Incidental Mutation 'R4855:Oprm1'
ID |
373896 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Oprm1
|
Ensembl Gene |
ENSMUSG00000000766 |
Gene Name |
opioid receptor, mu 1 |
Synonyms |
MOP-R, MOR-1, MOP receptor, mor, Oprm, muOR |
MMRRC Submission |
042466-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.110)
|
Stock # |
R4855 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
10 |
Chromosomal Location |
6708593-6988209 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 6788468 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Serine
at position 408
(C408S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000000783
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000783]
[ENSMUST00000052751]
[ENSMUST00000056385]
[ENSMUST00000063036]
[ENSMUST00000092729]
[ENSMUST00000092731]
[ENSMUST00000092734]
[ENSMUST00000147171]
[ENSMUST00000105607]
[ENSMUST00000105615]
[ENSMUST00000123861]
[ENSMUST00000129954]
[ENSMUST00000105597]
[ENSMUST00000105605]
[ENSMUST00000129221]
[ENSMUST00000105601]
[ENSMUST00000105604]
[ENSMUST00000144264]
[ENSMUST00000105611]
[ENSMUST00000135502]
[ENSMUST00000150374]
[ENSMUST00000152674]
[ENSMUST00000154906]
[ENSMUST00000154941]
|
AlphaFold |
P42866 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000000783
AA Change: C408S
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
SMART Domains |
Protein: ENSMUSP00000000783 Gene: ENSMUSG00000000766 AA Change: C408S
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
|
SMART Domains |
Protein: ENSMUSP00000060329 Gene: ENSMUSG00000000766
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
|
SMART Domains |
Protein: ENSMUSP00000060590 Gene: ENSMUSG00000000766
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: ENSMUST00000092729
|
SMART Domains |
Protein: ENSMUSP00000090405 Gene: ENSMUSG00000000766
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
|
SMART Domains |
Protein: ENSMUSP00000090407 Gene: ENSMUSG00000000766
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
|
SMART Domains |
Protein: ENSMUSP00000090410 Gene: ENSMUSG00000000766
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 |
noncoding transcript
Transcript: ENSMUST00000141897
|
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: ENSMUST00000105607
|
SMART Domains |
Protein: ENSMUSP00000101232 Gene: ENSMUSG00000000766
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: 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: ENSMUST00000123861
|
SMART Domains |
Protein: ENSMUSP00000120187 Gene: ENSMUSG00000000766
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: ENSMUST00000129954
|
SMART Domains |
Protein: ENSMUSP00000122385 Gene: ENSMUSG00000000766
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: ENSMUST00000105597
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105605
|
SMART Domains |
Protein: ENSMUSP00000101230 Gene: ENSMUSG00000000766
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: 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 benign
Transcript: ENSMUST00000105601
|
SMART Domains |
Protein: ENSMUSP00000101226 Gene: ENSMUSG00000000766
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: ENSMUST00000105604
|
SMART Domains |
Protein: ENSMUSP00000101229 Gene: ENSMUSG00000000766
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
|
SMART Domains |
Protein: ENSMUSP00000115836 Gene: ENSMUSG00000000766
