Incidental Mutation 'R3945:Or4f4b'
| ID |
307632 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or4f4b
|
| Ensembl Gene |
ENSMUSG00000061195 |
| Gene Name |
olfactory receptor family 4 subfamily F member 4B |
| Synonyms |
MOR245-6, GA_x6K02T2Q125-72534883-72535821, Olfr1289 |
| MMRRC Submission |
040926-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.154)
|
| Stock # |
R3945 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
111313777-111314673 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 111314032 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 86
(Q86*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000147119
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102551]
[ENSMUST00000104889]
[ENSMUST00000120021]
[ENSMUST00000207494]
[ENSMUST00000214816]
[ENSMUST00000217611]
|
| AlphaFold |
A0A288CFY5 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000102551
AA Change: Q86*
|
| SMART Domains |
Protein: ENSMUSP00000099611
Gene: ENSMUSG00000108908
AA Change: Q86*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
17 |
289 |
6e-45 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
20 |
288 |
1.4e-7 |
PFAM |
|
Pfam:7tm_1
|
27 |
273 |
7e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000104889
|
| SMART Domains |
Protein: ENSMUSP00000100485
Gene: ENSMUSG00000044039
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
304 |
1.3e-43 |
PFAM |
|
Pfam:7tm_1
|
41 |
287 |
2.5e-20 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000120021
AA Change: Q114*
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000207494
AA Change: Q86*
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214816
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217611
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225425
|
| Meta Mutation Damage Score |
0.9717 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.4%
|
| Validation Efficiency |
100% (54/54) |
| 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: 49 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930407I10Rik |
T |
C |
15: 81,949,601 (GRCm39) |
L1166P |
probably damaging |
Het |
| Actn4 |
T |
C |
7: 28,611,661 (GRCm39) |
|
probably null |
Het |
| Adamts17 |
A |
T |
7: 66,770,687 (GRCm39) |
E905V |
probably benign |
Het |
| Adck5 |
A |
G |
15: 76,479,400 (GRCm39) |
N485S |
probably damaging |
Het |
| Agr3 |
C |
A |
12: 35,997,512 (GRCm39) |
|
probably benign |
Het |
| Ankrd12 |
G |
A |
17: 66,283,098 (GRCm39) |
T1921I |
probably damaging |
Het |
| Ascl2 |
T |
C |
7: 142,521,708 (GRCm39) |
S247G |
probably benign |
Het |
| Atp7b |
T |
C |
8: 22,510,880 (GRCm39) |
E422G |
probably benign |
Het |
| Bltp2 |
T |
C |
11: 78,180,790 (GRCm39) |
I2229T |
probably damaging |
Het |
| C630050I24Rik |
C |
T |
8: 107,845,894 (GRCm39) |
R15* |
probably null |
Het |
| Cabin1 |
T |
G |
10: 75,581,093 (GRCm39) |
Q411P |
probably damaging |
Het |
| Chrne |
T |
C |
11: 70,507,869 (GRCm39) |
I277V |
possibly damaging |
Het |
| Coch |
A |
G |
12: 51,648,595 (GRCm39) |
|
probably null |
Het |
| Corin |
A |
G |
5: 72,515,767 (GRCm39) |
V429A |
probably damaging |
Het |
| Cpa3 |
A |
T |
3: 20,279,281 (GRCm39) |
N219K |
probably damaging |
Het |
| Creb3l1 |
T |
C |
2: 91,821,556 (GRCm39) |
E273G |
probably damaging |
Het |
| Csmd1 |
A |
C |
8: 15,960,619 (GRCm39) |
|
probably null |
Het |
| Ddx59 |
A |
G |
1: 136,362,356 (GRCm39) |
D527G |
probably damaging |
Het |
| Defa25 |
G |
A |
8: 21,574,506 (GRCm39) |
V17I |
probably null |
Het |
| Efs |
A |
G |
14: 55,158,108 (GRCm39) |
|
probably benign |
Het |
| Ern2 |
A |
G |
7: 121,775,753 (GRCm39) |
M447T |
probably benign |
Het |
| Fgfr2 |
C |
T |
7: 129,779,485 (GRCm39) |
E596K |
possibly damaging |
Het |
| Filip1 |
T |
C |
9: 79,725,649 (GRCm39) |
K990R |
probably benign |
Het |
| Ipo8 |
T |
A |
6: 148,719,615 (GRCm39) |
Q110L |
probably damaging |
Het |
| Kank4 |
T |
A |
4: 98,659,517 (GRCm39) |
I854F |
probably damaging |
Het |
| Mst1 |
G |
A |
9: 107,962,052 (GRCm39) |
C681Y |
probably damaging |
Het |
| Nr2c2 |
C |
T |
6: 92,140,119 (GRCm39) |
R464W |
probably damaging |
Het |
