Incidental Mutation 'R7485:Cdcp3'
ID |
580076 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cdcp3
|
Ensembl Gene |
ENSMUSG00000006204 |
Gene Name |
CUB domain containing protein 3 |
Synonyms |
5430419D17Rik |
MMRRC Submission |
045559-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7485 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
130776131-130908180 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 130830562 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Glutamine
at position 332
(P332Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000061529
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050586]
[ENSMUST00000124096]
[ENSMUST00000208921]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000050586
AA Change: P332Q
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000061529 Gene: ENSMUSG00000006204 AA Change: P332Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
low complexity region
|
85 |
105 |
N/A |
INTRINSIC |
SR
|
144 |
244 |
3.3e-57 |
SMART |
CUB
|
272 |
378 |
1.2e-16 |
SMART |
SR
|
428 |
528 |
3.9e-56 |
SMART |
low complexity region
|
533 |
548 |
N/A |
INTRINSIC |
CUB
|
556 |
667 |
5.1e-38 |
SMART |
SR
|
680 |
780 |
1.5e-57 |
SMART |
Pfam:CUB
|
795 |
840 |
3.1e-9 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000124096
|
SMART Domains |
Protein: ENSMUSP00000130971 Gene: ENSMUSG00000030849
Domain | Start | End | E-Value | Type |
Pfam:Pkinase
|
1 |
118 |
4.8e-19 |
PFAM |
Pfam:Pkinase_Tyr
|
1 |
118 |
1.7e-50 |
PFAM |
low complexity region
|
146 |
160 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000128522
AA Change: P205Q
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000208921
AA Change: P332Q
PolyPhen 2
Score 0.749 (Sensitivity: 0.85; Specificity: 0.92)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
99% (99/100) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat3 |
C |
T |
10: 80,442,234 (GRCm39) |
A24V |
probably benign |
Het |
Agbl1 |
A |
T |
7: 76,239,241 (GRCm39) |
E832D |
unknown |
Het |
Akap8l |
G |
A |
17: 32,554,545 (GRCm39) |
S347L |
probably benign |
Het |
Ankmy1 |
G |
T |
1: 92,804,379 (GRCm39) |
A868E |
probably damaging |
Het |
Ankrd49 |
A |
T |
9: 14,693,837 (GRCm39) |
L110* |
probably null |
Het |
Aoc3 |
A |
G |
11: 101,228,229 (GRCm39) |
T679A |
probably damaging |
Het |
Ap1s3 |
A |
G |
1: 79,592,018 (GRCm39) |
Y111H |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,402,659 (GRCm39) |
N777K |
probably damaging |
Het |
Atp4b |
A |
T |
8: 13,436,732 (GRCm39) |
M260K |
probably benign |
Het |
Bcl2l15 |
A |
T |
3: 103,740,729 (GRCm39) |
D65V |
probably damaging |
Het |
Bicdl1 |
G |
T |
5: 115,801,845 (GRCm39) |
S340* |
probably null |
Het |
Ccdc15 |
T |
C |
9: 37,226,574 (GRCm39) |
R467G |
probably benign |
Het |
Ccdc68 |
T |
A |
18: 70,102,084 (GRCm39) |
M327K |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,873,138 (GRCm39) |
T406A |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,468,232 (GRCm39) |
V55D |
probably damaging |
Het |
Cldn12 |
A |
G |
5: 5,558,008 (GRCm39) |
F140L |
probably benign |
Het |
Copb1 |
A |
C |
7: 113,844,720 (GRCm39) |
I213S |
possibly damaging |
Het |
Cps1 |
G |
A |
1: 67,179,016 (GRCm39) |
G76D |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,567,627 (GRCm39) |
W159R |
probably damaging |
Het |
Cul4a |
C |
T |
8: 13,190,279 (GRCm39) |
T572M |
