Incidental Mutation 'R7806:Ccdc180'
ID |
600762 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ccdc180
|
Ensembl Gene |
ENSMUSG00000035539 |
Gene Name |
coiled-coil domain containing 180 |
Synonyms |
LOC381522, E230008N13Rik |
MMRRC Submission |
045861-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7806 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
45890303-45950774 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 45912801 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Asparagine
at position 593
(K593N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136714
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000178561]
|
AlphaFold |
J3QNE4 |
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000119784 Gene: ENSMUSG00000035539 AA Change: K585N
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 |
possibly damaging
Transcript: ENSMUST00000178561
AA Change: K593N
PolyPhen 2
Score 0.847 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000136714 Gene: ENSMUSG00000035539 AA Change: K593N
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.8%
- 20x: 99.3%
|
Validation Efficiency |
98% (83/85) |
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: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810004N23Rik |
C |
A |
8: 125,569,143 (GRCm39) |
V144F |
probably benign |
Het |
Aar2 |
T |
A |
2: 156,393,031 (GRCm39) |
I140N |
possibly damaging |
Het |
Abca15 |
A |
G |
7: 119,932,059 (GRCm39) |
N104S |
probably damaging |
Het |
Adam22 |
A |
T |
5: 8,142,825 (GRCm39) |
N803K |
probably damaging |
Het |
Adk |
A |
G |
14: 21,376,679 (GRCm39) |
N26S |
|
Het |
Ak9 |
A |
C |
10: 41,309,080 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
C |
18: 65,482,487 (GRCm39) |
D40G |
probably benign |
Het |
Ankrd65 |
A |
T |
4: 155,877,437 (GRCm39) |
H316L |
probably benign |
Het |
Cabp7 |
C |
T |
11: 4,688,889 (GRCm39) |
A194T |
probably damaging |
Het |
Cd80 |
A |
G |
16: 38,294,315 (GRCm39) |
D66G |
probably benign |
Het |
Cdh5 |
T |
C |
8: 104,867,448 (GRCm39) |
V575A |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,737,809 (GRCm39) |
Q2678R |
probably benign |
Het |
Cideb |
G |
A |
14: 55,992,625 (GRCm39) |
T97M |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,638,157 (GRCm39) |
D35G |
probably benign |
Het |
Clpx |
T |
C |
9: 65,207,213 (GRCm39) |
V37A |
probably benign |
Het |
Cmya5 |
A |
C |
13: 93,230,770 (GRCm39) |
S1439R |
probably benign |
Het |
Cndp2 |
T |
A |
18: 84,688,945 (GRCm39) |
H279L |
probably benign |
Het |
Cngb1 |
A |
T |
8: 96,025,432 (GRCm39) |
|
probably null |
Het |
Cpq |
T |
A |
15: 33,497,443 (GRCm39) |
N394K |
possibly damaging |
Het |
Dedd |
T |
C |
1: 171,166,062 (GRCm39) |
L60P |
probably benign |
Het |
Dennd3 |
C |
A |
15: 73,442,624 (GRCm39) |
L1216M |
possibly damaging |
Het |
Dntt |
A |
T |
19: 41,018,071 (GRCm39) |
N65I |
probably benign |
Het |
Fap |
T |
A |
2: 62,333,758 (GRCm39) |
E662V |
probably damaging |
Het |
Fasn |
A |
T |
11: 120,700,821 (GRCm39) |
M2066K |
probably benign |
Het |
Fggy |
G |
A |
4: 95,489,203 (GRCm39) |
G69E |
probably benign |
Het |
Foxc1 |
G |
T |
13: 31,992,739 (GRCm39) |
G517C |
unknown |
Het |
Gas2l3 |
A |
G |
10: 89,249,232 (GRCm39) |
Y629H |
probably benign |
Het |
Gcnt2 |
A |
G |
13: 41,071,717 (GRCm39) |
N120S |
probably damaging |
Het |
Gfpt2 |
A |
G |
11: 49,714,142 (GRCm39) |
T300A |
probably benign |
Het |
Glud1 |
A |
G |
14: 34,065,606 (GRCm39) |
R535G |
probably damaging |
Het |
Gm3248 |
T |
A |
14: 5,943,883 (GRCm38) |
I114L |
probably benign |
Het |
Gm3278 |
G |
A |
14: 16,082,211 (GRCm39) |
|
probably null |
Het |
Gm3402 |
A |
C |
5: 146,451,090 (GRCm39) |
K44Q |
probably damaging |
Het |
Gm3696 |
C |
G |
14: 18,433,094 (GRCm39) |
R188S |
probably benign |
Het |
Gm3696 |
C |
A |
14: 18,433,095 (GRCm39) |
R188M |
probably benign |
Het |
Gmppa |
T |
C |
1: 75,415,581 (GRCm39) |
L113P |
probably damaging |
Het |
Gmps |
A |
G |
3: 63,890,091 (GRCm39) |
|
probably null |
Het |
Gnal |
T |
A |
18: 67,346,145 (GRCm39) |
M275K |
probably damaging |
Het |
Gopc |
G |
C |
10: 52,229,525 (GRCm39) |
N231K |
probably damaging |
