Incidental Mutation 'IGL03291:Or51ah3'
| ID |
415900 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or51ah3
|
| Ensembl Gene |
ENSMUSG00000073947 |
| Gene Name |
olfactory receptor family 51 subfamily AH member 3 |
| Synonyms |
MOR19-2, GA_x6K02T2PBJ9-6284902-6285843, Olfr615 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.051)
|
| Stock # |
IGL03291
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
103209686-103210627 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 103210119 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Lysine
at position 145
(M145K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150166
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098198]
[ENSMUST00000106886]
[ENSMUST00000214345]
[ENSMUST00000214806]
[ENSMUST00000215673]
[ENSMUST00000217293]
|
| AlphaFold |
Q8VGY4 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000098198
AA Change: M145K
PolyPhen 2
Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000095800
Gene: ENSMUSG00000073947
AA Change: M145K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
32 |
311 |
2.5e-105 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
36 |
253 |
8.5e-9 |
PFAM |
|
Pfam:7tm_1
|
42 |
293 |
8.2e-23 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000106886
|
| SMART Domains |
Protein: ENSMUSP00000102499
Gene: ENSMUSG00000047544
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
22 |
N/A |
INTRINSIC |
|
Pfam:7tm_4
|
33 |
311 |
1.1e-116 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
37 |
309 |
1.2e-6 |
PFAM |
|
Pfam:7tm_1
|
43 |
294 |
4.3e-19 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214345
AA Change: M145K
PolyPhen 2
Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214806
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215673
AA Change: M145K
PolyPhen 2
Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217293
|
| Coding Region Coverage |
|
| 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: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ano1 |
T |
A |
7: 144,175,412 (GRCm39) |
E502V |
probably damaging |
Het |
| Atic |
T |
C |
1: 71,610,081 (GRCm39) |
V364A |
probably benign |
Het |
| Cfap44 |
A |
T |
16: 44,227,674 (GRCm39) |
H125L |
possibly damaging |
Het |
| Ctnna2 |
T |
A |
6: 76,950,695 (GRCm39) |
E227V |
probably damaging |
Het |
| Ctsf |
A |
G |
19: 4,909,662 (GRCm39) |
I378V |
probably benign |
Het |
| Eya1 |
C |
T |
1: 14,254,572 (GRCm39) |
|
probably null |
Het |
| Fat2 |
C |
T |
11: 55,153,421 (GRCm39) |
R3597H |
probably benign |
Het |
| Gdpd5 |
T |
C |
7: 99,109,328 (GRCm39) |
|
probably benign |
Het |
| Glcci1 |
T |
A |
6: 8,579,678 (GRCm39) |
I293K |
probably damaging |
Het |
| Gm16503 |
T |
A |
4: 147,625,535 (GRCm39) |
Y10N |
unknown |
Het |
| Gm5930 |
A |
T |
14: 44,568,905 (GRCm39) |
I239N |
possibly damaging |
Het |
| Grm5 |
T |
C |
7: 87,780,004 (GRCm39) |
L1148P |
probably damaging |
Het |
| Kmt2e |
T |
A |
5: 23,704,289 (GRCm39) |
L1161I |
probably damaging |
Het |
| Megf9 |
C |
T |
4: 70,406,387 (GRCm39) |
V260I |
probably benign |
Het |
| Mme |
T |
A |
3: 63,253,525 (GRCm39) |
D456E |
probably benign |
Het |
| Mup8 |
T |
A |
4: 60,221,950 (GRCm39) |
E61V |
probably damaging |
Het |
| Olfml1 |
A |
G |
7: 107,189,436 (GRCm39) |
D167G |
probably damaging |
Het |
| Piezo2 |
T |
C |
18: 63,154,379 (GRCm39) |
K2467E |
probably damaging |
Het |
| Plscr1 |
T |
A |
9: 92,148,923 (GRCm39) |
F254L |
probably damaging |
Het |
| Prol1 |
A |
T |
5: 88,476,379 (GRCm39) |
K256N |
unknown |
Het |
| Rapgef4 |
A |
T |
