Incidental Mutation 'R1851:Cdon'
| ID |
208095 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cdon
|
| Ensembl Gene |
ENSMUSG00000038119 |
| Gene Name |
cell adhesion molecule-related/down-regulated by oncogenes |
| Synonyms |
CAM-related/down-regulated by oncogenes, CDO |
| MMRRC Submission |
039875-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.351)
|
| Stock # |
R1851 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
35332836-35418948 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 35394454 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Arginine
at position 900
(M900R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113977
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042842]
[ENSMUST00000119129]
|
| AlphaFold |
Q32MD9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000042842
AA Change: M900R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000045547
Gene: ENSMUSG00000038119
AA Change: M900R
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
103 |
1.35e-9 |
SMART |
|
IG
|
125 |
212 |
7.25e-1 |
SMART |
|
IGc2
|
233 |
296 |
1.38e-6 |
SMART |
|
IGc2
|
323 |
386 |
4.62e-17 |
SMART |
|
IGc2
|
416 |
506 |
5e-13 |
SMART |
|
FN3
|
573 |
660 |
2.18e-2 |
SMART |
|
FN3
|
717 |
800 |
1.89e-11 |
SMART |
|
FN3
|
822 |
909 |
7.01e-6 |
SMART |
|
transmembrane domain
|
962 |
984 |
N/A |
INTRINSIC |
|
low complexity region
|
1101 |
1111 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000119129
AA Change: M900R
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000113977
Gene: ENSMUSG00000038119
AA Change: M900R
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
103 |
1.35e-9 |
SMART |
|
IG
|
125 |
212 |
7.25e-1 |
SMART |
|
IGc2
|
233 |
296 |
1.38e-6 |
SMART |
|
IGc2
|
323 |
386 |
4.62e-17 |
SMART |
|
IGc2
|
416 |
506 |
5e-13 |
SMART |
|
FN3
|
573 |
660 |
2.18e-2 |
SMART |
|
FN3
|
717 |
800 |
1.89e-11 |
SMART |
|
FN3
|
822 |
909 |
7.01e-6 |
SMART |
|
transmembrane domain
|
962 |
984 |
N/A |
INTRINSIC |
|
low complexity region
|
1101 |
1111 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 94.9%
- 20x: 91.3%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a cell surface receptor that is a member of the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells and positively regulates myogenesis. [provided by RefSeq, Aug 2011]
PHENOTYPE: Homozygous null mice display facial defects characteristic of microform holoprosencephaly, are runted, and are prone to death prior to weaning. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 95 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 5730507C01Rik |
A |
G |
12: 18,583,687 (GRCm39) |
E225G |
possibly damaging |
Het |
| Abcb7 |
T |
C |
X: 103,349,005 (GRCm39) |
M153V |
probably benign |
Het |
| Abi1 |
A |
T |
2: 22,840,276 (GRCm39) |
V329D |
possibly damaging |
Het |
| Ablim3 |
G |
A |
18: 61,982,466 (GRCm39) |
H160Y |
probably benign |
Het |
| Acox3 |
A |
T |
5: 35,766,406 (GRCm39) |
D624V |
possibly damaging |
Het |
| Adam6b |
A |
G |
12: 113,455,442 (GRCm39) |
D753G |
probably benign |
Het |
| Ago1 |
C |
A |
4: 126,333,788 (GRCm39) |
R771L |
probably benign |
Het |
| Aktip |
A |
G |
8: 91,852,505 (GRCm39) |
V217A |
possibly damaging |
Het |
| Ankk1 |
A |
C |
9: 49,327,150 (GRCm39) |
H676Q |
probably benign |
Het |
| Arl1 |
G |
C |
10: 88,569,408 (GRCm39) |
|
probably benign |
Het |
| Asxl3 |
T |
A |
18: 22,650,796 (GRCm39) |
D928E |
probably damaging |
Het |
| AW209491 |
T |
