Incidental Mutation 'IGL02122:Cog6'
| ID |
280687 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Cog6
|
| Ensembl Gene |
ENSMUSG00000027742 |
| Gene Name |
component of oligomeric golgi complex 6 |
| Synonyms |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02122
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
3 |
| Chromosomal Location |
52889544-52924644 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 52905763 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 361
(I361V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000048603
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036665]
[ENSMUST00000193432]
[ENSMUST00000195183]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000036665
AA Change: I361V
PolyPhen 2
Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000048603
Gene: ENSMUSG00000027742
AA Change: I361V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
26 |
N/A |
INTRINSIC |
|
COG6
|
55 |
656 |
N/A |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192788
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193432
AA Change: I361V
PolyPhen 2
Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000141339
Gene: ENSMUSG00000027742
AA Change: I361V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
26 |
N/A |
INTRINSIC |
|
COG6
|
55 |
625 |
5e-289 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194779
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195183
AA Change: I89V
PolyPhen 2
Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000141733
Gene: ENSMUSG00000027742
AA Change: I89V
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
26 |
N/A |
INTRINSIC |
|
Pfam:COG6
|
39 |
174 |
5.5e-32 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi apparatus. The encoded protein is organized with conserved oligomeric Golgi complex components 5, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
C |
T |
12: 71,217,299 (GRCm39) |
T756I |
possibly damaging |
Het |
| Abi3bp |
T |
C |
16: 56,507,491 (GRCm39) |
|
probably benign |
Het |
| Adcy5 |
G |
A |
16: 35,103,982 (GRCm39) |
|
probably benign |
Het |
| Adcy6 |
T |
A |
15: 98,496,763 (GRCm39) |
H504L |
possibly damaging |
Het |
| Ank2 |
A |
G |
3: 126,731,523 (GRCm39) |
|
probably benign |
Het |
| Atxn2 |
A |
G |
5: 121,916,093 (GRCm39) |
D34G |
probably damaging |
Het |
| Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
| Carmil1 |
T |
C |
13: 24,220,541 (GRCm39) |
E657G |
possibly damaging |
Het |
| Cdc25c |
T |
C |
18: 34,877,038 (GRCm39) |
I212V |
probably benign |
Het |
| Chl1 |
A |
G |
6: 103,652,098 (GRCm39) |
D338G |
probably benign |
Het |
| Dip2c |
T |
C |
13: 9,556,695 (GRCm39) |
S80P |
possibly damaging |
Het |
| Dmrtc2 |
A |
T |
7: 24,572,008 (GRCm39) |
R34S |
possibly damaging |
Het |
| Exph5 |
A |
G |
9: 53,284,974 (GRCm39) |
N685S |
probably benign |
Het |
| Flnc |
A |
T |
6: 29,444,335 (GRCm39) |
I684L |
possibly damaging |
Het |
| Foxk1 |
T |
A |
5: 142,437,184 (GRCm39) |
|
probably benign |
Het |
| Gprc6a |
T |
C |
10: 51,502,819 (GRCm39) |
N348S |
probably benign |
Het |
| Gspt1 |
T |
C |
16: 11,047,080 (GRCm39) |
K445R |
probably damaging |
Het |
| Hace1 |
T |
C |
10: 45,494,700 (GRCm39) |
V170A |
probably damaging |
Het |
| Hydin |
T |
C |
8: 111,221,047 (GRCm39) |
I1481T |
possibly damaging |
Het |
| Ighv4-1 |
A |
T |
12: 113,912,145 (GRCm39) |
L36Q |
possibly damaging |
Het |
| Ints1 |
G |
A |
5: 139,750,905 (GRCm39) |
Q833* |
probably null |
Het |
| Myo15a |
T |
C |
11: 60,374,292 (GRCm39) |
F96L |
probably benign |
Het |
| Myom1 |
G |
T |
17: 71,399,132 (GRCm39) |
R998L |
probably damaging |
Het |
| Nacc2 |
A |
G |
2: 25,979,960 (GRCm39) |
S159P |
probably benign |
Het |
| Or5k15 |
T |
C |
16: 58,710,134 (GRCm39) |
T150A |
probably benign |
Het |
| Or5w10 |
A |
G |
2: 87,375,447 (GRCm39) |
V147A |
probably benign |
Het |
| Or7e177 |
T |
A |
9: 20,211,880 (GRCm39) |
L128Q |
probably damaging |
Het |
| Pbrm1 |
A |
G |
14: 30,811,573 (GRCm39) |
I1197V |
probably damaging |
Het |
| Pde4dip |
G |
A |
3: 97,674,737 (GRCm39) |
R60C |
probably damaging |
Het |
| Pfkfb4 |
C |
T |
9: 108,854,178 (GRCm39) |
R351W |
probably damaging |
Het |
| Pitpnm1 |
T |
C |
19: 4,157,796 (GRCm39) |
Y499H |
probably damaging |
Het |
| Plekhn1 |
C |
T |
4: 156,308,313 (GRCm39) |
|
probably null |
Het |
