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 |
CDO, CAM-related/down-regulated by oncogenes |
| MMRRC Submission |
038798-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.311)
|
| Stock # |
R0609 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
35421128-35507652 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 35478611 bp (GRCm38)
|
| 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: 35,811,461 (GRCm38) |
|
probably null |
Het |
| Abcb4 |
T |
A |
5: 8,947,376 (GRCm38) |
C952S |
probably damaging |
Het |
| Adamtsl2 |
A |
G |
2: 27,089,635 (GRCm38) |
D272G |
probably benign |
Het |
| Aim2 |
G |
A |
1: 173,461,964 (GRCm38) |
D158N |
probably damaging |
Het |
| Aldh3b1 |
C |
T |
19: 3,914,024 (GRCm38) |
R426H |
probably damaging |
Het |
| Apoc2 |
A |
G |
7: 19,673,353 (GRCm38) |
S28P |
probably benign |
Het |
| Arfgef3 |
G |
A |
10: 18,597,431 (GRCm38) |
T1628I |
probably benign |
Het |
| Atp10a |
G |
A |
7: 58,819,740 (GRCm38) |
|
probably null |
Het |
| Bcl2 |
G |
A |
1: 106,712,562 (GRCm38) |
R107C |
probably damaging |
Het |
| Bmp8b |
T |
A |
4: 123,121,899 (GRCm38) |
D226E |
probably benign |
Het |
| Brsk2 |
T |
C |
7: 141,998,492 (GRCm38) |
Y618H |
probably damaging |
Het |
| Casp12 |
T |
A |
9: 5,346,554 (GRCm38) |
F27Y |
probably damaging |
Het |
| Casp8 |
T |
A |
1: 58,844,792 (GRCm38) |
N439K |
probably benign |
Het |
| Ccdc175 |
T |
A |
12: 72,157,507 (GRCm38) |
K253N |
probably benign |
Het |
| Cdc42bpa |
A |
G |
1: 180,040,179 (GRCm38) |
H193R |
probably damaging |
Het |
| Cdk17 |
T |
C |
10: 93,216,472 (GRCm38) |
M105T |
probably benign |
Het |
| Cep44 |
A |
G |
8: 56,544,152 (GRCm38) |
M117T |
possibly damaging |
Het |
| Cep89 |
A |
T |
7: 35,435,530 (GRCm38) |
E674D |
probably damaging |
Het |
| Cit |
C |
T |
5: 115,873,943 (GRCm38) |
A203V |
probably damaging |
Het |
| Clstn1 |
C |
A |
4: 149,629,300 (GRCm38) |
|
probably null |
Het |
| Col7a1 |
T |
A |
9: 108,958,147 (GRCm38) |
D565E |
unknown |
Het |
| Cpb1 |
T |
A |
3: 20,262,474 (GRCm38) |
Y304F |
probably damaging |
Het |
| Cps1 |
T |
G |
1: 67,172,802 (GRCm38) |
Y710D |
probably damaging |
Het |
| Creb3l1 |
T |
C |
2: 91,987,053 (GRCm38) |
T372A |
possibly damaging |
Het |
| Dars |
A |
G |
1: 128,405,381 (GRCm38) |
V102A |
probably benign |
Het |
| Dhx35 |
C |
T |
2: 158,817,415 (GRCm38) |
T168I |
possibly damaging |
Het |
| Dnah5 |
T |
C |
15: 28,327,779 (GRCm38) |
S2100P |
probably benign |
Het |
| Dst |
T |
C |
1: 34,266,960 (GRCm38) |
|
probably null |
Het |
| Egflam |
A |
C |
15: 7,253,523 (GRCm38) |
L351R |
possibly damaging |
Het |
| Elp2 |
T |
A |
18: 24,626,156 (GRCm38) |
D523E |
probably benign |
Het |
| Exo5 |
C |
A |
4: 120,921,684 (GRCm38) |
G328V |
probably damaging |
Het |
| Fam208a |
C |
T |
14: 27,461,750 (GRCm38) |
T722I |
probably benign |
Het |
| Fut9 |
A |
G |
4: 25,620,811 (GRCm38) |
M1T |
probably null |
Het |
| Galnt5 |
A |
G |
2: 58,024,625 (GRCm38) |
N584S |
possibly damaging |
Het |
| Gbp3 |
T |
C |
3: 142,567,772 (GRCm38) |
V360A |
probably damaging |
Het |
| Gdf6 |
G |
A |
4: 9,859,977 (GRCm38) |
C353Y |
