Incidental Mutation 'IGL01674:Or14j5'
| ID |
103576 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or14j5
|
| Ensembl Gene |
ENSMUSG00000109212 |
| Gene Name |
olfactory receptor family 14 subfamily J member 5 |
| Synonyms |
Olfr126, GA_x6K02T2PSCP-2307164-2308123, MOR218-1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.198)
|
| Stock # |
IGL01674
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
17 |
| Chromosomal Location |
38161485-38162444 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 37920853 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Valine
at position 263
(D263V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000152714
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076936]
[ENSMUST00000221552]
[ENSMUST00000223366]
|
| AlphaFold |
Q8VGF0 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000076936
AA Change: D265V
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000076203
Gene: ENSMUSG00000092413
AA Change: D265V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srv
|
24 |
252 |
2.6e-7 |
PFAM |
|
Pfam:7tm_4
|
31 |
308 |
3.2e-45 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
2.3e-21 |
PFAM |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000133907
Gene: ENSMUSG00000092413
AA Change: D263V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
8.2e-46 |
PFAM |
|
Pfam:7TM_GPCR_Srx
|
32 |
307 |
2.9e-9 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
3.4e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
5.6e-20 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000207850
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000221552
AA Change: D263V
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000223366
AA Change: D263V
PolyPhen 2
Score 0.992 (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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arhgef39 |
A |
G |
4: 43,497,590 (GRCm39) |
L222P |
probably damaging |
Het |
| Art3 |
T |
A |
5: 92,551,473 (GRCm39) |
Y17* |
probably null |
Het |
| Cadps2 |
A |
G |
6: 23,355,851 (GRCm39) |
L859P |
probably damaging |
Het |
| Celsr2 |
A |
G |
3: 108,322,159 (GRCm39) |
Y218H |
probably damaging |
Het |
| Ces5a |
A |
G |
8: 94,228,847 (GRCm39) |
V461A |
probably damaging |
Het |
| Clic4 |
C |
A |
4: 134,966,204 (GRCm39) |
V51L |
probably benign |
Het |
| Col6a3 |
A |
G |
1: 90,730,236 (GRCm39) |
L1083P |
probably damaging |
Het |
| Cul5 |
T |
C |
9: 53,546,307 (GRCm39) |
E328G |
probably damaging |
Het |
| Erap1 |
T |
C |
13: 74,812,350 (GRCm39) |
|
probably benign |
Het |
| Fn1 |
G |
A |
1: 71,645,900 (GRCm39) |
P1527L |
probably damaging |
Het |
| Gm20547 |
T |
A |
17: 35,100,631 (GRCm39) |
Q63L |
probably benign |
Het |
| Gm5089 |
T |
C |
14: 122,673,575 (GRCm39) |
T49A |
unknown |
Het |
| Ippk |
T |
C |
13: 49,602,740 (GRCm39) |
L362S |
probably damaging |
Het |
| Krt23 |
T |
C |
11: 99,377,593 (GRCm39) |
M138V |
probably benign |
Het |
| Magi3 |
A |
G |
3: 104,013,037 (GRCm39) |
|
probably benign |
Het |
| Mcc |
T |
A |
18: 44,624,223 (GRCm39) |
I266F |
probably benign |
Het |
| Mcph1 |
A |
G |
8: 18,681,535 (GRCm39) |
E224G |
probably damaging |
Het |
| Neurod4 |
A |
T |
10: 130,106,887 (GRCm39) |
L129H |
probably damaging |
Het |
| Or4c123 |
T |
A |
2: 89,127,014 (GRCm39) |
N200I |
probably damaging |
Het |
| Or5b24 |
T |
C |
19: 12,912,926 (GRCm39) |
S275P |
probably damaging |
Het |
| Or8h7 |
T |
C |
2: 86,721,093 (GRCm39) |
Y142C |
probably benign |
Het |
| Piezo2 |
A |
T |
18: 63,160,630 (GRCm39) |
I2342N |
probably damaging |
Het |
| Pnpt1 |
A |
G |
11: 29,105,787 (GRCm39) |
Q632R |
probably benign |
Het |
| Ppp2r2c |
T |
C |
5: 37,097,570 (GRCm39) |
M252T |
possibly damaging |
Het |
| Ppp4r2 |
A |
G |
6: 100,841,644 (GRCm39) |
N142D |
possibly damaging |
Het |
| Prex2 |
G |
T |
1: 11,240,965 (GRCm39) |
K1024N |
probably damaging |
Het |
| Rimklb |
T |
A |
6: 122,436,129 (GRCm39) |
I150F |
probably damaging |
Het |
| Slco4c1 |
T |
C |
1: 96,770,218 (GRCm39) |
Q282R |
probably damaging |
Het |
| Tmem92 |
T |
C |
11: 94,669,519 (GRCm39) |
E148G |
probably damaging |
Het |
| Traf7 |
T |
C |
17: 24,729,349 (GRCm39) |
|
probably benign |
Het |
| Ubr5 |
G |
A |
15: 37,998,623 (GRCm39) |
T1622M |
probably damaging |
Het |
| Vmn1r5 |
T |
A |
6: 56,962,911 (GRCm39) |
S195R |
probably damaging |
Het |
| Vmn2r67 |
C |
T |
7: 84,785,651 (GRCm39) |
V785I |
probably damaging |
Het |
| Ythdc2 |
G |
A |
18: 44,993,471 (GRCm39) |
D839N |
probably benign |
Het |
| Zfp184 |
T |
C |
13: 22,134,395 (GRCm39) |
|
probably benign |
Het |
| Zfp654 |
T |
C |
16: 64,605,004 (GRCm39) |
N525S |
probably benign |
Het |
|
| Other mutations in Or14j5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01082:Or14j5
|
APN |
17 |
38,161,514 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01656:Or14j5
|
APN |
17 |
38,162,029 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
IGL01903:Or14j5
|
APN |
17 |
37,920,758 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL02262:Or14j5
|
APN |
17 |
38,162,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02445:Or14j5
|
APN |
17 |
38,162,008 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0559:Or14j5
|
UTSW |
17 |
38,161,746 (GRCm39) |
nonsense |
probably null |
|
|
R1164:Or14j5
|
UTSW |
17 |
38,161,575 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1828:Or14j5
|
UTSW |
17 |
38,161,966 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1840:Or14j5
|
UTSW |
17 |
38,161,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1882:Or14j5
|
UTSW |
17 |
38,161,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2368:Or14j5
|
UTSW |
17 |
38,161,509 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2377:Or14j5
|
UTSW |
17 |
38,161,498 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3832:Or14j5
|
UTSW |
17 |
38,162,071 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6589:Or14j5
|
UTSW |
17 |
38,161,727 (GRCm39) |
nonsense |
probably null |
|
|
R7794:Or14j5
|
UTSW |
17 |
38,161,678 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7853:Or14j5
|
UTSW |
17 |
38,161,714 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8009:Or14j5
|
UTSW |
17 |
38,161,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8501:Or14j5
|
UTSW |
17 |
38,161,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8874:Or14j5
|
UTSW |
17 |
38,161,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8902:Or14j5
|
UTSW |
17 |
38,162,101 (GRCm39) |
missense |
probably benign |
0.10 |
|
| Posted On |
2014-01-21 |
Incidental Mutation