Incidental Mutation 'IGL01123:Coq8b'
| ID |
51601 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Coq8b
|
| Ensembl Gene |
ENSMUSG00000003762 |
| Gene Name |
coenzyme Q8B |
| Synonyms |
0610012P18Rik, Adck4 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01123
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
26932448-26957375 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 26939509 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Isoleucine
at position 180
(V180I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000123309
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000003860]
[ENSMUST00000108378]
[ENSMUST00000128090]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000003860
AA Change: V180I
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000003860
Gene: ENSMUSG00000003762
AA Change: V180I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
93 |
109 |
N/A |
INTRINSIC |
|
Pfam:ABC1
|
198 |
314 |
4.9e-34 |
PFAM |
|
low complexity region
|
348 |
364 |
N/A |
INTRINSIC |
|
low complexity region
|
474 |
483 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108378
AA Change: V180I
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000104015
Gene: ENSMUSG00000003762
AA Change: V180I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
93 |
109 |
N/A |
INTRINSIC |
|
Pfam:ABC1
|
198 |
314 |
4.4e-34 |
PFAM |
|
low complexity region
|
348 |
364 |
N/A |
INTRINSIC |
|
low complexity region
|
474 |
483 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000128090
AA Change: V180I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000123309
Gene: ENSMUSG00000003762
AA Change: V180I
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
93 |
109 |
N/A |
INTRINSIC |
|
Pfam:ABC1
|
198 |
304 |
3.4e-32 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000143372
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206312
|
| 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 protein with two copies of a domain found in protein kinases. The encoded protein has a complete protein kinase catalytic domain, and a truncated domain that contains only the active and binding sites of the protein kinase domain, however, it is not known whether the protein has any kinase activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310057J18Rik |
G |
T |
10: 28,849,934 (GRCm39) |
D167E |
probably damaging |
Het |
| Aadat |
A |
T |
8: 60,979,648 (GRCm39) |
E170V |
probably benign |
Het |
| Acsf2 |
T |
C |
11: 94,461,276 (GRCm39) |
E300G |
probably benign |
Het |
| Agbl3 |
C |
T |
6: 34,823,911 (GRCm39) |
Q859* |
probably null |
Het |
| Arhgap11a |
T |
C |
2: 113,665,118 (GRCm39) |
|
probably benign |
Het |
| Arhgef40 |
C |
A |
14: 52,231,803 (GRCm39) |
Q730K |
probably damaging |
Het |
| Armc3 |
C |
T |
2: 19,206,616 (GRCm39) |
P13L |
possibly damaging |
Het |
| B3gnt2 |
T |
A |
11: 22,786,490 (GRCm39) |
T233S |
probably benign |
Het |
| Bnc1 |
G |
A |
7: 81,623,455 (GRCm39) |
Q591* |
probably null |
Het |
| Bsn |
A |
T |
9: 107,993,185 (GRCm39) |
F856I |
probably damaging |
Het |
| CK137956 |
T |
A |
4: 127,829,643 (GRCm39) |
T558S |
probably benign |
Het |
| Csmd1 |
A |
T |
8: 17,584,944 (GRCm39) |
L16Q |
possibly damaging |
Het |
| Dhx37 |
A |
G |
5: 125,496,152 (GRCm39) |
S769P |
possibly damaging |
Het |
| Diras1 |
T |
A |
10: 80,858,249 (GRCm39) |
M1L |
probably damaging |
Het |
| Fam161b |
A |
G |
12: 84,404,438 (GRCm39) |
W81R |
probably benign |
Het |
| Fat4 |
A |
T |
3: 39,011,418 (GRCm39) |
I2173L |
probably benign |
Het |
| Fbn2 |
T |
C |
18: 58,237,153 (GRCm39) |
T617A |
possibly damaging |
Het |
| Gabrq |
G |
A |
X: 71,880,439 (GRCm39) |
D311N |
probably benign |
Het |
| Isl2 |
G |
T |
9: 55,452,746 (GRCm39) |
G335C |
probably damaging |
Het |
| Kbtbd7 |
T |
C |
14: 79,666,052 (GRCm39) |
V628A |
probably damaging |
Het |
| Kmt2d |
T |
C |
15: 98,735,029 (GRCm39) |
M5378V |
unknown |
Het |
| Lrrc23 |
G |
T |
6: 124,755,782 (GRCm39) |
D75E |
probably benign |
Het |
| Mab21l3 |
G |
A |
3: 101,742,446 (GRCm39) |
T38M |
probably benign |
Het |
| Matn1 |
T |
C |
4: 130,677,322 (GRCm39) |
I177T |
possibly damaging |
Het |
| Mtor |
T |
C |
4: 148,537,494 (GRCm39) |
