Incidental Mutation 'R8687:Cog6'
| ID |
662082 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cog6
|
| Ensembl Gene |
ENSMUSG00000027742 |
| Gene Name |
component of oligomeric golgi complex 6 |
| Synonyms |
|
| MMRRC Submission |
068542-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8687 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
3 |
| Chromosomal Location |
52889544-52924644 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 52892338 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Isoleucine
at position 624
(V624I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000141339
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036665]
[ENSMUST00000193432]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000036665
|
| SMART Domains |
Protein: ENSMUSP00000048603
Gene: ENSMUSG00000027742
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
26 |
N/A |
INTRINSIC |
|
COG6
|
55 |
656 |
N/A |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193432
AA Change: V624I
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000141339
Gene: ENSMUSG00000027742
AA Change: V624I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
13 |
26 |
N/A |
INTRINSIC |
|
COG6
|
55 |
625 |
5e-289 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
| Validation Efficiency |
92% (22/24) |
| 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: 25 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arhgap45 |
C |
T |
10: 79,852,621 (GRCm39) |
|
probably benign |
Het |
| B3galt4 |
A |
G |
17: 34,169,819 (GRCm39) |
S140P |
probably damaging |
Het |
| Cysrt1 |
A |
G |
2: 25,129,399 (GRCm39) |
S38P |
possibly damaging |
Het |
| Eme2 |
C |
T |
17: 25,113,813 (GRCm39) |
V71M |
possibly damaging |
Het |
| Eva1c |
C |
A |
16: 90,687,433 (GRCm39) |
T223K |
probably benign |
Het |
| Gm3633 |
A |
T |
14: 42,462,648 (GRCm39) |
L81H |
|
Het |
| Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
| Iqch |
A |
T |
9: 63,432,067 (GRCm39) |
W443R |
probably damaging |
Het |
| Itgb1 |
T |
C |
8: 129,442,697 (GRCm39) |
V294A |
probably damaging |
Het |
| Kif1b |
T |
A |
4: 149,345,620 (GRCm39) |
K407* |
probably null |
Het |
| Kyat1 |
A |
G |
2: 30,075,759 (GRCm39) |
S377P |
probably benign |
Het |
| Mical3 |
A |
G |
6: 120,936,438 (GRCm39) |
S1363P |
probably benign |
Het |
| Muc4 |
C |
G |
16: 32,575,221 (GRCm39) |
Q1269E |
probably benign |
Het |
| Naip6 |
T |
A |
13: 100,435,636 (GRCm39) |
R962S |
probably benign |
Het |
| Pnma8a |
T |
G |
7: 16,694,520 (GRCm39) |
V125G |
probably damaging |
Het |
| Ptpdc1 |
G |
A |
13: 48,740,136 (GRCm39) |
P432S |
possibly damaging |
Het |
| Rhobtb2 |
G |
A |
14: 70,038,104 (GRCm39) |
T52I |
probably damaging |
Het |
| Slco1a8 |
C |
T |
6: 141,939,991 (GRCm39) |
G171S |
probably damaging |
Het |
| Spop |
G |
A |
11: 95,361,337 (GRCm39) |
|
probably benign |
Het |
| Stam |
TGCTGCTGCTGCTGCCGCTGCTGCTGCTG |
TGCTGCTGCTGCTG |
2: 14,151,096 (GRCm39) |
|
probably benign |
Het |
| Stam |
CCTGCTGCTGCTGCTGCTGCCGCTGCTGCTGCTG |
CCTGCCGCTGCTGCTGCTG |
2: 14,151,091 (GRCm39) |
|
probably benign |
Het |
| Tmem102 |
T |
C |
11: 69,695,441 (GRCm39) |
H177R |
probably benign |
Het |
| Trpc4ap |
T |
C |
2: 155,477,170 (GRCm39) |
T748A |
possibly damaging |
Het |
| Ttc27 |
T |
A |
17: 75,046,679 (GRCm39) |
Y247N |
probably benign |
Het |
| Ttc39a |
T |
C |
4: 109,288,776 (GRCm39) |
I292T |
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 |
|
|
IGL02122:Cog6
|
APN |
3 |
52,905,763 (GRCm39) |
missense |
probably benign |
0.04 |
|
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 |
|
|
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 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTCCTAAGCAGTCCTGGGTG -3'
(R):5'- GCATGGGCTTAGTGAAATAATTGG -3'
Sequencing Primer
(F):5'- AAGCAGTCCTGGGTGTTCCTAC -3'
(R):5'- GGGCTTAGTGAAATAATTGGTTTTTG -3'
|
| Posted On |
2021-03-08 |
Incidental Mutation