Incidental Mutation 'IGL01393:Or1j4'
| ID |
79276 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or1j4
|
| Ensembl Gene |
ENSMUSG00000050015 |
| Gene Name |
olfactory receptor family 1 subfamily J member 4 |
| Synonyms |
MOR136-13, Olfr350, GA_x6K02T2NLDC-33544602-33545540 |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.275)
|
| Stock # |
IGL01393
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
36740060-36740998 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 36740553 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glutamine
at position 165
(R165Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149667
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055130]
[ENSMUST00000214457]
[ENSMUST00000215100]
|
| AlphaFold |
Q8VFP8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000055130
AA Change: R165Q
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000053105
Gene: ENSMUSG00000050015
AA Change: R165Q
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
6.3e-61 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
1.3e-7 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
3e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214457
AA Change: R165Q
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215100
AA Change: R165Q
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| 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: 54 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930474N05Rik |
G |
A |
14: 35,818,379 (GRCm39) |
V126I |
possibly damaging |
Het |
| A630073D07Rik |
G |
T |
6: 132,603,577 (GRCm39) |
Q60K |
unknown |
Het |
| Alpk2 |
A |
G |
18: 65,440,779 (GRCm39) |
S205P |
possibly damaging |
Het |
| Ang4 |
T |
A |
14: 52,001,670 (GRCm39) |
I93L |
probably benign |
Het |
| Arpin |
A |
G |
7: 79,581,588 (GRCm39) |
V44A |
possibly damaging |
Het |
| Atxn3 |
A |
T |
12: 101,899,306 (GRCm39) |
C263* |
probably null |
Het |
| Cd209f |
T |
C |
8: 4,153,154 (GRCm39) |
N260S |
probably damaging |
Het |
| Cdh20 |
A |
G |
1: 104,861,969 (GRCm39) |
R50G |
probably benign |
Het |
| Cracd |
T |
C |
5: 77,006,818 (GRCm39) |
S1060P |
unknown |
Het |
| Csmd3 |
C |
T |
15: 48,320,995 (GRCm39) |
V272I |
possibly damaging |
Het |
| Dst |
A |
T |
1: 34,206,706 (GRCm39) |
Y1136F |
possibly damaging |
Het |
| Fam20c |
A |
G |
5: 138,793,026 (GRCm39) |
Y420C |
probably damaging |
Het |
| Fancd2 |
T |
A |
6: 113,554,321 (GRCm39) |
|
probably benign |
Het |
| Fat2 |
T |
C |
11: 55,160,135 (GRCm39) |
D3326G |
probably benign |
Het |
| Filip1l |
A |
G |
16: 57,392,586 (GRCm39) |
N820S |
probably damaging |
Het |
| Gm26566 |
G |
A |
4: 88,640,581 (GRCm39) |
|
probably benign |
Het |
| Gm4792 |
A |
G |
10: 94,134,304 (GRCm39) |
L22P |
unknown |
Het |
| Gpat2 |
A |
G |
2: 127,274,571 (GRCm39) |
E386G |
probably damaging |
Het |
| Grm3 |
T |
C |
5: 9,639,856 (GRCm39) |
D63G |
probably benign |
Het |
| Hdc |
A |
G |
2: 126,436,581 (GRCm39) |
V430A |
probably benign |
Het |
| Hnf4a |
T |
C |
2: 163,393,492 (GRCm39) |
|
probably benign |
Het |
| Il2ra |
A |
G |
2: 11,687,865 (GRCm39) |
D215G |
probably damaging |
Het |
| Kctd3 |
T |
C |
1: 188,732,487 (GRCm39) |
I74V |
probably benign |
Het |
| Kctd5 |
A |
T |
17: 24,278,292 (GRCm39) |
|
probably null |
Het |
| Lrsam1 |
A |
T |
2: 32,845,185 (GRCm39) |
|
probably benign |
Het |
| Mblac1 |
A |
G |
5: 138,193,036 (GRCm39) |
N126S |
possibly damaging |
Het |
| Mmrn1 |
T |
A |
6: 60,937,692 (GRCm39) |
|
probably benign |
Het |
| Mpp3 |
A |
T |
11: 101,916,304 (GRCm39) |
L16Q |
probably damaging |
Het |
| Mrgprb1 |
C |
A |
7: 48,097,754 (GRCm39) |
A53S |
possibly damaging |
Het |
| Nbea |
C |
A |
3: 55,912,729 (GRCm39) |
M1019I |
probably benign |
Het |
| Nlrp5 |
A |
G |
7: 23,103,599 (GRCm39) |
K22R |
probably null |
Het |
| Or2ag18 |
C |
T |
7: 106,405,642 (GRCm39) |
G9E |
probably benign |
Het |
| Or4k48 |
A |
G |
2: 111,475,601 (GRCm39) |
V247A |
probably damaging |
Het |
| Pard6b |
T |
A |
2: 167,929,298 (GRCm39) |
S35T |
probably benign |
Het |
| Peli1 |
T |
C |
11: 21,097,400 (GRCm39) |
V215A |
probably benign |
Het |
| Pkp4 |
A |
T |
2: 59,178,269 (GRCm39) |
D1003V |
probably damaging |
Het |
| Pot1a |
G |
A |
6: 25,744,630 (GRCm39) |
R625* |
probably null |
Het |
| Ppp1r16a |
T |
C |
15: 76,578,744 (GRCm39) |
S483P |
probably benign |
Het |
| Prpf8 |
C |
A |
11: 75,385,121 (GRCm39) |
A794D |
possibly damaging |
Het |
| Prrg3 |
T |
C |
X: 71,011,123 (GRCm39) |
V210A |
probably benign |
Het |
| Rev1 |
A |
G |
