Incidental Mutation 'IGL02362:Or1af1'
| ID |
290519 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or1af1
|
| Ensembl Gene |
ENSMUSG00000068947 |
| Gene Name |
olfactory receptor family 1 subfamily AF member 1 |
| Synonyms |
Olfr366, MOR138-5P, MOR138-6, GA_x6K02T2NLDC-33902472-33903401 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.081)
|
| Stock # |
IGL02362
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
37109503-37110432 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 37109681 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 60
(Y60C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150608
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000091001]
[ENSMUST00000214897]
|
| AlphaFold |
Q7TRY4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000091001
AA Change: Y60C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000088524
Gene: ENSMUSG00000068947
AA Change: Y60C
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
307 |
5e-62 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
3.7e-25 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000214897
AA Change: Y60C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| 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: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam3 |
C |
A |
8: 25,187,207 (GRCm39) |
C428F |
probably damaging |
Het |
| Alas1 |
T |
C |
9: 106,113,838 (GRCm39) |
Y469C |
probably damaging |
Het |
| Asxl1 |
C |
T |
2: 153,243,706 (GRCm39) |
L1419F |
probably benign |
Het |
| Bcan |
C |
T |
3: 87,901,449 (GRCm39) |
D418N |
possibly damaging |
Het |
| Cdc42bpg |
A |
G |
19: 6,360,839 (GRCm39) |
D199G |
possibly damaging |
Het |
| Chst15 |
T |
C |
7: 131,868,401 (GRCm39) |
N340D |
probably benign |
Het |
| Col12a1 |
T |
G |
9: 79,537,993 (GRCm39) |
|
probably benign |
Het |
| Cyp2c67 |
T |
A |
19: 39,631,849 (GRCm39) |
H116L |
probably benign |
Het |
| Cyp2c67 |
G |
A |
19: 39,605,826 (GRCm39) |
R357* |
probably null |
Het |
| Ears2 |
T |
C |
7: 121,643,773 (GRCm39) |
D395G |
probably benign |
Het |
| Fam227a |
A |
T |
15: 79,528,139 (GRCm39) |
|
probably benign |
Het |
| Fap |
A |
G |
2: 62,403,842 (GRCm39) |
V11A |
probably benign |
Het |
| Ganc |
A |
G |
2: 120,264,238 (GRCm39) |
D397G |
probably damaging |
Het |
| Gjb6 |
C |
A |
14: 57,361,752 (GRCm39) |
G170C |
possibly damaging |
Het |
| Gria2 |
A |
T |
3: 80,614,244 (GRCm39) |
W599R |
probably damaging |
Het |
| Gvin-ps5 |
T |
C |
7: 105,929,480 (GRCm39) |
|
noncoding transcript |
Het |
| Ighv1-64 |
A |
G |
12: 115,471,236 (GRCm39) |
S94P |
probably benign |
Het |
| Kifc3 |
C |
T |
8: 95,836,507 (GRCm39) |
A85T |
probably damaging |
Het |
| Lifr |
G |
A |
15: 7,194,174 (GRCm39) |
|
probably null |
Het |
| Lonp2 |
T |
G |
8: 87,350,874 (GRCm39) |
S21R |
probably benign |
Het |
| Nxpe3 |
A |
G |
16: 55,710,949 (GRCm39) |
V30A |
probably benign |
Het |
| Olfml1 |
T |
C |
7: 107,167,010 (GRCm39) |
V13A |
probably benign |
Het |
| Or10w1 |
T |
C |
19: 13,632,597 (GRCm39) |
V268A |
probably benign |
Het |
| Pcnt |
G |
A |
10: 76,210,996 (GRCm39) |
Q2376* |
probably null |
Het |
| Pglyrp2 |
A |
G |
17: 32,635,996 (GRCm39) |
L380P |
probably damaging |
Het |
| Plin3 |
A |
G |
17: 56,593,636 (GRCm39) |
V26A |
probably benign |
Het |
| Potefam1 |
T |
C |
2: 111,041,996 (GRCm39) |
|
probably benign |
Het |
| Pramel25 |
A |
G |
4: 143,519,580 (GRCm39) |
S114G |
probably damaging |
Het |
| Rims1 |
A |
G |
1: 22,522,288 (GRCm39) |
I470T |
probably damaging |
Het |
| Rora |
T |
C |
9: 69,281,374 (GRCm39) |
Y329H |
probably damaging |
Het |
| Scnn1b |
G |
A |
7: 121,516,770 (GRCm39) |
R503H |
probably damaging |
Het |
| Sec14l1 |
A |
G |
11: 117,035,675 (GRCm39) |
D237G |
possibly damaging |
Het |
| Selplg |
A |
G |
5: 113,957,467 (GRCm39) |
S280P |
probably benign |
Het |
| Serpina12 |
A |
G |
12: 104,004,140 (GRCm39) |
L164P |
probably benign |
Het |
| Sik2 |
C |
T |
9: 50,828,903 (GRCm39) |
W176* |
probably null |
Het |
| Slc2a1 |
