Incidental Mutation 'R5024:Ccdc141'
| ID |
391198 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ccdc141
|
| Ensembl Gene |
ENSMUSG00000044033 |
| Gene Name |
coiled-coil domain containing 141 |
| Synonyms |
ENSMUSG00000075261, CAMDI, 2610301F02Rik |
| MMRRC Submission |
042615-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R5024 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
76840246-77000980 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 76885047 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Lysine
at position 531
(N531K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000052945
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049544]
[ENSMUST00000164114]
|
| AlphaFold |
E9Q8Q6 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000028406
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000049544
AA Change: N531K
PolyPhen 2
Score 0.174 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000052945
Gene: ENSMUSG00000044033
AA Change: N531K
| 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 |
probably benign
Transcript: ENSMUST00000164114
AA Change: N531K
PolyPhen 2
Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
|
| SMART Domains |
Protein: ENSMUSP00000128736
Gene: ENSMUSG00000044033
AA Change: N531K
| 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 |
0.0898 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
| Validation Efficiency |
99% (95/96) |
| 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: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrd1 |
A |
G |
5: 129,248,959 (GRCm39) |
N575S |
probably damaging |
Het |
| Akap6 |
C |
T |
12: 53,189,345 (GRCm39) |
T2253M |
probably benign |
Het |
| Arhgef37 |
A |
C |
18: 61,639,511 (GRCm39) |
N289K |
probably damaging |
Het |
| Atad2b |
A |
C |
12: 4,987,534 (GRCm39) |
T121P |
probably benign |
Het |
| Atp4a |
A |
C |
7: 30,415,289 (GRCm39) |
D303A |
possibly damaging |
Het |
| Calu |
A |
T |
6: 29,374,518 (GRCm39) |
|
probably benign |
Het |
| Ccdc146 |
T |
C |
5: 21,604,612 (GRCm39) |
|
probably null |
Het |
| Cd207 |
G |
A |
6: 83,651,301 (GRCm39) |
T218I |
probably damaging |
Het |
| Cd2ap |
A |
C |
17: 43,116,236 (GRCm39) |
|
probably null |
Het |
| Ceacam23 |
A |
G |
7: 17,644,607 (GRCm39) |
I575V |
probably benign |
Het |
| Clip3 |
G |
A |
7: 29,991,644 (GRCm39) |
|
probably benign |
Het |
| Clstn1 |
G |
A |
4: 149,719,751 (GRCm39) |
R432H |
possibly damaging |
Het |
| Csmd2 |
A |
G |
4: 128,215,141 (GRCm39) |
Y521C |
possibly damaging |
Het |
| Dnah8 |
A |
T |
17: 30,955,070 (GRCm39) |
E2033V |
probably damaging |
Het |
| Eng |
T |
G |
2: 32,563,404 (GRCm39) |
V319G |
probably benign |
Het |
| Erp44 |
C |
T |
4: 48,241,296 (GRCm39) |
W57* |
probably null |
Het |
| Etv1 |
T |
A |
12: 38,904,233 (GRCm39) |
|
probably null |
Het |