| Or1s2 |
A |
G |
19: 13,758,786 (GRCm39) |
E270G |
probably benign |
Het |
| Pde11a |
T |
C |
2: 75,906,275 (GRCm39) |
|
probably benign |
Het |
| Ptprq |
A |
G |
10: 107,522,253 (GRCm39) |
|
probably benign |
Het |
| Rcbtb1 |
G |
A |
14: 59,462,225 (GRCm39) |
|
probably null |
Het |
| Rpl37 |
G |
A |
15: 5,147,176 (GRCm39) |
R72H |
probably benign |
Het |
| Samd9l |
A |
T |
6: 3,377,029 (GRCm39) |
S77R |
possibly damaging |
Het |
| Sin3b |
A |
G |
8: 73,460,067 (GRCm39) |
D218G |
possibly damaging |
Het |
| Slc22a23 |
A |
G |
13: 34,367,109 (GRCm39) |
I633T |
probably damaging |
Het |
| Spen |
T |
C |
4: 141,204,664 (GRCm39) |
D1321G |
unknown |
Het |
| Ssh2 |
T |
C |
11: 77,345,494 (GRCm39) |
S1160P |
possibly damaging |
Het |
| Synrg |
T |
A |
11: 83,914,232 (GRCm39) |
D952E |
probably damaging |
Het |
| Tigd3 |
A |
G |
19: 5,942,461 (GRCm39) |
F223S |
probably damaging |
Het |
| Trim66 |
G |
A |
7: 109,071,475 (GRCm39) |
T608I |
possibly damaging |
Het |
| Trmt13 |
A |
G |
3: 116,375,167 (GRCm39) |
F447S |
probably damaging |
Het |
| Trpc2 |
T |
C |
7: 101,737,486 (GRCm39) |
I800T |
possibly damaging |
Het |
| Ugt3a1 |
A |
T |
15: 9,370,184 (GRCm39) |
I443F |
possibly damaging |
Het |
| Vamp2 |
C |
A |
11: 68,980,000 (GRCm39) |
P24Q |
unknown |
Het |
| Vmn1r113 |
A |
G |
7: 20,521,637 (GRCm39) |
Y143C |
probably benign |
Het |
| Vmn1r14 |
T |
A |
6: 57,211,254 (GRCm39) |
N277K |
probably benign |
Het |
| Vmn1r181 |
T |
A |
7: 23,683,577 (GRCm39) |
V14E |
probably damaging |
Het |
| Wdfy4 |
A |
T |
14: 32,688,352 (GRCm39) |
I3086N |
probably damaging |
Het |
| Zfp988 |
A |
C |
4: 147,417,242 (GRCm39) |
K559Q |
probably benign |
Het |
|
| Other mutations in Or4f4b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01149:Or4f4b
|
APN |
2 |
111,314,446 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01682:Or4f4b
|
APN |
2 |
111,314,188 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02028:Or4f4b
|
APN |
2 |
111,313,816 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02731:Or4f4b
|
APN |
2 |
111,313,873 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03035:Or4f4b
|
APN |
2 |
111,314,168 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1214:Or4f4b
|
UTSW |
2 |
111,314,237 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1471:Or4f4b
|
UTSW |
2 |
111,314,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1714:Or4f4b
|
UTSW |
2 |
111,314,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2088:Or4f4b
|
UTSW |
2 |
111,314,623 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2136:Or4f4b
|
UTSW |
2 |
111,313,961 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2141:Or4f4b
|
UTSW |
2 |
111,313,975 (GRCm39) |
missense |
probably benign |
0.23 |
|
R4276:Or4f4b
|
UTSW |
2 |
111,313,849 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4562:Or4f4b
|
UTSW |
2 |
111,313,909 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4896:Or4f4b
|
UTSW |
2 |
111,314,005 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R4946:Or4f4b
|
UTSW |
2 |
111,314,311 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R5004:Or4f4b
|
UTSW |
2 |
111,314,005 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5686:Or4f4b
|
UTSW |
2 |
111,314,488 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6032:Or4f4b
|
UTSW |
2 |
111,314,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6032:Or4f4b
|
UTSW |
2 |
111,314,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6960:Or4f4b
|
UTSW |
2 |
111,314,071 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R7293:Or4f4b
|
UTSW |
2 |
111,313,699 (GRCm39) |
splice site |
probably null |
|
|
R7642:Or4f4b
|
UTSW |
2 |
111,313,823 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8429:Or4f4b
|
UTSW |
2 |
111,313,840 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R8447:Or4f4b
|
UTSW |
2 |
111,314,101 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATTCTCGGGAACTTCAGATCTTTC -3'
(R):5'- GTGTAGGAAGCCAATTGCCC -3'
Sequencing Primer
(F):5'- AGGCATTGTGTTTGGAAACC -3'
(R):5'- TGCCCATGCAGTAGCCAC -3'
|
| Posted On |
2015-04-17 |
Incidental Mutation