C |
13: 14,811,318 (GRCm39) |
V57A |
possibly damaging |
Het |
| B3galt4 |
G |
T |
17: 34,169,885 (GRCm39) |
Q118K |
probably benign |
Het |
| Ccdc187 |
A |
T |
2: 26,166,080 (GRCm39) |
M783K |
probably benign |
Het |
| Ceacam5 |
G |
A |
7: 17,448,835 (GRCm39) |
W67* |
probably null |
Het |
| Chd5 |
A |
G |
4: 152,462,727 (GRCm39) |
S1356G |
probably damaging |
Het |
| Chil3 |
C |
T |
3: 106,056,117 (GRCm39) |
|
probably null |
Het |
| Chmp7 |
C |
T |
14: 69,956,899 (GRCm39) |
M336I |
probably benign |
Het |
| Cntn1 |
C |
T |
15: 92,203,021 (GRCm39) |
R768C |
probably damaging |
Het |
| Col6a3 |
T |
A |
1: 90,735,256 (GRCm39) |
I798F |
possibly damaging |
Het |
| Cpxcr1 |
T |
A |
X: 115,387,758 (GRCm39) |
L223* |
probably null |
Het |
| Cpz |
C |
A |
5: 35,659,902 (GRCm39) |
R581L |
possibly damaging |
Het |
| Cxcr2 |
A |
G |
1: 74,198,438 (GRCm39) |
I311V |
probably benign |
Het |
| Cym |
T |
A |
3: 107,126,030 (GRCm39) |
I78F |
probably benign |
Het |
| Defb8 |
A |
T |
8: 19,495,899 (GRCm39) |
S54T |
probably benign |
Het |
| Dennd4a |
A |
G |
9: 64,769,312 (GRCm39) |
T433A |
probably damaging |
Het |
| Dhx29 |
A |
G |
13: 113,084,815 (GRCm39) |
T678A |
probably damaging |
Het |
| Dspp |
T |
C |
5: 104,321,951 (GRCm39) |
|
probably null |
Het |
| Enkur |
G |
T |
2: 21,193,988 (GRCm39) |
A195E |
probably benign |
Het |
| Ero1b |
T |
A |
13: 12,619,292 (GRCm39) |
S429T |
possibly damaging |
Het |
| Fh1 |
A |
G |
1: 175,435,452 (GRCm39) |
S344P |
probably damaging |
Het |
| Flnc |
G |
T |
6: 29,443,478 (GRCm39) |
G553V |
probably damaging |
Het |
| Fmo1 |
A |
T |
1: 162,657,554 (GRCm39) |
L529* |
probably null |
Het |
| Frem1 |
C |
A |
4: 82,868,737 (GRCm39) |
V1415F |
probably damaging |
Het |
| Gatb |
T |
G |
3: 85,526,184 (GRCm39) |
L354R |
probably damaging |
Het |
| Gdpgp1 |
A |
T |
7: 79,888,349 (GRCm39) |
N127Y |
probably damaging |
Het |
| Gpat2 |
A |
G |
2: 127,276,739 (GRCm39) |
T648A |
possibly damaging |
Het |
| Grk6 |
C |
T |
13: 55,599,591 (GRCm39) |
R225* |
probably null |
Het |
| Hells |
A |
T |
19: 38,948,120 (GRCm39) |
Q682L |
probably null |
Het |
| Hspa5 |
T |
A |
2: 34,664,690 (GRCm39) |
N381K |
possibly damaging |
Het |
| Ighmbp2 |
T |
C |
19: 3,312,075 (GRCm39) |
N893S |
probably benign |
Het |
| Ipo11 |
A |
T |
13: 106,948,765 (GRCm39) |
V914E |
possibly damaging |
Het |
| Lars1 |
T |
C |
18: 42,345,673 (GRCm39) |
N1001S |
probably benign |
Het |
| Lats2 |
A |
G |
14: 57,934,912 (GRCm39) |
L606P |
probably damaging |
Het |
| Map4k1 |
T |
C |
7: 28,699,209 (GRCm39) |
Y521H |
probably benign |
Het |
| Marchf11 |
T |
A |
15: 26,387,916 (GRCm39) |
V257E |
probably damaging |
Het |
| Med23 |
G |
A |
10: 24,786,768 (GRCm39) |
|
probably null |
Het |
| Meltf |
A |
G |
16: 31,715,395 (GRCm39) |
D696G |
probably benign |
Het |
| Ms4a7 |
T |
A |
19: 11,301,788 (GRCm39) |
M212L |
probably benign |
Het |
| Mx1 |
A |
T |
16: 97,249,403 (GRCm39) |
L608Q |
probably damaging |
Het |
| Myh1 |
T |
C |
11: 67,095,224 (GRCm39) |
Y195H |
probably damaging |
Het |
| Napb |
G |
T |
2: 148,548,909 (GRCm39) |
H110Q |
probably benign |
Het |
| Ngly1 |
C |
T |
14: 16,260,585 (GRCm38) |
P90S |
probably damaging |
Het |
| Nlrp1b |
T |
A |
11: 71,073,442 (GRCm39) |
I134L |
possibly damaging |
Het |
| Nup210 |
A |
G |
6: 90,993,036 (GRCm39) |
L1017P |
probably damaging |
Het |
| Nup85 |
T |
A |
11: 115,472,643 (GRCm39) |
I233N |
probably damaging |
Het |
| Obsl1 |
A |
G |
1: 75,469,537 (GRCm39) |