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
|
SMART Domains |
Protein: ENSMUSP00000101236 Gene: ENSMUSG00000000766
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
|
SMART Domains |
Protein: ENSMUSP00000135143 Gene: ENSMUSG00000000766
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 |
noncoding transcript
Transcript: ENSMUST00000148625
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150374
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152674
|
SMART Domains |
Protein: ENSMUSP00000115552 Gene: ENSMUSG00000000766
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: ENSMUST00000154906
|
SMART Domains |
Protein: ENSMUSP00000114342 Gene: ENSMUSG00000000766
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 |
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 |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.5%
|
Validation Efficiency |
98% (93/95) |
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: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Adad1 |
G |
T |
3: 37,139,260 (GRCm39) |
L443F |
probably damaging |
Het |
Amph |
T |
A |
13: 19,268,378 (GRCm39) |
M70K |
probably damaging |
Het |
Ankra2 |
T |
A |
13: 98,409,919 (GRCm39) |
L306H |
probably damaging |
Het |
Arc |
A |
C |
15: 74,543,592 (GRCm39) |
D210E |
probably benign |
Het |
Arhgap10 |
A |
G |
8: 78,159,367 (GRCm39) |
|
probably null |
Het |
Atp8b5 |
T |
A |
4: 43,344,449 (GRCm39) |
N445K |
probably benign |
Het |
C1qc |
G |
T |
4: 136,617,746 (GRCm39) |
Q117K |
probably benign |
Het |
Cadps |
T |
A |
14: 12,822,449 (GRCm38) |
E97V |
unknown |
Het |
Capn13 |
GCA |
G |
17: 73,658,501 (GRCm39) |
|
probably null |
Het |
Cdk13 |
A |
T |
13: 17,895,868 (GRCm39) |
W1014R |
probably damaging |
Het |
Cltb |
C |
T |
13: 54,746,908 (GRCm39) |
E23K |
probably damaging |
Het |
Clvs2 |
A |
T |
10: 33,498,642 (GRCm39) |
I96N |
probably damaging |
Het |
Cwf19l1 |
A |
G |
19: 44,103,006 (GRCm39) |
V403A |
probably damaging |
Het |
Ddr2 |
A |
T |
1: 169,816,066 (GRCm39) |
L547Q |
possibly damaging |
Het |
Ebf1 |
A |
T |
11: 44,863,735 (GRCm39) |
K354* |
probably null |
Het |
Fat4 |
A |
G |
3: 38,942,466 (GRCm39) |
Q453R |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gata6 |
A |
G |
18: 11,054,497 (GRCm39) |
E142G |
possibly damaging |
Het |
Gm14221 |
T |
C |
2: 160,416,600 (GRCm39) |
|
noncoding transcript |
Het |
Gm42791 |
C |
A |
5: 148,896,247 (GRCm39) |
|
probably benign |
Het |
Gm6370 |
G |
T |
5: 146,430,621 (GRCm39) |
V269L |
probably benign |
Het |
Gphn |
G |
A |
12: 78,673,984 (GRCm39) |
V526M |
probably damaging |
Het |
Gpt |
A |
T |
15: 76,583,485 (GRCm39) |
E206V |
probably damaging |
Het |
Grm3 |
G |
A |
5: 9,620,047 (GRCm39) |
A399V |
probably damaging |
Het |
Helq |
A |
T |
5: 100,931,025 (GRCm39) |
V575E |
possibly damaging |
Het |
Herc4 |
A |
G |
10: 63,151,437 (GRCm39) |
|
probably null |
Het |
Ifi207 |
A |
T |
1: 173,557,381 (GRCm39) |
N452K |
probably damaging |
Het |
Ikbke |
A |
G |
1: 131,184,848 (GRCm39) |
|
probably null |
Het |
Kbtbd2 |
A |
G |
6: 56,756,687 (GRCm39) |
F350L |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,519,555 (GRCm39) |
V2185A |
probably benign |
Het |
Lgi2 |
T |
C |
5: 52,695,849 (GRCm39) |
Q362R |
probably damaging |
Het |
Lrit1 |
G |
A |
14: 36,783,773 (GRCm39) |
G367E |
possibly damaging |
Het |
Lrp1 |
G |
A |
10: 127,446,311 (GRCm39) |
H78Y |
probably benign |
