Incidental Mutation 'R9589:Or51a39'
| ID |
722933 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or51a39
|
| Ensembl Gene |
ENSMUSG00000066273 |
| Gene Name |
olfactory receptor family 51 subfamily A member 39 |
| Synonyms |
MTPCR33, MOR11-2, GA_x6K02T2PBJ9-5431102-5430146, Olfr33 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.185)
|
| Stock # |
R9589 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
7 |
| Chromosomal Location |
102362662-102363618 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 102363372 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 83
(T83A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149588
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084817]
[ENSMUST00000094124]
[ENSMUST00000216312]
|
| AlphaFold |
Q8VGX7 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000084817
AA Change: T83A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000081877
Gene: ENSMUSG00000066273
AA Change: T83A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
37 |
317 |
2.1e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
41 |
211 |
7.5e-11 |
PFAM |
|
Pfam:7tm_1
|
47 |
299 |
2.4e-19 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000094124
|
| SMART Domains |
Protein: ENSMUSP00000091674
Gene: ENSMUSG00000070423
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
33 |
311 |
6.2e-117 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
308 |
2.4e-7 |
PFAM |
|
Pfam:7tm_1
|
43 |
293 |
2.4e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216312
AA Change: T83A
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrg3 |
A |
G |
8: 95,760,093 (GRCm39) |
D104G |
possibly damaging |
Het |
| Ahnak2 |
G |
T |
12: 112,746,831 (GRCm39) |
D1166E |
|
Het |
| C2cd3 |
T |
A |
7: 100,081,756 (GRCm39) |
S1133T |
|
Het |
| Ccdc17 |
A |
G |
4: 116,454,791 (GRCm39) |
Q168R |
probably benign |
Het |
| Fn1 |
A |
T |
1: 71,668,941 (GRCm39) |
I668N |
probably damaging |
Het |
| Fyb2 |
C |
A |
4: 104,872,833 (GRCm39) |
N735K |
probably damaging |
Het |
| Gad1 |
T |
C |
2: 70,416,284 (GRCm39) |
S248P |
possibly damaging |
Het |
| Gcnt1 |
G |
A |
19: 17,307,422 (GRCm39) |
A101V |
probably benign |
Het |
| Herc1 |
T |
A |
9: 66,372,840 (GRCm39) |
M3132K |
possibly damaging |
Het |
| Htra3 |
T |
C |
5: 35,821,409 (GRCm39) |
I323V |
probably damaging |
Het |
| Ighv11-2 |
A |
T |
12: 114,012,047 (GRCm39) |
V56D |
probably damaging |
Het |
| Itga8 |
C |
T |
2: 12,237,701 (GRCm39) |
G340R |
probably damaging |
Het |
| Kcnk15 |
C |
T |
2: 163,700,127 (GRCm39) |
T122M |
probably damaging |
Het |
| Kif13a |
G |
T |
13: 46,956,020 (GRCm39) |
Q658K |
probably benign |
Het |
| Kif13b |
T |
C |
14: 65,013,759 (GRCm39) |
I1303T |
possibly damaging |
Het |
| Kifc3 |
A |
T |
8: 95,861,372 (GRCm39) |
S94R |
possibly damaging |
Het |
| Lrrc63 |
A |
T |
14: 75,322,379 (GRCm39) |
F575Y |
possibly damaging |
Het |
| Map1a |
T |
C |
2: 121,136,398 (GRCm39) |
S2405P |
probably damaging |
Het |
| Map2 |
A |
G |
1: 66,449,753 (GRCm39) |
T159A |
probably benign |
Het |
| Mgam |
A |
T |
6: 40,727,519 (GRCm39) |
I1315F |
probably damaging |
Het |
| Pah |
T |
A |
10: 87,403,197 (GRCm39) |
F191I |
probably damaging |
Het |
| Plekhh2 |
G |
A |
17: 84,854,918 (GRCm39) |
D51N |
possibly damaging |
Het |
| Ppp4r2 |
C |
T |
6: 100,838,409 (GRCm39) |
T109M |
probably damaging |
Het |
| Rfx7 |
T |
C |
9: 72,525,122 (GRCm39) |
S771P |
possibly damaging |
Het |
| Sec11a |
T |
C |
7: 80,565,899 (GRCm39) |
*171W |
probably null |
Het |
| Secisbp2l |
C |
A |
2: 125,589,425 (GRCm39) |
V708L |
probably benign |
Het |
| Secisbp2l |
T |
G |
2: 125,589,430 (GRCm39) |
D706A |
probably damaging |
Het |
| Shpk |
C |
T |
11: 73,104,267 (GRCm39) |
P139S |
possibly damaging |
Het |
| Slc6a18 |
A |
G |
13: 73,816,323 (GRCm39) |
L352P |
possibly damaging |
Het |
| Slitrk3 |
T |
C |
3: 72,957,981 (GRCm39) |
T264A |
probably benign |
Het |
| Smg9 |
T |
G |
7: 24,120,246 (GRCm39) |
S407A |
probably damaging |
Het |
| Stmn4 |
A |
G |
14: 66,595,338 (GRCm39) |
E121G |
probably damaging |
Het |
| Tmem237 |
G |
A |
1: 59,159,146 (GRCm39) |
P10S |
probably benign |
Het |
| Vmn2r73 |
A |
G |
7: 85,519,659 (GRCm39) |
I433T |
probably benign |
Het |
| Zfp28 |
T |
A |
7: 6,392,816 (GRCm39) |
M164K |
probably benign |
Het |
| Zswim8 |
A |
G |
14: 20,763,171 (GRCm39) |
M357V |
probably damaging |
Het |
|
| Other mutations in Or51a39 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02064:Or51a39
|
APN |
7 |
102,362,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02349:Or51a39
|
APN |
7 |
102,363,333 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02739:Or51a39
|
APN |
7 |
102,363,521 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
IGL03110:Or51a39
|
APN |
7 |
102,363,090 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03014:Or51a39
|
UTSW |
7 |
102,362,753 (GRCm39) |
missense |
probably null |
0.91 |
|
R0158:Or51a39
|
UTSW |
7 |
102,363,162 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1455:Or51a39
|
UTSW |
7 |
102,363,205 (GRCm39) |
nonsense |
probably null |
|
|
R1996:Or51a39
|
UTSW |
7 |
102,362,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2032:Or51a39
|
UTSW |
7 |
102,363,083 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2152:Or51a39
|
UTSW |
7 |
102,362,788 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4852:Or51a39
|
UTSW |
7 |
102,362,750 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4965:Or51a39
|
UTSW |
7 |
102,362,702 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5264:Or51a39
|
UTSW |
7 |
102,363,558 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5464:Or51a39
|
UTSW |
7 |
102,362,889 (GRCm39) |
missense |
probably benign |
|
|
R6680:Or51a39
|
UTSW |
7 |
102,363,522 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R7195:Or51a39
|
UTSW |
7 |
102,362,873 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R7373:Or51a39
|
UTSW |
7 |
102,363,306 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7391:Or51a39
|
UTSW |
7 |
102,363,189 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7872:Or51a39
|
UTSW |
7 |
102,363,389 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7948:Or51a39
|
UTSW |
7 |
102,362,895 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8097:Or51a39
|
UTSW |
7 |
102,363,197 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8969:Or51a39
|
UTSW |
7 |
102,363,558 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9349:Or51a39
|
UTSW |
7 |
102,362,875 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CAAAGTAGCTCGGGTTGTAATGG -3'
(R):5'- AGTTTGCTCATGGCTGGATC -3'
Sequencing Primer
(F):5'- CCCAATCCTGATGATGACATTG -3'
(R):5'- GCTCATGGCTGGATCTCCATC -3'
|
| Posted On |
2022-08-09 |
Incidental Mutation