Incidental Mutation 'R0609:Cdon'
| ID |
54536 |
| 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 |
038798-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.351)
|
| Stock # |
R0609 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
35332836-35418948 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 35389907 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Threonine
at position 854
(P854T)
|
| 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: P854T
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000045547
Gene: ENSMUSG00000038119
AA Change: P854T
| 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 |
noncoding transcript
Transcript: ENSMUST00000084000
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000119129
AA Change: P854T
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000113977
Gene: ENSMUSG00000038119
AA Change: P854T
| 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: 99.4%
- 3x: 98.9%
- 10x: 97.6%
- 20x: 95.6%
|
| 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: 103 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930596D02Rik |
A |
T |
14: 35,533,418 (GRCm39) |
|
probably null |
Het |
| Abcb4 |
T |
A |
5: 8,997,376 (GRCm39) |
C952S |
probably damaging |
Het |
| Adamtsl2 |
A |
G |
2: 26,979,647 (GRCm39) |
D272G |
probably benign |
Het |
| Aim2 |
G |
A |
1: 173,289,530 (GRCm39) |
D158N |
probably damaging |
Het |
| Aldh3b1 |
C |
T |
19: 3,964,024 (GRCm39) |
R426H |
probably damaging |
Het |
| Apoc2 |
A |
G |
7: 19,407,278 (GRCm39) |
S28P |
probably benign |
Het |
| Arfgef3 |
G |
A |
10: 18,473,179 (GRCm39) |
T1628I |
probably benign |
Het |
| Atp10a |
G |
A |
7: 58,469,488 (GRCm39) |
|
probably null |
Het |
| Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
| Bmp8b |
T |
A |
4: 123,015,692 (GRCm39) |
D226E |
probably benign |
Het |
| Brsk2 |
T |
C |
7: 141,552,229 (GRCm39) |
Y618H |
probably damaging |
Het |
| Casp12 |
T |
A |
9: 5,346,554 (GRCm39) |
F27Y |
probably damaging |
Het |
| Casp8 |
T |
A |
1: 58,883,951 (GRCm39) |
N439K |
probably benign |
Het |
| Ccdc175 |
T |
A |
12: 72,204,281 (GRCm39) |
K253N |
probably benign |
Het |
| Cdc42bpa |
A |
G |
1: 179,867,744 (GRCm39) |
H193R |
probably damaging |
Het |
| Cdk17 |
T |
C |
10: 93,052,334 (GRCm39) |
M105T |
probably benign |
Het |
| Cep44 |
A |
G |
8: 56,997,187 (GRCm39) |
M117T |
possibly damaging |
Het |
| Cep89 |
A |
T |
7: 35,134,955 (GRCm39) |
E674D |
probably damaging |
Het |
| Cit |
C |
T |
5: 116,012,002 (GRCm39) |
A203V |
probably damaging |
Het |
| Clstn1 |
C |
A |
4: 149,713,757 (GRCm39) |
|
probably null |
Het |
| Col7a1 |
T |
A |
9: 108,787,215 (GRCm39) |
D565E |
unknown |
Het |
| Cpb1 |
T |
A |
3: 20,316,638 (GRCm39) |
Y304F |
probably damaging |
Het |
| Cps1 |
T |
G |
1: 67,211,961 (GRCm39) |
Y710D |
probably damaging |
Het |
| Creb3l1 |
T |
C |
2: 91,817,398 (GRCm39) |
T372A |
possibly damaging |
Het |
| Dars1 |
A |
G |
1: 128,333,118 (GRCm39) |
V102A |
probably benign |
Het |
| Dhx35 |
C |
T |
2: 158,659,335 (GRCm39) |
T168I |
possibly damaging |
Het |
| Dnah5 |
T |
C |
15: 28,327,925 (GRCm39) |
S2100P |
probably benign |