Het |
Matk |
A |
G |
10: 81,098,720 (GRCm39) |
|
probably benign |
Het |
Med21 |
G |
A |
6: 146,549,690 (GRCm39) |
G24S |
probably damaging |
Het |
Met |
G |
T |
6: 17,558,796 (GRCm39) |
L1141F |
probably damaging |
Het |
Mroh3 |
A |
T |
1: 136,128,677 (GRCm39) |
|
probably null |
Het |
Mrpl15 |
T |
C |
1: 4,844,683 (GRCm39) |
I203V |
probably benign |
Het |
Naip1 |
T |
C |
13: 100,559,728 (GRCm39) |
|
probably null |
Het |
Ndufa9 |
A |
C |
6: 126,804,505 (GRCm39) |
Y298* |
probably null |
Het |
Neb |
T |
C |
2: 52,188,906 (GRCm39) |
E808G |
probably damaging |
Het |
Nol4l |
C |
T |
2: 153,253,726 (GRCm39) |
G616S |
probably benign |
Het |
Or2ag18 |
T |
C |
7: 106,405,463 (GRCm39) |
M69V |
probably benign |
Het |
Or4f14 |
A |
G |
2: 111,742,444 (GRCm39) |
V277A |
probably benign |
Het |
Or4k42 |
T |
G |
2: 111,320,293 (GRCm39) |
D70A |
probably damaging |
Het |
Or52e7 |
T |
A |
7: 104,684,858 (GRCm39) |
I151N |
probably damaging |
Het |
Or5ak20 |
T |
C |
2: 85,183,793 (GRCm39) |
N159S |
possibly damaging |
Het |
Paqr3 |
A |
G |
5: 97,256,053 (GRCm39) |
I107T |
possibly damaging |
Het |
Pex5l |
G |
A |
3: 33,196,989 (GRCm39) |
|
probably benign |
Het |
Phf8-ps |
C |
T |
17: 33,285,713 (GRCm39) |
S363N |
probably benign |
Het |
Pik3ap1 |
T |
C |
19: 41,316,284 (GRCm39) |
D326G |
probably benign |
Het |
Plaa |
G |
T |
4: 94,474,645 (GRCm39) |
D252E |
probably damaging |
Het |
Plxna2 |
G |
A |
1: 194,480,040 (GRCm39) |
V1404I |
probably benign |
Het |
Ppargc1a |
G |
A |
5: 51,631,564 (GRCm39) |
A355V |
possibly damaging |
Het |
Primpol |
A |
G |
8: 47,039,726 (GRCm39) |
S350P |
probably benign |
Het |
Prlr |
T |
C |
15: 10,328,883 (GRCm39) |
S453P |
probably benign |
Het |
Psmd5 |
T |
C |
2: 34,742,564 (GRCm39) |
|
probably benign |
Het |
Robo2 |
A |
T |
16: 73,768,079 (GRCm39) |
V571E |
probably damaging |
Het |
Sbspon |
A |
T |
1: 15,929,264 (GRCm39) |
S176T |
possibly damaging |
Het |
Scyl2 |
G |
A |
10: 89,476,325 (GRCm39) |
|
probably benign |
Het |
Sema3e |
T |
A |
5: 14,280,144 (GRCm39) |
V341E |
probably damaging |
Het |
Serpinb3b |
A |
T |
1: 107,082,270 (GRCm39) |
F331L |
possibly damaging |
Het |
Setd2 |
A |
G |
9: 110,401,022 (GRCm39) |
H1736R |
probably benign |
Het |
Sidt2 |
A |
T |
9: 45,863,327 (GRCm39) |
D180E |
probably benign |
Het |
Skint9 |
A |
T |
4: 112,248,208 (GRCm39) |
Y179N |
probably benign |
Het |
Slc27a5 |
T |
C |
7: 12,722,560 (GRCm39) |
N638S |
probably benign |
Het |
Slc6a4 |
T |
A |
11: 76,904,135 (GRCm39) |
W197R |
probably damaging |
Het |
Spag17 |
A |
T |
3: 99,970,649 (GRCm39) |
M1278L |
probably benign |
Het |
Sptbn1 |
T |
A |
11: 30,092,353 (GRCm39) |
I471F |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,616,680 (GRCm39) |
|
probably null |
Het |
Teddm1a |
A |
G |
1: 153,768,382 (GRCm39) |
Q282R |
probably benign |
Het |
Tex35 |
A |
G |
1: 156,927,295 (GRCm39) |
L160P |
probably damaging |
Het |
Tfap2c |
T |
C |
2: 172,393,438 (GRCm39) |
Y118H |
probably damaging |
Het |
Tpp1 |
T |
C |
7: 105,395,930 (GRCm39) |
Q533R |
probably benign |
Het |
Ttc13 |
C |
T |
8: 125,401,174 (GRCm39) |
D730N |
probably damaging |
Het |
Ufc1 |
A |
G |
1: 171,122,375 (GRCm39) |
|
probably benign |
Het |
Vcpip1 |
A |
G |
1: 9,817,589 (GRCm39) |
W265R |
probably damaging |
Het |
Wdr11 |
C |
G |
7: 129,202,158 (GRCm39) |
|
probably null |
Het |
Xirp2 |
A |
G |
2: 67,341,408 (GRCm39) |
I1216M |
possibly damaging |
Het |
Zswim2 |
A |
G |
2: 83,747,187 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Oprm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01018:Oprm1
|
APN |
10 |
6,987,170 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01768:Oprm1
|
APN |
10 |
6,779,186 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Oprm1
|
APN |
10 |
6,780,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Oprm1
|
APN |
10 |
6,964,077 (GRCm39) |
intron |
probably benign |
|
IGL03410:Oprm1
|
APN |
10 |
6,780,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03048:Oprm1
|
UTSW |
10 |
6,779,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0189:Oprm1
|
UTSW |
10 |
6,739,071 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0321:Oprm1
|
UTSW |
10 |
6,779,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R0629:Oprm1
|
UTSW |
10 |
6,782,604 (GRCm39) |
splice site |
probably null |
|
R0730:Oprm1
|
UTSW |
10 |
6,782,652 (GRCm39) |
intron |
probably benign |
|
R1542:Oprm1
|
UTSW |
10 |
6,738,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Oprm1
|
UTSW |
10 |
6,780,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R1874:Oprm1
|
UTSW |
10 |
6,739,035 (GRCm39) |
missense |
probably benign |
0.17 |
R2864:Oprm1
|
UTSW |
10 |
6,744,226 (GRCm39) |
splice site |
probably null |
|
R2964:Oprm1
|
UTSW |
10 |
6,738,914 (GRCm39) |
missense |
probably damaging |
0.98 |
R3792:Oprm1
|
UTSW |
10 |
6,789,544 (GRCm39) |
missense |
probably benign |
0.00 |
R4008:Oprm1
|
UTSW |
10 |
6,782,520 (GRCm39) |
missense |
probably benign |
|
R4049:Oprm1
|
UTSW |
10 |
6,779,087 (GRCm39) |
missense |
probably benign |
0.36 |
R4088:Oprm1
|
UTSW |
10 |
6,780,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Oprm1
|
UTSW |
10 |
6,708,656 (GRCm39) |
nonsense |
probably null |
|
R4812:Oprm1
|
UTSW |
10 |
6,782,698 (GRCm39) |
intron |
probably benign |
|
R4822:Oprm1
|
UTSW |
10 |
6,779,036 (GRCm39) |
missense |
probably damaging |
0.99 |
R5072:Oprm1
|
UTSW |
10 |
6,782,550 (GRCm39) |
missense |
probably benign |
0.15 |
R5768:Oprm1
|
UTSW |
10 |
6,739,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5770:Oprm1
|
UTSW |
10 |
6,739,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Oprm1
|
UTSW |
10 |
6,782,520 (GRCm39) |
missense |
probably benign |
|
R6327:Oprm1
|
UTSW |
10 |
6,780,063 (GRCm39) |
missense |
probably damaging |
0.99 |
R7135:Oprm1
|
UTSW |
10 |
6,780,203 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7413:Oprm1
|
UTSW |
10 |
6,778,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Oprm1
|
UTSW |
10 |
6,780,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Oprm1
|
UTSW |
10 |
6,788,417 (GRCm39) |
missense |
probably benign |
0.04 |
R8210:Oprm1
|
UTSW |
10 |
6,780,442 (GRCm39) |
missense |
probably benign |
0.02 |
R8945:Oprm1
|
UTSW |
10 |
6,782,644 (GRCm39) |
intron |
probably benign |
|
R9054:Oprm1
|
UTSW |
10 |
6,773,914 (GRCm39) |
intron |
probably benign |
|
R9723:Oprm1
|
UTSW |
10 |
6,788,514 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9726:Oprm1
|
UTSW |
10 |
6,929,694 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Oprm1
|
UTSW |
10 |
6,780,462 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCTCTTTGATCCTAGAATGAAAGC -3'
(R):5'- ACCCATTTCAGCACTATGAGAAG -3'
Sequencing Primer
(F):5'- TCATTTGTCTATAGGAAGGAAGGG -3'
(R):5'- CCATTTCAGCACTATGAGAAGTTATC -3'
|
Posted On |
2016-03-01 |