
1 |
179,922,098 (GRCm39) |
intron |
probably benign |
|
R5196:Cdc42bpa
|
UTSW |
1 |
179,899,978 (GRCm39) |
missense |
probably benign |
0.09 |
R5276:Cdc42bpa
|
UTSW |
1 |
179,965,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5313:Cdc42bpa
|
UTSW |
1 |
179,911,998 (GRCm39) |
missense |
probably benign |
|
R5364:Cdc42bpa
|
UTSW |
1 |
179,894,747 (GRCm39) |
missense |
probably benign |
0.06 |
R5372:Cdc42bpa
|
UTSW |
1 |
179,892,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5405:Cdc42bpa
|
UTSW |
1 |
179,894,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Cdc42bpa
|
UTSW |
1 |
179,933,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R5713:Cdc42bpa
|
UTSW |
1 |
179,911,975 (GRCm39) |
missense |
probably benign |
0.03 |
R6012:Cdc42bpa
|
UTSW |
1 |
179,892,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Cdc42bpa
|
UTSW |
1 |
179,939,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Cdc42bpa
|
UTSW |
1 |
179,921,561 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6609:Cdc42bpa
|
UTSW |
1 |
179,928,839 (GRCm39) |
critical splice donor site |
probably null |
|
R7122:Cdc42bpa
|
UTSW |
1 |
179,892,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Cdc42bpa
|
UTSW |
1 |
179,889,362 (GRCm39) |
nonsense |
probably null |
|
R7670:Cdc42bpa
|
UTSW |
1 |
179,892,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R7912:Cdc42bpa
|
UTSW |
1 |
179,921,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8139:Cdc42bpa
|
UTSW |
1 |
179,896,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Cdc42bpa
|
UTSW |
1 |
179,989,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R8378:Cdc42bpa
|
UTSW |
1 |
179,989,709 (GRCm39) |
missense |
probably damaging |
0.98 |
R8794:Cdc42bpa
|
UTSW |
1 |
179,894,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R8835:Cdc42bpa
|
UTSW |
1 |
179,896,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Cdc42bpa
|
UTSW |
1 |
179,958,373 (GRCm39) |
intron |
probably benign |
|
R9012:Cdc42bpa
|
UTSW |
1 |
179,859,077 (GRCm39) |
missense |
|
|
R9110:Cdc42bpa
|
UTSW |
1 |
179,945,258 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9178:Cdc42bpa
|
UTSW |
1 |
179,958,401 (GRCm39) |
missense |
|
|
R9184:Cdc42bpa
|
UTSW |
1 |
179,972,301 (GRCm39) |
missense |
probably benign |
0.13 |
R9204:Cdc42bpa
|
UTSW |
1 |
179,939,460 (GRCm39) |
critical splice donor site |
probably null |
|
R9227:Cdc42bpa
|
UTSW |
1 |
179,933,638 (GRCm39) |
missense |
probably benign |
|
R9230:Cdc42bpa
|
UTSW |
1 |
179,933,638 (GRCm39) |
missense |
probably benign |
|
R9299:Cdc42bpa
|
UTSW |
1 |
179,972,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R9366:Cdc42bpa
|
UTSW |
1 |
179,921,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R9381:Cdc42bpa
|
UTSW |
1 |
179,969,048 (GRCm39) |
missense |
probably damaging |
0.97 |
R9461:Cdc42bpa
|
UTSW |
1 |
179,969,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R9559:Cdc42bpa
|
UTSW |
1 |
179,939,459 (GRCm39) |
critical splice donor site |
probably null |
|
X0026:Cdc42bpa
|
UTSW |
1 |
179,788,763 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cdc42bpa
|
UTSW |
1 |
179,892,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTGCAGTCTTAGCAGCGAGAG -3'
(R):5'- ATGTAGCTGTAGGGCTAAACCTG -3'
Sequencing Primer
(F):5'- TCTTAGCAGCGAGAGAGCAG -3'
(R):5'- CTGTAGGGCTAAACCTGAAAACTGAC -3'
|
Posted On |
2016-09-06 |