possibly damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,796,050 (GRCm39) |
Y109* |
probably null |
Het |
Dcc |
A |
G |
18: 71,553,317 (GRCm39) |
Y780H |
probably benign |
Het |
Dctn1 |
C |
T |
6: 83,166,887 (GRCm39) |
A283V |
possibly damaging |
Het |
Dio1 |
T |
C |
4: 107,154,874 (GRCm39) |
D134G |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,227,907 (GRCm39) |
L338Q |
probably damaging |
Het |
Dlg5 |
A |
T |
14: 24,198,390 (GRCm39) |
D1514E |
probably benign |
Het |
Dlgap2 |
A |
T |
8: 14,879,952 (GRCm39) |
K767N |
probably damaging |
Het |
Dst |
A |
T |
1: 34,313,270 (GRCm39) |
I4346F |
probably benign |
Het |
Dzip1l |
T |
C |
9: 99,543,065 (GRCm39) |
F507L |
probably benign |
Het |
Erich2 |
A |
T |
2: 70,362,109 (GRCm39) |
D300V |
probably damaging |
Het |
Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
Fam131a |
C |
T |
16: 20,520,444 (GRCm39) |
A299V |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,247,143 (GRCm39) |
|
probably null |
Het |
Fbn2 |
T |
C |
18: 58,204,912 (GRCm39) |
D1177G |
possibly damaging |
Het |
Fbxl6 |
T |
C |
15: 76,422,113 (GRCm39) |
|
probably null |
Het |
Frem3 |
A |
T |
8: 81,339,965 (GRCm39) |
I753F |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,288,744 (GRCm39) |
S234P |
probably damaging |
Het |
Gtse1 |
T |
A |
15: 85,752,901 (GRCm39) |
S339T |
probably benign |
Het |
Hdgfl3 |
T |
C |
7: 81,550,106 (GRCm39) |
N76S |
probably benign |
Het |
Herc6 |
A |
G |
6: 57,558,089 (GRCm39) |
E23G |
probably benign |
Het |
Hid1 |
T |
A |
11: 115,245,545 (GRCm39) |
H420L |
probably damaging |
Het |
Igsf21 |
G |
A |
4: 139,755,049 (GRCm39) |
T440I |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,468,451 (GRCm39) |
H676L |
unknown |
Het |
Il18r1 |
A |
G |
1: 40,520,140 (GRCm39) |
E177G |
probably benign |
Het |
Iqch |
A |
G |
9: 63,415,599 (GRCm39) |
Y558H |
possibly damaging |
Het |
Kif11 |
A |
T |
19: 37,399,072 (GRCm39) |
N752I |
possibly damaging |
Het |
Kntc1 |
T |
A |
5: 123,925,019 (GRCm39) |
C1111S |
possibly damaging |
Het |
Krtap9-5 |
A |
G |
11: 99,839,800 (GRCm39) |
K167R |
unknown |
Het |
Lgalsl2 |
C |
T |
7: 5,362,440 (GRCm39) |
R24C |
probably benign |
Het |
Lipe |
G |
T |
7: 25,080,036 (GRCm39) |
T704K |
probably benign |
Het |
Lrrc32 |
A |
T |
7: 98,147,414 (GRCm39) |
I65F |
possibly damaging |
Het |
Mogs |
C |
T |
6: 83,093,188 (GRCm39) |
H179Y |
probably damaging |
Het |
Mtnr1b |
A |
T |
9: 15,774,590 (GRCm39) |
Y156* |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,537,590 (GRCm39) |
H42R |
probably benign |
Het |
Mx2 |
T |
A |
16: 97,346,918 (GRCm39) |
D128E |
probably benign |
Het |
Myof |
A |
T |
19: 37,939,939 (GRCm39) |
L829* |
probably null |
Het |
Naip6 |
T |
C |
13: 100,420,359 (GRCm39) |
K1304E |
probably benign |
Het |
Neo1 |
A |
C |
9: 58,791,826 (GRCm39) |
S1307R |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,359,779 (GRCm39) |
D1475E |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 19,757,875 (GRCm39) |
F371I |
probably damaging |
Het |
Nrip1 |
A |
T |
16: 76,088,338 (GRCm39) |
M1073K |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,567,863 (GRCm39) |
N195D |
probably damaging |
Het |
Or13a18 |
T |
A |
7: 140,190,091 (GRCm39) |
I4K |
probably benign |
Het |
Or1j18 |
T |
A |
2: 36,624,650 (GRCm39) |
F106I |
probably benign |
Het |
Or5ac24 |
A |
T |
16: 59,165,687 (GRCm39) |
C126S |
probably damaging |
Het |
Or5b99 |
C |
T |