T |
C |
4: 118,993,612 (GRCm39) |
F483S |
possibly damaging |
Het |
| Speg |
A |
G |
1: 75,400,559 (GRCm39) |
D2573G |
possibly damaging |
Het |
| Stil |
C |
T |
4: 114,867,308 (GRCm39) |
S239L |
probably damaging |
Het |
| Tmem94 |
C |
A |
11: 115,685,571 (GRCm39) |
S941R |
probably damaging |
Het |
| Tnfrsf11b |
T |
A |
15: 54,115,778 (GRCm39) |
D273V |
probably damaging |
Het |
| Tns2 |
A |
G |
15: 102,020,725 (GRCm39) |
T864A |
probably benign |
Het |
| Zfpm2 |
A |
G |
15: 40,962,890 (GRCm39) |
H184R |
probably damaging |
Het |
|
| Other mutations in Or1af1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01691:Or1af1
|
APN |
2 |
37,110,038 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01925:Or1af1
|
APN |
2 |
37,110,058 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL02355:Or1af1
|
APN |
2 |
37,109,681 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02671:Or1af1
|
APN |
2 |
37,110,257 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02821:Or1af1
|
APN |
2 |
37,110,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0603:Or1af1
|
UTSW |
2 |
37,110,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0707:Or1af1
|
UTSW |
2 |
37,110,208 (GRCm39) |
nonsense |
probably null |
|
|
R1204:Or1af1
|
UTSW |
2 |
37,109,651 (GRCm39) |
missense |
probably benign |
|
|
R1457:Or1af1
|
UTSW |
2 |
37,109,671 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1509:Or1af1
|
UTSW |
2 |
37,109,966 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1676:Or1af1
|
UTSW |
2 |
37,109,653 (GRCm39) |
nonsense |
probably null |
|
|
R1823:Or1af1
|
UTSW |
2 |
37,110,344 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2163:Or1af1
|
UTSW |
2 |
37,110,089 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2909:Or1af1
|
UTSW |
2 |
37,110,188 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3696:Or1af1
|
UTSW |
2 |
37,110,188 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3698:Or1af1
|
UTSW |
2 |
37,110,188 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4004:Or1af1
|
UTSW |
2 |
37,109,960 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4655:Or1af1
|
UTSW |
2 |
37,109,885 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5311:Or1af1
|
UTSW |
2 |
37,109,633 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5385:Or1af1
|
UTSW |
2 |
37,109,599 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R5433:Or1af1
|
UTSW |
2 |
37,109,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5499:Or1af1
|
UTSW |
2 |
37,109,777 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R5707:Or1af1
|
UTSW |
2 |
37,109,901 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6330:Or1af1
|
UTSW |
2 |
37,110,136 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6338:Or1af1
|
UTSW |
2 |
37,109,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6666:Or1af1
|
UTSW |
2 |
37,110,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6872:Or1af1
|
UTSW |
2 |
37,109,989 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R7412:Or1af1
|
UTSW |
2 |
37,109,774 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R7789:Or1af1
|
UTSW |
2 |
37,109,672 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7831:Or1af1
|
UTSW |
2 |
37,109,723 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8220:Or1af1
|
UTSW |
2 |
37,109,791 (GRCm39) |
missense |
probably benign |
0.06 |
|
R8391:Or1af1
|
UTSW |
2 |
37,110,277 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8708:Or1af1
|
UTSW |
2 |
37,109,956 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9049:Or1af1
|
UTSW |
2 |
37,109,959 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9231:Or1af1
|
UTSW |
2 |
37,109,989 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R9294:Or1af1
|
UTSW |
2 |
37,110,122 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R9471:Or1af1
|
UTSW |
2 |
37,110,400 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9595:Or1af1
|
UTSW |
2 |
37,110,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation