Incidental Mutation 'IGL01523:Or1j1'
| ID |
89487 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or1j1
|
| Ensembl Gene |
ENSMUSG00000075384 |
| Gene Name |
olfactory receptor family 1 subfamily J member 1 |
| Synonyms |
GA_x6K02T2NLDC-33507606-33506665, Olfr3, MOR136-14, Y71 |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.251)
|
| Stock # |
IGL01523
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
36702161-36703102 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 36702415 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 230
(T230S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149118
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100151]
[ENSMUST00000213988]
|
| AlphaFold |
Q60879 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000100151
AA Change: T230S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000097728
Gene: ENSMUSG00000075384
AA Change: T230S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
1.3e-61 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
220 |
2.9e-7 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
6.3e-25 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000120418
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213988
AA Change: T230S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| 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: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca8b |
T |
C |
11: 109,867,320 (GRCm39) |
E246G |
probably damaging |
Het |
| B3galt5 |
T |
A |
16: 96,117,091 (GRCm39) |
D241E |
probably damaging |
Het |
| Camta1 |
A |
G |
4: 151,229,507 (GRCm39) |
F442L |
possibly damaging |
Het |
| Cntnap5b |
A |
T |
1: 100,359,504 (GRCm39) |
E709V |
probably benign |
Het |
| Ctnnal1 |
T |
C |
4: 56,835,243 (GRCm39) |
I345V |
probably damaging |
Het |
| Evpl |
T |
C |
11: 116,124,270 (GRCm39) |
N183S |
probably damaging |
Het |
| Fam90a1b |
T |
C |
X: 93,400,365 (GRCm39) |
D155G |
probably benign |
Het |
| Fsip2 |
G |
A |
2: 82,807,863 (GRCm39) |
S1394N |
probably benign |
Het |
| Gcnt2 |
A |
T |
13: 41,041,339 (GRCm39) |
Q166L |
probably benign |
Het |
| Gpatch1 |
T |
C |
7: 35,007,763 (GRCm39) |
D99G |
probably null |
Het |
| Grin2b |
A |
T |
6: 136,021,263 (GRCm39) |
W13R |
probably null |
Het |
| Hbb-bh1 |
C |
T |
7: 103,491,024 (GRCm39) |
V127M |
probably benign |
Het |
| Hc |
C |
T |
2: 34,929,250 (GRCm39) |
M282I |
probably benign |
Het |
| Hirip3 |
A |
G |
7: 126,461,876 (GRCm39) |
E57G |
probably damaging |
Het |
| Inpp5j |
C |
T |
11: 3,445,932 (GRCm39) |
|
probably null |
Het |
| Krt84 |
A |
T |
15: 101,437,179 (GRCm39) |
V328E |
probably damaging |
Het |
| Lrriq1 |
C |
A |
10: 103,053,977 (GRCm39) |
E247* |
probably null |
Het |
| Mmrn2 |
T |
A |
14: 34,125,174 (GRCm39) |
F918L |
probably damaging |
Het |
| Myh13 |
A |
G |
11: 67,238,769 (GRCm39) |
E704G |
possibly damaging |
Het |
| Myo16 |
T |
A |
8: 10,420,908 (GRCm39) |
N249K |
probably damaging |
Het |
| Nobox |
C |
A |
6: 43,281,057 (GRCm39) |
K472N |
probably damaging |
Het |
| Orc4 |
A |
T |
2: 48,807,236 (GRCm39) |
S232T |
probably benign |
Het |
| Pign |
A |
T |
1: 105,580,903 (GRCm39) |
Y159N |
probably damaging |
Het |
| Rere |
T |
A |
4: 150,700,012 (GRCm39) |
V1032E |
possibly damaging |
Het |
| Ror2 |
T |
C |
13: 53,272,999 (GRCm39) |
Q210R |
probably benign |
Het |
| Sh3tc2 |
G |
A |
18: 62,123,954 (GRCm39) |
R905Q |
probably benign |
Het |
| Ttn |
A |
G |
2: 76,785,327 (GRCm39) |
S683P |
possibly damaging |
Het |
|
| Other mutations in Or1j1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0501:Or1j1
|
UTSW |
2 |
36,702,492 (GRCm39) |
nonsense |
probably null |
|
|
R0519:Or1j1
|
UTSW |
2 |
36,702,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0890:Or1j1
|
UTSW |
2 |
36,702,586 (GRCm39) |
missense |
probably benign |
0.06 |
|
R1353:Or1j1
|
UTSW |
2 |
36,702,926 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R1543:Or1j1
|
UTSW |
2 |
36,703,069 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3435:Or1j1
|
UTSW |
2 |
36,702,690 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4378:Or1j1
|
UTSW |
2 |
36,702,481 (GRCm39) |
missense |
probably benign |
|
|
R4585:Or1j1
|
UTSW |
2 |
36,702,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4586:Or1j1
|
UTSW |
2 |
36,702,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4626:Or1j1
|
UTSW |
2 |
36,702,271 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4714:Or1j1
|
UTSW |
2 |
36,703,047 (GRCm39) |
missense |
probably benign |
0.37 |
|
R4720:Or1j1
|
UTSW |
2 |
36,702,484 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5390:Or1j1
|
UTSW |
2 |
36,702,444 (GRCm39) |
missense |
probably benign |
|
|
R5659:Or1j1
|
UTSW |
2 |
36,702,966 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5681:Or1j1
|
UTSW |
2 |
36,702,693 (GRCm39) |
missense |
probably benign |
0.18 |
|
R6750:Or1j1
|
UTSW |
2 |
36,702,954 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7003:Or1j1
|
UTSW |
2 |
36,703,047 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R7353:Or1j1
|
UTSW |
2 |
36,702,915 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7514:Or1j1
|
UTSW |
2 |
36,702,651 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8094:Or1j1
|
UTSW |
2 |
36,702,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8298:Or1j1
|
UTSW |
2 |
36,703,038 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9189:Or1j1
|
UTSW |
2 |
36,702,214 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9577:Or1j1
|
UTSW |
2 |
36,702,567 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9622:Or1j1
|
UTSW |
2 |
36,702,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-03 |
Incidental Mutation