19: 12,976,922 (GRCm39) |
H191Y |
probably benign |
Het |
Or5p64 |
C |
A |
7: 107,855,045 (GRCm39) |
C100F |
probably damaging |
Het |
Pax7 |
T |
C |
4: 139,511,880 (GRCm39) |
K232E |
probably benign |
Het |
Phldb3 |
C |
T |
7: 24,310,689 (GRCm39) |
|
probably benign |
Het |
Pkd1l1 |
C |
A |
11: 8,915,148 (GRCm39) |
V131L |
|
Het |
Ppp2r5a |
A |
G |
1: 191,128,532 (GRCm39) |
S28P |
probably benign |
Het |
Prl8a1 |
A |
G |
13: 27,758,068 (GRCm39) |
S214P |
probably damaging |
Het |
Prmt2 |
A |
T |
10: 76,056,838 (GRCm39) |
C228* |
probably null |
Het |
Prpf8 |
C |
T |
11: 75,399,738 (GRCm39) |
R2266* |
probably null |
Het |
Rabl6 |
A |
G |
2: 25,474,153 (GRCm39) |
S648P |
unknown |
Het |
Ralgapa1 |
T |
C |
12: 55,759,457 (GRCm39) |
K1022R |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,285,275 (GRCm39) |
D591E |
probably benign |
Het |
Rprd1a |
A |
G |
18: 24,639,889 (GRCm39) |
|
probably null |
Het |
Rsu1 |
T |
C |
2: 13,221,686 (GRCm39) |
R165G |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,842,491 (GRCm39) |
E334G |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,364,561 (GRCm39) |
Q804L |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,864,711 (GRCm39) |
D557G |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,427,501 (GRCm39) |
|
probably null |
Het |
Slc17a3 |
T |
A |
13: 24,039,832 (GRCm39) |
M290K |
|
Het |
Snd1 |
T |
A |
6: 28,531,449 (GRCm39) |
V330E |
probably benign |
Het |
Tceanc2 |
T |
C |
4: 107,022,852 (GRCm39) |
K45R |
probably damaging |
Het |
Tg |
A |
T |
15: 66,568,437 (GRCm39) |
I1375F |
probably benign |
Het |
Tmem116 |
T |
A |
5: 121,633,124 (GRCm39) |
I357K |
|
Het |
Tmem39a |
G |
T |
16: 38,408,658 (GRCm39) |
R407L |
possibly damaging |
Het |
Tmem74 |
A |
T |
15: 43,730,761 (GRCm39) |
M94K |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,398,751 (GRCm39) |
C226Y |
probably damaging |
Het |
Trbv21 |
T |
C |
6: 41,179,861 (GRCm39) |
I59T |
not run |
Het |
Trim11 |
A |
G |
11: 58,869,463 (GRCm39) |
D133G |
probably benign |
Het |
Uaca |
G |
A |
9: 60,753,282 (GRCm39) |
V76I |
probably damaging |
Het |
Ugt2a3 |
A |
G |
5: 87,475,539 (GRCm39) |
|
probably null |
Het |
Vmn2r104 |
G |
T |
17: 20,249,737 (GRCm39) |
H845N |
probably benign |
Het |
Wdr24 |
T |
C |
17: 26,045,101 (GRCm39) |
Y279H |
probably damaging |
Het |
Zbtb46 |
A |
G |
2: 181,065,512 (GRCm39) |
S213P |
probably benign |
Het |
Zdhhc13 |
C |
A |
7: 48,461,103 (GRCm39) |
Y346* |
probably null |
Het |
Zfp280b |
A |
T |
10: 75,875,075 (GRCm39) |
H318L |
probably damaging |
Het |
|
Other mutations in Cdcp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Cdcp3
|
APN |
7 |
130,839,823 (GRCm39) |
splice site |
probably null |
|
IGL00848:Cdcp3
|
APN |
7 |
130,848,453 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00966:Cdcp3
|
APN |
7 |
130,844,836 (GRCm39) |
nonsense |
probably null |
|
IGL01286:Cdcp3
|
APN |
7 |
130,848,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Cdcp3
|
APN |
7 |
130,796,060 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01585:Cdcp3
|
APN |
7 |
130,846,487 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01665:Cdcp3
|
APN |
7 |
130,848,386 (GRCm39) |
nonsense |
probably null |
|
IGL01953:Cdcp3
|
APN |
7 |
130,826,709 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02427:Cdcp3
|
APN |
7 |
130,846,517 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02508:Cdcp3
|