| Eva1c |
T |
C |
16: 90,673,081 (GRCm39) |
|
probably null |
Het |
| Fam221b |
T |
A |
4: 43,659,674 (GRCm39) |
N482I |
probably damaging |
Het |
| Fam83h |
T |
C |
15: 75,876,991 (GRCm39) |
H202R |
probably damaging |
Het |
| Fbxw13 |
T |
C |
9: 109,008,403 (GRCm39) |
T449A |
probably benign |
Het |
| Fbxw25 |
A |
T |
9: 109,492,442 (GRCm39) |
|
probably null |
Het |
| Frmd3 |
T |
A |
4: 74,016,381 (GRCm39) |
S99T |
probably benign |
Het |
| Gm5174 |
G |
T |
10: 86,492,451 (GRCm39) |
|
noncoding transcript |
Het |
| Gm815 |
C |
T |
19: 26,865,175 (GRCm39) |
Q49* |
probably null |
Het |
| H2-DMa |
A |
T |
17: 34,357,461 (GRCm39) |
I245F |
possibly damaging |
Het |
| Herc1 |
A |
T |
9: 66,377,608 (GRCm39) |
K3458M |
possibly damaging |
Het |
| Hirip3 |
A |
G |
7: 126,463,661 (GRCm39) |
|
probably null |
Het |
| Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
| Hmcn1 |
T |
A |
1: 150,556,439 (GRCm39) |
E2449V |
possibly damaging |
Het |
| Igll1 |
G |
T |
16: 16,681,657 (GRCm39) |
H33N |
probably benign |
Het |
| Il6 |
T |
C |
5: 30,224,512 (GRCm39) |
L184P |
probably damaging |
Het |
| Impg2 |
T |
A |
16: 56,080,463 (GRCm39) |
S756T |
probably damaging |
Het |
| Insyn2a |
A |
G |
7: 134,520,207 (GRCm39) |
S108P |
probably damaging |
Het |
| Kank4 |
T |
G |
4: 98,673,898 (GRCm39) |
D5A |
probably damaging |
Het |
| Kcna7 |
G |
A |
7: 45,056,015 (GRCm39) |
R77H |
probably damaging |
Het |
| Kcns2 |
A |
T |
15: 34,839,683 (GRCm39) |
T349S |
probably benign |
Het |
| Keap1 |
A |
G |
9: 21,148,522 (GRCm39) |
Y162H |
probably damaging |
Het |
| Kif9 |
T |
C |
9: 110,312,161 (GRCm39) |
F10L |
possibly damaging |
Het |
| Klhdc8b |
ACACGCACGCACGCACGCACGCACGCACGCACGCACGCAC |
ACACGCACGCACGCACGCACGCACGCACGCACGCACGCACGCAC |
9: 108,326,184 (GRCm39) |
|
probably benign |
Het |
| Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
| Lpar6 |
A |
G |
14: 73,476,809 (GRCm39) |
T257A |
probably damaging |
Het |
| Lpin1 |
A |
T |
12: 16,604,007 (GRCm39) |
L608Q |
probably benign |
Het |
| Lyst |
T |
C |
13: 13,808,989 (GRCm39) |
S220P |
probably benign |
Het |
| M1ap |
A |
G |
6: 83,005,339 (GRCm39) |
|
probably benign |
Het |
| Mbd6 |
C |
T |
10: 127,122,310 (GRCm39) |
V173I |
probably benign |
Het |
| Myo5b |
A |
T |
18: 74,849,105 (GRCm39) |
T1115S |
possibly damaging |
Het |
| Mysm1 |
C |
A |
4: 94,839,253 (GRCm39) |
V683F |
possibly damaging |
Het |
| Nlrp4g |
T |
A |
9: 124,350,155 (GRCm38) |
|
noncoding transcript |
Het |
| Odad2 |
T |
C |
18: 7,088,555 (GRCm39) |
M1005V |
probably benign |
Het |
| Or14c39 |
A |
T |
7: 86,344,089 (GRCm39) |
M142L |
probably benign |
Het |
| Or2ak5 |
T |
A |
11: 58,611,776 (GRCm39) |
I33F |
probably benign |
Het |
| Or5al6 |
G |
T |
2: 85,976,877 (GRCm39) |
A67E |
probably damaging |
Het |
| Or8j3c |
C |
T |
2: 86,253,805 (GRCm39) |
G72S |