2: 72,026,047 (GRCm39) |
L339F |
probably damaging |
Het |
| Slc27a2 |
T |
C |
2: 126,406,670 (GRCm39) |
I118T |
probably benign |
Het |
| Smim7 |
A |
T |
8: 73,323,838 (GRCm39) |
F19L |
possibly damaging |
Het |
| Svil |
T |
A |
18: 5,056,150 (GRCm39) |
L428* |
probably null |
Het |
| Tcof1 |
T |
C |
18: 60,962,133 (GRCm39) |
T699A |
possibly damaging |
Het |
| Thsd7b |
T |
A |
1: 129,688,092 (GRCm39) |
S668T |
possibly damaging |
Het |
| Tmprss7 |
T |
C |
16: 45,501,111 (GRCm39) |
D230G |
probably benign |
Het |
| Tyw1 |
A |
G |
5: 130,328,834 (GRCm39) |
D540G |
probably damaging |
Het |
| Zfp763 |
A |
G |
17: 33,238,860 (GRCm39) |
V95A |
probably damaging |
Het |
|
| Other mutations in Or51ah3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00742:Or51ah3
|
APN |
7 |
103,210,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01310:Or51ah3
|
APN |
7 |
103,210,008 (GRCm39) |
missense |
probably benign |
|
|
IGL01597:Or51ah3
|
APN |
7 |
103,210,349 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL01725:Or51ah3
|
APN |
7 |
103,210,282 (GRCm39) |
nonsense |
probably null |
|
|
R0055:Or51ah3
|
UTSW |
7 |
103,210,244 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0055:Or51ah3
|
UTSW |
7 |
103,210,244 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0189:Or51ah3
|
UTSW |
7 |
103,210,289 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0254:Or51ah3
|
UTSW |
7 |
103,209,829 (GRCm39) |
nonsense |
probably null |
|
|
R1395:Or51ah3
|
UTSW |
7 |
103,210,326 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1781:Or51ah3
|
UTSW |
7 |
103,209,773 (GRCm39) |
missense |
probably benign |
0.34 |
|
R2866:Or51ah3
|
UTSW |
7 |
103,210,064 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2958:Or51ah3
|
UTSW |
7 |
103,210,512 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R3922:Or51ah3
|
UTSW |
7 |
103,209,912 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4306:Or51ah3
|
UTSW |
7 |
103,210,380 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R4306:Or51ah3
|
UTSW |
7 |
103,210,379 (GRCm39) |
nonsense |
probably null |
|
|
R4818:Or51ah3
|
UTSW |
7 |
103,209,968 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4907:Or51ah3
|
UTSW |
7 |
103,210,241 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R4993:Or51ah3
|
UTSW |
7 |
103,210,524 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R5461:Or51ah3
|
UTSW |
7 |
103,209,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6225:Or51ah3
|
UTSW |
7 |
103,210,489 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6621:Or51ah3
|
UTSW |
7 |
103,210,085 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7174:Or51ah3
|
UTSW |
7 |
103,210,598 (GRCm39) |
nonsense |
probably null |
|
|
R7665:Or51ah3
|
UTSW |
7 |
103,210,523 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7684:Or51ah3
|
UTSW |
7 |
103,210,425 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8812:Or51ah3
|
UTSW |
7 |
103,209,816 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8934:Or51ah3
|
UTSW |
7 |
103,210,290 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9199:Or51ah3
|
UTSW |
7 |
103,210,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9243:Or51ah3
|
UTSW |
7 |
103,209,782 (GRCm39) |
missense |
probably benign |
|
|
R9276:Or51ah3
|
UTSW |
7 |
103,210,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Or51ah3
|
UTSW |
7 |
103,210,597 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Z1088:Or51ah3
|
UTSW |
7 |
103,210,266 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2016-08-02 |
Incidental Mutation