Incidental Mutation 'R0152:Or5b12'
| ID |
22807 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5b12
|
| Ensembl Gene |
ENSMUSG00000048456 |
| Gene Name |
olfactory receptor family 5 subfamily B member 12 |
| Synonyms |
GA_x6K02T2RE5P-3249780-3248836, MOR202-5, Olfr1448 |
| MMRRC Submission |
038435-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.114)
|
| Stock # |
R0152 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
(trace)
|
| Chromosome |
19 |
| Chromosomal Location |
12896727-12897671 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 12897472 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 67
(V67A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149296
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054737]
[ENSMUST00000213177]
[ENSMUST00000213713]
[ENSMUST00000216888]
|
| AlphaFold |
Q8VFX1 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000054737
AA Change: V67A
PolyPhen 2
Score 0.488 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000055664
Gene: ENSMUSG00000048456
AA Change: V67A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
306 |
3.2e-54 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
1e-21 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000208769
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213177
AA Change: V67A
PolyPhen 2
Score 0.488 (Sensitivity: 0.88; Specificity: 0.90)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213713
AA Change: V67A
PolyPhen 2
Score 0.488 (Sensitivity: 0.88; Specificity: 0.90)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216888
AA Change: V67A
PolyPhen 2
Score 0.488 (Sensitivity: 0.88; Specificity: 0.90)
|
| Meta Mutation Damage Score |
0.1777 |
| Coding Region Coverage |
- 1x: 98.9%
- 3x: 97.9%
- 10x: 95.3%
- 20x: 89.5%
|
| Validation Efficiency |
87% (40/46) |
| 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: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aass |
T |
C |
6: 23,074,688 (GRCm39) |
D834G |
probably damaging |
Het |
| Abca13 |
T |
A |
11: 9,531,724 (GRCm39) |
H4650Q |
probably damaging |
Het |
| Aqr |
T |
A |
2: 113,989,491 (GRCm39) |
T111S |
probably benign |
Het |
| Arfip2 |
G |
A |
7: 105,286,430 (GRCm39) |
T124M |
probably damaging |
Het |
| Arhgap44 |
G |
T |
11: 64,902,745 (GRCm39) |
A574E |
probably benign |
Het |
| Arhgef26 |
T |
C |
3: 62,330,965 (GRCm39) |
S560P |
probably damaging |
Het |
| Car5a |
T |
A |
8: 122,643,185 (GRCm39) |
N273I |
probably damaging |
Het |
| Cd4 |
G |
A |
6: 124,844,709 (GRCm39) |
Q359* |
probably null |
Het |
| Cgrrf1 |
G |
A |
14: 47,091,370 (GRCm39) |
C298Y |
probably damaging |
Het |
| Clip3 |
G |
A |
7: 30,002,857 (GRCm39) |
A416T |
probably benign |
Het |
| Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
| Eif3e |
G |
A |
15: 43,115,632 (GRCm39) |
A378V |
possibly damaging |
Het |
| Ercc6 |
C |
G |
14: 32,268,862 (GRCm39) |
|
probably benign |
Het |
| Eri2 |
A |
G |
7: 119,389,606 (GRCm39) |
V104A |
probably damaging |
Het |
| Exph5 |
T |
A |
9: 53,264,504 (GRCm39) |
|
probably null |
Het |
| Hmcn1 |
A |
T |
1: 150,539,630 (GRCm39) |
Y2954N |
probably benign |
Het |
| Itga2 |
C |
T |
13: 115,002,850 (GRCm39) |
G547R |
probably benign |
Het |
| Kbtbd11 |
T |
C |
8: 15,077,428 (GRCm39) |
V9A |
probably damaging |
Het |
| Ldb2 |
T |
C |
5: 44,699,141 (GRCm39) |
D99G |
possibly damaging |
Het |
| Mfsd12 |
G |
T |
10: 81,193,633 (GRCm39) |
D68Y |
probably damaging |
Het |
| Mgarp |
T |
C |
3: 51,296,384 (GRCm39) |
D228G |
probably benign |
Het |
| Myh14 |
A |
T |
7: 44,272,605 (GRCm39) |
L1441Q |
probably damaging |
Het |
| Obscn |
T |
C |
11: 58,943,402 (GRCm39) |
D4810G |
probably benign |
Het |
| Or10ak9 |
T |
A |
4: 118,726,083 (GRCm39) |
I34N |
possibly damaging |
Het |
| Or14c40 |
A |
T |
7: 86,313,719 (GRCm39) |
Y283F |
probably damaging |
Het |
| Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
| Or8g30 |
A |
G |
9: 39,230,757 (GRCm39) |
I51T |
probably benign |
Het |
| Pdhx |
A |
G |
2: 102,858,625 (GRCm39) |
V393A |
probably benign |
Het |
| Pdpk1 |
C |
T |
17: 24,325,920 (GRCm39) |
R92H |
possibly damaging |
Het |
| Pgr |
A |
T |
9: 8,965,023 (GRCm39) |
I889F |
probably benign |
Het |
| Pum2 |
T |
A |
12: 8,778,754 (GRCm39) |
I468K |
possibly damaging |
Het |
| Recql5 |
A |
G |
11: 115,785,499 (GRCm39) |
S666P |
probably benign |
Het |
| Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
| Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
| Slc26a4 |
T |
C |
12: 31,579,497 (GRCm39) |
I588M |
probably damaging |
Het |
| Slc9a2 |
A |
G |
1: 40,781,964 (GRCm39) |
T398A |
probably damaging |
Het |
| Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
| Tub |
A |
T |
7: 108,620,134 (GRCm39) |
N93Y |
probably damaging |
Het |
| Usp3 |
T |
C |
9: 66,447,432 (GRCm39) |
T181A |
probably damaging |
Het |
| Vars2 |
A |
G |
17: 35,970,919 (GRCm39) |
L637P |
probably damaging |
Het |
| Vmn2r1 |
T |
C |
3: 63,989,240 (GRCm39) |
S60P |
possibly damaging |
Het |
| Wdcp |
A |
G |
12: 4,901,583 (GRCm39) |
S480G |
probably benign |
Het |
| Zbtb38 |
T |
C |
9: 96,568,333 (GRCm39) |
Y917C |
probably damaging |
Het |
| Zfp68 |
T |
C |
5: 138,604,875 (GRCm39) |
K445E |
probably damaging |
Het |
| Zmynd10 |
A |
G |
9: 107,428,144 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Or5b12 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01318:Or5b12
|
APN |
19 |
12,897,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01730:Or5b12
|
APN |
19 |
12,896,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01901:Or5b12
|
APN |
19 |
12,896,947 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02055:Or5b12
|
APN |
19 |
12,896,930 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R0311:Or5b12
|
UTSW |
19 |
12,897,460 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0349:Or5b12
|
UTSW |
19 |
12,897,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1873:Or5b12
|
UTSW |
19 |
12,896,852 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2371:Or5b12
|
UTSW |
19 |
12,897,031 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3548:Or5b12
|
UTSW |
19 |
12,897,031 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4697:Or5b12
|
UTSW |
19 |
12,897,298 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5482:Or5b12
|
UTSW |
19 |
12,897,269 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5748:Or5b12
|
UTSW |
19 |
12,897,379 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5749:Or5b12
|
UTSW |
19 |
12,897,589 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5795:Or5b12
|
UTSW |
19 |
12,897,188 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5952:Or5b12
|
UTSW |
19 |
12,897,194 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6228:Or5b12
|
UTSW |
19 |
12,897,301 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6273:Or5b12
|
UTSW |
19 |
12,896,764 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6341:Or5b12
|
UTSW |
19 |
12,896,843 (GRCm39) |
missense |
probably benign |
0.29 |
|
R6343:Or5b12
|
UTSW |
19 |
12,896,946 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6454:Or5b12
|
UTSW |
19 |
12,897,395 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7666:Or5b12
|
UTSW |
19 |
12,897,526 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7810:Or5b12
|
UTSW |
19 |
12,897,229 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7859:Or5b12
|
UTSW |
19 |
12,897,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7869:Or5b12
|
UTSW |
19 |
12,896,911 (GRCm39) |
missense |
probably benign |
0.26 |
|
R8518:Or5b12
|
UTSW |
19 |
12,896,959 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9011:Or5b12
|
UTSW |
19 |
12,897,479 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9043:Or5b12
|
UTSW |
19 |
12,897,667 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9162:Or5b12
|
UTSW |
19 |
12,897,024 (GRCm39) |
nonsense |
probably null |
|
|
R9273:Or5b12
|
UTSW |
19 |
12,897,446 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9279:Or5b12
|
UTSW |
19 |
12,897,309 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGCTGCATAGCGGTCATAAGCC -3'
(R):5'- TGCTGGAAAGGAACATTGCATCCTG -3'
Sequencing Primer
(F):5'- CATGGCAGCCAAGAGAAAGC -3'
(R):5'- TCTCTTTGATACAGGGCAGC -3'
|
| Posted On |
2013-04-16 |
Incidental Mutation