Incidental Mutation 'R1892:Cobl'
ID |
211628 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cobl
|
Ensembl Gene |
ENSMUSG00000020173 |
Gene Name |
cordon-bleu WH2 repeat |
Synonyms |
C530045F18Rik |
MMRRC Submission |
039912-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1892 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
12186676-12415022 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to C
at 12203258 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Tryptophan
at position 1066
(S1066W)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000105277
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046755]
[ENSMUST00000109650]
[ENSMUST00000109651]
[ENSMUST00000172919]
[ENSMUST00000172956]
[ENSMUST00000174874]
|
AlphaFold |
Q5NBX1 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000046755
AA Change: S1148W
PolyPhen 2
Score 0.961 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000045693 Gene: ENSMUSG00000020173 AA Change: S1148W
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
30 |
N/A |
INTRINSIC |
Pfam:Cobl
|
144 |
235 |
2.2e-46 |
PFAM |
low complexity region
|
328 |
333 |
N/A |
INTRINSIC |
low complexity region
|
360 |
376 |
N/A |
INTRINSIC |
low complexity region
|
408 |
433 |
N/A |
INTRINSIC |
low complexity region
|
468 |
482 |
N/A |
INTRINSIC |
low complexity region
|
526 |
541 |
N/A |
INTRINSIC |
coiled coil region
|
564 |
589 |
N/A |
INTRINSIC |
WH2
|
1185 |
1205 |
1.32e0 |
SMART |
WH2
|
1225 |
1245 |
6.36e-3 |
SMART |
low complexity region
|
1276 |
1296 |
N/A |
INTRINSIC |
WH2
|
1313 |
1333 |
3.91e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109650
AA Change: S1066W
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000105277 Gene: ENSMUSG00000020173 AA Change: S1066W
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
30 |
N/A |
INTRINSIC |
Pfam:Cobl
|
182 |
260 |
1.6e-40 |
PFAM |
low complexity region
|
303 |
308 |
N/A |
INTRINSIC |
low complexity region
|
335 |
351 |
N/A |
INTRINSIC |
low complexity region
|
386 |
400 |
N/A |
INTRINSIC |
low complexity region
|
444 |
459 |
N/A |
INTRINSIC |
coiled coil region
|
482 |
507 |
N/A |
INTRINSIC |
WH2
|
1103 |
1123 |
1.32e0 |
SMART |
WH2
|
1143 |
1163 |
6.36e-3 |
SMART |
low complexity region
|
1194 |
1214 |
N/A |
INTRINSIC |
WH2
|
1231 |
1251 |
3.91e-3 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109651
AA Change: S1123W
PolyPhen 2
Score 0.959 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000105278 Gene: ENSMUSG00000020173 AA Change: S1123W
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
30 |
N/A |
INTRINSIC |
Pfam:Cobl
|
182 |
260 |
1.2e-40 |
PFAM |
low complexity region
|
303 |
308 |
N/A |
INTRINSIC |
low complexity region
|
335 |
351 |
N/A |
INTRINSIC |
low complexity region
|
383 |
408 |
N/A |
INTRINSIC |
low complexity region
|
443 |
457 |
N/A |
INTRINSIC |
low complexity region
|
501 |
516 |
N/A |
INTRINSIC |
coiled coil region
|
539 |
564 |
N/A |
INTRINSIC |
WH2
|
1160 |
1180 |
1.32e0 |
SMART |
WH2
|
1200 |
1220 |
6.36e-3 |
SMART |
low complexity region
|
1251 |
1271 |
N/A |
INTRINSIC |
WH2
|
1288 |
1308 |
3.91e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000172919
|
SMART Domains |
Protein: ENSMUSP00000133669 Gene: ENSMUSG00000020173
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
30 |
N/A |
INTRINSIC |
Pfam:Cobl
|
182 |
260 |
2.6e-41 |
PFAM |
low complexity region
|
328 |
333 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000172956
|
SMART Domains |
Protein: ENSMUSP00000134372 Gene: ENSMUSG00000020173
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
30 |
N/A |
INTRINSIC |
Pfam:Cobl
|
182 |
260 |
2.4e-41 |
PFAM |
low complexity region
|
303 |
308 |
N/A |
INTRINSIC |
low complexity region
|
335 |
351 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000174874
AA Change: S1141W
PolyPhen 2
Score 0.961 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000133470 Gene: ENSMUSG00000020173 AA Change: S1141W
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
23 |
N/A |
INTRINSIC |
Pfam:Cobl
|
175 |
253 |
1.2e-40 |
PFAM |
low complexity region
|
321 |
326 |
N/A |
INTRINSIC |
low complexity region
|
353 |
369 |
N/A |
INTRINSIC |
low complexity region
|
401 |
426 |
N/A |
INTRINSIC |
low complexity region
|
461 |
475 |
N/A |
INTRINSIC |
low complexity region
|
519 |
534 |
N/A |
INTRINSIC |
coiled coil region
|
557 |
582 |
N/A |
INTRINSIC |
WH2
|
1178 |
1198 |
1.32e0 |
SMART |
WH2
|
1218 |
1238 |
6.36e-3 |
SMART |
low complexity region
|
1269 |
1289 |
N/A |
INTRINSIC |
WH2
|
1306 |
1326 |
3.91e-3 |
SMART |
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 93.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that contains WH2 domains (WASP, Wiskott-Aldrich syndrome protein, homology domain-2) that interact with actin. The encoded actin regulator protein is required for growth and assembly of brush border microvilli that play a role in maintaining intestinal homeostasis. A similar protein in mouse functions in midbrain neural tube closure. A pseudogene of this gene is located on chromosome X. [provided by RefSeq, Oct 2016] PHENOTYPE: Animals homozygous for this mutation do not display a phenotype. However, the allele exacerbates the neural tube defects seen in the loop tail mouse. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
G |
A |
7: 119,815,561 (GRCm39) |
A270T |
probably benign |
Het |
Abcb7 |
A |
T |
X: 103,386,142 (GRCm39) |
H97Q |
probably damaging |
Het |
Adat3 |
T |
C |
10: 80,442,249 (GRCm39) |
L29P |
probably damaging |
Het |
AI987944 |
A |
T |
7: 41,024,020 (GRCm39) |
C320S |
probably damaging |
Het |
Asic4 |
C |
T |
1: 75,446,126 (GRCm39) |
R285W |
probably damaging |
Het |
Asic5 |
A |
T |
3: 81,928,293 (GRCm39) |
I419L |
probably damaging |
Het |
Batf |
A |
G |
12: 85,736,102 (GRCm39) |
K42E |
probably damaging |
Het |
Bcar3 |
A |
G |
3: 122,301,785 (GRCm39) |
N160S |
probably benign |
Het |
Bco2 |
C |
A |
9: 50,461,863 (GRCm39) |
G47V |
probably damaging |
Het |
Bicc1 |
T |
G |
10: 70,794,614 (GRCm39) |
K181T |
probably damaging |
Het |
Brinp2 |
A |
G |
1: 158,082,542 (GRCm39) |
|
probably null |
Het |
Cacng8 |
A |
G |
7: 3,463,568 (GRCm39) |
D240G |
possibly damaging |
Het |
Calca |
A |
G |
7: 114,232,962 (GRCm39) |
Y96H |
probably damaging |
