Incidental Mutation 'R0104:Or14j2'
| ID |
16292 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or14j2
|
| Ensembl Gene |
ENSMUSG00000092292 |
| Gene Name |
olfactory receptor family 14 subfamily J member 2 |
| Synonyms |
Olfr113, GA_x6K02T2PSCP-2034880-2033942, MOR218-9 |
| MMRRC Submission |
038390-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.083)
|
| Stock # |
R0104 (G1)
|
| Quality Score |
|
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
37885374-37886312 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 37885817 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 166
(I166F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149739
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000174139]
[ENSMUST00000216181]
|
| AlphaFold |
Q8VEU4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000174139
AA Change: I166F
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000134080
Gene: ENSMUSG00000109212
AA Change: I166F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
3.7e-46 |
PFAM |
|
Pfam:7TM_GPCR_Srx
|
32 |
307 |
3.4e-7 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
4.2e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.9e-20 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216181
AA Change: I166F
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| Meta Mutation Damage Score |
0.6467 |
| Coding Region Coverage |
- 1x: 75.5%
- 3x: 52.6%
- 10x: 7.5%
- 20x: 3.0%
|
| Validation Efficiency |
100% (37/37) |
| 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: 23 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3100002H09Rik |
C |
A |
4: 124,504,469 (GRCm39) |
A28S |
probably damaging |
Het |
| Arhgap5 |
A |
T |
12: 52,563,500 (GRCm39) |
D157V |
probably damaging |
Het |
| Cfap54 |
G |
T |
10: 92,864,514 (GRCm39) |
H142N |
probably damaging |
Het |
| Dpp10 |
A |
T |
1: 123,295,572 (GRCm39) |
M525K |
probably benign |
Het |
| Fsip2 |
A |
T |
2: 82,809,317 (GRCm39) |
T1879S |
possibly damaging |
Het |
| Gm14129 |
T |
C |
2: 148,773,493 (GRCm39) |
|
noncoding transcript |
Het |
| Ighv2-7 |
A |
T |
12: 113,771,088 (GRCm39) |
W66R |
probably damaging |
Het |
| Kif11 |
T |
A |
19: 37,401,663 (GRCm39) |
V880D |
probably benign |
Het |
| Mcpt1 |
T |
A |
14: 56,256,888 (GRCm39) |
M142K |
possibly damaging |
Het |
| Mlst8 |
T |
C |
17: 24,695,091 (GRCm39) |
N264S |
possibly damaging |
Het |
| Nmrk1 |
T |
A |
19: 18,618,582 (GRCm39) |
S88R |
probably benign |
Het |
| Or8d23 |
A |
G |
9: 38,842,261 (GRCm39) |
S265G |
possibly damaging |
Het |
| Rtn1 |
A |
T |
12: 72,355,619 (GRCm39) |
I109N |
probably damaging |
Het |
| Slc15a2 |
T |
A |
16: 36,594,997 (GRCm39) |
L156F |
possibly damaging |
Het |
| Slc22a21 |
A |
C |
11: 53,842,635 (GRCm39) |
M498R |
probably null |
Het |
| Ssc5d |
T |
C |
7: 4,939,285 (GRCm39) |
S574P |
probably benign |
Het |
| Taf2 |
T |
C |
15: 54,901,734 (GRCm39) |
D820G |
probably benign |
Het |
| Tas2r135 |
A |
T |
6: 42,383,258 (GRCm39) |
I266F |
possibly damaging |
Het |
| Trgv4 |
C |
T |
13: 19,369,480 (GRCm39) |
H75Y |
probably damaging |
Het |
| Vil1 |
A |
G |
1: 74,457,525 (GRCm39) |
K53E |
probably benign |
Het |
| Zfc3h1 |
T |
A |
10: 115,251,192 (GRCm39) |
M1261K |
possibly damaging |
Het |
| Zfp655 |
T |
C |
5: 145,180,825 (GRCm39) |
S228P |
probably damaging |
Het |
| Zfyve9 |
C |
A |
4: 108,575,360 (GRCm39) |
D574Y |
probably damaging |
Het |
|
| Other mutations in Or14j2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00088:Or14j2
|
APN |
17 |
37,885,808 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01061:Or14j2
|
APN |
17 |
37,885,795 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
IGL01293:Or14j2
|
APN |
17 |
37,886,308 (GRCm39) |
missense |
probably benign |
|
|
IGL01370:Or14j2
|
APN |
17 |
37,885,412 (GRCm39) |
splice site |
probably null |
|
|
IGL01535:Or14j2
|
APN |
17 |
37,885,679 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02134:Or14j2
|
APN |
17 |
37,886,249 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02536:Or14j2
|
APN |
17 |
37,885,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02640:Or14j2
|
APN |
17 |
37,885,912 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL02652:Or14j2
|
APN |
17 |
37,885,836 (GRCm39) |
nonsense |
probably null |
|
|
IGL02963:Or14j2
|
APN |
17 |
37,885,745 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1662:Or14j2
|
UTSW |
17 |
37,886,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2904:Or14j2
|
UTSW |
17 |
37,885,705 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5129:Or14j2
|
UTSW |
17 |
37,886,071 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5197:Or14j2
|
UTSW |
17 |
37,886,111 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5347:Or14j2
|
UTSW |
17 |
37,885,618 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6044:Or14j2
|
UTSW |
17 |
37,885,426 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7048:Or14j2
|
UTSW |
17 |
37,886,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7064:Or14j2
|
UTSW |
17 |
37,885,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8123:Or14j2
|
UTSW |
17 |
37,885,653 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8205:Or14j2
|
UTSW |
17 |
37,885,892 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8710:Or14j2
|
UTSW |
17 |
37,885,540 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8989:Or14j2
|
UTSW |
17 |
37,885,542 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9323:Or14j2
|
UTSW |
17 |
37,886,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9439:Or14j2
|
UTSW |
17 |
37,885,825 (GRCm39) |
missense |
probably benign |
0.00 |
|
X0062:Or14j2
|
UTSW |
17 |
37,885,388 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2013-01-20 |
Incidental Mutation