Het |
Gpr152 |
T |
C |
19: 4,193,487 (GRCm39) |
S343P |
probably benign |
Het |
Gpr17 |
T |
C |
18: 32,080,593 (GRCm39) |
I157V |
probably benign |
Het |
Grm7 |
T |
A |
6: 111,223,314 (GRCm39) |
Y451* |
probably null |
Het |
Ikbke |
T |
C |
1: 131,199,635 (GRCm39) |
E286G |
probably damaging |
Het |
Inpp5b |
A |
T |
4: 124,678,881 (GRCm39) |
|
probably null |
Het |
Iqgap2 |
G |
A |
13: 95,818,765 (GRCm39) |
L664F |
probably benign |
Het |
Kif17 |
A |
G |
4: 138,015,507 (GRCm39) |
E552G |
possibly damaging |
Het |
Lamtor1 |
T |
A |
7: 101,555,220 (GRCm39) |
Y5* |
probably null |
Het |
Lpin2 |
A |
G |
17: 71,552,166 (GRCm39) |
I829V |
probably damaging |
Het |
Lrg1 |
T |
G |
17: 56,426,967 (GRCm39) |
D335A |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 154,804,444 (GRCm39) |
Y35H |
probably damaging |
Het |
Mkx |
T |
A |
18: 7,000,607 (GRCm39) |
M112L |
probably benign |
Het |
Mlxipl |
A |
C |
5: 135,163,397 (GRCm39) |
D760A |
possibly damaging |
Het |
Muc6 |
T |
C |
7: 141,217,387 (GRCm39) |
T2429A |
possibly damaging |
Het |
N4bp2l2 |
A |
G |
5: 150,566,715 (GRCm39) |
C134R |
unknown |
Het |
Nanos1 |
A |
G |
19: 60,744,972 (GRCm39) |
E90G |
probably benign |
Het |
Nckap1 |
T |
C |
2: 80,371,843 (GRCm39) |
D329G |
probably damaging |
Het |
Or13a18 |
T |
C |
7: 140,190,685 (GRCm39) |
I194T |
probably benign |
Het |
Or14j9 |
A |
C |
17: 37,875,112 (GRCm39) |
L30R |
probably damaging |
Het |
Or8b12c |
T |
C |
9: 37,715,872 (GRCm39) |
S222P |
probably damaging |
Het |
Or8g51 |
G |
T |
9: 38,609,567 (GRCm39) |
L32I |
probably benign |
Het |
Osbpl7 |
A |
G |
11: 96,946,954 (GRCm39) |
H419R |
probably benign |
Het |
Otog |
C |
T |
7: 45,935,200 (GRCm39) |
T1395I |
probably benign |
Het |
Pigq |
T |
A |
17: 26,150,700 (GRCm39) |
I451F |
probably benign |
Het |
Ptgfrn |
A |
G |
3: 100,984,448 (GRCm39) |
V248A |
possibly damaging |
Het |
Rdh19 |
G |
T |
10: 127,692,740 (GRCm39) |
V136L |
probably damaging |
Het |
Rfesd |
T |
C |
13: 76,156,308 (GRCm39) |
T33A |
possibly damaging |
Het |
Rnf213 |
G |
A |
11: 119,302,371 (GRCm39) |
V432M |
|
Het |
Rpl22l1 |
T |
A |
3: 28,860,962 (GRCm39) |
L60Q |
probably benign |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,127 (GRCm39) |
|
probably benign |
Het |
Samd3 |
A |
G |
10: 26,120,425 (GRCm39) |
T140A |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,189,623 (GRCm39) |
V419A |
possibly damaging |
Het |
Serpinb6a |
T |
C |
13: 34,119,548 (GRCm39) |
|
probably null |
Het |
Slc22a4 |
A |
G |
11: 53,881,476 (GRCm39) |
L414P |
probably damaging |
Het |
Smarcd3 |
A |
T |
5: 24,798,260 (GRCm39) |
V420D |
probably benign |
Het |
Tcaim |
A |
G |
9: 122,663,995 (GRCm39) |
D495G |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,074,266 (GRCm39) |
V1873A |
possibly damaging |
Het |
Tmcc2 |
T |
C |
1: 132,288,527 (GRCm39) |
N387D |
probably damaging |
Het |
Tmed8 |
A |
T |
12: 87,219,204 (GRCm39) |
I322N |
probably damaging |
Het |
Tmod4 |
A |
C |
3: 95,034,915 (GRCm39) |
D168A |
probably benign |
Het |
Trgc2 |
A |
T |
13: 19,491,390 (GRCm39) |
|
probably benign |
Het |
Trp53bp1 |
C |
T |
2: 121,035,542 (GRCm39) |
E1520K |
probably damaging |
Het |
Trpv5 |
T |
A |
6: 41,651,867 (GRCm39) |
I183F |
probably damaging |
Het |
Vmn2r70 |
A |
T |
7: 85,208,401 (GRCm39) |
I692K |
probably benign |
Het |
Vmn2r87 |
T |
A |
10: 130,315,679 (GRCm39) |
Y129F |
probably benign |
Het |
Vps8 |
A |
G |
16: 21,278,501 (GRCm39) |
D253G |
probably damaging |
Het |
Ythdc2 |
T |
C |
18: 44,977,353 (GRCm39) |
I383T |
possibly damaging |
Het |
Ythdc2 |
T |
C |
18: 44,983,491 (GRCm39) |
S553P |
probably benign |
Het |
Zfyve26 |
A |
G |
12: 79,327,129 (GRCm39) |
|
probably null |
Het |
Zic1 |
G |
A |
9: 91,247,024 (GRCm39) |
T16I |
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 |
R0276:Ccdc180
|
UTSW |
4 |
45,923,534 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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'- AGAGTTCCCTTCACACAGTGG -3'
(R):5'- CCTTGACATCCTGACATGGAATTC -3'
Sequencing Primer
(F):5'- ACACAGTGGTCTCATCTCCC -3'
(R):5'- GCAGACTTAAGGATGGCTTCC -3'
|
Posted On |
2019-11-26 |