Incidental Mutation 'R3805:Or4b1'
| ID |
274537 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4b1
|
| Ensembl Gene |
ENSMUSG00000075065 |
| Gene Name |
olfactory receptor family 4 subfamily B member 1 |
| Synonyms |
Olfr1270, GA_x6K02T2Q125-51584440-51583526, MOR227-1 |
| MMRRC Submission |
040762-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.092)
|
| Stock # |
R3805 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
89979363-89980380 bp(-) (GRCm39) |
| Type of Mutation |
utr 3 prime |
| DNA Base Change (assembly) |
T to G
at 89978805 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150561
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099754]
[ENSMUST00000213946]
[ENSMUST00000215578]
[ENSMUST00000215975]
[ENSMUST00000216354]
[ENSMUST00000217139]
|
| AlphaFold |
Q8VGP3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099754
|
| SMART Domains |
Protein: ENSMUSP00000097343
Gene: ENSMUSG00000075065
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
303 |
2.3e-54 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
33 |
300 |
7.5e-6 |
PFAM |
|
Pfam:7tm_1
|
39 |
285 |
2e-24 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000165784
|
| SMART Domains |
Protein: ENSMUSP00000126140
Gene: ENSMUSG00000091703
| Domain | Start | End | E-Value | Type |
|---|
|
HOX
|
19 |
81 |
1.29e-3 |
SMART |
|
low complexity region
|
118 |
128 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000213946
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215578
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215975
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216354
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217139
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.7%
- 20x: 96.1%
|
| Validation Efficiency |
100% (41/41) |
| 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 |
|---|
| 1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
| Aebp2 |
GCGGCC |
GCGGCCGGCC |
6: 140,589,675 (GRCm39) |
|
probably null |
Het |
| Ano5 |
T |
C |
7: 51,226,398 (GRCm39) |
F584L |
probably benign |
Het |
| Ap1b1 |
T |
A |
11: 4,983,225 (GRCm39) |
|
probably null |
Het |
| Bicd1 |
T |
A |
6: 149,420,489 (GRCm39) |
L780M |
probably damaging |
Het |
| Ccdc138 |
T |
C |
10: 58,397,819 (GRCm39) |
I553T |
possibly damaging |
Het |
| Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
| Crct1 |
C |
A |
3: 92,922,014 (GRCm39) |
|
probably benign |
Het |
| Ctu1 |
T |
C |
7: 43,326,097 (GRCm39) |
L252P |
probably damaging |
Het |
| Dhrs2 |
A |
T |
14: 55,472,205 (GRCm39) |
N32I |
probably benign |
Het |
| Dnah1 |
A |
T |
14: 31,016,720 (GRCm39) |
M1599K |
possibly damaging |
Het |
| Eri2 |
A |
T |
7: 119,385,231 (GRCm39) |
C423* |
probably null |
Het |
| Fam169a |
G |
A |
13: 97,234,192 (GRCm39) |
V155I |
probably benign |
Het |
| Get4 |
G |
T |
5: 139,238,286 (GRCm39) |
V23F |
probably damaging |
Het |
| Hdac3 |
A |
G |
18: 38,078,745 (GRCm39) |
|
probably null |
Het |
| Herc3 |
C |
A |
6: 58,893,835 (GRCm39) |
H970Q |
probably damaging |
Het |
| Htt |
A |
G |
5: 35,034,548 (GRCm39) |
|
probably null |
Het |
| Ifit1 |
A |
G |
19: 34,625,556 (GRCm39) |
I231V |
probably damaging |
Het |
| Lingo4 |
A |
G |
3: 94,309,407 (GRCm39) |
D115G |
probably damaging |
Het |
| Lrrc7 |
T |
C |
3: 157,891,130 (GRCm39) |
I346V |
probably benign |
Het |
| Map7d1 |
A |
T |
4: 126,131,084 (GRCm39) |
|
probably null |
Het |
| Morf4l1 |
A |
G |
9: 89,977,196 (GRCm39) |
S203P |
probably benign |
Het |
| Naaladl1 |
A |
G |
19: 6,164,895 (GRCm39) |
T628A |
probably benign |
Het |
| Nlrp9a |
T |
A |
7: 26,264,277 (GRCm39) |
C643* |
probably null |
Het |
| Or4ac1-ps1 |
A |
T |
2: 88,370,700 (GRCm39) |
|
noncoding transcript |
Het |
| Oxtr |
T |
C |
6: 112,454,147 (GRCm39) |
K39R |
probably benign |
Het |
| Ppp4r4 |
T |
A |
12: 103,566,625 (GRCm39) |
M24K |
probably damaging |
Het |
| Ppp6r2 |
T |
C |
15: 89,149,842 (GRCm39) |
F256L |
probably benign |
Het |
| Robo4 |
A |
T |
9: 37,315,734 (GRCm39) |
D329V |
possibly damaging |
Het |
| Rsph10b |
G |
A |
5: 143,895,206 (GRCm39) |
|
probably null |
Het |
| Slc9b2 |
T |
C |
3: 135,030,349 (GRCm39) |
L222P |
probably damaging |
Het |
| Speer4a1 |
C |
T |
5: 26,240,082 (GRCm39) |
E223K |
possibly damaging |
Het |
| St18 |
T |
A |
1: 6,872,577 (GRCm39) |
L104H |
probably damaging |
Het |
| Tmem184c |
C |
A |
8: 78,323,504 (GRCm39) |
D453Y |
unknown |
Het |
| Trpv1 |
A |
T |
11: 73,143,879 (GRCm39) |
N237I |
probably damaging |
Het |
| Vmn2r77 |
T |
A |
7: 86,444,368 (GRCm39) |
L7* |
probably null |
Het |
|
| Other mutations in Or4b1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02648:Or4b1
|
APN |
2 |
89,979,697 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
IGL03034:Or4b1
|
APN |
2 |
89,980,177 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0726:Or4b1
|
UTSW |
2 |
89,979,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1573:Or4b1
|
UTSW |
2 |
89,979,068 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R1965:Or4b1
|
UTSW |
2 |
89,979,748 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1966:Or4b1
|
UTSW |
2 |
89,979,748 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2353:Or4b1
|
UTSW |
2 |
89,980,062 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4606:Or4b1
|
UTSW |
2 |
89,979,160 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4662:Or4b1
|
UTSW |
2 |
89,980,222 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6198:Or4b1
|
UTSW |
2 |
89,979,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6596:Or4b1
|
UTSW |
2 |
89,979,622 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6957:Or4b1
|
UTSW |
2 |
89,979,494 (GRCm39) |
nonsense |
probably null |
|
|
R7408:Or4b1
|
UTSW |
2 |
89,980,188 (GRCm39) |
missense |
probably benign |
|
|
R7418:Or4b1
|
UTSW |
2 |
89,979,831 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7454:Or4b1
|
UTSW |
2 |
89,979,763 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7935:Or4b1
|
UTSW |
2 |
89,979,928 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9006:Or4b1
|
UTSW |
2 |
89,980,327 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9157:Or4b1
|
UTSW |
2 |
89,979,522 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R9454:Or4b1
|
UTSW |
2 |
89,979,820 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9478:Or4b1
|
UTSW |
2 |
89,979,595 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTACTCCAGCCATAATAGAAGCAGG -3'
(R):5'- CGCTGAGTGATGAACCAGGATC -3'
Sequencing Primer
(F):5'- CCAGCCATAATAGAAGCAGGTATCAG -3'
(R):5'- AACCAGGATCTGATGAGGTCTTTC -3'
|
| Posted On |
2015-04-02 |
Incidental Mutation