Incidental Mutation 'R1542:Oprm1'
| ID |
171832 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Oprm1
|
| Ensembl Gene |
ENSMUSG00000000766 |
| Gene Name |
opioid receptor, mu 1 |
| Synonyms |
Oprm, MOP receptor, mor, muOR, MOR-1, MOP-R |
| MMRRC Submission |
039581-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.146)
|
| Stock # |
R1542 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
6758506-7038198 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 6788960 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Leucine
at position 29
(W29L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000115552
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000783]
[ENSMUST00000052751]
[ENSMUST00000056385]
[ENSMUST00000063036]
[ENSMUST00000078634]
[ENSMUST00000092729]
[ENSMUST00000092731]
[ENSMUST00000092734]
[ENSMUST00000105597]
[ENSMUST00000105601]
[ENSMUST00000105602]
[ENSMUST00000152674]
[ENSMUST00000105604]
[ENSMUST00000144264]
[ENSMUST00000105611]
[ENSMUST00000135502]
[ENSMUST00000105607]
[ENSMUST00000105603]
[ENSMUST00000105605]
[ENSMUST00000129954]
[ENSMUST00000129221]
[ENSMUST00000123861]
[ENSMUST00000154941]
[ENSMUST00000154906]
[ENSMUST00000147171]
[ENSMUST00000105615]
[ENSMUST00000143875]
[ENSMUST00000150374]
|
| AlphaFold |
P42866 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000000783
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000000783
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
339 |
1.6e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1.3e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
4e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000052751
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000060329
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.1e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.2e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000056385
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000060590
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.7e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.3e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000063036
|
| SMART Domains |
Protein: ENSMUSP00000053498
Gene: ENSMUSG00000000766
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
24 |
268 |
8.7e-64 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000078634
AA Change: W29L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000077704
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
339 |
2.1e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
2.4e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
9e-60 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000092729
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000090405
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.7e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
9.6e-11 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.1e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000092731
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000090407
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
9.9e-11 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.2e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000092734
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000090410
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.7e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.3e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105597
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000105601
AA Change: W29L
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000101226
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
SCOP:d1l9ha_
|
46 |
100 |
3e-9 |
SMART |
|
PDB:4DKL|A
|
52 |
100 |
3e-21 |
PDB |
|
low complexity region
|
119 |
131 |
N/A |
INTRINSIC |
|
low complexity region
|
173 |
184 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105602
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000101227
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.8e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
