Incidental Mutation 'R0276:Ccdc180'
ID |
35358 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ccdc180
|
Ensembl Gene |
ENSMUSG00000035539 |
Gene Name |
coiled-coil domain containing 180 |
Synonyms |
LOC381522, E230008N13Rik |
MMRRC Submission |
038498-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0276 (G1)
|
Quality Score |
169 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
45890303-45950774 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 45923534 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 1105
(D1105G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136714
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000178561]
|
AlphaFold |
J3QNE4 |
Predicted Effect |
unknown
Transcript: ENSMUST00000149903
AA Change: D929G
|
SMART Domains |
Protein: ENSMUSP00000119784 Gene: ENSMUSG00000035539 AA Change: D929G
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
42 |
N/A |
INTRINSIC |
coiled coil region
|
90 |
117 |
N/A |
INTRINSIC |
Pfam:DUF4455
|
141 |
609 |
2e-189 |
PFAM |
low complexity region
|
628 |
642 |
N/A |
INTRINSIC |
low complexity region
|
658 |
675 |
N/A |
INTRINSIC |
coiled coil region
|
710 |
780 |
N/A |
INTRINSIC |
coiled coil region
|
945 |
979 |
N/A |
INTRINSIC |
low complexity region
|
1100 |
1123 |
N/A |
INTRINSIC |
Pfam:DUF4456
|
1169 |
1372 |
9.5e-77 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151024
|
SMART Domains |
Protein: ENSMUSP00000122332 Gene: ENSMUSG00000035539
Domain | Start | End | E-Value | Type |
low complexity region
|
8 |
22 |
N/A |
INTRINSIC |
low complexity region
|
38 |
55 |
N/A |
INTRINSIC |
coiled coil region
|
90 |
160 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000178561
AA Change: D1105G
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000136714 Gene: ENSMUSG00000035539 AA Change: D1105G
Domain | Start | End | E-Value | Type |
low complexity region
|
32 |
49 |
N/A |
INTRINSIC |
coiled coil region
|
98 |
125 |
N/A |
INTRINSIC |
Pfam:DUF4455
|
148 |
616 |
7.3e-189 |
PFAM |
low complexity region
|
635 |
649 |
N/A |
INTRINSIC |
low complexity region
|
665 |
682 |
N/A |
INTRINSIC |
coiled coil region
|
718 |
788 |
N/A |
INTRINSIC |
coiled coil region
|
1121 |
1155 |
N/A |
INTRINSIC |
low complexity region
|
1275 |
1298 |
N/A |
INTRINSIC |
Pfam:DUF4456
|
1344 |
1547 |
2.2e-76 |
PFAM |
|
Meta Mutation Damage Score |
0.4360 |
Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.8%
- 10x: 96.2%
- 20x: 93.8%
|
Validation Efficiency |
98% (101/103) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a coiled-coil domain. Alternative splicing results in multiple transcript variants encoding different isoforms. A single nucleotide polymorphism (SNP) in this gene has been associated with increased susceptibility to Behcet's Disease (PMID: 19442274). [provided by RefSeq, Dec 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts13 |
A |
G |
2: 26,865,772 (GRCm39) |
N109S |
possibly damaging |
Het |
Adcy10 |
T |
A |
1: 165,400,160 (GRCm39) |
M1523K |
possibly damaging |
Het |
Agtpbp1 |
C |
T |
13: 59,609,845 (GRCm39) |
S1095N |
possibly damaging |
Het |
Ang2 |
C |
T |
14: 51,432,975 (GRCm39) |
V136I |