Het |
| Dst |
T |
C |
1: 34,306,041 (GRCm39) |
|
probably null |
Het |
| Egflam |
A |
C |
15: 7,283,004 (GRCm39) |
L351R |
possibly damaging |
Het |
| Elp2 |
T |
A |
18: 24,759,213 (GRCm39) |
D523E |
probably benign |
Het |
| Exo5 |
C |
A |
4: 120,778,881 (GRCm39) |
G328V |
probably damaging |
Het |
| Fut9 |
A |
G |
4: 25,620,811 (GRCm39) |
M1T |
probably null |
Het |
| Galnt5 |
A |
G |
2: 57,914,637 (GRCm39) |
N584S |
possibly damaging |
Het |
| Gbp3 |
T |
C |
3: 142,273,533 (GRCm39) |
V360A |
probably damaging |
Het |
| Gdf6 |
G |
A |
4: 9,859,977 (GRCm39) |
C353Y |
probably damaging |
Het |
| Hace1 |
A |
G |
10: 45,524,965 (GRCm39) |
T244A |
probably damaging |
Het |
| Hr |
T |
C |
14: 70,797,097 (GRCm39) |
I500T |
probably benign |
Het |
| Ifnl2 |
A |
T |
7: 28,208,707 (GRCm39) |
L115Q |
probably damaging |
Het |
| Iigp1 |
T |
C |
18: 60,522,896 (GRCm39) |
F5L |
probably benign |
Het |
| Inhbb |
A |
G |
1: 119,345,146 (GRCm39) |
L381P |
probably damaging |
Het |
| Irx3 |
A |
T |
8: 92,527,721 (GRCm39) |
S50T |
probably benign |
Het |
| Ivns1abp |
C |
T |
1: 151,235,896 (GRCm39) |
T363I |
probably benign |
Het |
| Izumo1 |
A |
T |
7: 45,272,323 (GRCm39) |
T35S |
probably benign |
Het |
| Kank4 |
A |
G |
4: 98,665,342 (GRCm39) |
S651P |
probably damaging |
Het |
| Kit |
T |
C |
5: 75,771,539 (GRCm39) |
V232A |
probably benign |
Het |
| Klhl11 |
T |
C |
11: 100,354,540 (GRCm39) |
Y427C |
probably damaging |
Het |
| Laptm4b |
T |
A |
15: 34,258,835 (GRCm39) |
N36K |
probably damaging |
Het |
| Lrrk1 |
T |
C |
7: 65,916,363 (GRCm39) |
|
probably null |
Het |
| Mamdc4 |
G |
T |
2: 25,454,205 (GRCm39) |
Q1042K |
probably benign |
Het |
| Mical2 |
A |
G |
7: 111,920,647 (GRCm39) |
|
probably null |
Het |
| Ms4a3 |
C |
A |
19: 11,608,725 (GRCm39) |
V176F |
possibly damaging |
Het |
| Myo3a |
T |
C |
2: 22,338,324 (GRCm39) |
V427A |
probably benign |
Het |
| Myo3a |
A |
C |
2: 22,401,110 (GRCm39) |
E626D |
possibly damaging |
Het |
| Nckap5 |
A |
T |
1: 125,955,025 (GRCm39) |
L509* |
probably null |
Het |
| Ndufa5 |
A |
T |
6: 24,519,248 (GRCm39) |
D64E |
possibly damaging |
Het |
| Nedd4l |
T |
C |
18: 65,341,532 (GRCm39) |
Y753H |
probably damaging |
Het |
| Nynrin |
T |
C |
14: 56,110,218 (GRCm39) |
V1775A |
probably damaging |
Het |
| Oplah |
A |
G |
15: 76,187,192 (GRCm39) |
S570P |
probably benign |
Het |
| Or14c39 |
T |
C |
7: 86,344,084 (GRCm39) |
V140A |
possibly damaging |
Het |
| Or2ag1b |
A |
T |
7: 106,288,205 (GRCm39) |
H244Q |
probably damaging |
Het |
| Or4q3 |
T |
C |
14: 50,583,383 (GRCm39) |
Y141C |
probably damaging |
Het |
| Or5t18 |
A |
G |
2: 86,637,205 (GRCm39) |
L46S |
probably damaging |
Het |
| Or9r3 |
G |
A |
10: 129,948,449 (GRCm39) |
S70F |
probably damaging |
Het |
| Osbpl11 |
C |
A |
16: 33,054,814 (GRCm39) |
Y632* |
probably null |
Het |
| Osbpl5 |
A |
T |
7: 143,248,558 (GRCm39) |
L644Q |
probably damaging |
Het |
| Pcdhb19 |
T |
C |
18: 37,631,005 (GRCm39) |
W267R |
probably benign |
Het |
| Pkhd1l1 |
A |
C |
15: 44,330,820 (GRCm39) |
S132R |
possibly damaging |
Het |
| Pramel23 |
A |
T |
4: 143,425,073 (GRCm39) |
D123E |
probably benign |