9.8e-11 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.1e-67 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000152674
AA Change: W29L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000115552
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
SCOP:d1l9ha_
|
46 |
94 |
8e-8 |
SMART |
|
PDB:4DKL|A
|
52 |
94 |
7e-23 |
PDB |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105604
AA Change: W29L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000101229
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
332 |
5.1e-8 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
9.9e-11 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.8e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000144264
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000115836
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.7e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.4e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105611
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000101236
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
338 |
1.7e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1.4e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
4.4e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135502
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000135143
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
339 |
2.2e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1.9e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
7.5e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105607
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000101232
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1.7e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.3e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105603
AA Change: W29L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000101228
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
6.7e-8 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
9.6e-11 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.6e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105605
AA Change: W29L
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000101230
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
325 |
1e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
9.8e-11 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.2e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000129954
AA Change: W29L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000122385
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
338 |
6.9e-8 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1.5e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
5.4e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000129221
|
| SMART Domains |
Protein: ENSMUSP00000123117
Gene: ENSMUSG00000000766
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
12 |
261 |
1.1e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
15 |
287 |
7.3e-11 |
PFAM |
|
Pfam:7tm_1
|
21 |
272 |
2.4e-67 |
PFAM |
|
low complexity region
|
340 |
351 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000123861
AA Change: W29L
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000120187
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
SCOP:d1l9ha_
|
46 |
100 |
3e-9 |
SMART |
|
PDB:4DKL|A
|
52 |
100 |
3e-21 |
PDB |
|
low complexity region
|
119 |
131 |
N/A |
INTRINSIC |
|
low complexity region
|
173 |
184 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000154941
|
| SMART Domains |
Protein: ENSMUSP00000115413
Gene: ENSMUSG00000000766
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
12 |
261 |
9.6e-8 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
15 |
287 |
6.1e-11 |
PFAM |
|
Pfam:7tm_1
|
21 |
272 |
2e-67 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000154906
AA Change: W29L
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000114342
Gene: ENSMUSG00000000766
AA Change: W29L
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srx