possibly damaging |
Het |
| Otud6b |
T |
A |
4: 14,826,293 (GRCm39) |
Q34L |
probably damaging |
Het |
| Parp11 |
C |
T |
6: 127,448,599 (GRCm39) |
T72I |
probably damaging |
Het |
| Pbx1 |
T |
A |
1: 168,011,158 (GRCm39) |
D343V |
possibly damaging |
Het |
| Phf11 |
T |
C |
14: 59,495,932 (GRCm39) |
|
probably null |
Het |
| Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
| Pramel15 |
C |
A |
4: 144,099,878 (GRCm39) |
E296* |
probably null |
Het |
| Ranbp9 |
A |
T |
13: 43,588,331 (GRCm39) |
I67N |
probably damaging |
Het |
| Rasgrp4 |
A |
G |
7: 28,847,832 (GRCm39) |
E414G |
probably damaging |
Het |
| Rbbp5 |
A |
G |
1: 132,418,226 (GRCm39) |
H15R |
possibly damaging |
Het |
| Scd2 |
A |
G |
19: 44,289,710 (GRCm39) |
Y235C |
probably benign |
Het |
| Sdr16c5 |
C |
T |
4: 4,010,365 (GRCm39) |
G170S |
probably damaging |
Het |
| Sh3bp4 |
G |
T |
1: 89,073,317 (GRCm39) |
G722C |
probably damaging |
Het |
| Shmt1 |
A |
T |
11: 60,688,305 (GRCm39) |
|
probably benign |
Het |
| Slc12a1 |
A |
G |
2: 125,008,057 (GRCm39) |
I206V |
probably benign |
Het |
| Slc26a3 |
A |
G |
12: 31,503,907 (GRCm39) |
D304G |
probably benign |
Het |
| Slc26a7 |
T |
A |
4: 14,532,572 (GRCm39) |
D434V |
possibly damaging |
Het |
| Slc6a16 |
G |
T |
7: 44,909,390 (GRCm39) |
M185I |
probably benign |
Het |
| Stat4 |
A |
G |
1: 52,121,729 (GRCm39) |
I363V |
possibly damaging |
Het |
| Tgfb1i1 |
G |
T |
7: 127,847,389 (GRCm39) |
M1I |
probably null |
Het |
| Thoc2l |
A |
G |
5: 104,670,124 (GRCm39) |
K1549E |
possibly damaging |
Het |
| Tmem225 |
T |
C |
9: 40,060,639 (GRCm39) |
V66A |
probably benign |
Het |
| Tmtc4 |
T |
C |
14: 123,178,714 (GRCm39) |
|
probably null |
Het |
| Trpc4 |
T |
A |
3: 54,102,217 (GRCm39) |
N38K |
probably benign |
Het |
| Ttll12 |
A |
T |
15: 83,471,314 (GRCm39) |
Y218N |
probably damaging |
Het |
| Ttn |
A |
T |
2: 76,778,769 (GRCm39) |
|
probably null |
Het |
| Tulp1 |
A |
C |
17: 28,570,969 (GRCm39) |
Y178* |
probably null |
Het |
| Vmn2r58 |
A |
G |
7: 41,513,746 (GRCm39) |
V299A |
probably damaging |
Het |
| Washc4 |
C |
A |
10: 83,419,200 (GRCm39) |
Q911K |
possibly damaging |
Het |
| Wdr3 |
T |
C |
3: 100,062,252 (GRCm39) |
D221G |
probably benign |
Het |
| Zan |
A |
T |
5: 137,460,155 (GRCm39) |
C1245* |
probably null |
Het |
| Zfyve9 |
A |
C |
4: 108,548,866 (GRCm39) |
S773A |
probably benign |
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 |
|
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 |
|
|
R7014:Ccdc141
|
UTSW |
2 |
76,962,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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'- AAGATGGACAGAGGCCATCC -3'
(R):5'- AGATGGCTTTCAGATTCAAGTGCC -3'
Sequencing Primer
(F):5'- ACAGAGGCCATCCTGCTGAAG -3'
(R):5'- AGTTACACCTTTCTTTGATTGAGG -3'
|
| Posted On |
2016-06-06 |
Incidental Mutation