V965A |
probably damaging |
Het |
| Or4c12 |
A |
C |
2: 89,774,158 (GRCm39) |
Y100* |
probably null |
Het |
| Or4f6 |
T |
C |
2: 111,839,036 (GRCm39) |
D165G |
probably benign |
Het |
| Or6c5c |
T |
C |
10: 129,299,370 (GRCm39) |
L275P |
probably damaging |
Het |
| Pak1ip1 |
A |
G |
13: 41,164,708 (GRCm39) |
T264A |
possibly damaging |
Het |
| Pard6g |
C |
T |
18: 80,160,357 (GRCm39) |
R157C |
probably damaging |
Het |
| Pcdhb7 |
A |
T |
18: 37,475,631 (GRCm39) |
T256S |
possibly damaging |
Het |
| Phrf1 |
T |
C |
7: 140,820,831 (GRCm39) |
F153L |
probably damaging |
Het |
| Pigw |
A |
T |
11: 84,768,874 (GRCm39) |
F152I |
probably damaging |
Het |
| Pip4k2c |
A |
G |
10: 127,036,744 (GRCm39) |
S222P |
probably damaging |
Het |
| Pjvk |
A |
G |
2: 76,487,775 (GRCm39) |
|
probably null |
Het |
| Plxnd1 |
C |
T |
6: 115,940,875 (GRCm39) |
V1355M |
probably damaging |
Het |
| Pramel26 |
T |
C |
4: 143,539,396 (GRCm39) |
I32M |
probably benign |
Het |
| Prss22 |
G |
A |
17: 24,215,288 (GRCm39) |
P163S |
probably damaging |
Het |
| Prune2 |
A |
G |
19: 17,176,503 (GRCm39) |
I154V |
probably damaging |
Het |
| Rapgef6 |
T |
A |
11: 54,533,637 (GRCm39) |
D362E |
probably benign |
Het |
| Retreg2 |
A |
G |
1: 75,123,319 (GRCm39) |
K416E |
probably benign |
Het |
| Scn7a |
T |
C |
2: 66,510,635 (GRCm39) |
I1256V |
probably benign |
Het |
| Sema4d |
A |
G |
13: 51,865,258 (GRCm39) |
V362A |
possibly damaging |
Het |
| Septin4 |
T |
A |
11: 87,459,741 (GRCm39) |
D496E |
probably damaging |
Het |
| Slc25a34 |
G |
A |
4: 141,349,579 (GRCm39) |
T192I |
probably benign |
Het |
| Tacc3 |
G |
T |
5: 33,825,544 (GRCm39) |
V425L |
probably benign |
Het |
| Tfdp2 |
A |
T |
9: 96,179,762 (GRCm39) |
K125I |
probably damaging |
Het |
| Tjp2 |
C |
T |
19: 24,076,899 (GRCm39) |
R952Q |
possibly damaging |
Het |
| Tk2 |
G |
T |
8: 104,975,077 (GRCm39) |
S30* |
probably null |
Het |
| Tmem74 |
A |
T |
15: 43,730,559 (GRCm39) |
D161E |
probably benign |
Het |
| Tmprss9 |
G |
A |
10: 80,728,119 (GRCm39) |
V570M |
probably damaging |
Het |
| Tnk2 |
C |
A |
16: 32,498,280 (GRCm39) |
P26Q |
probably damaging |
Het |
| Tnpo2 |
T |
G |
8: 85,778,401 (GRCm39) |
V610G |
probably damaging |
Het |
| Trim37 |
T |
C |
11: 87,109,132 (GRCm39) |
F953S |
probably damaging |
Het |
| U2surp |
T |
A |
9: 95,364,150 (GRCm39) |
K589* |
probably null |
Het |
| Usp2 |
G |
A |
9: 43,987,263 (GRCm39) |
R187H |
probably benign |
Het |
| Vmn2r1 |
C |
T |
3: 64,008,926 (GRCm39) |
T535I |
probably benign |
Het |
| Wdr20rt |
T |
A |
12: 65,273,925 (GRCm39) |
S463T |
possibly damaging |
Het |
| Zbtb25 |
C |
A |
12: 76,396,488 (GRCm39) |
G245W |
probably damaging |
Het |
| Zc3h14 |
T |
A |
12: 98,726,613 (GRCm39) |
L27* |
probably null |
Het |
| Zfp2 |
T |
C |
11: 50,791,915 (GRCm39) |
K43E |
probably benign |
Het |
| Zfp268 |
T |
G |
4: 145,350,820 (GRCm39) |
|
probably benign |
Het |
| Zfp654 |
A |
G |
16: 64,605,491 (GRCm39) |
Y904H |
probably benign |
Het |
|
| Other mutations in Cdon |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00832:Cdon
|
APN |
9 |
35,389,412 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01307:Cdon
|
APN |
9 |
35,368,860 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01528:Cdon
|
APN |
9 |
35,381,403 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01663:Cdon
|
APN |
9 |
35,394,510 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
IGL01723:Cdon
|
APN |
9 |
