Incidental Mutation 'R0268:Cdcp3'
ID |
35071 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cdcp3
|
Ensembl Gene |
ENSMUSG00000006204 |
Gene Name |
CUB domain containing protein 3 |
Synonyms |
5430419D17Rik |
MMRRC Submission |
038494-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0268 (G1)
|
Quality Score |
218 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
130776131-130908180 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 130839905 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 609
(D609G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000150784
(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: D493G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000061529 Gene: ENSMUSG00000006204 AA Change: D493G
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 benign
Transcript: ENSMUST00000128522
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000208921
AA Change: D609G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.7%
- 10x: 95.9%
- 20x: 93.0%
|
Validation Efficiency |
98% (93/95) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
T |
A |
7: 29,274,027 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl4 |
A |
T |
4: 144,349,565 (GRCm39) |
H274L |
probably benign |
Het |
Aldh1a7 |
T |
A |
19: 20,686,866 (GRCm39) |
|
probably null |
Het |
Ap3m1 |
A |
C |
14: 21,087,170 (GRCm39) |
|
probably benign |
Het |
Atp5f1a |
C |
A |
18: 77,867,895 (GRCm39) |
N356K |
probably damaging |
Het |
AU021092 |
A |
T |
16: 5,040,031 (GRCm39) |
M31K |
possibly damaging |
Het |
Avpr1a |
T |
C |
10: 122,285,614 (GRCm39) |
V302A |
probably damaging |
Het |
Bicral |
A |
G |
17: 47,124,978 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
Casp8ap2 |
A |
T |
4: 32,644,079 (GRCm39) |
I1051F |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,899,125 (GRCm39) |
I196V |
probably benign |
Het |
Cdc42bpa |
G |
T |
1: 179,983,347 (GRCm39) |
|
probably benign |
Het |
Clec16a |
T |
A |
16: 10,462,692 (GRCm39) |
L670* |
probably null |
Het |
Cmtm2b |
A |
G |
8: 105,049,066 (GRCm39) |
E27G |
probably damaging |
Het |
Col4a1 |
T |
A |
8: 11,317,588 (GRCm39) |
|
probably benign |
Het |
Cyp26b1 |
A |
T |
6: 84,551,554 (GRCm39) |
F221I |
probably damaging |
Het |
D430041D05Rik |
G |
C |
2: 103,998,295 (GRCm39) |
P1836R |
probably damaging |
Het |
Dennd6b |
T |
C |
15: 89,080,432 (GRCm39) |
Q56R |
probably benign |
Het |
Dip2c |
G |
A |
13: 9,687,186 (GRCm39) |
R1270H |
probably damaging |
Het |
Dlg1 |
T |
C |
16: 31,503,011 (GRCm39) |
C73R |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,988,681 (GRCm39) |
D3217G |
probably damaging |
Het |
Dtx1 |
T |
C |
5: 120,819,356 (GRCm39) |
E614G |
probably damaging |
Het |
Dut |
C |
A |
2: 125,099,011 (GRCm39) |
A166E |
probably damaging |
Het |
Ebf1 |
C |
A |
11: 44,534,240 (GRCm39) |
D166E |
probably damaging |
Het |
Egln2 |
A |
T |
7: 26,864,672 (GRCm39) |
D84E |
possibly damaging |
Het |
Exosc7 |
T |
A |
9: 122,948,025 (GRCm39) |
S65T |
probably benign |
Het |
Fam83e |
G |
A |
7: 45,376,334 (GRCm39) |
R349Q |
probably benign |
Het |
Fbxl17 |
G |
A |
17: 63,692,062 (GRCm39) |
|
probably benign |
Het |
Fras1 |
A |
G |
5: 96,884,868 (GRCm39) |
N2582S |
probably damaging |
Het |
Fubp1 |
T |
C |
3: 151,925,350 (GRCm39) |
V164A |
probably damaging |
Het |
Gfral |
A |
T |
9: 76,104,383 (GRCm39) |
C210S |
probably damaging |
Het |
Gls |
GGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTGCTGCTGCTG |
1: 52,271,853 (GRCm39) |
|
probably benign |
Het |
Hcn4 |
A |
C |
9: 58,767,445 (GRCm39) |
E1002A |
unknown |
Het |
Hcrtr2 |
A |
G |
9: 76,135,470 (GRCm39) |
V449A |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,815,891 (GRCm39) |
S1394G |
possibly damaging |
Het |
Hectd1 |
C |
A |
12: 51,815,890 (GRCm39) |
S1394I |
probably damaging |
Het |
Hecw2 |
A |
G |
1: 53,965,857 (GRCm39) |
|
probably benign |
Het |
Herc3 |
A |
G |
6: 58,845,613 (GRCm39) |
|
probably benign |
Het |
Ipo4 |