probably damaging |
Het |
| Gm13089 |
A |
T |
4: 143,698,503 (GRCm38) |
D123E |
probably benign |
Het |
| Hace1 |
A |
G |
10: 45,648,869 (GRCm38) |
T244A |
probably damaging |
Het |
| Hr |
T |
C |
14: 70,559,657 (GRCm38) |
I500T |
probably benign |
Het |
| Ifnl2 |
A |
T |
7: 28,509,282 (GRCm38) |
L115Q |
probably damaging |
Het |
| Iigp1 |
T |
C |
18: 60,389,824 (GRCm38) |
F5L |
probably benign |
Het |
| Inhbb |
A |
G |
1: 119,417,416 (GRCm38) |
L381P |
probably damaging |
Het |
| Irx3 |
A |
T |
8: 91,801,093 (GRCm38) |
S50T |
probably benign |
Het |
| Ivns1abp |
C |
T |
1: 151,360,145 (GRCm38) |
T363I |
probably benign |
Het |
| Izumo1 |
A |
T |
7: 45,622,899 (GRCm38) |
T35S |
probably benign |
Het |
| Kank4 |
A |
G |
4: 98,777,105 (GRCm38) |
S651P |
probably damaging |
Het |
| Kit |
T |
C |
5: 75,610,879 (GRCm38) |
V232A |
probably benign |
Het |
| Klhl11 |
T |
C |
11: 100,463,714 (GRCm38) |
Y427C |
probably damaging |
Het |
| Laptm4b |
T |
A |
15: 34,258,689 (GRCm38) |
N36K |
probably damaging |
Het |
| Lrrk1 |
T |
C |
7: 66,266,615 (GRCm38) |
|
probably null |
Het |
| Mamdc4 |
G |
T |
2: 25,564,193 (GRCm38) |
Q1042K |
probably benign |
Het |
| Mical2 |
A |
G |
7: 112,321,440 (GRCm38) |
|
probably null |
Het |
| Ms4a3 |
C |
A |
19: 11,631,361 (GRCm38) |
V176F |
possibly damaging |
Het |
| Myo3a |
T |
C |
2: 22,333,513 (GRCm38) |
V427A |
probably benign |
Het |
| Myo3a |
A |
C |
2: 22,396,299 (GRCm38) |
E626D |
possibly damaging |
Het |
| Nckap5 |
A |
T |
1: 126,027,288 (GRCm38) |
L509* |
probably null |
Het |
| Ndufa5 |
A |
T |
6: 24,519,249 (GRCm38) |
D64E |
possibly damaging |
Het |
| Nedd4l |
T |
C |
18: 65,208,461 (GRCm38) |
Y753H |
probably damaging |
Het |
| Nynrin |
T |
C |
14: 55,872,761 (GRCm38) |
V1775A |
probably damaging |
Het |
| Olfr141 |
A |
G |
2: 86,806,861 (GRCm38) |
L46S |
probably damaging |
Het |
| Olfr292 |
T |
C |
7: 86,694,876 (GRCm38) |
V140A |
possibly damaging |
Het |
| Olfr694 |
A |
T |
7: 106,688,998 (GRCm38) |
H244Q |
probably damaging |
Het |
| Olfr735 |
T |
C |
14: 50,345,926 (GRCm38) |
Y141C |
probably damaging |
Het |
| Olfr823 |
G |
A |
10: 130,112,580 (GRCm38) |
S70F |
probably damaging |
Het |
| Oplah |
A |
G |
15: 76,302,992 (GRCm38) |
S570P |
probably benign |
Het |
| Osbpl11 |
C |
A |
16: 33,234,444 (GRCm38) |
Y632* |
probably null |
Het |
| Osbpl5 |
A |
T |
7: 143,694,821 (GRCm38) |
L644Q |
probably damaging |
Het |
| Pcdhb19 |
T |
C |
18: 37,497,952 (GRCm38) |
W267R |
probably benign |
Het |
| Pkhd1l1 |
A |
C |
15: 44,467,424 (GRCm38) |
S132R |
possibly damaging |
Het |
| Ptpn13 |
T |
A |
5: 103,556,145 (GRCm38) |
S1348T |
probably benign |
Het |
| Rc3h1 |
T |
A |
1: 160,930,135 (GRCm38) |
W8R |
probably damaging |
Het |
| Rgs3 |
T |
G |
4: 62,625,936 (GRCm38) |
V315G |
probably damaging |
Het |
| Rora |
T |
A |
9: 69,361,869 (GRCm38) |
M82K |
probably damaging |
Het |
| Rph3al |
T |
C |
11: 75,908,969 (GRCm38) |
I55V |
probably benign |
Het |
| Sag |
T |
C |
1: 87,812,991 (GRCm38) |
V45A |
probably damaging |
Het |
| Scn3a |
T |
C |
2: 65,536,510 (GRCm38) |
E56G |
probably damaging |
Het |
| Sec24c |