35,414,634 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02200:Cdon
|
APN |
9 |
35,394,405 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL02444:Cdon
|
APN |
9 |
35,384,744 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL02547:Cdon
|
APN |
9 |
35,389,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02620:Cdon
|
APN |
9 |
35,364,095 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02861:Cdon
|
APN |
9 |
35,398,253 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02894:Cdon
|
APN |
9 |
35,366,722 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03153:Cdon
|
APN |
9 |
35,389,255 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03206:Cdon
|
APN |
9 |
35,414,602 (GRCm39) |
missense |
probably benign |
|
|
IGL03374:Cdon
|
APN |
9 |
35,389,299 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
corleone
|
UTSW |
9 |
35,398,252 (GRCm39) |
nonsense |
probably null |
|
|
indentured
|
UTSW |
9 |
35,363,402 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
Molar
|
UTSW |
9 |
35,375,191 (GRCm39) |
missense |
probably benign |
0.15 |
|
Servitude
|
UTSW |
9 |
35,388,244 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4280001:Cdon
|
UTSW |
9 |
35,398,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0045:Cdon
|
UTSW |
9 |
35,398,103 (GRCm39) |
missense |
probably benign |
|
|
R0045:Cdon
|
UTSW |
9 |
35,398,103 (GRCm39) |
missense |
probably benign |
|
|
R0064:Cdon
|
UTSW |
9 |
35,400,523 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0396:Cdon
|
UTSW |
9 |
35,381,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0403:Cdon
|
UTSW |
9 |
35,384,796 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0490:Cdon
|
UTSW |
9 |
35,363,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0547:Cdon
|
UTSW |
9 |
35,368,794 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R0609:Cdon
|
UTSW |
9 |
35,389,907 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0645:Cdon
|
UTSW |
9 |
35,388,379 (GRCm39) |
splice site |
probably null |
|
|
R0781:Cdon
|
UTSW |
9 |
35,367,733 (GRCm39) |
splice site |
probably benign |
|
|
R1110:Cdon
|
UTSW |
9 |
35,367,733 (GRCm39) |
splice site |
probably benign |
|
|
R1391:Cdon
|
UTSW |
9 |
35,415,485 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R1574:Cdon
|
UTSW |
9 |
35,364,233 (GRCm39) |
splice site |
probably benign |
|
|
R2031:Cdon
|
UTSW |
9 |
35,415,370 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2230:Cdon
|
UTSW |
9 |
35,403,222 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3683:Cdon
|
UTSW |
9 |
35,400,328 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3684:Cdon
|
UTSW |
9 |
35,400,328 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3685:Cdon
|
UTSW |
9 |
35,400,328 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R3941:Cdon
|
UTSW |
9 |
35,375,467 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4030:Cdon
|
UTSW |
9 |
35,403,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4084:Cdon
|
UTSW |
9 |
35,389,427 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4462:Cdon
|
UTSW |
9 |
35,368,876 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4569:Cdon
|
UTSW |
9 |
35,388,265 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4677:Cdon
|
UTSW |
9 |
35,389,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4869:Cdon
|
UTSW |
9 |
35,364,200 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R5032:Cdon
|
UTSW |
9 |
35,400,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5047:Cdon