probably damaging |
Het |
Arhgap10 |
A |
T |
8: 78,140,210 (GRCm39) |
M250K |
probably benign |
Het |
Arhgap33 |
A |
T |
7: 30,222,669 (GRCm39) |
W1088R |
probably benign |
Het |
Arhgef15 |
T |
C |
11: 68,844,298 (GRCm39) |
|
probably benign |
Het |
Aspm |
T |
C |
1: 139,406,209 (GRCm39) |
S1699P |
possibly damaging |
Het |
Atp12a |
C |
A |
14: 56,625,151 (GRCm39) |
D1014E |
probably damaging |
Het |
Atp1a4 |
T |
A |
1: 172,085,468 (GRCm39) |
K45M |
probably damaging |
Het |
Atp8a1 |
A |
T |
5: 67,944,016 (GRCm39) |
|
probably benign |
Het |
Baiap3 |
A |
C |
17: 25,462,661 (GRCm39) |
F1099C |
probably damaging |
Het |
Bcas3 |
T |
A |
11: 85,361,663 (GRCm39) |
|
probably null |
Het |
Bms1 |
G |
A |
6: 118,385,095 (GRCm39) |
T371M |
possibly damaging |
Het |
Camta1 |
C |
A |
4: 151,159,597 (GRCm39) |
R1614L |
probably damaging |
Het |
Capn3 |
T |
C |
2: 120,318,546 (GRCm39) |
|
probably benign |
Het |
Ccdc33 |
G |
T |
9: 57,965,675 (GRCm39) |
P364Q |
probably damaging |
Het |
Clstn3 |
A |
G |
6: 124,408,699 (GRCm39) |
|
probably benign |
Het |
Cntrl |
A |
T |
2: 35,041,744 (GRCm39) |
Y619F |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,538,023 (GRCm39) |
Y2514* |
probably null |
Het |
Cpt1b |
T |
C |
15: 89,304,162 (GRCm39) |
H503R |
probably benign |
Het |
Crb1 |
T |
A |
1: 139,251,073 (GRCm39) |
T293S |
possibly damaging |
Het |
D130043K22Rik |
C |
T |
13: 25,042,028 (GRCm39) |
T319I |
possibly damaging |
Het |
Dnaaf10 |
T |
C |
11: 17,179,821 (GRCm39) |
I274T |
probably benign |
Het |
Dzip1l |
G |
A |
9: 99,543,051 (GRCm39) |
R502Q |
probably benign |
Het |
Efcab5 |
A |
G |
11: 77,020,702 (GRCm39) |
M673T |
probably damaging |
Het |
Efcab5 |
G |
A |
11: 77,031,749 (GRCm39) |
R42W |
probably damaging |
Het |
F2rl3 |
A |
G |
8: 73,489,426 (GRCm39) |
T218A |
probably benign |
Het |
Fam135a |
C |
T |
1: 24,107,045 (GRCm39) |
R31H |
probably damaging |
Het |
Fcer2a |
A |
T |
8: 3,739,811 (GRCm39) |
N53K |
possibly damaging |
Het |
Golgb1 |
A |
C |
16: 36,734,238 (GRCm39) |
K1162Q |
probably damaging |
Het |
Gpr137b |
A |
T |
13: 13,542,160 (GRCm39) |
|
probably benign |
Het |
Haspin |
A |
T |
11: 73,027,313 (GRCm39) |
L592Q |
probably damaging |
Het |
Helq |
A |
G |
5: 100,938,013 (GRCm39) |
F478L |
probably damaging |
Het |
Iho1 |
A |
T |
9: 108,305,639 (GRCm39) |
M11K |
possibly damaging |
Het |
Il17rb |
T |
A |
14: 29,726,337 (GRCm39) |
T84S |
probably damaging |
Het |
Itga4 |
T |
C |
2: 79,151,837 (GRCm39) |
L880P |
probably damaging |
Het |
Itih5 |
A |
G |
2: 10,190,375 (GRCm39) |
I61V |
possibly damaging |
Het |
Ivl |
G |
A |
3: 92,478,821 (GRCm39) |
L415F |
unknown |
Het |
Kif2a |
A |
G |
13: 107,113,158 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
T |
C |
15: 98,748,192 (GRCm39) |
|
probably benign |
Het |
Lars2 |
A |
G |
9: 123,267,186 (GRCm39) |
|
probably benign |
Het |
Lilrb4a |
T |
C |
10: 51,367,677 (GRCm39) |
V73A |
probably benign |
Het |
Lratd2 |
G |
T |
15: 60,695,523 (GRCm39) |
Y74* |
probably null |
Het |
Lrrc8a |
A |
G |
2: 30,146,800 (GRCm39) |
D538G |
possibly damaging |
Het |
Lrrk1 |
G |
A |
7: 65,946,011 (GRCm39) |
|
probably benign |
Het |
Mc2r |
A |
T |