|
76 |
332 |
1.5e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
79 |
351 |
1.1e-10 |
PFAM |
|
Pfam:7tm_1
|
85 |
336 |
3.6e-67 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148625
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141897
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133486
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000147171
|
| SMART Domains |
Protein: ENSMUSP00000117950
Gene: ENSMUSG00000000766
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
24 |
268 |
9.2e-64 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105615
|
| SMART Domains |
Protein: ENSMUSP00000101240
Gene: ENSMUSG00000000766
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
24 |
268 |
1.3e-63 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000143875
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000150374
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.5%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes the mu opioid receptor which is where drugs such as morphine and other opioids have pharmacological effects. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]
PHENOTYPE: Homozygotes for null mutations exhibit isoform dependent loss of behavioral and gastrointestinal opioid responses and may also show impaired spatial memory, heightened nociception, reduced locomotor activity, increased hematopoietic proliferation, and decreased male fertility. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700006A11Rik |
A |
G |
3: 124,414,406 (GRCm38) |
M208T |
possibly damaging |
Het |
| Acsbg2 |
T |
A |
17: 56,849,791 (GRCm38) |
I416F |
probably damaging |
Het |
| Adam6b |
G |
A |
12: 113,490,939 (GRCm38) |
D459N |
possibly damaging |
Het |
| Adprh |
A |
T |
16: 38,445,924 (GRCm38) |
D285E |
probably damaging |
Het |
| Aggf1 |
A |
T |
13: 95,370,942 (GRCm38) |
C112S |
probably benign |
Het |
| Als2cl |
T |
C |
9: 110,894,034 (GRCm38) |
V602A |
probably benign |
Het |
| Angptl2 |
G |
T |
2: 33,228,885 (GRCm38) |
V224F |
probably benign |
Het |
| Ap3b2 |
A |
T |
7: 81,478,077 (GRCm38) |
|
probably null |
Het |
| Aqp2 |
A |
C |
15: 99,583,842 (GRCm38) |
I206L |
probably benign |
Het |
| Asap2 |
A |
G |
12: 21,265,997 (GRCm38) |
D930G |
probably damaging |
Het |
| Cacna1e |
T |
A |
1: 154,477,779 (GRCm38) |
M682L |
probably benign |
Het |
| Ccdc18 |
A |
G |
5: 108,212,188 (GRCm38) |
N1146S |
probably benign |
Het |
| Ccr4 |
G |
A |
9: 114,492,005 (GRCm38) |
H331Y |
probably benign |
Het |
| Cd33 |
A |
G |
7: 43,532,106 (GRCm38) |
L210P |
probably damaging |
Het |
| Cep85l |
T |
C |
10: 53,301,584 (GRCm38) |
E351G |
probably damaging |
Het |
| Cntn6 |
C |
A |
6: 104,848,100 (GRCm38) |
T867K |
probably damaging |
Het |
| Cpeb2 |
C |
T |
5: 43,285,875 (GRCm38) |
R970C |
probably damaging |
Het |
| Cul7 |
T |
A |
17: 46,663,190 (GRCm38) |
L1467H |
probably damaging |
Het |
| Dscaml1 |
T |
A |
9: 45,749,440 (GRCm38) |
I1693K |
possibly damaging |
Het |
| Ebf4 |
A |
T |
2: 130,365,498 (GRCm38) |
M621L |
probably benign |
Het |
| Elp4 |
G |
T |
2: 105,794,609 (GRCm38) |
T313N |
probably benign |
Het |
| Epas1 |
T |
A |
17: 86,824,490 (GRCm38) |
I373N |
possibly damaging |
Het |
| Etnk1 |
A |
T |
6: 143,180,641 (GRCm38) |
M71L |
probably benign |
Het |
| Fry |
C |
T |
5: 150,404,966 (GRCm38) |
T1257I |
probably benign |
Het |
| Gm21834 |
A |
G |
17: 57,741,951 (GRCm38) |
F90S |
possibly damaging |
Het |
| Gm8674 |
T |
A |
13: 49,900,003 (GRCm38) |
|
noncoding transcript |
Het |
| Gna11 |
T |
C |
10: 81,533,328 (GRCm38) |
T134A |
probably benign |
Het |
| Golga5 |
C |
T |
12: 102,474,720 (GRCm38) |
S238F |
probably damaging |
Het |
| Grin2a |
T |
A |
16: 9,579,203 (GRCm38) |
N1007Y |
probably damaging |
Het |
| Hist1h3e |
A |
G |
13: 23,562,164 (GRCm38) |
F68L |
probably damaging |
Het |
| Ifnar2 |
G |
A |
16: 91,399,265 (GRCm38) |
V253M |
possibly damaging |
Het |
| Insl5 |
A |
T |
4: 103,018,185 (GRCm38) |
S123T |
probably damaging |
Het |
| Itgb2 |
T |
C |
10: 77,559,486 (GRCm38) |
S474P |
probably benign |
Het |
| Kcnb2 |
A |
G |
1: 15,710,788 (GRCm38) |
H628R |
probably benign |
Het |
| L3mbtl2 |
G |
A |
15: 81,682,151 (GRCm38) |
D392N |
probably null |
Het |
| Lrp1b |
G |
T |
2: 41,123,712 (GRCm38) |
T1813K |
probably damaging |
Het |
| Map3k4 |
A |
G |
17: 12,235,906 (GRCm38) |
L1399P |
probably damaging |
Het |
| Mbtps1 |
A |
C |
8: 119,546,247 (GRCm38) |
|
probably null |
Het |
| Mettl25 |
A |
T |
10: 105,826,120 (GRCm38) |
S330T |
probably benign |
Het |
| Mical2 |
T |
C |
7: 112,309,468 (GRCm38) |
L211P |
probably damaging |
Het |
| Mmrn1 |
T |
A |
6: 60,945,118 (GRCm38) |
S186R |
probably damaging |
Het |
| Mob3b |
C |
A |
4: 35,084,046 (GRCm38) |
V48L |
possibly damaging |
Het |
| Mpp6 |
A |
G |
6: 50,198,326 (GRCm38) |
Y539C |
probably damaging |
Het |
| Napsa |
A |
T |
7: 44,581,689 (GRCm38) |
H114L |
probably damaging |
Het |
| Nsmce4a |
A |
T |
7: 130,545,893 (GRCm38) |
|
probably null |
Het |
| Nup62 |
A |
G |
7: 44,829,929 (GRCm38) |
K456R |
possibly damaging |
Het |
| Nwd2 |
T |
A |
5: 63,806,975 (GRCm38) |
W1301R |
probably damaging |
Het |
| Olfr1141 |
A |
G |
2: 87,753,318 (GRCm38) |
V225A |
probably damaging |
Het |
| Olfr118 |
A |
T |
17: 37,672,251 (GRCm38) |
E76V |
probably damaging |
Het |
| Olfr15 |
T |
A |
16: 3,839,832 (GRCm38) |
N286K |
probably damaging |
Het |
| Olfr364-ps1 |
T |
A |
2: 37,146,966 (GRCm38) |
S251R |
probably damaging |
Het |
| Pcnt |
T |
G |
10: 76,389,387 (GRCm38) |
N1761T |
probably benign |
Het |
| Pcnt |
C |
T |
10: 76,401,386 (GRCm38) |
M1355I |
probably benign |
Het |
| Pde11a |
A |
T |
2: 76,046,855 (GRCm38) |
S757T |
probably benign |
Het |
| Pde6a |
T |
A |
18: 61,257,045 (GRCm38) |
I490N |
possibly damaging |
Het |
| Pgap1 |
A |
G |
1: 54,492,090 (GRCm38) |
V742A |
probably benign |
Het |
| Pik3c2b |
T |
C |
1: 133,090,034 (GRCm38) |
L915P |
probably damaging |
Het |
| Pkd1l1 |
A |
G |
11: 8,874,179 (GRCm38) |
C1129R |
possibly damaging |
Het |
| Pkhd1l1 |
A |
T |
15: 44,528,191 (GRCm38) |
H1551L |
probably benign |
Het |
| Plxnb2 |
C |
T |
15: 89,165,921 (GRCm38) |
C491Y |
probably damaging |
Het |
| Ppt1 |
C |
A |
4: 122,857,609 (GRCm38) |
H300N |
probably benign |
Het |
| Prpf3 |
T |
A |
3: 95,836,470 (GRCm38) |
Q457L |
probably benign |
Het |
| Ranbp17 |
C |
T |
11: 33,264,672 (GRCm38) |
V914I |
probably benign |
Het |
| Rasal2 |
T |
C |
1: 157,175,851 (GRCm38) |
I413V |
possibly damaging |
Het |
| Rb1cc1 |
G |
A |
1: 6,244,249 (GRCm38) |
V382I |
possibly damaging |
Het |
| Rere |
T |
A |
4: 150,615,942 (GRCm38) |
F1125I |
probably damaging |
Het |
| Rprd2 |
A |
T |
3: 95,765,676 (GRCm38) |
V805E |
possibly damaging |
Het |
| Sept10 |
T |
G |
10: 59,166,606 (GRCm38) |
E162A |
probably damaging |
Het |
| Sept12 |
G |
T |
16: 4,992,295 (GRCm38) |
D125E |
probably benign |
Het |
| Serpina6 |
A |
G |
12: 103,654,473 (GRCm38) |
Y6H |
probably benign |
Het |
| Serpinb3c |
T |
C |
1: 107,272,787 (GRCm38) |
M209V |
probably damaging |
Het |
| Slc2a7 |
A |
T |
4: 150,168,471 (GRCm38) |
T523S |
probably damaging |
Het |
| Smdt1 |
T |
C |
15: 82,346,175 (GRCm38) |
V31A |
possibly damaging |
Het |
| Snrnp48 |
T |
C |
13: 38,220,704 (GRCm38) |
I245T |
probably damaging |
Het |
| Spink2 |
G |
A |
5: 77,206,965 (GRCm38) |
T33I |
probably damaging |
Het |
| Sptan1 |
A |
G |
2: 30,027,127 (GRCm38) |
T2204A |
probably damaging |
Het |
| Synj2 |
A |
G |
17: 6,025,017 (GRCm38) |
D306G |
probably benign |
Het |
| Tas2r109 |
A |
G |
6: 132,980,910 (GRCm38) |
I19T |
possibly damaging |
Het |
| Tbk1 |
C |
T |
10: 121,559,935 (GRCm38) |
V418M |
probably benign |
Het |
| Tcerg1 |
A |
G |
18: 42,553,430 (GRCm38) |
E684G |
probably damaging |
Het |
| Tenm2 |
T |
C |
11: 36,300,220 (GRCm38) |
N308S |
probably damaging |
Het |
| Tfb2m |
A |
T |
1: 179,537,861 (GRCm38) |
|
probably null |
Het |
| Tmc1 |
T |
A |
19: 20,816,122 (GRCm38) |
L558F |
probably damaging |
Het |
| Tmprss5 |
T |
A |
9: 49,109,134 (GRCm38) |
I80N |
possibly damaging |
Het |
| Trappc2l |
G |
A |
8: 122,615,407 (GRCm38) |
V131M |
probably damaging |
Het |
| Trpm7 |
A |
C |
2: 126,822,599 (GRCm38) |
Y953* |
probably null |
Het |
| Ttn |
T |
C |
2: 76,753,515 (GRCm38) |
R22383G |
probably damaging |
Het |
| Ugt1a6b |
G |
A |
1: 88,107,261 (GRCm38) |
G107D |
probably benign |
Het |
| Vmn1r197 |
A |
T |
13: 22,328,350 (GRCm38) |
Y147F |
probably benign |
Het |
| Zfp507 |
A |
T |
7: 35,794,801 (GRCm38) |
N272K |
possibly damaging |
Het |
| Zfp526 |
G |
A |
7: 25,226,262 (GRCm38) |
E649K |
probably benign |
Het |
| Zswim6 |
G |
A |
13: 107,727,234 (GRCm38) |
|
noncoding transcript |
Het |
|
| Other mutations in Oprm1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01018:Oprm1
|
APN |
10 |
7,037,170 (GRCm38) |
utr 3 prime |
probably benign |
|
|
IGL01768:Oprm1
|
APN |
10 |
6,829,186 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02455:Oprm1
|
APN |
10 |
6,830,219 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03391:Oprm1
|
APN |
10 |
7,014,077 (GRCm38) |
intron |
probably benign |
|
|
IGL03410:Oprm1
|
APN |
10 |
6,830,051 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03048:Oprm1
|
UTSW |
10 |
6,829,064 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0189:Oprm1
|
UTSW |
10 |
6,789,071 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R0321:Oprm1
|
UTSW |
10 |
6,829,183 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0629:Oprm1
|
UTSW |
10 |
6,832,604 (GRCm38) |
splice site |
probably null |
|
|
R0730:Oprm1
|
UTSW |
10 |
6,832,652 (GRCm38) |
intron |
probably benign |
|
|
R1743:Oprm1
|
UTSW |
10 |
6,830,105 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1874:Oprm1
|
UTSW |
10 |
6,789,035 (GRCm38) |
missense |
probably benign |
0.17 |
|
R2864:Oprm1
|
UTSW |
10 |
6,794,226 (GRCm38) |
splice site |
probably null |
|
|
R2964:Oprm1
|
UTSW |
10 |
6,788,914 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R3792:Oprm1
|
UTSW |
10 |
6,839,544 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4008:Oprm1
|
UTSW |
10 |
6,832,520 (GRCm38) |
missense |
probably benign |
|
|
R4049:Oprm1
|
UTSW |
10 |
6,829,087 (GRCm38) |
missense |
probably benign |
0.36 |
|
R4088:Oprm1
|
UTSW |
10 |
6,830,234 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4724:Oprm1
|
UTSW |
10 |
6,758,656 (GRCm38) |
nonsense |
probably null |
|
|
R4812:Oprm1
|
UTSW |
10 |
6,832,698 (GRCm38) |
intron |
probably benign |
|
|
R4822:Oprm1
|
UTSW |
10 |
6,829,036 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4855:Oprm1
|
UTSW |
10 |
6,838,468 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5072:Oprm1
|
UTSW |
10 |
6,832,550 (GRCm38) |
missense |
probably benign |
0.15 |
|
R5768:Oprm1
|
UTSW |
10 |
6,789,026 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5770:Oprm1
|
UTSW |
10 |
6,789,026 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5995:Oprm1
|
UTSW |
10 |
6,832,520 (GRCm38) |
missense |
probably benign |
|
|
R6327:Oprm1
|
UTSW |
10 |
6,830,063 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7135:Oprm1
|
UTSW |
10 |
6,830,203 (GRCm38) |
missense |
possibly damaging |
0.77 |
|
R7413:Oprm1
|
UTSW |
10 |
6,828,919 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7455:Oprm1
|
UTSW |
10 |
6,830,204 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8192:Oprm1
|
UTSW |
10 |
6,838,417 (GRCm38) |
missense |
probably benign |
0.04 |
|
R8210:Oprm1
|
UTSW |
10 |
6,830,442 (GRCm38) |
missense |
probably benign |
0.02 |
|
R8945:Oprm1
|
UTSW |
10 |
6,832,644 (GRCm38) |
intron |
probably benign |
|
|
R9054:Oprm1
|
UTSW |
10 |
6,823,914 (GRCm38) |
intron |
probably benign |
|
|
R9723:Oprm1
|
UTSW |
10 |
6,838,514 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R9726:Oprm1
|
UTSW |
10 |
6,979,694 (GRCm38) |
missense |
probably benign |
0.00 |
|
X0066:Oprm1
|
UTSW |
10 |
6,830,462 (GRCm38) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGGAACCCGAACACTCTTGAGTGC -3'
(R):5'- AGCTCATCCAGAGGGAGGATTGAC -3'
Sequencing Primer
(F):5'- AGTGCTCTCAGTTACAGCC -3'
(R):5'- CCTGCGGAACTAGGTATTCAG -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation