Incidental Mutation 'R5266:Opa1'
| ID |
401726 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Opa1
|
| Ensembl Gene |
ENSMUSG00000038084 |
| Gene Name |
OPA1, mitochondrial dynamin like GTPase |
| Synonyms |
optic atrophy 1, lilr3, 1200011N24Rik |
| MMRRC Submission |
042858-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R5266 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
29398152-29473702 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 29436948 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 637
(I637N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124739
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038867]
[ENSMUST00000160475]
[ENSMUST00000160597]
[ENSMUST00000161186]
|
| AlphaFold |
P58281 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000038867
AA Change: I637N
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000036993
Gene: ENSMUSG00000038084
AA Change: I637N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
63 |
76 |
N/A |
INTRINSIC |
|
low complexity region
|
91 |
101 |
N/A |
INTRINSIC |
|
low complexity region
|
189 |
205 |
N/A |
INTRINSIC |
|
coiled coil region
|
228 |
271 |
N/A |
INTRINSIC |
|
DYNc
|
283 |
533 |
2.18e-10 |
SMART |
|
coiled coil region
|
918 |
967 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159036
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160101
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160153
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160475
AA Change: I637N
PolyPhen 2
Score 0.185 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000124739
Gene: ENSMUSG00000038084
AA Change: I637N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
63 |
76 |
N/A |
INTRINSIC |
|
low complexity region
|
91 |
101 |
N/A |
INTRINSIC |
|
low complexity region
|
189 |
205 |
N/A |
INTRINSIC |
|
coiled coil region
|
228 |
271 |
N/A |
INTRINSIC |
|
DYNc
|
283 |
533 |
2.18e-10 |
SMART |
|
Blast:DYNc
|
608 |
632 |
1e-5 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000160597
AA Change: I619N
PolyPhen 2
Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000124223
Gene: ENSMUSG00000038084
AA Change: I619N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
63 |
76 |
N/A |
INTRINSIC |
|
low complexity region
|
91 |
101 |
N/A |
INTRINSIC |
|
coiled coil region
|
210 |
253 |
N/A |
INTRINSIC |
|
DYNc
|
265 |
515 |
2.18e-10 |
SMART |
|
coiled coil region
|
900 |
949 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000161186
AA Change: I656N
PolyPhen 2
Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000123880
Gene: ENSMUSG00000038084
AA Change: I656N
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
63 |
76 |
N/A |
INTRINSIC |
|
low complexity region
|
91 |
101 |
N/A |
INTRINSIC |
|
coiled coil region
|
207 |
290 |
N/A |
INTRINSIC |
|
DYNc
|
302 |
552 |
2.18e-10 |
SMART |
|
coiled coil region
|
937 |
986 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.1479 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.6%
|
| Validation Efficiency |
97% (56/58) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
PHENOTYPE: Mice homozygous for an ENU mutation exhibit embryonic lethality, embryonic growth retardation and morphological abnormalities. Mice heterozygous for an ENU mutation exhibit abnormal cellular morphology, altered optic nerve myelination, abnormal responseto a new environment and decreased vision. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930503L19Rik |
T |
C |
18: 70,591,455 (GRCm39) |
N457S |
probably damaging |
Het |
| Asic4 |
G |
A |
1: 75,427,567 (GRCm39) |
G31E |
probably benign |
Het |
| Atp2a3 |
A |
G |
11: 72,866,223 (GRCm39) |
D281G |
probably damaging |
Het |
| Azin1 |
T |
C |
15: 38,491,795 (GRCm39) |
D387G |
probably benign |
Het |
| Bdp1 |
T |
C |
13: 100,204,043 (GRCm39) |
M660V |
probably benign |
Het |
| Catsperg2 |
G |
A |
7: 29,416,491 (GRCm39) |
T307M |
probably damaging |
Het |
| Cfap54 |
T |
G |
10: 92,651,764 (GRCm39) |
K3095N |
probably benign |
Het |
| Chl1 |
A |
G |
6: 103,677,504 (GRCm39) |
N706S |
probably damaging |
Het |
| Crym |
A |
G |
7: 119,798,517 (GRCm39) |
V113A |
probably benign |
Het |
| Cux1 |
A |
G |
5: 136,341,548 (GRCm39) |
S607P |
probably damaging |
Het |
| Cyp3a44 |
T |
C |
5: 145,731,207 (GRCm39) |
N198D |
possibly damaging |
Het |
| Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
| Elac1 |
A |
G |
18: 73,875,740 (GRCm39) |
V97A |
probably benign |
Het |
| Erbb3 |
G |
A |
10: 128,405,505 (GRCm39) |
T1251M |
probably damaging |
Het |
| Gask1b |
T |
A |
3: 79,843,910 (GRCm39) |
N12K |
probably damaging |
Het |
| Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
| Hydin |
A |
G |
8: 111,061,416 (GRCm39) |
H316R |
possibly damaging |
Het |
| Ikzf3 |
A |
T |
11: 98,381,406 (GRCm39) |
M58K |
probably benign |
Het |
| Lyst |
T |
C |
13: 13,835,555 (GRCm39) |
Y1746H |
probably damaging |
Het |
| Map3k11 |
T |
A |
19: 5,750,622 (GRCm39) |
N613K |
probably benign |
Het |
| Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
| Mrm1 |
A |
T |
11: 84,710,086 (GRCm39) |
L38Q |
possibly damaging |
Het |
| Myo7b |
A |
G |
18: 32,131,787 (GRCm39) |
F470L |
probably damaging |
Het |
| Ndst2 |
G |
A |
14: 20,774,555 (GRCm39) |
R834W |
probably damaging |
Het |
| Or52h9 |
A |
T |
7: 104,203,026 (GRCm39) |
Q300L |
probably benign |
Het |
| Or5d43 |
T |
C |
2: 88,104,565 (GRCm39) |
Y276C |
possibly damaging |
Het |
| Padi4 |
A |
G |
4: 140,473,442 (GRCm39) |
V665A |
possibly damaging |
Het |
| Pcdh1 |
A |
G |
18: 38,325,252 (GRCm39) |
Y897H |
probably damaging |
Het |
| Pkp3 |
A |
G |
7: 140,663,190 (GRCm39) |
D345G |
probably damaging |
Het |
| Pla2g4a |
T |
C |
1: 149,740,918 (GRCm39) |
M366V |
possibly damaging |
Het |
| Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
| Pon3 |
T |
C |
6: 5,240,860 (GRCm39) |
D34G |
possibly damaging |
Het |
| Ppargc1b |
A |
T |
18: 61,448,876 (GRCm39) |
S133T |
probably damaging |
Het |
| Ppp4r3b |
T |
C |
11: 29,123,309 (GRCm39) |
S2P |
possibly damaging |
Het |
| Rbm20 |
A |
G |
19: 53,801,818 (GRCm39) |
T109A |
probably damaging |
Het |
| Rexo5 |
C |
A |
7: 119,443,660 (GRCm39) |
H690Q |
probably benign |
Het |
| Scube2 |
C |
T |
7: 109,408,437 (GRCm39) |
G670D |
probably damaging |
Het |
| Sipa1l2 |
T |
C |
8: 126,218,865 (GRCm39) |
I157M |
probably damaging |
Het |
| Slbp |
A |
T |
5: 33,801,210 (GRCm39) |
I167N |
probably damaging |
Het |
| Sry |
C |
G |
Y: 2,662,975 (GRCm39) |
Q228H |
unknown |
Het |
| Stk36 |
T |
C |
1: 74,650,317 (GRCm39) |
V283A |
probably benign |
Het |
| Tead1 |
A |
G |
7: 112,358,673 (GRCm39) |
|
probably benign |
Het |
| Tecpr2 |
G |
C |
12: 110,881,836 (GRCm39) |
W135S |
probably damaging |
Het |
| Tha1 |
A |
C |
11: 117,760,502 (GRCm39) |
S241A |
probably damaging |
Het |
| Ttc39a |
A |
T |
4: 109,279,701 (GRCm39) |
I112F |
probably benign |
Het |
| Vmn1r128 |
A |
T |
7: 21,083,328 (GRCm39) |
T11S |
probably benign |
Het |
| Vnn1 |
G |
A |
10: 23,779,303 (GRCm39) |
C404Y |
probably damaging |
Het |
| Wdr41 |
T |
C |
13: 95,131,759 (GRCm39) |
F57L |
probably damaging |
Het |
| Zfp975 |
T |
G |
7: 42,311,654 (GRCm39) |
T320P |
probably damaging |
Het |
| Zfp985 |
A |
T |
4: 147,667,289 (GRCm39) |
|
probably null |
Het |
| Zfpm2 |
T |
C |
15: 40,962,865 (GRCm39) |
S176P |
probably benign |
Het |
|
| Other mutations in Opa1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01082:Opa1
|
APN |
16 |
29,436,933 (GRCm39) |
splice site |
probably benign |
|
|
IGL01087:Opa1
|
APN |
16 |
29,405,815 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01799:Opa1
|
APN |
16 |
29,435,476 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
IGL01927:Opa1
|
APN |
16 |
29,405,813 (GRCm39) |
missense |
probably benign |
0.35 |
|
IGL02067:Opa1
|
APN |
16 |
29,435,473 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02317:Opa1
|
APN |
16 |
29,433,984 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02567:Opa1
|
APN |
16 |
29,407,104 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02826:Opa1
|
APN |
16 |
29,429,705 (GRCm39) |
missense |
probably null |
|
|
Longshanks
|
UTSW |
16 |
29,437,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0032:Opa1
|
UTSW |
16 |
29,433,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0032:Opa1
|
UTSW |
16 |
29,433,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0092:Opa1
|
UTSW |
16 |
29,444,412 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0114:Opa1
|
UTSW |
16 |
29,448,453 (GRCm39) |
missense |
probably benign |
0.35 |
|
R0200:Opa1
|
UTSW |
16 |
29,432,947 (GRCm39) |
missense |
probably benign |
0.08 |
|
R0308:Opa1
|
UTSW |
16 |
29,440,349 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0427:Opa1
|
UTSW |
16 |
29,430,279 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0671:Opa1
|
UTSW |
16 |
29,421,025 (GRCm39) |
splice site |
probably benign |
|
|
R1768:Opa1
|
UTSW |
16 |
29,439,628 (GRCm39) |
missense |
probably benign |
|
|
R1889:Opa1
|
UTSW |
16 |
29,444,403 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R3932:Opa1
|
UTSW |
16 |
29,429,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3933:Opa1
|
UTSW |
16 |
29,429,698 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4434:Opa1
|
UTSW |
16 |
29,430,801 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4618:Opa1
|
UTSW |
16 |
29,405,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4926:Opa1
|
UTSW |
16 |
29,467,791 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5163:Opa1
|
UTSW |
16 |
29,416,438 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5249:Opa1
|
UTSW |
16 |
29,437,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5275:Opa1
|
UTSW |
16 |
29,430,397 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5372:Opa1
|
UTSW |
16 |
29,404,937 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5990:Opa1
|
UTSW |
16 |
29,405,836 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6054:Opa1
|
UTSW |
16 |
29,433,952 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6483:Opa1
|
UTSW |
16 |
29,447,525 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6522:Opa1
|
UTSW |
16 |
29,444,332 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6889:Opa1
|
UTSW |
16 |
29,439,686 (GRCm39) |
missense |
probably benign |
0.22 |
|
R7225:Opa1
|
UTSW |
16 |
29,432,857 (GRCm39) |
splice site |
probably null |
|
|
R7243:Opa1
|
UTSW |
16 |
29,405,814 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7324:Opa1
|
UTSW |
16 |
29,405,799 (GRCm39) |
missense |
probably benign |
|
|
R7831:Opa1
|
UTSW |
16 |
29,467,755 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8304:Opa1
|
UTSW |
16 |
29,416,489 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R8317:Opa1
|
UTSW |
16 |
29,432,962 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8353:Opa1
|
UTSW |
16 |
29,439,686 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8453:Opa1
|
UTSW |
16 |
29,439,686 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8795:Opa1
|
UTSW |
16 |
29,448,450 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8919:Opa1
|
UTSW |
16 |
29,424,340 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9053:Opa1
|
UTSW |
16 |
29,404,836 (GRCm39) |
nonsense |
probably null |
|
|
R9087:Opa1
|
UTSW |
16 |
29,437,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9172:Opa1
|
UTSW |
16 |
29,439,232 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9355:Opa1
|
UTSW |
16 |
29,432,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9434:Opa1
|
UTSW |
16 |
29,404,874 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9511:Opa1
|
UTSW |
16 |
29,429,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9612:Opa1
|
UTSW |
16 |
29,430,255 (GRCm39) |
missense |
|
|
|
R9784:Opa1
|
UTSW |
16 |
29,437,029 (GRCm39) |
nonsense |
probably null |
|
|
RF012:Opa1
|
UTSW |
16 |
29,432,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
T0722:Opa1
|
UTSW |
16 |
29,429,748 (GRCm39) |
critical splice donor site |
probably null |
|
|
X0065:Opa1
|
UTSW |
16 |
29,439,602 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
| Predicted Primers |
PCR Primer
(F):5'- CATGCCTCGGTTATCTTCTAATAAGC -3'
(R):5'- ACATTATATCCTAACCTCGACTGC -3'
Sequencing Primer
(F):5'- TCGGTTATCTTCTAATAAGCCTGTAG -3'
(R):5'- ACCTCGACTGCTTTATTAGGAAG -3'
|
| Posted On |
2016-07-06 |
Incidental Mutation