Incidental Mutation 'IGL02492:Or4n4b'
| ID |
295694 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or4n4b
|
| Ensembl Gene |
ENSMUSG00000090874 |
| Gene Name |
olfactory receptor family 4 subfamily N member 4B |
| Synonyms |
Olfr733, GA_x6K02T2PMLR-5992342-5991416, MOR241-2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.116)
|
| Stock # |
IGL02492
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
50535794-50536787 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 50536060 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Asparagine
at position 235
(K235N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149807
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000163469]
[ENSMUST00000214372]
[ENSMUST00000214756]
[ENSMUST00000216195]
|
| AlphaFold |
Q14AK5 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000163469
AA Change: K235N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000128332
Gene: ENSMUSG00000090874
AA Change: K235N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
305 |
6.4e-41 |
PFAM |
|
Pfam:7tm_1
|
41 |
288 |
1e-19 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000214372
AA Change: K235N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000214756
AA Change: K235N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000216195
AA Change: K235N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| 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: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Atm |
A |
G |
9: 53,367,159 (GRCm39) |
L2482P |
probably damaging |
Het |
| Bcl11b |
T |
C |
12: 107,881,945 (GRCm39) |
Y718C |
probably damaging |
Het |
| Bltp1 |
A |
G |
3: 37,102,262 (GRCm39) |
E1320G |
probably benign |
Het |
| Ccrl2 |
A |
G |
9: 110,884,871 (GRCm39) |
I209T |
probably benign |
Het |
| Cd200r2 |
A |
G |
16: 44,729,903 (GRCm39) |
K149R |
probably damaging |
Het |
| Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
| Col18a1 |
A |
G |
10: 76,907,855 (GRCm39) |
|
probably benign |
Het |
| Cops5 |
T |
A |
1: 10,097,377 (GRCm39) |
T291S |
probably benign |
Het |
| Csmd1 |
C |
A |
8: 16,052,597 (GRCm39) |
V2176F |
probably benign |
Het |
| Ctse |
C |
A |
1: 131,595,972 (GRCm39) |
S221R |
probably damaging |
Het |
| Cxcl3 |
A |
G |
5: 90,934,199 (GRCm39) |
|
probably null |
Het |
| Cyp51 |
C |
T |
5: 4,154,304 (GRCm39) |
V2I |
probably benign |
Het |
| Dennd5a |
A |
G |
7: 109,532,844 (GRCm39) |
F285L |
probably benign |
Het |
| Dst |
T |
G |
1: 34,191,274 (GRCm39) |
|
probably benign |
Het |
| Frzb |
A |
T |
2: 80,254,935 (GRCm39) |
|
probably benign |
Het |
| Gm5070 |
A |
T |
3: 95,318,354 (GRCm39) |
|
noncoding transcript |
Het |
| Gm9637 |
A |
G |
14: 19,402,182 (GRCm38) |
|
noncoding transcript |
Het |
| Grip1 |
A |
G |
10: 119,765,945 (GRCm39) |
|
probably benign |
Het |
| Itga4 |
C |
T |
2: 79,086,001 (GRCm39) |
|
probably benign |
Het |
| Ltbp2 |
A |
T |
12: 84,856,439 (GRCm39) |
I675N |
probably damaging |
Het |
| Pcdhb20 |
G |
T |
18: 37,639,453 (GRCm39) |
V660L |
probably benign |
Het |
| Prex2 |
T |
G |
1: 11,194,069 (GRCm39) |
L484R |
possibly damaging |
Het |
| Prkg1 |
A |
T |
19: 30,701,602 (GRCm39) |
V305D |
probably damaging |
Het |
| Rab44 |
A |
G |
17: 29,365,023 (GRCm39) |
|
probably benign |
Het |
| Smpd4 |
C |
T |
16: 17,457,215 (GRCm39) |
A391V |
probably damaging |
Het |
| Smyd4 |
T |
C |
11: 75,294,252 (GRCm39) |
L711P |
probably benign |
Het |
| Spag16 |
T |
G |
1: 69,926,688 (GRCm39) |
M261R |
probably benign |
Het |
| Steap1 |
A |
G |
5: 5,790,561 (GRCm39) |
V129A |
possibly damaging |
Het |
| Tbcd |
A |
T |
11: 121,387,960 (GRCm39) |
I364L |
probably benign |
Het |
| Trmt13 |
C |
T |
3: 116,376,192 (GRCm39) |
D400N |
possibly damaging |
Het |
| Vps13a |
A |
G |
19: 16,625,001 (GRCm39) |
S2753P |
probably damaging |
Het |
| Xirp2 |
T |
G |
2: 67,346,511 (GRCm39) |
S2917R |
probably damaging |
Het |
| Zfp983 |
G |
A |
17: 21,876,528 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Or4n4b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01879:Or4n4b
|
APN |
14 |
50,535,969 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02247:Or4n4b
|
APN |
14 |
50,536,571 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02307:Or4n4b
|
APN |
14 |
50,536,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4378001:Or4n4b
|
UTSW |
14 |
50,536,355 (GRCm39) |
missense |
probably benign |
|
|
R0544:Or4n4b
|
UTSW |
14 |
50,536,139 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1603:Or4n4b
|
UTSW |
14 |
50,536,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1881:Or4n4b
|
UTSW |
14 |
50,536,472 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3731:Or4n4b
|
UTSW |
14 |
50,535,962 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4271:Or4n4b
|
UTSW |
14 |
50,535,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4512:Or4n4b
|
UTSW |
14 |
50,536,453 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5601:Or4n4b
|
UTSW |
14 |
50,536,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6468:Or4n4b
|
UTSW |
14 |
50,535,924 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6614:Or4n4b
|
UTSW |
14 |
50,536,494 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7013:Or4n4b
|
UTSW |
14 |
50,536,656 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7083:Or4n4b
|
UTSW |
14 |
50,536,736 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R7274:Or4n4b
|
UTSW |
14 |
50,535,879 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7493:Or4n4b
|
UTSW |
14 |
50,536,281 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7653:Or4n4b
|
UTSW |
14 |
50,536,604 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R7659:Or4n4b
|
UTSW |
14 |
50,536,698 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7885:Or4n4b
|
UTSW |
14 |
50,536,041 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9138:Or4n4b
|
UTSW |
14 |
50,536,494 (GRCm39) |
missense |
probably benign |
|
|
R9497:Or4n4b
|
UTSW |
14 |
50,536,362 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2015-04-16 |
Incidental Mutation