18: 68,541,203 (GRCm39) |
I30K |
possibly damaging |
Het |
Mybbp1a |
C |
A |
11: 72,340,933 (GRCm39) |
|
probably null |
Het |
Napg |
C |
T |
18: 63,120,034 (GRCm39) |
R149C |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,314,517 (GRCm39) |
|
probably benign |
Het |
Nlk |
T |
C |
11: 78,462,301 (GRCm39) |
I509V |
probably benign |
Het |
Nlrp2 |
A |
T |
7: 5,331,108 (GRCm39) |
N429K |
probably benign |
Het |
Nlrp9b |
A |
G |
7: 19,762,423 (GRCm39) |
T247A |
probably benign |
Het |
Noxo1 |
A |
T |
17: 24,919,136 (GRCm39) |
|
probably null |
Het |
Or1n1b |
A |
T |
2: 36,780,035 (GRCm39) |
M275K |
probably benign |
Het |
Or2ag2b |
A |
T |
7: 106,417,904 (GRCm39) |
I205L |
probably benign |
Het |
Or3a10 |
A |
G |
11: 73,935,944 (GRCm39) |
I52T |
probably damaging |
Het |
Or4c107 |
T |
A |
2: 88,789,099 (GRCm39) |
C96* |
probably null |
Het |
Or4m1 |
C |
A |
14: 50,557,636 (GRCm39) |
A219S |
probably benign |
Het |
Oxr1 |
T |
C |
15: 41,683,458 (GRCm39) |
S294P |
probably damaging |
Het |
Pfpl |
A |
G |
19: 12,406,601 (GRCm39) |
Y284C |
probably damaging |
Het |
Pi16 |
A |
T |
17: 29,545,917 (GRCm39) |
T232S |
probably benign |
Het |
Plcxd2 |
A |
T |
16: 45,830,070 (GRCm39) |
N50K |
probably benign |
Het |
Plekhn1 |
T |
A |
4: 156,312,703 (GRCm39) |
N52Y |
probably damaging |
Het |
Prl2c5 |
T |
C |
13: 13,357,634 (GRCm39) |
|
probably benign |
Het |
Prrc2b |
G |
A |
2: 32,109,666 (GRCm39) |
V1080I |
probably damaging |
Het |
Psg28 |
A |
T |
7: 18,164,321 (GRCm39) |
N130K |
probably benign |
Het |
Psme4 |
C |
A |
11: 30,761,980 (GRCm39) |
T440K |
probably damaging |
Het |
Ptcd2 |
T |
C |
13: 99,458,104 (GRCm39) |
K296E |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,378,596 (GRCm39) |
|
probably null |
Het |
Rab5b |
A |
C |
10: 128,522,615 (GRCm39) |
|
probably null |
Het |
Rft1 |
T |
A |
14: 30,412,540 (GRCm39) |
S534T |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rsu1 |
A |
T |
2: 13,174,946 (GRCm39) |
|
probably benign |
Het |
Senp6 |
A |
G |
9: 80,044,029 (GRCm39) |
M887V |
probably benign |
Het |
Sgcz |
T |
A |
8: 38,420,073 (GRCm39) |
M60L |
probably benign |
Het |
Siglec1 |
G |
A |
2: 130,925,861 (GRCm39) |
Q282* |
probably null |
Het |
Sipa1l2 |
T |
C |
8: 126,148,679 (GRCm39) |
T1655A |
probably damaging |
Het |
Slc28a2b |
T |
A |
2: 122,352,409 (GRCm39) |
S389T |
probably damaging |
Het |
Slc43a3 |
G |
A |
2: 84,768,007 (GRCm39) |
|
probably benign |
Het |
Snx29 |
T |
C |
16: 11,556,237 (GRCm39) |
V756A |
probably benign |
Het |
Spta1 |
T |
A |
1: 174,045,460 (GRCm39) |
H1539Q |
probably damaging |
Het |
Stk3 |
A |
C |
15: 35,099,615 (GRCm39) |
S104A |
probably damaging |
Het |
Stk38 |
C |
A |
17: 29,211,390 (GRCm39) |
|
probably null |
Het |
Stx6 |
T |
C |
1: 155,049,909 (GRCm39) |
|
probably benign |
Het |
Thbs4 |
G |
A |
13: 92,912,040 (GRCm39) |
T230I |
probably benign |
Het |
Thrsp |
A |
G |
7: 97,066,709 (GRCm39) |
M1T |
probably null |
Het |
Tmem63b |
A |
T |
17: 45,986,299 (GRCm39) |
|
probably benign |
Het |
Top2a |
A |
G |
11: 98,900,733 (GRCm39) |
|
probably benign |
Het |
Tpd52l2 |
T |
C |
2: 181,143,852 (GRCm39) |
|
probably null |
Het |
Trak1 |
A |
G |
