Incidental Mutation 'R7894:Cdon'
| ID |
609524 |
| 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 |
045946-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.351)
|
| Stock # |
R7894 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
35332836-35418948 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to G
at 35388244 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glycine
at position 740
(R740G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000045547
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042842]
[ENSMUST00000119129]
|
| AlphaFold |
Q32MD9 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000042842
AA Change: R740G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000045547
Gene: ENSMUSG00000038119
AA Change: R740G
| 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: R740G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000113977
Gene: ENSMUSG00000038119
AA Change: R740G
| 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 |
|
| Meta Mutation Damage Score |
0.5478 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
99% (81/82) |
| 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: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca9 |
A |
G |
11: 109,997,415 (GRCm39) |
M1551T |
possibly damaging |
Het |
| Abcc9 |
A |
G |
6: 142,539,733 (GRCm39) |
*1547Q |
probably null |
Het |
| Adamts20 |
A |
C |
15: 94,249,641 (GRCm39) |
C459G |
probably damaging |
Het |
| Adamts5 |
C |
T |
16: 85,674,808 (GRCm39) |
W452* |
probably null |
Het |
| Adcy8 |
G |
T |
15: 64,792,054 (GRCm39) |
Q301K |
possibly damaging |
Het |
| Adgrv1 |
A |
C |
13: 81,715,570 (GRCm39) |
C873G |
probably benign |
Het |
| Ak9 |
A |
G |
10: 41,296,535 (GRCm39) |
D1427G |
unknown |
Het |
| Amy2a1 |
T |
A |
3: 113,324,190 (GRCm39) |
M117L |
possibly damaging |
Het |
| Ap5z1 |
G |
T |
5: 142,452,039 (GRCm39) |
R23L |
probably benign |
Het |
| Ap5z1 |
C |
T |
5: 142,456,191 (GRCm39) |
Q337* |
probably null |
Het |
| Astn1 |
C |
A |
1: 158,429,508 (GRCm39) |
Q759K |
probably damaging |
Het |
| Cd276 |
T |
A |
9: 58,444,762 (GRCm39) |
T70S |
possibly damaging |
Het |
| Cd38 |
C |
T |
5: 44,057,746 (GRCm39) |
T106I |
probably damaging |
Het |
| Clk2 |
C |
T |
3: 89,076,201 (GRCm39) |
R124W |
possibly damaging |
Het |
| Cyp1b1 |
C |
T |
17: 80,021,644 (GRCm39) |
V33M |
possibly damaging |
Het |
| Dab1 |
T |
A |
4: 104,589,335 (GRCm39) |
D547E |
probably benign |
Het |
| Degs1 |
A |
T |
1: 182,104,416 (GRCm39) |
Y290N |
probably damaging |
Het |
| Degs1 |
G |
C |
1: 182,104,417 (GRCm39) |
H289Q |
probably benign |
Het |
| Dop1b |
T |
A |
16: 93,607,092 (GRCm39) |
C2249S |
probably benign |
Het |
| Ecpas |
T |
C |
4: 58,853,708 (GRCm39) |
N361S |
probably damaging |
Het |
| Ehd4 |
A |
C |
2: 119,932,909 (GRCm39) |
Y172* |
probably null |
Het |
| Erc2 |
A |
G |
14: 27,499,165 (GRCm39) |
D347G |
probably damaging |
Het |
| Espl1 |
T |
G |
15: 102,212,460 (GRCm39) |
V522G |
probably damaging |
Het |
| Fabp9 |
T |
A |
3: 10,262,227 (GRCm39) |
T10S |
probably benign |
Het |
| Fam193a |
T |
C |
5: 34,597,877 (GRCm39) |
I558T |
possibly damaging |
Het |
| Fhod1 |
T |
C |
8: 106,057,789 (GRCm39) |
E912G |
probably damaging |
Het |
| Gja1 |
T |
C |
10: 56,264,645 (GRCm39) |
F335L |
possibly damaging |
Het |
| Gm29106 |
A |
G |
1: 118,127,265 (GRCm39) |
H319R |
probably damaging |
Het |
| Hunk |
C |
T |
16: 90,269,353 (GRCm39) |
S299F |
probably damaging |
Het |
| Hydin |
C |
T |
8: 111,239,642 (GRCm39) |
T1974M |
possibly damaging |
Het |
| Ighv10-1 |
T |
A |
12: 114,442,650 (GRCm39) |
T112S |
probably damaging |
Het |
| Ireb2 |
T |
A |
9: 54,789,620 (GRCm39) |
V98E |
probably damaging |
Het |
| Irf4 |
A |
C |
13: 30,937,435 (GRCm39) |
H167P |
probably benign |
Het |
| Irf6 |
C |
T |
1: 192,845,021 (GRCm39) |
P164L |
probably benign |
Het |
| Josd1 |
A |
G |
15: 79,561,451 (GRCm39) |
I119T |
probably damaging |
Het |
| Kcna5 |
G |
T |
6: 126,512,011 (GRCm39) |
T39K |
probably damaging |
Het |
| Klhl24 |
A |
G |
16: 19,941,750 (GRCm39) |
D566G |
probably damaging |
Het |
| Kmt2a |
T |
A |
9: 44,761,154 (GRCm39) |
K232* |
probably null |
Het |
| Krt36 |
A |
G |
11: 99,996,061 (GRCm39) |
L121P |
probably damaging |
Het |
| Lama3 |
A |
T |
18: 12,595,864 (GRCm39) |
H931L |
probably benign |
Het |
| Lamp3 |
A |
T |
16: 19,474,141 (GRCm39) |
I411N |
probably damaging |
Het |
| Lingo3 |
C |
T |
10: 80,670,610 (GRCm39) |
W440* |
probably null |
Het |
| Mia2 |
T |
C |
12: 59,236,433 (GRCm39) |
Y712H |
probably damaging |
Het |
| Mlh1 |
T |
A |
9: 111,059,145 (GRCm39) |
|
probably null |
Het |
| Mta3 |
T |
A |
17: 84,070,363 (GRCm39) |
S174T |
probably benign |
Het |
| Myo15a |
A |
G |
11: 60,381,963 (GRCm39) |
T347A |
|
Het |
| Naaladl2 |
C |
T |
3: 23,900,718 (GRCm39) |
R704H |
possibly damaging |
Het |
| Nfib |
T |
C |
4: 82,246,030 (GRCm39) |
N394S |
probably benign |
Het |
| Nr2f2 |
A |
G |
7: 70,009,681 (GRCm39) |
Y133H |
probably damaging |
Het |
| Or2ak7 |
C |
T |
11: 58,575,500 (GRCm39) |
S267F |
possibly damaging |
Het |
| Or2i1 |
C |
T |
17: 37,508,047 (GRCm39) |
E196K |
probably damaging |
Het |
| Or4c115 |
A |
G |
2: 88,927,932 (GRCm39) |
V113A |
possibly damaging |
Het |
| Or4f61 |
A |
T |
2: 111,922,822 (GRCm39) |
C75S |
probably benign |
Het |
| Or5p62 |
T |
A |
7: 107,771,391 (GRCm39) |
M187L |
probably benign |
Het |
| Phgdh |
C |
A |
3: 98,247,124 (GRCm39) |
V9L |
probably damaging |
Het |
| Pkd2 |
T |
A |
5: 104,628,103 (GRCm39) |
D392E |
probably damaging |
Het |
| Plekhm3 |
A |
G |
1: 64,960,874 (GRCm39) |
S461P |
probably benign |
Het |
| Prss39 |
A |
G |
1: 34,539,308 (GRCm39) |
T183A |
probably benign |
Het |
| Pter |
T |
A |
2: 12,999,566 (GRCm39) |
I235K |
probably damaging |
Het |
| Ptp4a3 |
T |
C |
15: 73,628,756 (GRCm39) |
V172A |
probably benign |
Het |
| Rasa2 |
T |
C |
9: 96,484,780 (GRCm39) |
N145D |
probably benign |
Het |
| Rasal2 |
A |
T |
1: 157,071,218 (GRCm39) |
H45Q |
probably benign |
Het |
| Rbm43 |
A |
G |
2: 51,815,909 (GRCm39) |
V104A |
probably damaging |
Het |
| Rhbdd2 |
C |
A |
5: 135,667,969 (GRCm39) |
|
probably null |
Het |
| Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
| Rimbp2 |
T |
A |
5: 128,838,528 (GRCm39) |
N1023I |
probably damaging |
Het |
| Rtl1 |
A |
T |
12: 109,561,031 (GRCm39) |
D269E |
possibly damaging |
Het |
| Sbp |
A |
G |
17: 24,161,163 (GRCm39) |
|
probably benign |
Het |
| Sorbs1 |
T |
A |
19: 40,316,020 (GRCm39) |
T374S |
probably benign |
Het |
| Tgs1 |
A |
T |
4: 3,598,652 (GRCm39) |
K655I |
probably benign |
Het |
| Thsd1 |
A |
C |
8: 22,749,585 (GRCm39) |
T819P |
probably damaging |
Het |
| Tmprss11c |
C |
T |
5: 86,379,655 (GRCm39) |
V418M |
probably damaging |
Het |
| Top2a |
A |
T |
11: 98,900,431 (GRCm39) |
D645E |
probably damaging |
Het |
| Top2b |
G |
A |
14: 16,413,081 (GRCm38) |
V997I |
possibly damaging |
Het |
| Ttc34 |
A |
G |
4: 154,943,840 (GRCm39) |
D118G |
probably damaging |
Het |
| Ttll5 |
A |
G |
12: 85,935,948 (GRCm39) |
D353G |
probably damaging |
Het |
| Uba6 |
A |
T |
5: 86,265,924 (GRCm39) |
Y994* |
probably null |
Het |
| Vinac1 |
A |
C |
2: 128,879,049 (GRCm39) |
V959G |
unknown |
Het |
| Vmn1r189 |
A |
T |
13: 22,285,906 (GRCm39) |
Y310* |
probably null |
Het |
| Vps13c |
T |
A |
9: 67,834,265 (GRCm39) |
I1644N |
probably damaging |
Het |
| Zfp811 |
T |
C |
17: 33,017,821 (GRCm39) |
D73G |
possibly damaging |
Het |
| Zfp951 |
A |
T |
5: 104,962,838 (GRCm39) |
C243S |
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 |
|
|
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 |
|
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'- GGGCCTTTTAACACCAGGTCTG -3'
(R):5'- TATACTGTGCATGAATGGGTAGAG -3'
Sequencing Primer
(F):5'- GTCTGGAATTACCTACCCCTCAGAG -3'
(R):5'- GCATGAATGGGTAGAGTTGATATAAC -3'
|
| Posted On |
2019-12-20 |
Incidental Mutation