Incidental Mutation 'R5242:Or51a25'
| ID |
400920 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or51a25
|
| Ensembl Gene |
ENSMUSG00000066272 |
| Gene Name |
olfactory receptor family 51 subfamily A member 25 |
| Synonyms |
MOR11-1, Olfr559, GA_x6K02T2PBJ9-5441154-5440198 |
| MMRRC Submission |
042813-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.068)
|
| Stock # |
R5242 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
102372739-102373695 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 102373483 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Isoleucine
at position 71
(M71I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151100
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084816]
[ENSMUST00000215657]
|
| AlphaFold |
Q8VH14 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000084816
AA Change: M71I
PolyPhen 2
Score 0.411 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000095820
Gene: ENSMUSG00000066272
AA Change: M71I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
37 |
317 |
1.1e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
41 |
215 |
1e-10 |
PFAM |
|
Pfam:7tm_1
|
47 |
299 |
3e-18 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215657
AA Change: M71I
PolyPhen 2
Score 0.411 (Sensitivity: 0.89; Specificity: 0.90)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 43 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrl1 |
T |
C |
8: 84,657,711 (GRCm39) |
V439A |
possibly damaging |
Het |
| Aldh6a1 |
A |
G |
12: 84,483,157 (GRCm39) |
V390A |
probably damaging |
Het |
| Alox5 |
T |
C |
6: 116,437,927 (GRCm39) |
D20G |
probably damaging |
Het |
| Atp2a2 |
A |
T |
5: 122,600,009 (GRCm39) |
F487I |
probably damaging |
Het |
| BC048679 |
G |
A |
7: 81,145,091 (GRCm39) |
T84M |
probably damaging |
Het |
| C2cd3 |
T |
C |
7: 100,039,373 (GRCm39) |
S191P |
probably benign |
Het |
| Cdh6 |
A |
G |
15: 13,064,497 (GRCm39) |
V131A |
probably benign |
Het |
| Chrna9 |
A |
G |
5: 66,134,423 (GRCm39) |
T425A |
probably benign |
Het |
| Cplane2 |
T |
C |
4: 140,947,158 (GRCm39) |
Y180H |
probably damaging |
Het |
| Ddx39a |
A |
G |
8: 84,448,440 (GRCm39) |
S231G |
probably benign |
Het |
| Diaph1 |
C |
T |
18: 37,984,688 (GRCm39) |
G1176R |
probably damaging |
Het |
| Dnah10 |
G |
T |
5: 124,864,484 (GRCm39) |
V2230L |
probably benign |
Het |
| Foxo1 |
T |
C |
3: 52,176,676 (GRCm39) |
S152P |
probably damaging |
Het |
| Fras1 |
T |
A |
5: 96,805,109 (GRCm39) |
D1250E |
probably benign |
Het |
| G6pd2 |
A |
G |
5: 61,966,785 (GRCm39) |
I187V |
probably benign |
Het |
| Gm10113 |
T |
C |
13: 46,330,992 (GRCm39) |
|
noncoding transcript |
Het |
| Hoxd1 |
A |
G |
2: 74,593,792 (GRCm39) |
D116G |
probably damaging |
Het |
| Igkv13-85 |
A |
T |
6: 68,907,544 (GRCm39) |
I19K |
probably benign |
Het |
| Jag2 |
C |
T |
12: 112,880,486 (GRCm39) |
V288M |
probably damaging |
Het |
| Ndrg2 |
A |
G |
14: 52,148,541 (GRCm39) |
|
probably null |
Het |
| Neurl3 |
G |
A |
1: 36,308,501 (GRCm39) |
Q104* |
probably null |
Het |
| Nudt16l1 |
C |
T |
16: 4,757,485 (GRCm39) |
R133W |
probably damaging |
Het |
| Oasl2 |
A |
T |
5: 115,043,122 (GRCm39) |
Q298L |
possibly damaging |
Het |
| Or3a10 |
A |
T |
11: 73,935,848 (GRCm39) |
M84K |
possibly damaging |
Het |
| Pnma2 |
C |
A |
14: 67,153,746 (GRCm39) |
Q57K |
probably benign |
Het |
| Pramel22 |
A |
T |
4: 143,382,181 (GRCm39) |
L172I |
probably benign |
Het |
| Rps7 |
T |
A |
12: 28,681,136 (GRCm39) |
E188D |
probably benign |
Het |
| Rrp1b |
T |
C |
17: 32,270,677 (GRCm39) |
V212A |
possibly damaging |
Het |
| Serpina9 |
C |
A |
12: 103,974,644 (GRCm39) |
A170S |
probably benign |
Het |
| Shmt2 |
C |
T |
10: 127,354,789 (GRCm39) |
V299I |
probably benign |
Het |
| Siae |
C |
T |
9: 37,556,148 (GRCm39) |
P435S |
probably damaging |
Het |
| Smarcal1 |
T |
C |
1: 72,630,242 (GRCm39) |
S99P |
probably benign |
Het |
| Sntb1 |
C |
G |
15: 55,506,191 (GRCm39) |
G461R |
probably damaging |
Het |
| Stimate |
T |
A |
14: 30,547,793 (GRCm39) |
F36I |
probably damaging |
Het |
| Tas2r124 |
T |
C |
6: 132,732,503 (GRCm39) |
Y271H |
possibly damaging |
Het |
| Thsd7a |
A |
T |
6: 12,327,582 (GRCm39) |
I1430K |
probably damaging |
Het |
| Trmt9b |
A |
G |
8: 36,979,084 (GRCm39) |
K229R |
probably benign |
Het |
| Tsc22d2 |
T |
A |
3: 58,323,360 (GRCm39) |
V84E |
possibly damaging |
Het |
| Ube2s |
C |
T |
7: 4,813,434 (GRCm39) |
R110Q |
possibly damaging |
Het |
| Usp3 |
C |
T |
9: 66,434,432 (GRCm39) |
C283Y |
probably damaging |
Het |
| Vmn2r81 |
T |
A |
10: 79,129,309 (GRCm39) |
Y733* |
probably null |
Het |
| Wdr75 |
T |
A |
1: 45,856,487 (GRCm39) |
C503* |
probably null |
Het |
| Zfp764 |
T |
C |
7: 127,004,541 (GRCm39) |
M197V |
probably benign |
Het |
|
| Other mutations in Or51a25 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02832:Or51a25
|
APN |
7 |
102,372,858 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0505:Or51a25
|
UTSW |
7 |
102,373,236 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1131:Or51a25
|
UTSW |
7 |
102,372,887 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1449:Or51a25
|
UTSW |
7 |
102,373,397 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3788:Or51a25
|
UTSW |
7 |
102,372,694 (GRCm39) |
splice site |
probably null |
|
|
R3915:Or51a25
|
UTSW |
7 |
102,373,409 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3980:Or51a25
|
UTSW |
7 |
102,372,959 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4647:Or51a25
|
UTSW |
7 |
102,373,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5404:Or51a25
|
UTSW |
7 |
102,372,807 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5464:Or51a25
|
UTSW |
7 |
102,373,124 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5807:Or51a25
|
UTSW |
7 |
102,373,409 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5965:Or51a25
|
UTSW |
7 |
102,373,467 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6008:Or51a25
|
UTSW |
7 |
102,373,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6036:Or51a25
|
UTSW |
7 |
102,373,692 (GRCm39) |
missense |
probably benign |
|
|
R6036:Or51a25
|
UTSW |
7 |
102,373,692 (GRCm39) |
missense |
probably benign |
|
|
R6493:Or51a25
|
UTSW |
7 |
102,373,287 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6756:Or51a25
|
UTSW |
7 |
102,373,295 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7201:Or51a25
|
UTSW |
7 |
102,373,692 (GRCm39) |
missense |
probably benign |
|
|
R7460:Or51a25
|
UTSW |
7 |
102,373,028 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7695:Or51a25
|
UTSW |
7 |
102,372,866 (GRCm39) |
missense |
probably benign |
0.37 |
|
R8145:Or51a25
|
UTSW |
7 |
102,372,937 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8371:Or51a25
|
UTSW |
7 |
102,372,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8499:Or51a25
|
UTSW |
7 |
102,372,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9185:Or51a25
|
UTSW |
7 |
102,373,409 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9230:Or51a25
|
UTSW |
7 |
102,372,795 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
X0025:Or51a25
|
UTSW |
7 |
102,373,022 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TAGCCACAAAGCGGTCAAATG -3'
(R):5'- CCAAGGATGATCCCTTCTGG -3'
Sequencing Primer
(F):5'- GCGGTCAAATGACATGGCC -3'
(R):5'- GGGCCATTCATCAACATCTCC -3'
|
| Posted On |
2016-07-06 |
Incidental Mutation