Het |
Cdh1 |
A |
T |
8: 107,390,882 (GRCm39) |
K666I |
possibly damaging |
Het |
Cdh16 |
A |
T |
8: 105,344,631 (GRCm39) |
I500N |
possibly damaging |
Het |
Chst14 |
A |
G |
2: 118,757,830 (GRCm39) |
Y208C |
probably damaging |
Het |
Chst9 |
T |
C |
18: 15,586,017 (GRCm39) |
H182R |
probably damaging |
Het |
Clk2 |
A |
G |
3: 89,082,502 (GRCm39) |
I367M |
possibly damaging |
Het |
Ctcfl |
A |
G |
2: 172,960,478 (GRCm39) |
V35A |
probably benign |
Het |
Dchs1 |
G |
T |
7: 105,413,363 (GRCm39) |
H1151N |
probably benign |
Het |
Dennd1c |
T |
C |
17: 57,374,083 (GRCm39) |
T529A |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,070,209 (GRCm39) |
V1532D |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,612,738 (GRCm39) |
Y2871C |
probably damaging |
Het |
Dytn |
T |
C |
1: 63,716,420 (GRCm39) |
E51G |
probably benign |
Het |
Esd |
C |
T |
14: 74,987,113 (GRCm39) |
A266V |
probably damaging |
Het |
Gli1 |
T |
C |
10: 127,165,975 (GRCm39) |
M1093V |
possibly damaging |
Het |
Gm15446 |
A |
G |
5: 110,091,253 (GRCm39) |
K502E |
probably damaging |
Het |
Gm4076 |
T |
A |
13: 85,275,447 (GRCm39) |
|
noncoding transcript |
Het |
Gm9830 |
A |
G |
9: 44,375,825 (GRCm39) |
|
noncoding transcript |
Het |
Gm9938 |
G |
A |
19: 23,701,955 (GRCm39) |
|
probably benign |
Het |
Grhl1 |
G |
A |
12: 24,634,909 (GRCm39) |
R245H |
probably damaging |
Het |
Hnrnpul1 |
A |
T |
7: 25,426,191 (GRCm39) |
D553E |
probably benign |
Het |
Hpn |
G |
A |
7: 30,798,468 (GRCm39) |
Q415* |
probably null |
Het |
Hsd11b1 |
T |
G |
1: 192,906,068 (GRCm39) |
M175L |
probably benign |
Het |
Htra1 |
G |
A |
7: 130,586,799 (GRCm39) |
V461I |
possibly damaging |
Het |
Il1rl2 |
A |
G |
1: 40,366,694 (GRCm39) |
H76R |
probably damaging |
Het |
Insrr |
G |
A |
3: 87,721,184 (GRCm39) |
V1112M |
probably damaging |
Het |
Ints9 |
T |
C |
14: 65,257,872 (GRCm39) |
S351P |
probably benign |
Het |
Itgav |
T |
A |
2: 83,601,680 (GRCm39) |
N350K |
probably damaging |
Het |
Kdm4d |
C |
A |
9: 14,375,613 (GRCm39) |
V82L |
probably benign |
Het |
Klc1 |
T |
C |
12: 111,748,261 (GRCm39) |
|
probably null |
Het |
Kmt5c |
T |
A |
7: 4,745,714 (GRCm39) |
C69* |
probably null |
Het |
Lgals3 |
T |
G |
14: 47,622,164 (GRCm39) |
N193K |
possibly damaging |
Het |
Morc2b |
T |
A |
17: 33,354,748 (GRCm39) |
D1008V |
probably damaging |
Het |
Mpg |
C |
T |
11: 32,181,720 (GRCm39) |
Q243* |
probably null |
Het |
Muc15 |
C |
T |
2: 110,567,697 (GRCm39) |
R281* |
probably null |
Het |
Ncstn |
CAGCTCCACGAAG |
CAG |
1: 171,899,038 (GRCm39) |
|
probably null |
Het |
Nek5 |
A |
G |
8: 22,597,745 (GRCm39) |
M278T |
probably benign |
Het |
Npas2 |
A |
G |
1: 39,384,503 (GRCm39) |
T599A |
probably benign |
Het |
Nrf1 |
A |
G |
6: 30,144,787 (GRCm39) |
D519G |
probably null |
Het |
Nup43 |
A |
G |
10: 7,549,373 (GRCm39) |
H176R |
probably damaging |
Het |
Nxpe2 |
T |
C |
9: 48,237,914 (GRCm39) |
T114A |
probably damaging |
Het |
Or10j3 |
T |
C |
1: 173,031,795 (GRCm39) |
Y291H |
probably damaging |
Het |
Or5p72 |
A |
T |
7: 108,022,147 (GRCm39) |
Y123F |
possibly damaging |
Het |
Or6c75 |
A |
C |
10: 129,336,902 (GRCm39) |