| Prmt8 |
A |
G |
6: 127,667,680 (GRCm39) |
Y332H |
probably benign |
Het |
| Prpf38a |
A |
G |
4: 108,436,238 (GRCm39) |
I25T |
possibly damaging |
Het |
| Rpf1 |
T |
C |
3: 146,227,022 (GRCm39) |
K44E |
probably benign |
Het |
| Rusc2 |
T |
C |
4: 43,421,685 (GRCm39) |
F702L |
possibly damaging |
Het |
| Ryr2 |
A |
T |
13: 11,756,755 (GRCm39) |
I1633K |
probably damaging |
Het |
| Slc39a10 |
G |
A |
1: 46,857,288 (GRCm39) |
A696V |
probably damaging |
Het |
| Tkt |
T |
C |
14: 30,293,158 (GRCm39) |
V510A |
possibly damaging |
Het |
| Tmem106a |
C |
A |
11: 101,481,240 (GRCm39) |
N249K |
probably damaging |
Het |
| Tmpo |
A |
T |
10: 90,999,998 (GRCm39) |
S157T |
possibly damaging |
Het |
| Tspan32 |
A |
T |
7: 142,569,372 (GRCm39) |
I144F |
probably damaging |
Het |
| Ufsp2 |
G |
A |
8: 46,448,685 (GRCm39) |
V429I |
probably benign |
Het |
| Unc13c |
T |
A |
9: 73,641,679 (GRCm39) |
|
probably benign |
Het |
| Usp47 |
A |
T |
7: 111,706,115 (GRCm39) |
K1259M |
probably damaging |
Het |
| Zdhhc18 |
A |
T |
4: 133,340,946 (GRCm39) |
|
probably benign |
Het |
| Zfp507 |
G |
T |
7: 35,475,520 (GRCm39) |
L898I |
probably damaging |
Het |
|
| Other mutations in Cog6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01922:Cog6
|
APN |
3 |
52,893,846 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01946:Cog6
|
APN |
3 |
52,909,825 (GRCm39) |
intron |
probably benign |
|
|
IGL02589:Cog6
|
APN |
3 |
52,914,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02819:Cog6
|
APN |
3 |
52,916,966 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0045:Cog6
|
UTSW |
3 |
52,900,171 (GRCm39) |
splice site |
probably null |
|
|
R0045:Cog6
|
UTSW |
3 |
52,900,171 (GRCm39) |
splice site |
probably null |
|
|
R0086:Cog6
|
UTSW |
3 |
52,900,991 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0545:Cog6
|
UTSW |
3 |
52,903,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0707:Cog6
|
UTSW |
3 |
52,921,283 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R0718:Cog6
|
UTSW |
3 |
52,918,050 (GRCm39) |
missense |
probably benign |
0.35 |
|
R1169:Cog6
|
UTSW |
3 |
52,921,265 (GRCm39) |
missense |
probably benign |
0.30 |
|
R1451:Cog6
|
UTSW |
3 |
52,916,534 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R1891:Cog6
|
UTSW |
3 |
52,890,601 (GRCm39) |
missense |
probably benign |
|
|
R2249:Cog6
|
UTSW |
3 |
52,907,900 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2264:Cog6
|
UTSW |
3 |
52,900,332 (GRCm39) |
nonsense |
probably null |
|
|
R3745:Cog6
|
UTSW |
3 |
52,900,240 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4027:Cog6
|
UTSW |
3 |
52,909,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4230:Cog6
|
UTSW |
3 |
52,900,229 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4400:Cog6
|
UTSW |
3 |
52,920,362 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4551:Cog6
|
UTSW |
3 |
52,905,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4866:Cog6
|
UTSW |
3 |
52,918,019 (GRCm39) |
missense |
probably benign |
0.10 |
|
R5326:Cog6
|
UTSW |
3 |
52,921,237 (GRCm39) |
missense |
probably null |
0.12 |
|
R6169:Cog6
|
UTSW |
3 |
52,914,722 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6273:Cog6
|
UTSW |
3 |
52,903,473 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7169:Cog6
|
UTSW |
3 |
52,897,387 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7199:Cog6
|
UTSW |
3 |
52,890,610 (GRCm39) |
missense |
probably benign |
0.21 |
|
R7243:Cog6
|
UTSW |
3 |
52,909,736 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7299:Cog6
|
UTSW |
3 |
52,909,928 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8254:Cog6
|
UTSW |
3 |
52,900,938 (GRCm39) |
missense |
probably benign |
|
|
R8687:Cog6
|
UTSW |
3 |
52,892,338 (GRCm39) |
missense |
probably benign |
|
|
R8759:Cog6
|
UTSW |
3 |
52,897,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8827:Cog6
|
UTSW |
3 |
52,890,535 (GRCm39) |
missense |
probably benign |
|
|
R9539:Cog6
|
UTSW |
3 |
52,914,722 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9688:Cog6
|
UTSW |
3 |
52,916,528 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9729:Cog6
|
UTSW |
3 |
52,900,907 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1177:Cog6
|
UTSW |
3 |
52,921,285 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2015-04-16 |
Incidental Mutation