APN |
7 |
130,824,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02678:Cdcp3
|
APN |
7 |
130,830,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03092:Cdcp3
|
APN |
7 |
130,803,527 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03122:Cdcp3
|
APN |
7 |
130,798,243 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03343:Cdcp3
|
APN |
7 |
130,848,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Cdcp3
|
UTSW |
7 |
130,831,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R0011:Cdcp3
|
UTSW |
7 |
130,831,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R0234:Cdcp3
|
UTSW |
7 |
130,796,032 (GRCm39) |
splice site |
probably null |
|
R0234:Cdcp3
|
UTSW |
7 |
130,796,032 (GRCm39) |
splice site |
probably null |
|
R0268:Cdcp3
|
UTSW |
7 |
130,839,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Cdcp3
|
UTSW |
7 |
130,841,268 (GRCm39) |
missense |
probably benign |
0.05 |
R0973:Cdcp3
|
UTSW |
7 |
130,839,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Cdcp3
|
UTSW |
7 |
130,839,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Cdcp3
|
UTSW |
7 |
130,839,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Cdcp3
|
UTSW |
7 |
130,846,560 (GRCm39) |
nonsense |
probably null |
|
R1911:Cdcp3
|
UTSW |
7 |
130,839,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2032:Cdcp3
|
UTSW |
7 |
130,844,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R2097:Cdcp3
|
UTSW |
7 |
130,783,693 (GRCm39) |
nonsense |
probably null |
|
R2221:Cdcp3
|
UTSW |
7 |
130,849,186 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2223:Cdcp3
|
UTSW |
7 |
130,849,186 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2254:Cdcp3
|
UTSW |
7 |
130,824,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R2913:Cdcp3
|
UTSW |
7 |
130,783,753 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2991:Cdcp3
|
UTSW |
7 |
130,848,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R3439:Cdcp3
|
UTSW |
7 |
130,790,508 (GRCm39) |
critical splice donor site |
probably null |
|
R4418:Cdcp3
|
UTSW |
7 |
130,849,194 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4916:Cdcp3
|
UTSW |
7 |
130,776,206 (GRCm39) |
splice site |
probably null |
|
R5488:Cdcp3
|
UTSW |
7 |
130,848,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Cdcp3
|
UTSW |
7 |
130,841,252 (GRCm39) |
missense |
probably benign |
0.12 |
R5897:Cdcp3
|
UTSW |
7 |
130,798,280 (GRCm39) |
splice site |
probably null |
|
R5898:Cdcp3
|
UTSW |
7 |
130,843,696 (GRCm39) |
splice site |
probably null |
|
R5940:Cdcp3
|
UTSW |
7 |
130,839,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Cdcp3
|
UTSW |
7 |
130,776,216 (GRCm39) |
splice site |
probably null |
|
R6187:Cdcp3
|
UTSW |
7 |
130,872,328 (GRCm39) |
intron |
probably benign |
|
R6321:Cdcp3
|
UTSW |
7 |
130,858,735 (GRCm39) |
critical splice donor site |
probably null |
|
R6409:Cdcp3
|
UTSW |
7 |
130,863,800 (GRCm39) |
intron |
probably benign |
|
R6432:Cdcp3
|
UTSW |
7 |
130,846,601 (GRCm39) |
critical splice donor site |
probably null |
|
R6481:Cdcp3
|
UTSW |
7 |
130,858,530 (GRCm39) |
missense |
probably benign |
0.05 |
R6750:Cdcp3
|
UTSW |
7 |
130,889,974 (GRCm39) |
intron |
probably benign |
|
R6783:Cdcp3
|
UTSW |
7 |
130,828,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R6836:Cdcp3
|
UTSW |
7 |
130,798,233 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6925:Cdcp3
|
UTSW |
7 |