I50L |
probably benign |
Het |
Perm1 |
C |
T |
4: 156,302,340 (GRCm39) |
R295C |
probably benign |
Het |
Pik3ip1 |
G |
T |
11: 3,283,304 (GRCm39) |
A135S |
probably damaging |
Het |
Pira13 |
A |
C |
7: 3,827,573 (GRCm39) |
C195G |
probably benign |
Het |
Ppp4c |
A |
G |
7: 126,385,452 (GRCm39) |
V119A |
probably damaging |
Het |
Prepl |
A |
G |
17: 85,395,878 (GRCm39) |
Y35H |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,649,545 (GRCm39) |
Y316C |
possibly damaging |
Het |
Pxk |
C |
T |
14: 8,151,507 (GRCm38) |
R441* |
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,299,921 (GRCm39) |
V491A |
probably benign |
Het |
Ranbp9 |
C |
A |
13: 43,569,933 (GRCm39) |
C495F |
possibly damaging |
Het |
Rfx8 |
A |
T |
1: 39,709,746 (GRCm39) |
|
probably null |
Het |
Rnf111 |
T |
A |
9: 70,383,656 (GRCm39) |
K92N |
probably damaging |
Het |
Rtn1 |
A |
G |
12: 72,259,337 (GRCm39) |
I772T |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,673,844 (GRCm39) |
K72* |
probably null |
Het |
Sergef |
A |
T |
7: 46,264,040 (GRCm39) |
|
probably null |
Het |
Sez6l |
T |
C |
5: 112,620,665 (GRCm39) |
N305S |
probably damaging |
Het |
Slc40a1 |
A |
T |
1: 45,950,302 (GRCm39) |
C383* |
probably null |
Het |
Stab2 |
C |
T |
10: 86,773,913 (GRCm39) |
C806Y |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,524,189 (GRCm39) |
T795A |
probably benign |
Het |
Stk31 |
T |
C |
6: 49,415,408 (GRCm39) |
I536T |
probably damaging |
Het |
Stox1 |
T |
A |
10: 62,501,178 (GRCm39) |
T461S |
possibly damaging |
Het |
Suv39h2 |
T |
C |
2: 3,460,805 (GRCm39) |
Y219C |
probably damaging |
Het |
Tap1 |
T |
G |
17: 34,413,915 (GRCm39) |
D643E |
probably damaging |
Het |
Tbc1d2b |
T |
A |
9: 90,100,996 (GRCm39) |
I665F |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,935,696 (GRCm39) |
N1784S |
probably benign |
Het |
Tmem14c |
T |
C |
13: 41,174,633 (GRCm39) |
F81L |
possibly damaging |
Het |
Tnrc6c |
A |
G |
11: 117,605,188 (GRCm39) |
N108D |
probably benign |
Het |
Tox3 |
A |
T |
8: 90,996,869 (GRCm39) |
N131K |
probably benign |
Het |
Tspear |
T |
A |
10: 77,706,308 (GRCm39) |
D359E |
probably benign |
Het |
Ttc9 |
A |
G |
12: 81,678,551 (GRCm39) |
I125V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,728,531 (GRCm39) |
|
probably benign |
Het |
Ubn2 |
C |
T |
6: 38,468,226 (GRCm39) |
S980F |
probably damaging |
Het |
Vcf1 |
G |
T |
11: 113,554,212 (GRCm39) |
P161H |
probably damaging |
Het |
Zfp362 |
T |
A |
4: 128,684,057 (GRCm39) |
T30S |
probably benign |
Het |
Zfp385c |
A |
C |
11: 100,528,630 (GRCm39) |
H32Q |
probably damaging |
Het |
Zfp870 |
A |
T |
17: 33,102,863 (GRCm39) |
H156Q |
possibly damaging |
Het |
Zfp873 |
T |
C |
10: 81,897,080 (GRCm39) |
C641R |
probably damaging |
Het |
Zfp950 |
A |
T |
19: 61,107,549 (GRCm39) |
H511Q |
probably benign |
Het |
|
Other mutations in Cobl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00338:Cobl
|
APN |
11 |
12,325,813 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00698:Cobl
|
APN |
11 |
12,203,722 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00772:Cobl
|
APN |
11 |
