Incidental Mutation 'IGL02184:Or4a73'
| ID |
284283 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4a73
|
| Ensembl Gene |
ENSMUSG00000111715 |
| Gene Name |
olfactory receptor family 4 subfamily A member 73 |
| Synonyms |
GA_x6K02T2Q125-51034790-51033846, Olfr1246, MOR231-9 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.156)
|
| Stock # |
IGL02184
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
89420413-89421490 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 89420637 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 274
(T274I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150876
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000187990]
[ENSMUST00000213221]
[ENSMUST00000217192]
[ENSMUST00000217254]
|
| AlphaFold |
Q7TQZ6 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000187990
AA Change: T274I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000140066
Gene: ENSMUSG00000111715
AA Change: T274I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
39 |
285 |
2.7e-28 |
PFAM |
|
Pfam:7tm_4
|
137 |
278 |
3.5e-37 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000191053
AA Change: T274I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000140823
Gene: ENSMUSG00000100828
AA Change: T274I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_1
|
39 |
285 |
1.9e-29 |
PFAM |
|
Pfam:7tm_4
|
137 |
278 |
1.1e-38 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000213221
AA Change: T274I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217192
AA Change: T274I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000217254
AA Change: T274I
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
| 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: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam15 |
C |
T |
3: 89,253,241 (GRCm39) |
|
probably benign |
Het |
| Antxr2 |
A |
C |
5: 98,125,454 (GRCm39) |
|
probably null |
Het |
| Aopep |
T |
G |
13: 63,215,925 (GRCm39) |
I399S |
possibly damaging |
Het |
| Atp8b3 |
A |
C |
10: 80,363,067 (GRCm39) |
|
probably benign |
Het |
| Brwd1 |
A |
T |
16: 95,815,029 (GRCm39) |
M1417K |
probably damaging |
Het |
| Camk2d |
A |
T |
3: 126,591,422 (GRCm39) |
R297S |
probably damaging |
Het |
| Cntnap1 |
A |
T |
11: 101,069,191 (GRCm39) |
H215L |
probably damaging |
Het |
| Cytip |
T |
C |
2: 58,023,750 (GRCm39) |
S357G |
probably damaging |
Het |
| Eif1ad15 |
T |
C |
12: 88,287,951 (GRCm39) |
R101G |
probably benign |
Het |
| Fancg |
A |
G |
4: 43,006,872 (GRCm39) |
Y273H |
possibly damaging |
Het |
| Fbxo36 |
A |
G |
1: 84,858,885 (GRCm39) |
S57G |
probably benign |
Het |
| Fgf8 |
A |
T |
19: 45,725,655 (GRCm39) |
L141Q |
probably damaging |
Het |
| Grm5 |
C |
T |
7: 87,675,650 (GRCm39) |
T388M |
probably damaging |
Het |
| Hipk1 |
A |
G |
3: 103,666,066 (GRCm39) |
L589P |
possibly damaging |
Het |
| Kiz |
T |
C |
2: 146,731,520 (GRCm39) |
S337P |
probably benign |
Het |
| Lrrc37a |
A |
T |
11: 103,388,435 (GRCm39) |
I2330K |
unknown |
Het |
| Mdfic |
T |
A |
6: 15,770,366 (GRCm39) |
I124K |
possibly damaging |
Het |
| Mdfic2 |
T |
C |
6: 98,225,059 (GRCm39) |
S75G |
possibly damaging |
Het |
| Mttp |
A |
G |
3: 137,821,761 (GRCm39) |
|
probably null |
Het |
| Myom1 |
G |
A |
17: 71,379,132 (GRCm39) |
S632N |
possibly damaging |
Het |
| Nlrp12 |
T |
C |
7: 3,289,094 (GRCm39) |
K473E |
probably damaging |
Het |
| Nrp2 |
C |
A |
1: 62,758,099 (GRCm39) |
C28* |
probably null |
Het |
| Nwd2 |
G |
T |
5: 63,963,020 (GRCm39) |
G868V |
probably damaging |
Het |
| Or4c58 |
G |
A |
2: 89,674,729 (GRCm39) |
A196V |
probably damaging |
Het |
| Or5w1 |
A |
G |
2: 87,487,136 (GRCm39) |
L43P |
probably damaging |
Het |
| Pappa |
A |
T |
4: 65,258,928 (GRCm39) |
M1559L |
possibly damaging |
Het |
| Pmm2 |
T |
A |
16: 8,455,668 (GRCm39) |
D10E |
possibly damaging |
Het |
| Polm |
T |
C |
11: 5,780,137 (GRCm39) |
Q300R |
probably benign |
Het |
| Prrc2b |
T |
A |
2: 32,111,467 (GRCm39) |
N1208K |
probably benign |
Het |