T |
C |
14: 55,863,399 (GRCm39) |
Q1073R |
possibly damaging |
Het |
Itsn2 |
G |
A |
12: 4,750,333 (GRCm39) |
R1199Q |
probably benign |
Het |
Kcnj3 |
C |
A |
2: 55,484,971 (GRCm39) |
Y356* |
probably null |
Het |
Klb |
T |
A |
5: 65,506,180 (GRCm39) |
D142E |
probably benign |
Het |
Klhl35 |
T |
A |
7: 99,120,958 (GRCm39) |
S409T |
probably benign |
Het |
Krt16 |
T |
A |
11: 100,137,351 (GRCm39) |
|
probably benign |
Het |
Krt82 |
C |
A |
15: 101,450,148 (GRCm39) |
R516L |
probably benign |
Het |
Lce3a |
A |
T |
3: 92,833,038 (GRCm39) |
C21S |
unknown |
Het |
Lims2 |
A |
G |
18: 32,077,573 (GRCm39) |
E103G |
probably benign |
Het |
Map2 |
A |
T |
1: 66,419,881 (GRCm39) |
K71* |
probably null |
Het |
Mthfr |
C |
G |
4: 148,139,885 (GRCm39) |
S618W |
probably damaging |
Het |
Mycbp2 |
T |
A |
14: 103,551,761 (GRCm39) |
R157* |
probably null |
Het |
Nat10 |
C |
A |
2: 103,558,262 (GRCm39) |
|
probably benign |
Het |
Obscn |
G |
A |
11: 58,958,098 (GRCm39) |
T3810M |
possibly damaging |
Het |
Or13a19 |
G |
A |
7: 139,903,068 (GRCm39) |
S152N |
possibly damaging |
Het |
Or1x6 |
T |
A |
11: 50,939,768 (GRCm39) |
M278K |
probably damaging |
Het |
Or5d35 |
A |
T |
2: 87,855,812 (GRCm39) |
I249F |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,645 (GRCm39) |
T254A |
possibly damaging |
Het |
Or6c209 |
A |
T |
10: 129,483,045 (GRCm39) |
D16V |
possibly damaging |
Het |
Or7a38 |
C |
T |
10: 78,753,439 (GRCm39) |
T255I |
probably damaging |
Het |
Park7 |
A |
G |
4: 150,992,806 (GRCm39) |
V20A |
possibly damaging |
Het |
Pgm2 |
T |
A |
5: 64,263,151 (GRCm39) |
V266E |
probably damaging |
Het |
Phip |
G |
A |
9: 82,753,341 (GRCm39) |
T1801I |
probably damaging |
Het |
Pkhd1l1 |
C |
A |
15: 44,460,407 (GRCm39) |
H4205Q |
probably benign |
Het |
Ppp1r12a |
T |
A |
10: 108,109,242 (GRCm39) |
|
probably benign |
Het |
Pramel26 |
A |
T |
4: 143,537,338 (GRCm39) |
I331N |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,541,409 (GRCm39) |
D372E |
probably benign |
Het |
Ptprr |
G |
A |
10: 116,088,868 (GRCm39) |
V340I |
possibly damaging |
Het |
Qki |
A |
G |
17: 10,428,575 (GRCm39) |
|
probably benign |
Het |
Qpct |
T |
A |
17: 79,385,081 (GRCm39) |
D240E |
probably benign |
Het |
Ren1 |
A |
G |
1: 133,283,349 (GRCm39) |
T162A |
possibly damaging |
Het |
Rif1 |
T |
C |
2: 51,980,298 (GRCm39) |
|
probably null |
Het |
Sart3 |
A |
G |
5: 113,890,460 (GRCm39) |
V461A |
probably damaging |
Het |
Saxo4 |
A |
G |
19: 10,454,449 (GRCm39) |
V329A |
possibly damaging |
Het |
Scgb1b24 |
G |
A |
7: 33,443,278 (GRCm39) |
G19R |
probably null |
Het |
Spen |
A |
T |
4: 141,204,868 (GRCm39) |
I1253N |
unknown |
Het |
Sspo |
C |
A |
6: 48,442,489 (GRCm39) |
H1995N |
probably benign |
Het |
Tfap2c |
A |
G |
2: 172,393,423 (GRCm39) |
T113A |
probably benign |
Het |
Togaram2 |
T |
C |
17: 72,004,993 (GRCm39) |
|
probably null |
Het |
Trim65 |
T |
A |
11: 116,017,470 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
T |
A |
19: 22,874,885 (GRCm39) |
|
probably null |
Het |
Ubxn7 |
T |
C |
16: 32,178,864 (GRCm39) |
I87T |
probably benign |
Het |
Vav1 |
T |
C |
17: 57,603,090 (GRCm39) |
F81L |
probably damaging |
Het |
Vmn2r102 |
A |
G |
17: 19,898,112 (GRCm39) |
T376A |
probably benign |
Het |
Vmn2r105 |
A |
T |
17: 20,428,938 (GRCm39) |
C713S |
probably benign |
Het |
Zbtb45 |
C |
T |
7: 12,742,254 (GRCm39) |
M1I |
probably null |
Het |
Zfp229 |
A |
T |
17: 21,964,822 (GRCm39) |
M351L |
probably benign |
Het |
Zfp932 |
T |
C |
5: 110,156,929 (GRCm39) |
I176T |
probably benign |
Het |
Zswim1 |
G |
A |
2: 164,668,046 (GRCm39) |
E433K |
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 |
|
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 |
|
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'- TCAGGACGAGTGGAAATCCTCTACC -3'
(R):5'- TGGAATCCTTACTGCAATGCCCC -3'
Sequencing Primer
(F):5'- TGGAAATCCTCTACCAGGGAGTC -3'
(R):5'- TTACTGCAATGCCCCAGAGTG -3'
|
Posted On |
2013-05-09 |