T |
G |
14: 20,686,948 (GRCm38) |
V324G |
probably damaging |
Het |
| Sptbn1 |
A |
G |
11: 30,138,979 (GRCm38) |
L748S |
probably damaging |
Het |
| Stard9 |
A |
T |
2: 120,706,306 (GRCm38) |
D4186V |
probably damaging |
Het |
| Stk39 |
T |
C |
2: 68,366,167 (GRCm38) |
E306G |
probably damaging |
Het |
| Sycp1 |
C |
A |
3: 102,898,849 (GRCm38) |
|
probably null |
Het |
| Taf2 |
A |
C |
15: 55,060,050 (GRCm38) |
L277R |
probably damaging |
Het |
| Tbc1d23 |
T |
A |
16: 57,173,106 (GRCm38) |
I566F |
possibly damaging |
Het |
| Tekt5 |
T |
C |
16: 10,361,304 (GRCm38) |
T400A |
possibly damaging |
Het |
| Tgfbrap1 |
T |
C |
1: 43,060,141 (GRCm38) |
H401R |
probably benign |
Het |
| Tie1 |
T |
A |
4: 118,476,147 (GRCm38) |
I841L |
possibly damaging |
Het |
| Tln1 |
T |
G |
4: 43,544,645 (GRCm38) |
T1095P |
possibly damaging |
Het |
| Tmem147 |
A |
G |
7: 30,728,102 (GRCm38) |
Y72H |
probably benign |
Het |
| Tnfaip2 |
A |
G |
12: 111,453,507 (GRCm38) |
N691S |
probably benign |
Het |
| Trim24 |
G |
A |
6: 37,957,783 (GRCm38) |
C811Y |
probably damaging |
Het |
| Trim30b |
T |
A |
7: 104,357,976 (GRCm38) |
|
probably benign |
Het |
| Trpc4 |
T |
G |
3: 54,194,768 (GRCm38) |
L29R |
probably damaging |
Het |
| Trpm6 |
A |
T |
19: 18,825,862 (GRCm38) |
I890F |
probably damaging |
Het |
| Ttc23l |
C |
T |
15: 10,504,536 (GRCm38) |
E442K |
probably benign |
Het |
| Uggt2 |
A |
G |
14: 119,095,336 (GRCm38) |
V62A |
probably damaging |
Het |
| Ugt1a6a |
C |
A |
1: 88,138,884 (GRCm38) |
S137R |
probably benign |
Het |
| Unc13a |
A |
G |
8: 71,658,467 (GRCm38) |
Y367H |
probably damaging |
Het |
| Vmn2r49 |
A |
G |
7: 9,976,306 (GRCm38) |
I833T |
probably benign |
Het |
| Vmn2r7 |
T |
C |
3: 64,716,479 (GRCm38) |
D231G |
probably benign |
Het |
| Ythdc2 |
A |
T |
18: 44,864,357 (GRCm38) |
M994L |
probably benign |
Het |
| Zcchc6 |
A |
T |
13: 59,799,782 (GRCm38) |
C506* |
probably null |
Het |
| Zfp804a |
G |
A |
2: 82,257,588 (GRCm38) |
S587N |
probably damaging |
Het |
| Zswim2 |
A |
G |
2: 83,923,659 (GRCm38) |
I219T |
probably benign |
Het |
|
| Other mutations in Cdon |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00832:Cdon
|
APN |
9 |
35,478,116 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01307:Cdon
|
APN |
9 |
35,457,564 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL01528:Cdon
|
APN |
9 |
35,470,107 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
IGL01663:Cdon
|
APN |
9 |
35,483,214 (GRCm38) |
missense |
possibly damaging |
0.57 |
|
IGL01723:Cdon
|
APN |
9 |
35,503,338 (GRCm38) |
missense |
probably benign |
0.05 |
|
IGL02200:Cdon
|
APN |
9 |
35,483,109 (GRCm38) |
missense |
probably benign |
0.28 |
|
IGL02444:Cdon
|
APN |
9 |
35,473,448 (GRCm38) |
missense |
probably benign |
0.09 |
|
IGL02547:Cdon
|
APN |
9 |
35,478,654 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02620:Cdon
|
APN |
9 |
35,452,799 (GRCm38) |
missense |
probably benign |
0.00 |
|
IGL02861:Cdon
|
APN |
9 |
35,486,957 (GRCm38) |
missense |
probably damaging |
0.96 |
|
IGL02894:Cdon
|
APN |
9 |
35,455,426 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL03153:Cdon
|
APN |
9 |
35,477,959 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03206:Cdon
|
APN |
9 |
35,503,306 (GRCm38) |
missense |
probably benign |
|
|
IGL03374:Cdon
|
APN |
9 |
35,478,003 (GRCm38) |
missense |
possibly damaging |
0.46 |
|
corleone
|
UTSW |
9 |
35,486,956 (GRCm38) |
nonsense |
probably null |
|
|
indentured
|
UTSW |
9 |
35,452,106 (GRCm38) |
start codon destroyed |
probably null |
1.00 |
|
Molar
|
UTSW |
9 |
35,463,895 (GRCm38) |
missense |
probably benign |
0.15 |
|
Servitude
|
UTSW |
9 |
35,476,948 (GRCm38) |
missense |
probably damaging |
1.00 |
|
PIT4280001:Cdon
|
UTSW |
9 |
35,486,935 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0045:Cdon
|
UTSW |
9 |
35,486,807 (GRCm38) |
missense |
probably benign |
|
|
R0045:Cdon
|
UTSW |
9 |
35,486,807 (GRCm38) |
missense |
probably benign |
|
|
R0064:Cdon
|
UTSW |
9 |
35,489,227 (GRCm38) |
missense |
probably benign |
0.03 |
|
R0396:Cdon
|
UTSW |
9 |
35,470,130 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0403:Cdon
|
UTSW |
9 |
35,473,500 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0490:Cdon
|
UTSW |
9 |
35,452,682 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0547:Cdon
|
UTSW |
9 |
35,457,498 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
R0645:Cdon
|
UTSW |
9 |
35,477,083 (GRCm38) |
splice site |
probably null |
|
|
R0781:Cdon
|
UTSW |
9 |
35,456,437 (GRCm38) |
splice site |
probably benign |
|
|
R1110:Cdon
|
UTSW |
9 |
35,456,437 (GRCm38) |
splice site |
probably benign |
|
|
R1391:Cdon
|
UTSW |
9 |
35,504,189 (GRCm38) |
missense |
possibly damaging |
0.51 |
|
R1574:Cdon
|
UTSW |
9 |
35,452,937 (GRCm38) |
splice site |
probably benign |
|
|
R1851:Cdon
|
UTSW |
9 |
35,483,158 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2031:Cdon
|
UTSW |
9 |
35,504,074 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R2230:Cdon
|
UTSW |
9 |
35,491,926 (GRCm38) |
critical splice donor site |
probably null |
|
|
R3683:Cdon
|
UTSW |
9 |
35,489,032 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R3684:Cdon
|
UTSW |
9 |
35,489,032 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R3685:Cdon
|
UTSW |
9 |
35,489,032 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R3941:Cdon
|
UTSW |
9 |
35,464,171 (GRCm38) |
missense |
probably benign |
0.09 |
|
R4030:Cdon
|
UTSW |
9 |
35,491,906 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4084:Cdon
|
UTSW |
9 |
35,478,131 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R4462:Cdon
|
UTSW |
9 |
35,457,580 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R4569:Cdon
|
UTSW |
9 |
35,476,969 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4677:Cdon
|
UTSW |
9 |
35,478,605 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4869:Cdon
|
UTSW |
9 |
35,452,904 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R5032:Cdon
|
UTSW |
9 |
35,489,034 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5047:Cdon
|
UTSW |
9 |
35,478,639 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5214:Cdon
|
UTSW |
9 |
35,483,208 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5341:Cdon