S60P |
probably benign |
Het |
| Naip6 |
T |
C |
13: 100,440,946 (GRCm39) |
E278G |
probably benign |
Het |
| Nsun6 |
T |
C |
2: 15,053,789 (GRCm39) |
I7V |
possibly damaging |
Het |
| Pabpc6 |
A |
T |
17: 9,887,076 (GRCm39) |
S492T |
probably benign |
Het |
| Pakap |
C |
T |
4: 57,757,627 (GRCm39) |
Q188* |
probably null |
Het |
| Pom121 |
A |
T |
5: 135,420,560 (GRCm39) |
V287D |
unknown |
Het |
| Ptprq |
A |
T |
10: 107,522,079 (GRCm39) |
F624Y |
probably damaging |
Het |
| Ptprr |
A |
G |
10: 116,024,222 (GRCm39) |
T178A |
probably benign |
Het |
| Pygm |
A |
G |
19: 6,441,424 (GRCm39) |
N473S |
probably benign |
Het |
| Ros1 |
A |
T |
10: 51,996,905 (GRCm39) |
Y1256N |
probably damaging |
Het |
| Scpep1 |
T |
C |
11: 88,832,154 (GRCm39) |
N192S |
possibly damaging |
Het |
| Serpina1f |
A |
G |
12: 103,660,265 (GRCm39) |
S6P |
possibly damaging |
Het |
| Sgca |
T |
A |
11: 94,863,113 (GRCm39) |
Q80L |
probably damaging |
Het |
| Skint6 |
A |
G |
4: 112,661,879 (GRCm39) |
L1235P |
possibly damaging |
Het |
| Slc23a2 |
A |
C |
2: 131,898,736 (GRCm39) |
N600K |
probably benign |
Het |
| Spata20 |
T |
C |
11: 94,374,221 (GRCm39) |
T350A |
probably benign |
Het |
| Syne1 |
G |
T |
10: 5,294,921 (GRCm39) |
Y1227* |
probably null |
Het |
| Unc13c |
T |
C |
9: 73,840,479 (GRCm39) |
Y124C |
probably benign |
Het |
| Usp40 |
G |
A |
1: 87,913,845 (GRCm39) |
T416I |
probably benign |
Het |
| Vmn1r200 |
T |
C |
13: 22,579,571 (GRCm39) |
W116R |
probably benign |
Het |
| Vps4a |
T |
C |
8: 107,765,851 (GRCm39) |
|
probably benign |
Het |
| Zfyve16 |
A |
G |
13: 92,629,030 (GRCm39) |
V1469A |
probably damaging |
Het |
|
| Other mutations in Coq8b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00490:Coq8b
|
APN |
7 |
26,956,902 (GRCm39) |
missense |
probably benign |
|
|
IGL01116:Coq8b
|
APN |
7 |
26,939,282 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02949:Coq8b
|
APN |
7 |
26,956,038 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R0067:Coq8b
|
UTSW |
7 |
26,932,906 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R0690:Coq8b
|
UTSW |
7 |
26,941,674 (GRCm39) |
missense |
probably benign |
0.15 |
|
R1307:Coq8b
|
UTSW |
7 |
26,950,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1470:Coq8b
|
UTSW |
7 |
26,951,734 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1470:Coq8b
|
UTSW |
7 |
26,951,734 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1551:Coq8b
|
UTSW |
7 |
26,956,907 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1682:Coq8b
|
UTSW |
7 |
26,939,549 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1895:Coq8b
|
UTSW |
7 |
26,939,299 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1945:Coq8b
|
UTSW |
7 |
26,933,406 (GRCm39) |
small insertion |
probably benign |
|
|
R1945:Coq8b
|
UTSW |
7 |
26,933,405 (GRCm39) |
small insertion |
probably benign |
|
|
R1946:Coq8b
|
UTSW |
7 |
26,939,299 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2069:Coq8b
|
UTSW |
7 |
26,956,802 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3758:Coq8b
|
UTSW |
7 |
26,941,652 (GRCm39) |
nonsense |
probably null |
|
|
R4545:Coq8b
|
UTSW |
7 |
26,932,930 (GRCm39) |
missense |
probably benign |
0.45 |
|
R4838:Coq8b
|
UTSW |
7 |
26,950,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5181:Coq8b
|
UTSW |
7 |
26,951,747 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5345:Coq8b
|
UTSW |
7 |
26,949,773 (GRCm39) |
missense |
probably benign |
|
|
R5806:Coq8b
|
UTSW |
7 |
26,950,050 (GRCm39) |
nonsense |
probably null |
|
|
R5943:Coq8b
|
UTSW |
7 |
26,933,428 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6005:Coq8b
|
UTSW |
7 |
26,956,750 (GRCm39) |
nonsense |
probably null |
|
|
R7028:Coq8b
|
UTSW |
7 |
26,939,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7709:Coq8b
|
UTSW |
7 |
26,949,962 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8300:Coq8b
|
UTSW |
7 |
26,941,671 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9039:Coq8b
|
UTSW |
7 |
26,950,011 (GRCm39) |
missense |
probably benign |
0.19 |
|
R9310:Coq8b
|
UTSW |
7 |
26,941,486 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-06-21 |
Incidental Mutation