9: 121,283,404 (GRCm39) |
E390G |
probably damaging |
Het |
Trappc3 |
T |
A |
4: 126,167,745 (GRCm39) |
D101E |
possibly damaging |
Het |
Trhr |
A |
G |
15: 44,060,482 (GRCm39) |
M1V |
probably null |
Het |
Triobp |
T |
A |
15: 78,857,876 (GRCm39) |
I1159K |
probably benign |
Het |
Unc45a |
A |
G |
7: 79,976,045 (GRCm39) |
|
probably benign |
Het |
Usb1 |
A |
G |
8: 96,060,085 (GRCm39) |
D12G |
probably damaging |
Het |
Ushbp1 |
C |
T |
8: 71,847,293 (GRCm39) |
C113Y |
possibly damaging |
Het |
Vim |
A |
G |
2: 13,579,670 (GRCm39) |
K143R |
probably benign |
Het |
Vmn2r75 |
T |
C |
7: 85,797,515 (GRCm39) |
K766R |
probably benign |
Het |
Xpo5 |
T |
G |
17: 46,552,433 (GRCm39) |
C1089G |
probably damaging |
Het |
|
Other mutations in Ccdc180 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01369:Ccdc180
|
APN |
4 |
45,900,256 (GRCm39) |
missense |
probably benign |
|
IGL01713:Ccdc180
|
APN |
4 |
45,921,025 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01915:Ccdc180
|
APN |
4 |
45,904,544 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01935:Ccdc180
|
APN |
4 |
45,906,889 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02539:Ccdc180
|
APN |
4 |
45,921,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Ccdc180
|
APN |
4 |
45,903,840 (GRCm39) |
splice site |
probably benign |
|
IGL03071:Ccdc180
|
APN |
4 |
45,903,840 (GRCm39) |
splice site |
probably benign |
|
IGL03146:Ccdc180
|
APN |
4 |
45,903,840 (GRCm39) |
splice site |
probably benign |
|
PIT4687001:Ccdc180
|
UTSW |
4 |
45,949,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Ccdc180
|
UTSW |
4 |
45,930,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0049:Ccdc180
|
UTSW |
4 |
45,930,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0054:Ccdc180
|
UTSW |
4 |
45,890,900 (GRCm39) |
missense |
probably benign |
0.01 |
R0054:Ccdc180
|
UTSW |
4 |
45,890,900 (GRCm39) |
missense |
probably benign |
0.01 |
R0080:Ccdc180
|
UTSW |
4 |
45,896,205 (GRCm39) |
missense |
probably null |
0.00 |
R0082:Ccdc180
|
UTSW |
4 |
45,896,205 (GRCm39) |
missense |
probably null |
0.00 |
R0126:Ccdc180
|
UTSW |
4 |
45,912,866 (GRCm39) |
critical splice donor site |
probably null |
|
R0193:Ccdc180
|
UTSW |
4 |
45,914,803 (GRCm39) |
missense |
probably benign |
0.01 |
R0362:Ccdc180
|
UTSW |
4 |
45,923,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0380:Ccdc180
|
UTSW |
4 |
45,930,197 (GRCm39) |
critical splice donor site |
probably null |
|
R0468:Ccdc180
|
UTSW |
4 |
45,923,271 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0539:Ccdc180
|
UTSW |
4 |
45,922,010 (GRCm39) |
missense |
probably damaging |
0.97 |
R0543:Ccdc180
|
UTSW |
4 |
45,900,041 (GRCm39) |
nonsense |
probably null |
|
R0546:Ccdc180
|
UTSW |
4 |
45,904,597 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0612:Ccdc180
|
UTSW |
4 |
45,927,969 (GRCm39) |
missense |
probably damaging |
0.98 |
R0792:Ccdc180
|
UTSW |
4 |
45,927,975 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1056:Ccdc180
|
UTSW |
4 |
45,916,375 (GRCm39) |
missense |
probably benign |
0.01 |
R1099:Ccdc180
|
UTSW |
4 |
45,914,225 (GRCm39) |
missense |
probably benign |
0.03 |
R1136:Ccdc180
|