|
UTSW |
9 |
35,470,135 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5410:Cdon
|
UTSW |
9 |
35,470,035 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5581:Cdon
|
UTSW |
9 |
35,504,081 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5696:Cdon
|
UTSW |
9 |
35,491,866 (GRCm38) |
missense |
possibly damaging |
0.69 |
|
R5757:Cdon
|
UTSW |
9 |
35,452,772 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R5802:Cdon
|
UTSW |
9 |
35,454,420 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5845:Cdon
|
UTSW |
9 |
35,457,466 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5949:Cdon
|
UTSW |
9 |
35,486,951 (GRCm38) |
missense |
probably benign |
0.32 |
|
R6106:Cdon
|
UTSW |
9 |
35,455,408 (GRCm38) |
nonsense |
probably null |
|
|
R6245:Cdon
|
UTSW |
9 |
35,476,939 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6845:Cdon
|
UTSW |
9 |
35,486,956 (GRCm38) |
nonsense |
probably null |
|
|
R6896:Cdon
|
UTSW |
9 |
35,452,106 (GRCm38) |
start codon destroyed |
probably null |
1.00 |
|
R7060:Cdon
|
UTSW |
9 |
35,486,909 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7076:Cdon
|
UTSW |
9 |
35,504,150 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7184:Cdon
|
UTSW |
9 |
35,463,895 (GRCm38) |
missense |
probably benign |
0.15 |
|
R7382:Cdon
|
UTSW |
9 |
35,478,648 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7763:Cdon
|
UTSW |
9 |
35,454,415 (GRCm38) |
nonsense |
probably null |
|
|
R7857:Cdon
|
UTSW |
9 |
35,456,612 (GRCm38) |
missense |
possibly damaging |
0.79 |
|
R7885:Cdon
|
UTSW |
9 |
35,456,522 (GRCm38) |
missense |
probably benign |
0.01 |
|
R7894:Cdon
|
UTSW |
9 |
35,476,948 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7984:Cdon
|
UTSW |
9 |
35,503,302 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8287:Cdon
|
UTSW |
9 |
35,463,929 (GRCm38) |
missense |
probably benign |
|
|
R8428:Cdon
|
UTSW |
9 |
35,491,867 (GRCm38) |
missense |
probably benign |
0.21 |
|
R8519:Cdon
|
UTSW |
9 |
35,478,654 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8698:Cdon
|
UTSW |
9 |
35,486,973 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8797:Cdon
|
UTSW |
9 |
35,478,635 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8995:Cdon
|
UTSW |
9 |
35,486,797 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9090:Cdon
|
UTSW |
9 |
35,491,879 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9177:Cdon
|
UTSW |
9 |
35,469,934 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9200:Cdon
|
UTSW |
9 |
35,503,321 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9271:Cdon
|
UTSW |
9 |
35,491,879 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9330:Cdon
|
UTSW |
9 |
35,488,979 (GRCm38) |
nonsense |
probably null |
|
|
R9477:Cdon
|
UTSW |
9 |
35,491,905 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9612:Cdon
|
UTSW |
9 |
35,486,905 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9730:Cdon
|
UTSW |
9 |
35,486,967 (GRCm38) |
missense |
probably benign |
0.00 |
|
Z1177:Cdon
|
UTSW |
9 |
35,491,900 (GRCm38) |
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