|
UTSW |
9 |
35,389,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5214:Cdon
|
UTSW |
9 |
35,394,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5341:Cdon
|
UTSW |
9 |
35,381,431 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5410:Cdon
|
UTSW |
9 |
35,381,331 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5581:Cdon
|
UTSW |
9 |
35,415,377 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5696:Cdon
|
UTSW |
9 |
35,403,162 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R5757:Cdon
|
UTSW |
9 |
35,364,068 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5802:Cdon
|
UTSW |
9 |
35,365,716 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5845:Cdon
|
UTSW |
9 |
35,368,762 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5949:Cdon
|
UTSW |
9 |
35,398,247 (GRCm39) |
missense |
probably benign |
0.32 |
|
R6106:Cdon
|
UTSW |
9 |
35,366,704 (GRCm39) |
nonsense |
probably null |
|
|
R6245:Cdon
|
UTSW |
9 |
35,388,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6845:Cdon
|
UTSW |
9 |
35,398,252 (GRCm39) |
nonsense |
probably null |
|
|
R6896:Cdon
|
UTSW |
9 |
35,363,402 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R7060:Cdon
|
UTSW |
9 |
35,398,205 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7076:Cdon
|
UTSW |
9 |
35,415,446 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7184:Cdon
|
UTSW |
9 |
35,375,191 (GRCm39) |
missense |
probably benign |
0.15 |
|
R7382:Cdon
|
UTSW |
9 |
35,389,944 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7763:Cdon
|
UTSW |
9 |
35,365,711 (GRCm39) |
nonsense |
probably null |
|
|
R7857:Cdon
|
UTSW |
9 |
35,367,908 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7885:Cdon
|
UTSW |
9 |
35,367,818 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7894:Cdon
|
UTSW |
9 |
35,388,244 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7984:Cdon
|
UTSW |
9 |
35,414,598 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8287:Cdon
|
UTSW |
9 |
35,375,225 (GRCm39) |
missense |
probably benign |
|
|
R8428:Cdon
|
UTSW |
9 |
35,403,163 (GRCm39) |
missense |
probably benign |
0.21 |
|
R8519:Cdon
|
UTSW |
9 |
35,389,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8698:Cdon
|
UTSW |
9 |
35,398,269 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8797:Cdon
|
UTSW |
9 |
35,389,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8995:Cdon
|
UTSW |
9 |
35,398,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9090:Cdon
|
UTSW |
9 |
35,403,175 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9177:Cdon
|
UTSW |
9 |
35,381,230 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9200:Cdon
|
UTSW |
9 |
35,414,617 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9271:Cdon
|
UTSW |
9 |
35,403,175 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9330:Cdon
|
UTSW |
9 |
35,400,275 (GRCm39) |
nonsense |
probably null |
|
|
R9477:Cdon
|
UTSW |
9 |
35,403,201 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9612:Cdon
|
UTSW |
9 |
35,398,201 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9730:Cdon
|
UTSW |
9 |
35,398,263 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1177:Cdon
|
UTSW |
9 |
35,403,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCACAAGCTGTATGAAATGGCAAG -3'
(R):5'- TGAATGCTCTAGCCGACACC -3'
Sequencing Primer
(F):5'- CTGTATGAAATGGCAAGGGATTC -3'
(R):5'- GACACCATGGACTTCTATAGGGTAC -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation