Incidental Mutation 'R7014:Ccdc141'
| ID |
545157 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ccdc141
|
| Ensembl Gene |
ENSMUSG00000044033 |
| Gene Name |
coiled-coil domain containing 141 |
| Synonyms |
ENSMUSG00000075261, CAMDI, 2610301F02Rik |
| MMRRC Submission |
045115-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7014 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
76840246-77000980 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 76962641 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 101
(V101A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000128736
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049544]
[ENSMUST00000133503]
[ENSMUST00000164114]
|
| AlphaFold |
E9Q8Q6 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000028406
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000049544
AA Change: V101A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000052945
Gene: ENSMUSG00000044033
AA Change: V101A
| Domain | Start | End | E-Value | Type |
|---|
|
SPEC
|
26 |
128 |
2.87e-1 |
SMART |
|
Blast:SPEC
|
132 |
222 |
1e-40 |
BLAST |
|
low complexity region
|
223 |
251 |
N/A |
INTRINSIC |
|
SPEC
|
252 |
353 |
3.61e-1 |
SMART |
|
Blast:SPEC
|
356 |
453 |
2e-49 |
BLAST |
|
Blast:SPEC
|
461 |
562 |
1e-16 |
BLAST |
|
low complexity region
|
569 |
583 |
N/A |
INTRINSIC |
|
Blast:SPEC
|
688 |
772 |
7e-30 |
BLAST |
|
low complexity region
|
773 |
785 |
N/A |
INTRINSIC |
|
Blast:SPEC
|
790 |
894 |
2e-24 |
BLAST |
|
Blast:SPEC
|
907 |
1009 |
4e-44 |
BLAST |
|
Blast:SPEC
|
1012 |
1118 |
9e-63 |
BLAST |
|
low complexity region
|
1203 |
1231 |
N/A |
INTRINSIC |
|
Blast:IG
|
1305 |
1416 |
5e-54 |
BLAST |
|
SCOP:d1g1ca_
|
1406 |
1443 |
1e-9 |
SMART |
|
Blast:IG
|
1416 |
1444 |
2e-9 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131660
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000133503
|
| SMART Domains |
Protein: ENSMUSP00000120312
Gene: ENSMUSG00000044033
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:SPEC
|
26 |
60 |
4e-17 |
BLAST |
|
low complexity region
|
61 |
76 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000164114
AA Change: V101A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000128736
Gene: ENSMUSG00000044033
AA Change: V101A
| Domain | Start | End | E-Value | Type |
|---|
|
SPEC
|
26 |
128 |
2.87e-1 |
SMART |
|
Blast:SPEC
|
132 |
222 |
2e-40 |
BLAST |
|
low complexity region
|
223 |
251 |
N/A |
INTRINSIC |
|
SPEC
|
252 |
353 |
3.61e-1 |
SMART |
|
Blast:SPEC
|
356 |
453 |
2e-49 |
BLAST |
|
Blast:SPEC
|
461 |
562 |
1e-16 |
BLAST |
|
low complexity region
|
569 |
583 |
N/A |
INTRINSIC |
|
Blast:SPEC
|
688 |
772 |
7e-30 |
BLAST |
|
low complexity region
|
773 |
785 |
N/A |
INTRINSIC |
|
Blast:SPEC
|
790 |
894 |
3e-24 |
BLAST |
|
Blast:SPEC
|
907 |
1009 |
4e-44 |
BLAST |
|
Blast:SPEC
|
1012 |
1118 |
1e-62 |
BLAST |
|
low complexity region
|
1203 |
1231 |
N/A |
INTRINSIC |
|
IGc2
|
1422 |
1489 |
1.27e-5 |
SMART |
|
transmembrane domain
|
1510 |
1529 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1587 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
99% (80/81) |
| MGI Phenotype |
PHENOTYPE: Homozygous knockout impairs migration of neurons in the somatosensory cortex, resulting in increased anxiety and hyperactivity. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310022A10Rik |
C |
T |
7: 27,278,198 (GRCm39) |
Q156* |
probably null |
Het |
| 2700097O09Rik |
A |
G |
