Incidental Mutation 'R7980:Cdcp3'
ID |
651147 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cdcp3
|
Ensembl Gene |
ENSMUSG00000006204 |
Gene Name |
CUB domain containing protein 3 |
Synonyms |
5430419D17Rik |
MMRRC Submission |
046021-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7980 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
130776131-130908180 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 130836506 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Glutamic Acid
at position 400
(V400E)
|
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: V400E
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000061529 Gene: ENSMUSG00000006204 AA Change: V400E
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 |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000208921
AA Change: V400E
PolyPhen 2
Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
100% (87/87) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
A |
G |
4: 88,786,315 (GRCm39) |
L101P |
unknown |
Het |
Actn3 |
G |
A |
19: 4,917,950 (GRCm39) |
P339L |
probably damaging |
Het |
Adamts12 |
G |
A |
15: 11,263,423 (GRCm39) |
C595Y |
probably damaging |
Het |
Adrm1b |
T |
A |
3: 92,336,406 (GRCm39) |
K99* |
probably null |
Het |
Agl |
A |
T |
3: 116,585,830 (GRCm39) |
N99K |
probably benign |
Het |
Aplp1 |
A |
T |
7: 30,134,992 (GRCm39) |
M592K |
probably benign |
Het |
Arhgef11 |
C |
T |
3: 87,605,297 (GRCm39) |
R251C |
probably benign |
Het |
Arhgef12 |
A |
T |
9: 42,882,595 (GRCm39) |
C1416* |
probably null |
Het |
Asah1 |
A |
G |
8: 41,807,067 (GRCm39) |
M119T |
|
Het |
Asxl2 |
A |
T |
12: 3,546,630 (GRCm39) |
Q471H |
probably damaging |
Het |
Atp6v1c2 |
A |
T |
12: 17,371,613 (GRCm39) |
D61E |
probably damaging |
Het |
Btbd16 |
C |
A |
7: 130,426,097 (GRCm39) |
P520Q |
probably damaging |
Het |
Cacnb2 |
A |
G |
2: 14,609,326 (GRCm39) |
E22G |
probably benign |
Het |
Catspere2 |
G |
T |
1: 177,830,610 (GRCm39) |
|
probably null |
Het |
Cdc25a |
T |
A |
9: 109,708,949 (GRCm39) |
D124E |
probably damaging |
Het |
Cdc42se1 |
A |
T |
3: 95,139,166 (GRCm39) |
|
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,817,922 (GRCm39) |
K1265E |
possibly damaging |
Het |
Chaf1b |
A |
G |
16: 93,681,415 (GRCm39) |
H11R |
probably damaging |
Het |
Chil4 |
T |
C |
3: 106,110,060 (GRCm39) |
K345E |
probably damaging |
Het |
Cntnap1 |
A |
G |
11: 101,079,719 (GRCm39) |
I1283V |
probably benign |
Het |
Dagla |
C |
T |
19: 10,229,406 (GRCm39) |
C618Y |
possibly damaging |
Het |
Ddx19b |
C |
T |
8: 111,738,077 (GRCm39) |
V224M |
possibly damaging |
Het |
Dohh |
C |
T |
10: 81,223,726 (GRCm39) |
R260* |
probably null |
Het |
Dsg3 |
A |
T |
18: 20,664,417 (GRCm39) |
N472Y |
probably benign |
Het |
Duox1 |
T |
A |
2: 122,177,801 (GRCm39) |
N1528K |
possibly damaging |
Het |
Eml6 |
A |
G |
11: 29,783,205 (GRCm39) |
Y559H |
probably damaging |
Het |
Esp4 |
A |
G |
17: 40,913,192 (GRCm39) |
T20A |
possibly damaging |
Het |
Fbxw21 |
T |
C |
9: 108,985,639 (GRCm39) |
|
probably null |
Het |
Gcc2 |
T |
A |
10: 58,114,574 (GRCm39) |
|
probably null |
Het |
Grin3b |
C |
T |
10: 79,811,559 (GRCm39) |
A715V |
possibly damaging |
Het |
Gxylt2 |
A |
T |
6: 100,764,170 (GRCm39) |
|
probably null |
Het |
Hspa4 |
A |
T |
11: 53,171,404 (GRCm39) |
S267T |
probably benign |
Het |
Hspd1 |
A |
G |
1: 55,117,785 (GRCm39) |
V491A |
possibly damaging |
Het |
Idua |
A |
G |
5: 108,828,486 (GRCm39) |
E280G |
probably benign |
Het |
Ift172 |
T |
A |
5: 31,417,988 (GRCm39) |
E1267V |
probably benign |
Het |
Itsn1 |
T |
A |
16: 91,702,182 (GRCm39) |
V1448E |
unknown |
Het |
Kat6a |
A |
G |
8: 23,416,432 (GRCm39) |
M647V |
possibly damaging |
Het |
Kcnq4 |
A |
T |
4: 120,568,494 (GRCm39) |
D407E |
probably benign |
Het |
Kif1b |
A |
T |
4: 149,354,378 (GRCm39) |
F221I |
probably damaging |
Het |
Lama2 |
G |
T |
10: 27,239,609 (GRCm39) |
D315E |
probably damaging |
Het |
Lrrn4 |
G |
A |
2: 132,720,096 (GRCm39) |
L235F |
probably damaging |