1: 38,131,144 (GRCm39) |
V168A |
probably damaging |
Het |
| Sez6l |
G |
T |
5: 112,586,261 (GRCm39) |
|
probably benign |
Het |
| Spag17 |
A |
G |
3: 99,934,926 (GRCm39) |
T711A |
possibly damaging |
Het |
| Spice1 |
A |
G |
16: 44,186,993 (GRCm39) |
I163M |
probably benign |
Het |
| Tex13c1 |
C |
T |
X: 42,680,233 (GRCm39) |
A66V |
probably damaging |
Het |
| Tmem132d |
A |
T |
5: 127,861,702 (GRCm39) |
S806R |
probably benign |
Het |
| Tnc |
A |
G |
4: 63,932,291 (GRCm39) |
|
probably benign |
Het |
| Tpbg |
T |
A |
9: 85,726,145 (GRCm39) |
V38E |
unknown |
Het |
| Unc13c |
T |
A |
9: 73,447,552 (GRCm39) |
I1883F |
probably benign |
Het |
| Vmn2r61 |
A |
C |
7: 41,916,258 (GRCm39) |
Q290H |
probably benign |
Het |
| Vps39 |
A |
G |
2: 120,180,719 (GRCm39) |
|
probably benign |
Het |
| Zfp369 |
T |
C |
13: 65,442,288 (GRCm39) |
V294A |
possibly damaging |
Het |
| Zfp821 |
T |
A |
8: 110,436,110 (GRCm39) |
|
probably benign |
Het |
| Zfp941 |
C |
T |
7: 140,391,841 (GRCm39) |
G506E |
probably damaging |
Het |
|
| Other mutations in Or1j4 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01068:Or1j4
|
APN |
2 |
36,740,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01113:Or1j4
|
APN |
2 |
36,740,631 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02302:Or1j4
|
APN |
2 |
36,740,715 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02316:Or1j4
|
APN |
2 |
36,740,294 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB007:Or1j4
|
UTSW |
2 |
36,740,285 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB017:Or1j4
|
UTSW |
2 |
36,740,285 (GRCm39) |
missense |
probably damaging |
1.00 |
|
F6893:Or1j4
|
UTSW |
2 |
36,740,819 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4402001:Or1j4
|
UTSW |
2 |
36,740,316 (GRCm39) |
missense |
probably benign |
|
|
R0312:Or1j4
|
UTSW |
2 |
36,740,372 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0525:Or1j4
|
UTSW |
2 |
36,740,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0557:Or1j4
|
UTSW |
2 |
36,740,760 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R0665:Or1j4
|
UTSW |
2 |
36,740,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2019:Or1j4
|
UTSW |
2 |
36,740,418 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2107:Or1j4
|
UTSW |
2 |
36,740,355 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R2108:Or1j4
|
UTSW |
2 |
36,740,355 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R2848:Or1j4
|
UTSW |
2 |
36,740,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3964:Or1j4
|
UTSW |
2 |
36,740,729 (GRCm39) |
missense |
probably benign |
0.12 |
|
R4822:Or1j4
|
UTSW |
2 |
36,740,888 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4907:Or1j4
|
UTSW |
2 |
36,740,270 (GRCm39) |
missense |
probably benign |
0.28 |
|
R5134:Or1j4
|
UTSW |
2 |
36,740,488 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5144:Or1j4
|
UTSW |
2 |
36,740,156 (GRCm39) |
missense |
probably benign |
|
|
R5702:Or1j4
|
UTSW |
2 |
36,740,946 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5727:Or1j4
|
UTSW |
2 |
36,740,544 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5786:Or1j4
|
UTSW |
2 |
36,740,061 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
|
R6179:Or1j4
|
UTSW |
2 |
36,740,846 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R6862:Or1j4
|
UTSW |
2 |
36,740,234 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7258:Or1j4
|
UTSW |
2 |
36,740,352 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7307:Or1j4
|
UTSW |
2 |
36,740,137 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7353:Or1j4
|
UTSW |
2 |
36,740,081 (GRCm39) |
missense |
probably benign |
|
|
R7412:Or1j4
|
UTSW |
2 |
36,740,478 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7851:Or1j4
|
UTSW |
2 |
36,740,428 (GRCm39) |
nonsense |
probably null |
|
|
R7930:Or1j4
|
UTSW |
2 |
36,740,285 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8005:Or1j4
|
UTSW |
2 |
36,740,156 (GRCm39) |
missense |
probably benign |
|
|
R8346:Or1j4
|
UTSW |
2 |
36,740,351 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8692:Or1j4
|
UTSW |
2 |
36,740,096 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9120:Or1j4
|
UTSW |
2 |
36,740,143 (GRCm39) |
nonsense |
probably null |
|
|
R9318:Or1j4
|
UTSW |
2 |
36,740,565 (GRCm39) |
missense |
probably benign |
0.12 |
|
Z1177:Or1j4
|
UTSW |
2 |
36,740,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Or1j4
|
UTSW |
2 |
36,740,251 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2013-11-05 |
Incidental Mutation