12: 55,092,727 (GRCm39) |
I264T |
probably benign |
Het |
| Arid3a |
G |
T |
10: 79,786,718 (GRCm39) |
M488I |
possibly damaging |
Het |
| Auts2 |
A |
G |
5: 131,494,961 (GRCm39) |
F331S |
probably damaging |
Het |
| Axdnd1 |
T |
C |
1: 156,158,532 (GRCm39) |
|
probably null |
Het |
| Bpifb5 |
C |
A |
2: 154,066,876 (GRCm39) |
S43* |
probably null |
Het |
| Carhsp1 |
A |
G |
16: 8,478,869 (GRCm39) |
V128A |
probably benign |
Het |
| Cdk6 |
C |
G |
5: 3,523,152 (GRCm39) |
L191V |
probably damaging |
Het |
| Cgnl1 |
T |
G |
9: 71,632,416 (GRCm39) |
K312Q |
possibly damaging |
Het |
| Col6a1 |
T |
C |
10: 76,557,277 (GRCm39) |
E225G |
probably damaging |
Het |
| Copg1 |
T |
A |
6: 87,879,322 (GRCm39) |
L456Q |
probably damaging |
Het |
| Ctif |
T |
A |
18: 75,570,279 (GRCm39) |
D540V |
possibly damaging |
Het |
| Cyfip1 |
T |
C |
7: 55,569,241 (GRCm39) |
I917T |
probably benign |
Het |
| Cyth1 |
T |
C |
11: 118,103,477 (GRCm39) |
D9G |
probably benign |
Het |
| Dnajb1 |
T |
C |
8: 84,336,884 (GRCm39) |
I118T |
probably damaging |
Het |
| Ebna1bp2 |
T |
A |
4: 118,480,575 (GRCm39) |
Y139* |
probably null |
Het |
| Efcab3 |
A |
G |
11: 104,584,248 (GRCm39) |
T100A |
probably benign |
Het |
| Fam162a |
A |
T |
16: 35,870,302 (GRCm39) |
V59E |
probably damaging |
Het |
| Fhad1 |
CGG |
CG |
4: 141,645,602 (GRCm39) |
|
probably null |
Het |
| Fmo6 |
C |
G |
1: 162,753,877 (GRCm39) |
R112T |
probably benign |
Het |
| Gm17087 |
T |
A |
17: 8,785,304 (GRCm39) |
D133V |
probably benign |
Het |
| Gm42669 |
A |
G |
5: 107,656,142 (GRCm39) |
I802V |
probably benign |
Het |
| Gp2 |
T |
C |
7: 119,050,868 (GRCm39) |
N288D |
probably damaging |
Het |
| Gstm7 |
C |
T |
3: 107,834,278 (GRCm39) |
D196N |
probably benign |
Het |
| Hsph1 |
A |
T |
5: 149,553,865 (GRCm39) |
V201D |
probably damaging |
Het |
| Il20ra |
T |
C |
10: 19,588,458 (GRCm39) |
L26P |
unknown |
Het |
| Itpr1 |
T |
A |
6: 108,408,459 (GRCm39) |
|
probably null |
Het |
| Kcns3 |
A |
T |
12: 11,141,688 (GRCm39) |
I337N |
probably damaging |
Het |
| Kdm4d |
A |
G |
9: 14,375,475 (GRCm39) |
Y128H |
probably damaging |
Het |
| Kirrel2 |
A |
G |
7: 30,153,999 (GRCm39) |
I200T |
probably benign |
Het |
| Klhdc10 |
T |
A |
6: 30,450,502 (GRCm39) |
I294N |
probably damaging |
Het |
| Map1a |
A |
C |
2: 121,130,720 (GRCm39) |
N512T |
probably damaging |
Het |
| Marchf8 |
C |
G |
6: 116,380,504 (GRCm39) |
C118W |
probably damaging |
Het |
| Marchf8 |
T |
G |
6: 116,380,505 (GRCm39) |
C119G |
probably damaging |
Het |
| Mrpl38 |
G |
T |
11: 116,025,741 (GRCm39) |
P195Q |
probably damaging |
Het |
| Ms4a4d |
A |
T |
19: 11,525,947 (GRCm39) |
Q27L |
probably benign |
Het |
| Muc16 |
T |
A |
9: 18,569,532 (GRCm39) |
T996S |
unknown |
Het |
| Mug1 |
C |
T |
6: 121,838,084 (GRCm39) |
A438V |
probably benign |
Het |
| Mup7 |
T |
A |
4: 60,069,866 (GRCm39) |
I33F |
probably damaging |
Het |
| Ndufa5 |
C |
T |
6: 24,519,190 (GRCm39) |
|
probably null |
Het |
| Or2b7 |
A |
G |
13: 21,740,108 (GRCm39) |
F28S |
probably benign |
Het |
| Or2l5 |
A |
T |
16: 19,334,206 (GRCm39) |
F60Y |
probably benign |
Het |
| Or5w17 |
T |
C |
2: 87,584,215 (GRCm39) |
I41V |
probably benign |
Het |
| Or5w1b |
A |
T |
2: 87,476,320 (GRCm39) |
L49Q |
probably damaging |
Het |
| Or7e177 |
T |
A |
9: 20,211,959 (GRCm39) |
C154* |
probably null |
Het |
| Parp9 |
T |
A |
16: 35,780,433 (GRCm39) |
|
probably null |
Het |
| Pate8 |
C |
A |
9: 36,493,854 (GRCm39) |