UTSW |
4 |
45,914,589 (GRCm39) |
missense |
probably benign |
0.00 |
R1263:Ccdc180
|
UTSW |
4 |
45,903,887 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1331:Ccdc180
|
UTSW |
4 |
45,909,359 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1522:Ccdc180
|
UTSW |
4 |
45,927,975 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1819:Ccdc180
|
UTSW |
4 |
45,926,195 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2022:Ccdc180
|
UTSW |
4 |
45,944,418 (GRCm39) |
missense |
probably benign |
0.18 |
R2056:Ccdc180
|
UTSW |
4 |
45,932,477 (GRCm39) |
missense |
probably benign |
0.03 |
R2219:Ccdc180
|
UTSW |
4 |
45,944,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Ccdc180
|
UTSW |
4 |
45,948,856 (GRCm39) |
critical splice donor site |
probably null |
|
R2229:Ccdc180
|
UTSW |
4 |
45,948,856 (GRCm39) |
critical splice donor site |
probably null |
|
R2255:Ccdc180
|
UTSW |
4 |
45,921,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R2427:Ccdc180
|
UTSW |
4 |
45,929,545 (GRCm39) |
missense |
probably benign |
0.03 |
R3001:Ccdc180
|
UTSW |
4 |
45,899,988 (GRCm39) |
missense |
probably benign |
|
R3002:Ccdc180
|
UTSW |
4 |
45,899,988 (GRCm39) |
missense |
probably benign |
|
R3003:Ccdc180
|
UTSW |
4 |
45,899,988 (GRCm39) |
missense |
probably benign |
|
R3110:Ccdc180
|
UTSW |
4 |
45,900,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3111:Ccdc180
|
UTSW |
4 |
45,900,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3112:Ccdc180
|
UTSW |
4 |
45,900,470 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3898:Ccdc180
|
UTSW |
4 |
45,912,799 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4022:Ccdc180
|
UTSW |
4 |
45,904,560 (GRCm39) |
nonsense |
probably null |
|
R4084:Ccdc180
|
UTSW |
4 |
45,950,632 (GRCm39) |
missense |
probably benign |
0.19 |
R4377:Ccdc180
|
UTSW |
4 |
45,941,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R4595:Ccdc180
|
UTSW |
4 |
45,945,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R4637:Ccdc180
|
UTSW |
4 |
45,914,443 (GRCm39) |
missense |
probably benign |
|
R4811:Ccdc180
|
UTSW |
4 |
45,928,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Ccdc180
|
UTSW |
4 |
45,912,794 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4858:Ccdc180
|
UTSW |
4 |
45,923,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Ccdc180
|
UTSW |
4 |
45,909,308 (GRCm39) |
missense |
probably damaging |
0.98 |
R4940:Ccdc180
|
UTSW |
4 |
45,917,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Ccdc180
|
UTSW |
4 |
45,917,453 (GRCm39) |
missense |
probably damaging |
0.96 |
R5042:Ccdc180
|
UTSW |
4 |
45,916,255 (GRCm39) |
missense |
probably damaging |
0.98 |
R5119:Ccdc180
|
UTSW |
4 |
45,914,603 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5177:Ccdc180
|
UTSW |
4 |
45,917,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Ccdc180
|
UTSW |
4 |
45,917,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R5333:Ccdc180
|
UTSW |
4 |
45,890,935 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5448:Ccdc180
|
UTSW |
4 |
45,920,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R5510:Ccdc180
|
UTSW |
4 |
45,928,046 (GRCm39) |
missense |
probably damaging |
0.96 |
R6018:Ccdc180
|
UTSW |
4 |
45,926,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R6108:Ccdc180
|
UTSW |
4 |
45,911,389 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6283:Ccdc180
|
UTSW |
4 |
45,902,486 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6483:Ccdc180
|
UTSW |
4 |
45,921,950 (GRCm39) |
missense |
probably benign |
0.32 |
R6618:Ccdc180
|
UTSW |
4 |
45,950,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Ccdc180
|
UTSW |
4 |
45,940,934 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7205:Ccdc180
|
UTSW |
4 |
45,914,588 (GRCm39) |
missense |
probably benign |
|
R7341:Ccdc180
|
UTSW |
4 |
45,898,644 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7351:Ccdc180
|
UTSW |
4 |
45,903,887 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7418:Ccdc180
|
UTSW |
4 |
45,904,616 (GRCm39) |
missense |
probably damaging |
0.98 |
R7492:Ccdc180
|
UTSW |
4 |
45,930,009 (GRCm39) |
splice site |
probably null |
|
R7573:Ccdc180
|
UTSW |
4 |
45,922,015 (GRCm39) |
missense |
probably benign |
0.33 |
R7639:Ccdc180
|
UTSW |
4 |
45,928,043 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7792:Ccdc180
|
UTSW |
4 |
45,890,389 (GRCm39) |
critical splice donor site |
probably null |
|
R7806:Ccdc180
|
UTSW |
4 |
45,912,801 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7812:Ccdc180
|
UTSW |
4 |
45,906,952 (GRCm39) |
critical splice donor site |
probably null |
|
R7840:Ccdc180
|
UTSW |
4 |
45,900,461 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7842:Ccdc180
|
UTSW |
4 |
45,909,428 (GRCm39) |
missense |
probably benign |
0.00 |
R8712:Ccdc180
|
UTSW |
4 |
45,920,842 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8818:Ccdc180
|
UTSW |
4 |
45,900,484 (GRCm39) |
missense |
probably benign |
0.02 |
R8961:Ccdc180
|
UTSW |
4 |
45,929,573 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8983:Ccdc180
|
UTSW |
4 |
45,909,359 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9035:Ccdc180
|
UTSW |
4 |
45,906,922 (GRCm39) |
nonsense |
probably null |
|
R9095:Ccdc180
|
UTSW |
4 |
45,949,466 (GRCm39) |
nonsense |
probably null |
|
R9240:Ccdc180
|
UTSW |
4 |
45,917,566 (GRCm39) |
critical splice donor site |
probably null |
|
R9293:Ccdc180
|
UTSW |
4 |
45,944,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Ccdc180
|
UTSW |
4 |
45,902,447 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9346:Ccdc180
|
UTSW |
4 |
45,927,953 (GRCm39) |
missense |
probably benign |
0.09 |
R9521:Ccdc180
|
UTSW |
4 |
45,916,283 (GRCm39) |
missense |
probably null |
0.50 |
R9653:Ccdc180
|
UTSW |
4 |
45,923,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R9667:Ccdc180
|
UTSW |
4 |
45,920,861 (GRCm39) |
nonsense |
probably null |
|
X0017:Ccdc180
|
UTSW |
4 |
45,909,350 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Ccdc180
|
UTSW |
4 |
45,920,910 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ccdc180
|
UTSW |
4 |
45,916,406 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TCCCCTGAAGAAGTTGAGACGCTG -3'
(R):5'- TGGTACAACCATCACCCTGTGGAC -3'
Sequencing Primer
(F):5'- AGTTGAGACGCTGTGCCAC -3'
(R):5'- GAAGATTTGTCATCAGCCGC -3'
|
Posted On |
2013-05-09 |