Het |
| Ptpn13 |
T |
A |
5: 103,704,011 (GRCm39) |
S1348T |
probably benign |
Het |
| Rc3h1 |
T |
A |
1: 160,757,705 (GRCm39) |
W8R |
probably damaging |
Het |
| Rgs3 |
T |
G |
4: 62,544,173 (GRCm39) |
V315G |
probably damaging |
Het |
| Rora |
T |
A |
9: 69,269,151 (GRCm39) |
M82K |
probably damaging |
Het |
| Rph3al |
T |
C |
11: 75,799,795 (GRCm39) |
I55V |
probably benign |
Het |
| Sag |
T |
C |
1: 87,740,713 (GRCm39) |
V45A |
probably damaging |
Het |
| Scn3a |
T |
C |
2: 65,366,854 (GRCm39) |
E56G |
probably damaging |
Het |
| Sec24c |
T |
G |
14: 20,737,016 (GRCm39) |
V324G |
probably damaging |
Het |
| Sptbn1 |
A |
G |
11: 30,088,979 (GRCm39) |
L748S |
probably damaging |
Het |
| Stard9 |
A |
T |
2: 120,536,787 (GRCm39) |
D4186V |
probably damaging |
Het |
| Stk39 |
T |
C |
2: 68,196,511 (GRCm39) |
E306G |
probably damaging |
Het |
| Sycp1 |
C |
A |
3: 102,806,165 (GRCm39) |
|
probably null |
Het |
| Taf2 |
A |
C |
15: 54,923,446 (GRCm39) |
L277R |
probably damaging |
Het |
| Tasor |
C |
T |
14: 27,183,707 (GRCm39) |
T722I |
probably benign |
Het |
| Tbc1d23 |
T |
A |
16: 56,993,469 (GRCm39) |
I566F |
possibly damaging |
Het |
| Tekt5 |
T |
C |
16: 10,179,168 (GRCm39) |
T400A |
possibly damaging |
Het |
| Tgfbrap1 |
T |
C |
1: 43,099,301 (GRCm39) |
H401R |
probably benign |
Het |
| Tie1 |
T |
A |
4: 118,333,344 (GRCm39) |
I841L |
possibly damaging |
Het |
| Tln1 |
T |
G |
4: 43,544,645 (GRCm39) |
T1095P |
possibly damaging |
Het |
| Tmem147 |
A |
G |
7: 30,427,527 (GRCm39) |
Y72H |
probably benign |
Het |
| Tnfaip2 |
A |
G |
12: 111,419,941 (GRCm39) |
N691S |
probably benign |
Het |
| Trim24 |
G |
A |
6: 37,934,718 (GRCm39) |
C811Y |
probably damaging |
Het |
| Trim30b |
T |
A |
7: 104,007,183 (GRCm39) |
|
probably benign |
Het |
| Trpc4 |
T |
G |
3: 54,102,189 (GRCm39) |
L29R |
probably damaging |
Het |
| Trpm6 |
A |
T |
19: 18,803,226 (GRCm39) |
I890F |
probably damaging |
Het |
| Ttc23l |
C |
T |
15: 10,504,622 (GRCm39) |
E442K |
probably benign |
Het |
| Tut7 |
A |
T |
13: 59,947,596 (GRCm39) |
C506* |
probably null |
Het |
| Uggt2 |
A |
G |
14: 119,332,748 (GRCm39) |
V62A |
probably damaging |
Het |
| Ugt1a6a |
C |
A |
1: 88,066,606 (GRCm39) |
S137R |
probably benign |
Het |
| Unc13a |
A |
G |
8: 72,111,111 (GRCm39) |
Y367H |
probably damaging |
Het |
| Vmn2r49 |
A |
G |
7: 9,710,233 (GRCm39) |
I833T |
probably benign |
Het |
| Vmn2r7 |
T |
C |
3: 64,623,900 (GRCm39) |
D231G |
probably benign |
Het |
| Ythdc2 |
A |
T |
18: 44,997,424 (GRCm39) |
M994L |
probably benign |
Het |
| Zfp804a |
G |
A |
2: 82,087,932 (GRCm39) |
S587N |
probably damaging |
Het |
| Zswim2 |
A |
G |
2: 83,754,003 (GRCm39) |
I219T |
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 |
|
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 |
|
|
R1851:Cdon
|
UTSW |
9 |
35,394,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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'- CGGTATGTGAGCGAACACCTTCTTG -3'
(R):5'- ACCCAGTCTTAGCCCGTGAAGATG -3'
Sequencing Primer
(F):5'- AGCGAACACCTTCTTGGTGAG -3'
(R):5'- GCCCGTGAAGATGGGTTTG -3'
|
| Posted On |
2013-07-11 |
Incidental Mutation