Het |
Map2k6 |
T |
A |
11: 110,390,210 (GRCm39) |
I248N |
|
Het |
Mgat5 |
A |
G |
1: 127,407,248 (GRCm39) |
Q638R |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,155,651 (GRCm39) |
K455E |
probably damaging |
Het |
Mrs2 |
A |
G |
13: 25,204,221 (GRCm39) |
C3R |
possibly damaging |
Het |
Nprl3 |
A |
G |
11: 32,187,357 (GRCm39) |
I325T |
probably damaging |
Het |
Nr1h3 |
T |
A |
2: 91,021,229 (GRCm39) |
Q186L |
probably benign |
Het |
Oas1f |
A |
G |
5: 120,989,538 (GRCm39) |
E159G |
probably benign |
Het |
Or2g7 |
A |
T |
17: 38,378,412 (GRCm39) |
M117L |
possibly damaging |
Het |
Or4k15b |
T |
A |
14: 50,272,252 (GRCm39) |
S203C |
probably damaging |
Het |
Or52ae7 |
T |
A |
7: 103,119,504 (GRCm39) |
F86Y |
probably damaging |
Het |
Or52e19b |
T |
A |
7: 103,032,970 (GRCm39) |
I80F |
probably damaging |
Het |
Or52s1b |
T |
A |
7: 102,822,242 (GRCm39) |
S201C |
probably damaging |
Het |
Or5m12 |
A |
G |
2: 85,734,942 (GRCm39) |
F152S |
probably benign |
Het |
Or8g4 |
T |
C |
9: 39,662,417 (GRCm39) |
I245T |
probably damaging |
Het |
Or9a4 |
T |
A |
6: 40,549,154 (GRCm39) |
I278N |
probably benign |
Het |
Pbxip1 |
G |
C |
3: 89,353,648 (GRCm39) |
S267T |
probably benign |
Het |
Pcdhga10 |
A |
T |
18: 37,881,645 (GRCm39) |
I469F |
possibly damaging |
Het |
Pkd1l1 |
A |
G |
11: 8,804,375 (GRCm39) |
S1739P |
probably damaging |
Het |
Plcd4 |
A |
C |
1: 74,604,464 (GRCm39) |
N788T |
probably benign |
Het |
Pms2 |
T |
A |
5: 143,867,909 (GRCm39) |
W838R |
probably damaging |
Het |
Pnpla6 |
T |
A |
8: 3,586,562 (GRCm39) |
V926D |
probably damaging |
Het |
Pros1 |
A |
T |
16: 62,748,516 (GRCm39) |
H663L |
possibly damaging |
Het |
Prss55 |
T |
C |
14: 64,316,138 (GRCm39) |
|
probably null |
Het |
Pum2 |
T |
C |
12: 8,763,904 (GRCm39) |
Y283H |
probably damaging |
Het |
Rad21 |
A |
G |
15: 51,828,422 (GRCm39) |
S549P |
probably benign |
Het |
Sap130 |
T |
A |
18: 31,781,182 (GRCm39) |
|
probably null |
Het |
Sertad4 |
C |
T |
1: 192,529,189 (GRCm39) |
S209N |
probably benign |
Het |
Sez6 |
A |
G |
11: 77,844,668 (GRCm39) |
T164A |
probably benign |
Het |
Slc22a28 |
C |
T |
19: 8,078,837 (GRCm39) |
R284Q |
probably damaging |
Het |
Slco4c1 |
T |
C |
1: 96,764,650 (GRCm39) |
K474R |
probably benign |
Het |
Stx5a |
T |
C |
19: 8,719,802 (GRCm39) |
S56P |
probably damaging |
Het |
Svopl |
T |
C |
6: 37,991,744 (GRCm39) |
T379A |
probably damaging |
Het |
Sypl2 |
A |
G |
3: 108,125,008 (GRCm39) |
F118L |
probably damaging |
Het |
Tfrc |
G |
A |
16: 32,435,967 (GRCm39) |
V215M |
probably benign |
Het |
Thnsl2 |
T |
C |
6: 71,115,652 (GRCm39) |
N185S |
probably damaging |
Het |
Tmem104 |
T |
C |
11: 115,134,580 (GRCm39) |
I372T |
probably damaging |
Het |
Tnfaip6 |
G |
A |
2: 51,941,070 (GRCm39) |
G204S |
probably damaging |
Het |
Trim12a |
C |
T |
7: 103,953,335 (GRCm39) |
E259K |
probably benign |
Het |
Tubgcp6 |
G |
A |
15: 88,986,232 (GRCm39) |
R1436C |
probably benign |
Het |
Tyrp1 |
C |
T |
4: 80,758,864 (GRCm39) |
L246F |
probably damaging |
Het |
Ubr4 |
G |
T |
4: 139,145,717 (GRCm39) |
V216F |
|
Het |
Unc5a |
A |
G |
13: 55,147,319 (GRCm39) |
I409V |
possibly damaging |
Het |
Vmn1r15 |
T |
C |
6: 57,235,399 (GRCm39) |
L89P |
probably damaging |
Het |
Vmn1r32 |
A |
T |
6: 66,530,305 (GRCm39) |
L157* |
probably null |
Het |
Zcchc24 |
A |
G |
14: 25,720,185 (GRCm39) |
Y160H |
probably damaging |
Het |
Zfp184 |
A |
T |
13: 22,144,376 (GRCm39) |
H694L |
probably damaging |
Het |
Zfp345 |
A |
C |
2: 150,314,723 (GRCm39) |
Y271* |
probably null |
Het |
Zranb3 |
T |
C |
1: 128,030,671 (GRCm39) |
|
probably benign |
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 |
|
R7485:Cdcp3
|
UTSW |
7 |
130,830,562 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|
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'- GCTGCTGGGCTACATTAGAC -3'
(R):5'- AGGTGAGATGTTCCCACTGG -3'
Sequencing Primer
(F):5'- GGCTACATTAGACCCATGTGAAG -3'
(R):5'- CCACTGGGAGTATTTGAGAATTCTG -3'
|
Posted On |
2020-09-15 |