130,824,436 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6995:Cdcp3
|
UTSW |
7 |
130,824,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Cdcp3
|
UTSW |
7 |
130,837,641 (GRCm39) |
nonsense |
probably null |
|
R7205:Cdcp3
|
UTSW |
7 |
130,879,352 (GRCm39) |
critical splice donor site |
probably null |
|
R7340:Cdcp3
|
UTSW |
7 |
130,879,344 (GRCm39) |
missense |
unknown |
|
R7354:Cdcp3
|
UTSW |
7 |
130,873,762 (GRCm39) |
missense |
unknown |
|
R7354:Cdcp3
|
UTSW |
7 |
130,858,458 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7434:Cdcp3
|
UTSW |
7 |
130,881,212 (GRCm39) |
missense |
unknown |
|
R7513:Cdcp3
|
UTSW |
7 |
130,873,800 (GRCm39) |
missense |
unknown |
|
R7562:Cdcp3
|
UTSW |
7 |
130,904,426 (GRCm39) |
missense |
unknown |
|
R7623:Cdcp3
|
UTSW |
7 |
130,879,295 (GRCm39) |
splice site |
probably null |
|
R7782:Cdcp3
|
UTSW |
7 |
130,904,466 (GRCm39) |
splice site |
probably null |
|
R7879:Cdcp3
|
UTSW |
7 |
130,844,871 (GRCm39) |
missense |
probably damaging |
0.98 |
R7935:Cdcp3
|
UTSW |
7 |
130,852,205 (GRCm39) |
missense |
probably damaging |
0.96 |
R7949:Cdcp3
|
UTSW |
7 |
130,895,324 (GRCm39) |
splice site |
probably null |
|
R7964:Cdcp3
|
UTSW |
7 |
130,899,963 (GRCm39) |
missense |
unknown |
|
R7980:Cdcp3
|
UTSW |
7 |
130,836,506 (GRCm39) |
missense |
probably damaging |
0.98 |
R8145:Cdcp3
|
UTSW |
7 |
130,898,045 (GRCm39) |
missense |
unknown |
|
R8673:Cdcp3
|
UTSW |
7 |
130,844,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:Cdcp3
|
UTSW |
7 |
130,837,688 (GRCm39) |
nonsense |
probably null |
|
R8721:Cdcp3
|
UTSW |
7 |
130,879,335 (GRCm39) |
missense |
unknown |
|
R8725:Cdcp3
|
UTSW |
7 |
130,875,485 (GRCm39) |
missense |
unknown |
|
R8727:Cdcp3
|
UTSW |
7 |
130,875,485 (GRCm39) |
missense |
unknown |
|
R8742:Cdcp3
|
UTSW |
7 |
130,783,741 (GRCm39) |
missense |
unknown |
|
R8807:Cdcp3
|
UTSW |
7 |
130,846,507 (GRCm39) |
missense |
probably damaging |
0.97 |
R8822:Cdcp3
|
UTSW |
7 |
130,843,706 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8861:Cdcp3
|
UTSW |
7 |
130,861,690 (GRCm39) |
nonsense |
probably null |
|
R8897:Cdcp3
|
UTSW |
7 |
130,867,566 (GRCm39) |
missense |
unknown |
|
R8900:Cdcp3
|
UTSW |
7 |
130,904,197 (GRCm39) |
intron |
probably benign |
|
R9214:Cdcp3
|
UTSW |
7 |
130,824,481 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9218:Cdcp3
|
UTSW |
7 |
130,863,728 (GRCm39) |
missense |
unknown |
|
R9311:Cdcp3
|
UTSW |
7 |
130,859,490 (GRCm39) |
missense |
unknown |
|
R9323:Cdcp3
|
UTSW |
7 |
130,828,401 (GRCm39) |
missense |
probably damaging |
0.96 |
R9384:Cdcp3
|
UTSW |
7 |
130,904,404 (GRCm39) |
missense |
unknown |
|
R9387:Cdcp3
|
UTSW |
7 |
130,863,620 (GRCm39) |
missense |
unknown |
|
R9417:Cdcp3
|
UTSW |
7 |
130,852,218 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9502:Cdcp3
|
UTSW |
7 |
130,836,815 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9603:Cdcp3
|
UTSW |
7 |
130,830,643 (GRCm39) |
missense |
probably damaging |
0.98 |
R9642:Cdcp3
|
UTSW |
7 |
130,848,257 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Cdcp3
|
UTSW |
7 |
130,848,362 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cdcp3
|
UTSW |
7 |
130,867,595 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- ACATCACAGACAGGCTTTGG -3'
(R):5'- GTCAAGTGTCTTGTCCAAAGTC -3'
Sequencing Primer
(F):5'- CAGGCTTTGGGCTTGCTCC -3'
(R):5'- TGTCTTGTCCAAAGTCACAGAAC -3'
|
Posted On |
2019-10-07 |