| Serpinb3c |
T |
C |
1: 107,199,648 (GRCm39) |
D291G |
probably damaging |
Het |
| Skic3 |
A |
G |
13: 76,259,810 (GRCm39) |
K37E |
probably damaging |
Het |
| Slc1a2 |
T |
C |
2: 102,578,889 (GRCm39) |
F268S |
probably damaging |
Het |
| Slc26a4 |
A |
G |
12: 31,599,948 (GRCm39) |
Y127H |
probably damaging |
Het |
| Slc29a4 |
A |
G |
5: 142,703,506 (GRCm39) |
Y260C |
probably damaging |
Het |
| Sorbs3 |
C |
T |
14: 70,421,455 (GRCm39) |
|
probably null |
Het |
| Spen |
T |
C |
4: 141,214,917 (GRCm39) |
Y534C |
unknown |
Het |
| Tmem237 |
T |
C |
1: 59,159,270 (GRCm39) |
|
probably null |
Het |
| Tnfrsf21 |
A |
T |
17: 43,396,354 (GRCm39) |
N546I |
probably benign |
Het |
| Tpgs2 |
T |
A |
18: 25,273,630 (GRCm39) |
D177V |
probably damaging |
Het |
| Tpx2 |
C |
T |
2: 152,724,240 (GRCm39) |
R339* |
probably null |
Het |
| Trim12c |
T |
C |
7: 103,997,430 (GRCm39) |
Y42C |
probably benign |
Het |
| Trip10 |
A |
T |
17: 57,564,272 (GRCm39) |
E341V |
probably damaging |
Het |
| Trpm8 |
A |
T |
1: 88,258,416 (GRCm39) |
|
probably null |
Het |
| Ubr1 |
T |
A |
2: 120,730,989 (GRCm39) |
I1221F |
probably benign |
Het |
| Ucp2 |
C |
T |
7: 100,148,529 (GRCm39) |
A301V |
probably benign |
Het |
| Zfyve1 |
T |
C |
12: 83,605,467 (GRCm39) |
I411V |
probably benign |
Het |
|
| Other mutations in Or4a73 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02140:Or4a73
|
APN |
2 |
89,420,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03383:Or4a73
|
APN |
2 |
89,420,656 (GRCm39) |
missense |
probably benign |
0.24 |
|
PIT4283001:Or4a73
|
UTSW |
2 |
89,420,572 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0453:Or4a73
|
UTSW |
2 |
89,421,095 (GRCm39) |
nonsense |
probably null |
|
|
R1614:Or4a73
|
UTSW |
2 |
89,421,040 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R2310:Or4a73
|
UTSW |
2 |
89,420,794 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2436:Or4a73
|
UTSW |
2 |
89,421,117 (GRCm39) |
missense |
probably benign |
0.42 |
|
R3683:Or4a73
|
UTSW |
2 |
89,421,099 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3685:Or4a73
|
UTSW |
2 |
89,421,099 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4037:Or4a73
|
UTSW |
2 |
89,421,379 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5219:Or4a73
|
UTSW |
2 |
89,421,046 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5350:Or4a73
|
UTSW |
2 |
89,421,432 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R5383:Or4a73
|
UTSW |
2 |
89,421,457 (GRCm39) |
start codon destroyed |
probably null |
0.91 |
|
R5639:Or4a73
|
UTSW |
2 |
89,421,069 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5927:Or4a73
|
UTSW |
2 |
89,421,444 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6056:Or4a73
|
UTSW |
2 |
89,421,445 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6177:Or4a73
|
UTSW |
2 |
89,420,661 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7351:Or4a73
|
UTSW |
2 |
89,420,857 (GRCm39) |
missense |
probably benign |
0.32 |
|
R7496:Or4a73
|
UTSW |
2 |
89,421,040 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7583:Or4a73
|
UTSW |
2 |
89,421,095 (GRCm39) |
nonsense |
probably null |
|
|
R7973:Or4a73
|
UTSW |
2 |
89,421,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8770:Or4a73
|
UTSW |
2 |
89,421,171 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8813:Or4a73
|
UTSW |
2 |
89,420,730 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8821:Or4a73
|
UTSW |
2 |
89,420,880 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9037:Or4a73
|
UTSW |
2 |
89,421,051 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9062:Or4a73
|
UTSW |
2 |
89,420,923 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9262:Or4a73
|
UTSW |
2 |
89,421,435 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9554:Or4a73
|
UTSW |
2 |
89,420,710 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9623:Or4a73
|
UTSW |
2 |
89,421,261 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2015-04-16 |
Incidental Mutation