W26C |
unknown |
Het |
| Pbx1 |
T |
A |
1: 168,258,949 (GRCm39) |
D42V |
probably damaging |
Het |
| Pde4dip |
G |
T |
3: 97,622,738 (GRCm39) |
N1490K |
possibly damaging |
Het |
| Pdzd2 |
T |
C |
15: 12,372,647 (GRCm39) |
N2496S |
probably benign |
Het |
| Pdzd2 |
A |
G |
15: 12,373,061 (GRCm39) |
M2358T |
probably benign |
Het |
| Pglyrp2 |
C |
A |
17: 32,634,904 (GRCm39) |
C486F |
probably damaging |
Het |
| Pi4ka |
A |
G |
16: 17,114,931 (GRCm39) |
|
probably benign |
Het |
| Pknox2 |
T |
A |
9: 36,820,963 (GRCm39) |
T300S |
probably damaging |
Het |
| Plekhm3 |
A |
G |
1: 64,922,429 (GRCm39) |
I582T |
probably damaging |
Het |
| Prtg |
T |
C |
9: 72,799,267 (GRCm39) |
Y766H |
possibly damaging |
Het |
| Prxl2a |
T |
C |
14: 40,724,451 (GRCm39) |
E71G |
probably benign |
Het |
| Rabgap1 |
A |
G |
2: 37,450,575 (GRCm39) |
E901G |
probably benign |
Het |
| Rabgap1l |
A |
T |
1: 160,169,642 (GRCm39) |
N60K |
probably damaging |
Het |
| Rnf150 |
C |
T |
8: 83,769,292 (GRCm39) |
T359I |
probably benign |
Het |
| Rps6ka2 |
C |
T |
17: 7,523,331 (GRCm39) |
H236Y |
probably benign |
Het |
| Rrp1b |
T |
A |
17: 32,268,401 (GRCm39) |
L120Q |
probably damaging |
Het |
| Scn7a |
C |
A |
2: 66,572,303 (GRCm39) |
G223C |
probably null |
Het |
| Sema6a |
T |
A |
18: 47,431,284 (GRCm39) |
N138I |
probably damaging |
Het |
| Septin5 |
T |
A |
16: 18,443,659 (GRCm39) |
I97F |
probably damaging |
Het |
| Shcbp1 |
T |
A |
8: 4,804,234 (GRCm39) |
E225D |
probably damaging |
Het |
| Slc25a19 |
A |
G |
11: 115,511,792 (GRCm39) |
C124R |
probably damaging |
Het |
| Slc37a2 |
C |
T |
9: 37,145,183 (GRCm39) |
A428T |
probably damaging |
Het |
| Slc5a12 |
A |
G |
2: 110,474,709 (GRCm39) |
I538V |
probably benign |
Het |
| Slco4c1 |
A |
T |
1: 96,751,506 (GRCm39) |
|
probably null |
Het |
| Smarcad1 |
T |
C |
6: 65,029,654 (GRCm39) |
S81P |
probably damaging |
Het |
| Smyd1 |
T |
C |
6: 71,215,611 (GRCm39) |
D116G |
probably damaging |
Het |
| Themis |
T |
C |
10: 28,665,703 (GRCm39) |
Y589H |
probably benign |
Het |
| Trim30d |
T |
C |
7: 104,132,543 (GRCm39) |
K248R |
probably benign |
Het |
| Tspan12 |
C |
T |
6: 21,772,918 (GRCm39) |
M210I |
probably benign |
Het |
| Vmn2r11 |
T |
C |
5: 109,201,289 (GRCm39) |
Y405C |
probably damaging |
Het |
| Wdfy3 |
A |
G |
5: 102,042,775 (GRCm39) |
|
probably null |
Het |
| Wiz |
C |
A |
17: 32,580,840 (GRCm39) |
A83S |
probably damaging |
Het |
| Zfp1002 |
A |
T |
2: 150,097,182 (GRCm39) |
C82* |
probably null |
Het |
| Zmym6 |
T |
A |
4: 127,017,337 (GRCm39) |
Y947* |
probably null |
Het |
|
| Other mutations in Ccdc141 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00517:Ccdc141
|
APN |
2 |
76,884,988 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01396:Ccdc141
|
APN |
2 |
76,958,669 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL01408:Ccdc141
|
APN |
2 |
76,876,023 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01633:Ccdc141
|
APN |
2 |
76,919,593 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01982:Ccdc141
|
APN |
2 |
76,861,003 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02105:Ccdc141
|
APN |
2 |
76,879,921 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02307:Ccdc141
|
APN |
2 |
76,859,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02645:Ccdc141
|
APN |
2 |
76,905,211 (GRCm39) |
nonsense |
probably null |
|
|
IGL02737:Ccdc141
|
APN |
2 |
76,888,268 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02740:Ccdc141
|
APN |
2 |
76,884,953 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02949:Ccdc141
|
APN |
2 |
76,857,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03127:Ccdc141
|
APN |
2 |
76,859,579 (GRCm39) |
critical splice donor site |
probably null |
|
|
Verloren
|
UTSW |
2 |
76,857,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Verschied
|
UTSW |
2 |
76,938,700 (GRCm39) |
splice site |
probably benign |
|
|
R0153:Ccdc141
|
UTSW |
2 |
76,995,582 (GRCm39) |
intron |
probably benign |
|
|
R0384:Ccdc141
|
UTSW |
2 |
76,857,992 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0423:Ccdc141
|
UTSW |
2 |
76,869,794 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0573:Ccdc141
|
UTSW |
2 |
76,869,837 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1332:Ccdc141
|
UTSW |
2 |
76,844,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1336:Ccdc141
|
UTSW |
2 |
76,844,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1355:Ccdc141
|
UTSW |
2 |
76,860,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1416:Ccdc141
|
UTSW |
2 |
76,845,140 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1659:Ccdc141
|
UTSW |
2 |
76,885,027 (GRCm39) |
missense |
probably benign |
0.41 |
|
R1726:Ccdc141
|
UTSW |
2 |
76,938,700 (GRCm39) |
splice site |
probably benign |
|
|
R1799:Ccdc141
|
UTSW |
2 |
76,842,015 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1837:Ccdc141
|
UTSW |
2 |
76,842,009 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1839:Ccdc141
|
UTSW |
2 |
76,842,009 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1918:Ccdc141
|
UTSW |
2 |
76,845,047 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2019:Ccdc141
|
UTSW |
2 |
76,841,909 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2133:Ccdc141
|
UTSW |
2 |
76,889,951 (GRCm39) |
missense |
probably benign |
0.28 |
|
R2158:Ccdc141
|
UTSW |
2 |
76,861,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2256:Ccdc141
|
UTSW |
2 |
76,962,606 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2359:Ccdc141
|
UTSW |
2 |
77,000,746 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2382:Ccdc141
|
UTSW |
2 |
76,905,342 (GRCm39) |
missense |
probably benign |
0.11 |
|
R2382:Ccdc141
|
UTSW |
2 |
76,841,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3110:Ccdc141
|
UTSW |
2 |
76,869,830 (GRCm39) |
missense |
probably benign |
0.31 |
|
R3112:Ccdc141
|
UTSW |
2 |
76,869,830 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4334:Ccdc141
|
UTSW |
2 |
77,000,776 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4493:Ccdc141
|
UTSW |
2 |
76,962,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4494:Ccdc141
|
UTSW |
2 |
76,962,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4628:Ccdc141
|
UTSW |
2 |
76,890,024 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4748:Ccdc141
|
UTSW |
2 |
76,888,324 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R4810:Ccdc141
|
UTSW |
2 |
76,876,099 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R4824:Ccdc141
|
UTSW |
2 |
76,954,680 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4829:Ccdc141
|
UTSW |
2 |
76,905,260 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4920:Ccdc141
|
UTSW |
2 |
76,998,907 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5024:Ccdc141
|
UTSW |
2 |
76,885,047 (GRCm39) |
missense |
probably benign |
0.17 |
|
R5073:Ccdc141
|
UTSW |
2 |
76,954,722 (GRCm39) |
splice site |
probably null |
|
|
R5251:Ccdc141
|
UTSW |
2 |
76,858,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5252:Ccdc141
|
UTSW |
2 |
76,962,593 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5534:Ccdc141
|
UTSW |
2 |
76,888,241 (GRCm39) |
missense |
probably benign |
|
|
R5539:Ccdc141
|
UTSW |
2 |
76,845,437 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5551:Ccdc141
|
UTSW |
2 |
76,844,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5784:Ccdc141
|
UTSW |
2 |
76,859,671 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5837:Ccdc141
|
UTSW |
2 |
76,938,781 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R5850:Ccdc141
|
UTSW |
2 |
76,859,747 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6050:Ccdc141
|
UTSW |
2 |
76,842,075 (GRCm39) |
missense |
probably benign |
0.33 |
|
R6263:Ccdc141
|
UTSW |
2 |
76,938,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6502:Ccdc141
|
UTSW |
2 |
77,000,745 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6580:Ccdc141
|
UTSW |
2 |
76,842,099 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6865:Ccdc141
|
UTSW |
2 |
76,859,579 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7094:Ccdc141
|
UTSW |
2 |
76,871,797 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7195:Ccdc141
|
UTSW |
2 |
76,879,927 (GRCm39) |
missense |
probably benign |
0.39 |
|
R7300:Ccdc141
|
UTSW |
2 |
76,845,038 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7654:Ccdc141
|
UTSW |
2 |
76,872,822 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7834:Ccdc141
|
UTSW |
2 |
76,889,889 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R7868:Ccdc141
|
UTSW |
2 |
76,938,756 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7986:Ccdc141
|
UTSW |
2 |
76,845,461 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8059:Ccdc141
|
UTSW |
2 |
76,875,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8082:Ccdc141
|
UTSW |
2 |
76,954,588 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8439:Ccdc141
|
UTSW |
2 |
76,889,894 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8508:Ccdc141
|
UTSW |
2 |
76,962,588 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8695:Ccdc141
|
UTSW |
2 |
76,879,963 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8880:Ccdc141
|
UTSW |
2 |
76,845,556 (GRCm39) |
missense |
probably benign |
0.28 |
|
R8992:Ccdc141
|
UTSW |
2 |
76,844,739 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9048:Ccdc141
|
UTSW |
2 |
76,853,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9260:Ccdc141
|
UTSW |
2 |
76,844,795 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9297:Ccdc141
|
UTSW |
2 |
76,842,028 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9418:Ccdc141
|
UTSW |
2 |
76,871,766 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9601:Ccdc141
|
UTSW |
2 |
76,885,073 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9628:Ccdc141
|
UTSW |
2 |
76,844,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9763:Ccdc141
|
UTSW |
2 |
76,869,919 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Ccdc141
|
UTSW |
2 |
76,958,616 (GRCm39) |
missense |
probably benign |
0.03 |
|
Z1177:Ccdc141
|
UTSW |
2 |
76,845,493 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATCCTGCCATTTTGAACATGTATGC -3'
(R):5'- AGGAGGGAATAATGAACCTTCTC -3'
Sequencing Primer
(F):5'- GCAACATTTGTTTTAGGATGTCAAAC -3'
(R):5'- TAGACCTTCCTGGATCACATACGG -3'
|
| Posted On |
2019-05-13 |
Incidental Mutation