Incidental Mutation 'IGL01331:Or51ai2'
| ID |
74514 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or51ai2
|
| Ensembl Gene |
ENSMUSG00000073938 |
| Gene Name |
olfactory receptor family 51 subfamily AI member 2 |
| Synonyms |
GA_x6K02T2PBJ9-6671256-6672209, MOR2-1, Olfr632 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.055)
|
| Stock # |
IGL01331
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
103586589-103587542 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 103586782 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 65
(Y65C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149598
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098189]
[ENSMUST00000214711]
|
| AlphaFold |
Q9EPN9 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000098189
AA Change: Y65C
PolyPhen 2
Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000095791
Gene: ENSMUSG00000073938
AA Change: Y65C
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
313 |
2.5e-109 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
39 |
232 |
7.5e-11 |
PFAM |
|
Pfam:7tm_1
|
45 |
296 |
1.4e-16 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000211625
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214509
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000214711
AA Change: Y65C
PolyPhen 2
Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
|
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Clca3a1 |
G |
A |
3: 144,453,273 (GRCm39) |
T517M |
probably damaging |
Het |
| Clec4g |
T |
C |
8: 3,767,190 (GRCm39) |
|
probably benign |
Het |
| Cmya5 |
C |
T |
13: 93,233,454 (GRCm39) |
E545K |
possibly damaging |
Het |
| Cntn6 |
A |
T |
6: 104,751,484 (GRCm39) |
D380V |
probably damaging |
Het |
| Col9a2 |
C |
T |
4: 120,902,389 (GRCm39) |
P209S |
possibly damaging |
Het |
| Cyp2b9 |
T |
C |
7: 25,887,140 (GRCm39) |
V183A |
probably damaging |
Het |
| Dpt |
T |
C |
1: 164,624,379 (GRCm39) |
Y27H |
unknown |
Het |
| Dusp16 |
T |
C |
6: 134,695,067 (GRCm39) |
Q588R |
possibly damaging |
Het |
| Emg1 |
A |
G |
6: 124,682,033 (GRCm39) |
S164P |
probably benign |
Het |
| Foxk1 |
G |
A |
5: 142,439,344 (GRCm39) |
R428Q |
probably damaging |
Het |
| Frmd4a |
T |
A |
2: 4,607,036 (GRCm39) |
M667K |
probably benign |
Het |
| Gpr55 |
T |
A |
1: 85,868,915 (GRCm39) |
|
probably benign |
Het |
| Gtpbp8 |
A |
G |
16: 44,560,494 (GRCm39) |
I162T |
probably benign |
Het |
| Ighv1-59 |
C |
T |
12: 115,298,992 (GRCm39) |
V21I |
possibly damaging |
Het |
| Ipo11 |
T |
A |
13: 106,932,254 (GRCm39) |
Y938F |
possibly damaging |
Het |
| Map4 |
G |
T |
9: 109,863,869 (GRCm39) |
V365L |
probably benign |
Het |
| Mboat1 |
C |
A |
13: 30,403,684 (GRCm39) |
|
probably benign |
Het |
| Med12 |
A |
G |
X: 100,324,360 (GRCm39) |
E649G |
possibly damaging |
Het |
| Nfkbie |
T |
C |
17: 45,869,495 (GRCm39) |
V150A |
probably benign |
Het |
| Or8k22 |
A |
C |
2: 86,163,048 (GRCm39) |
Y217* |
probably null |
Het |
| Prdm1 |
T |
A |
10: 44,317,970 (GRCm39) |
K299N |
possibly damaging |
Het |
| Ribc1 |
T |
C |
X: 150,788,102 (GRCm39) |
T291A |
probably benign |
Het |
| Rps6kc1 |
G |
T |
1: 190,532,549 (GRCm39) |
N484K |
possibly damaging |
Het |
| Serpina3k |
C |
A |
12: 104,309,369 (GRCm39) |
A271D |
probably benign |
Het |
| Spata18 |
G |
T |
5: 73,827,024 (GRCm39) |
R321L |
probably damaging |
Het |
| Styxl2 |
C |
A |
1: 165,935,749 (GRCm39) |
V150L |
probably damaging |
Het |
| Syne2 |
C |
A |
12: 75,976,027 (GRCm39) |
|
probably benign |
Het |
| Syt17 |
T |
A |
7: 118,007,389 (GRCm39) |
I302F |
probably damaging |
Het |
| Tgm6 |
A |
G |
2: 129,985,538 (GRCm39) |
|
probably null |
Het |
| Tmc2 |
A |
G |
2: 130,074,276 (GRCm39) |
Y323C |
probably damaging |
Het |
| Tnc |
T |
C |
4: 63,901,112 (GRCm39) |
D1452G |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,620,022 (GRCm39) |
I7555T |
probably damaging |
Het |
| Ugt2b36 |
A |
T |
5: 87,238,801 (GRCm39) |
W131R |
probably damaging |
Het |
| Vmn2r75 |
A |
T |
7: 85,820,870 (GRCm39) |
C21* |
probably null |
Het |
| Zfp592 |
T |
A |
7: 80,691,296 (GRCm39) |
C1158* |
probably null |
Het |
|
| Other mutations in Or51ai2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01817:Or51ai2
|
APN |
7 |
103,587,030 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02303:Or51ai2
|
APN |
7 |
103,586,770 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL03392:Or51ai2
|
APN |
7 |
103,587,232 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0092:Or51ai2
|
UTSW |
7 |
103,586,934 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0492:Or51ai2
|
UTSW |
7 |
103,586,971 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0711:Or51ai2
|
UTSW |
7 |
103,587,024 (GRCm39) |
missense |
probably benign |
0.29 |
|
R2893:Or51ai2
|
UTSW |
7 |
103,587,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3911:Or51ai2
|
UTSW |
7 |
103,586,616 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4825:Or51ai2
|
UTSW |
7 |
103,586,710 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6106:Or51ai2
|
UTSW |
7 |
103,587,400 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6254:Or51ai2
|
UTSW |
7 |
103,586,741 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6383:Or51ai2
|
UTSW |
7 |
103,587,030 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6821:Or51ai2
|
UTSW |
7 |
103,586,793 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6890:Or51ai2
|
UTSW |
7 |
103,587,066 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R7646:Or51ai2
|
UTSW |
7 |
103,587,504 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8041:Or51ai2
|
UTSW |
7 |
103,586,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8232:Or51ai2
|
UTSW |
7 |
103,586,980 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8266:Or51ai2
|
UTSW |
7 |
103,586,746 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8326:Or51ai2
|
UTSW |
7 |
103,586,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8783:Or51ai2
|
UTSW |
7 |
103,586,751 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
Z1177:Or51ai2
|
UTSW |
7 |
103,586,965 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
| Posted On |
2013-10-07 |
Incidental Mutation