12,216,985 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00922:Cobl
|
APN |
11 |
12,204,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00985:Cobl
|
APN |
11 |
12,204,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01641:Cobl
|
APN |
11 |
12,259,641 (GRCm39) |
nonsense |
probably null |
|
IGL01722:Cobl
|
APN |
11 |
12,203,987 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01734:Cobl
|
APN |
11 |
12,204,980 (GRCm39) |
splice site |
probably benign |
|
IGL01924:Cobl
|
APN |
11 |
12,204,596 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02105:Cobl
|
APN |
11 |
12,199,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02326:Cobl
|
APN |
11 |
12,336,712 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02342:Cobl
|
APN |
11 |
12,203,672 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02426:Cobl
|
APN |
11 |
12,204,351 (GRCm39) |
nonsense |
probably null |
|
IGL02754:Cobl
|
APN |
11 |
12,204,370 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02754:Cobl
|
APN |
11 |
12,204,371 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02811:Cobl
|
APN |
11 |
12,203,285 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02859:Cobl
|
APN |
11 |
12,319,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02999:Cobl
|
APN |
11 |
12,293,869 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03030:Cobl
|
APN |
11 |
12,204,241 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03191:Cobl
|
APN |
11 |
12,203,364 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4418001:Cobl
|
UTSW |
11 |
12,206,240 (GRCm39) |
missense |
possibly damaging |
0.79 |
PIT4480001:Cobl
|
UTSW |
11 |
12,203,592 (GRCm39) |
missense |
probably benign |
|
PIT4495001:Cobl
|
UTSW |
11 |
12,204,596 (GRCm39) |
missense |
probably benign |
0.00 |
R0031:Cobl
|
UTSW |
11 |
12,204,945 (GRCm39) |
missense |
probably benign |
0.36 |
R0241:Cobl
|
UTSW |
11 |
12,204,524 (GRCm39) |
missense |
probably benign |
0.25 |
R0241:Cobl
|
UTSW |
11 |
12,204,524 (GRCm39) |
missense |
probably benign |
0.25 |
R0322:Cobl
|
UTSW |
11 |
12,217,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Cobl
|
UTSW |
11 |
12,204,699 (GRCm39) |
missense |
probably benign |
0.24 |
R0733:Cobl
|
UTSW |
11 |
12,315,167 (GRCm39) |
missense |
probably benign |
0.31 |
R0734:Cobl
|
UTSW |
11 |
12,325,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Cobl
|
UTSW |
11 |
12,216,843 (GRCm39) |
splice site |
probably benign |
|
R0884:Cobl
|
UTSW |
11 |
12,325,908 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1065:Cobl
|
UTSW |
11 |
12,204,327 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1331:Cobl
|
UTSW |
11 |
12,325,853 (GRCm39) |
missense |
probably damaging |
0.96 |
R2847:Cobl
|
UTSW |
11 |
12,328,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2848:Cobl
|
UTSW |
11 |
12,328,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R3407:Cobl
|
UTSW |
11 |
12,325,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Cobl
|
UTSW |
11 |
12,201,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Cobl
|
UTSW |
11 |
12,203,672 (GRCm39) |
missense |
probably benign |
0.08 |
R4677:Cobl
|
UTSW |
11 |
12,336,665 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4844:Cobl
|
UTSW |
11 |
12,204,740 (GRCm39) |
missense |
probably benign |
0.10 |
R4942:Cobl
|
UTSW |
11 |
12,204,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R5158:Cobl
|
UTSW |
11 |
12,206,198 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5195:Cobl
|
UTSW |
11 |
12,203,565 (GRCm39) |
missense |
probably benign |
0.02 |
R5255:Cobl
|
UTSW |
11 |
12,325,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Cobl
|
UTSW |
11 |
12,293,886 (GRCm39) |
nonsense |
probably null |
|
R5637:Cobl
|
UTSW |
11 |
12,246,531 (GRCm39) |
intron |
probably benign |
|
R5643:Cobl
|
UTSW |
11 |
12,256,948 (GRCm39) |
splice site |
probably benign |
|
R5749:Cobl
|
UTSW |
11 |
12,216,965 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5953:Cobl
|
UTSW |
11 |
12,206,220 (GRCm39) |
missense |
probably benign |
0.00 |
R6000:Cobl
|
UTSW |
11 |
12,319,684 (GRCm39) |
missense |
probably benign |
0.08 |
R6373:Cobl
|
UTSW |
11 |
12,203,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Cobl
|
UTSW |
11 |
12,204,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R7071:Cobl
|
UTSW |
11 |
12,204,795 (GRCm39) |
missense |
probably benign |
0.00 |
R7077:Cobl
|
UTSW |
11 |
12,203,441 (GRCm39) |
missense |
probably benign |
0.04 |
R7078:Cobl
|
UTSW |
11 |
12,328,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Cobl
|
UTSW |
11 |
12,246,540 (GRCm39) |
missense |
|
|
R7153:Cobl
|
UTSW |
11 |
12,204,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Cobl
|
UTSW |
11 |
12,206,225 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7519:Cobl
|
UTSW |
11 |
12,203,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Cobl
|
UTSW |
11 |
12,362,117 (GRCm39) |
start gained |
probably benign |
|
R7772:Cobl
|
UTSW |
11 |
12,204,488 (GRCm39) |
missense |
probably benign |
0.29 |
R7841:Cobl
|
UTSW |
11 |
12,203,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7845:Cobl
|
UTSW |
11 |
12,315,139 (GRCm39) |
missense |
probably benign |
0.35 |
R8026:Cobl
|
UTSW |
11 |
12,203,459 (GRCm39) |
missense |
probably benign |
0.01 |
R8118:Cobl
|
UTSW |
11 |
12,204,834 (GRCm39) |
missense |
probably benign |
0.03 |
R8192:Cobl
|
UTSW |
11 |
12,199,745 (GRCm39) |
missense |
probably benign |
0.07 |
R8320:Cobl
|
UTSW |
11 |
12,217,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Cobl
|
UTSW |
11 |
12,203,696 (GRCm39) |
missense |
probably benign |
0.41 |
R9319:Cobl
|
UTSW |
11 |
12,203,648 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Cobl
|
UTSW |
11 |
12,203,501 (GRCm39) |
missense |
probably benign |
0.00 |
R9501:Cobl
|
UTSW |
11 |
12,328,235 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Cobl
|
UTSW |
11 |
12,325,827 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cobl
|
UTSW |
11 |
12,319,645 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cobl
|
UTSW |
11 |
12,203,433 (GRCm39) |
missense |
probably benign |
0.02 |
|
Predicted Primers |
PCR Primer
(F):5'- ACCACATTCACCTTCCGGAG -3'
(R):5'- AGAGCTGTGGTTTCAATGAAAAGC -3'
Sequencing Primer
(F):5'- GAGCTTTTCTCTCCCTCCTGATGAG -3'
(R):5'- ATTCAACATCTAACTTCTCGCAGG -3'
|
Posted On |
2014-06-30 |