Incidental Mutation 'R8875:Or52h7'
| ID |
676523 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or52h7
|
| Ensembl Gene |
ENSMUSG00000073927 |
| Gene Name |
olfactory receptor family 52 subfamily H member 7 |
| Synonyms |
MOR31-8, Olfr652, GA_x6K02T2PBJ9-7191524-7192471 |
| MMRRC Submission |
068687-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
R8875 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
104213359-104214419 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 104213670 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 81
(T81A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000149718
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000098175]
[ENSMUST00000215410]
[ENSMUST00000216131]
[ENSMUST00000219111]
|
| AlphaFold |
B9EHE6 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000098175
AA Change: T81A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
| SMART Domains |
Protein: ENSMUSP00000095777
Gene: ENSMUSG00000073927
AA Change: T81A
| Domain | Start | End | E-Value | Type |
|---|
|
transmembrane domain
|
7 |
25 |
N/A |
INTRINSIC |
|
Pfam:7tm_4
|
36 |
315 |
2.6e-105 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
40 |
312 |
6.9e-9 |
PFAM |
|
Pfam:7tm_1
|
46 |
297 |
4.7e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000215410
AA Change: T81A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216131
AA Change: T81A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000219111
AA Change: T81A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.8%
|
| Validation Efficiency |
100% (49/49) |
| 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: 50 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 0610010K14Rik |
A |
G |
11: 70,126,380 (GRCm39) |
V140A |
|
Het |
| Ablim1 |
G |
T |
19: 57,119,386 (GRCm39) |
H233N |
probably benign |
Het |
| Adra1a |
A |
T |
14: 66,875,214 (GRCm39) |
Y63F |
possibly damaging |
Het |
| Ank3 |
A |
G |
10: 69,660,233 (GRCm39) |
D245G |
unknown |
Het |
| Ap4e1 |
T |
C |
2: 126,877,100 (GRCm39) |
I279T |
probably damaging |
Het |
| Bap1 |
T |
G |
14: 30,975,522 (GRCm39) |
F122C |
probably damaging |
Het |
| Cdc5l |
T |
C |
17: 45,703,915 (GRCm39) |
|
probably benign |
Het |
| Chd2 |
A |
T |
7: 73,151,783 (GRCm39) |
I309N |
probably damaging |
Het |
| Cnpy3 |
T |
C |
17: 47,048,185 (GRCm39) |
I177V |
probably damaging |
Het |
| Cp |
A |
G |
3: 20,027,994 (GRCm39) |
K467E |
possibly damaging |
Het |
| D630039A03Rik |
T |
G |
4: 57,910,320 (GRCm39) |
N164T |
probably benign |
Het |
| Dnah7a |
C |
A |
1: 53,682,682 (GRCm39) |
A263S |
probably benign |
Het |
| Eif2s1 |
G |
A |
12: 78,913,461 (GRCm39) |
R54Q |
probably damaging |
Het |
| Fasn |
A |
T |
11: 120,703,224 (GRCm39) |
D1600E |
possibly damaging |
Het |
| Fat1 |
T |
A |
8: 45,493,600 (GRCm39) |
F3915L |
probably damaging |
Het |
| Fiz1 |
A |
T |
7: 5,012,093 (GRCm39) |
S142T |
probably benign |
Het |
| Fnip1 |
A |
G |
11: 54,406,380 (GRCm39) |
Y1159C |
probably damaging |
Het |
| Fsip2 |
T |
A |
2: 82,820,782 (GRCm39) |
V5505D |
possibly damaging |
Het |
| Gabrg3 |
A |
G |
7: 56,379,514 (GRCm39) |
M296T |
probably damaging |
Het |
| Gm11562 |
A |
T |
11: 99,511,177 (GRCm39) |
S8T |
unknown |
Het |
| Hoxd11 |
A |
G |
2: 74,513,365 (GRCm39) |
D210G |
probably benign |
Het |
| Hsd17b2 |
T |
C |
8: 118,469,101 (GRCm39) |
V171A |
possibly damaging |
Het |
| Ifi206 |
T |
C |
1: 173,301,353 (GRCm39) |
Y775C |
unknown |
Het |
| Nherf2 |
T |
A |
17: 24,866,703 (GRCm39) |
|
probably null |
Het |
| Nr2f1 |
A |
C |
13: 78,337,970 (GRCm39) |
I382S |
probably damaging |
Het |
| Nrp1 |
T |
A |
8: 129,207,472 (GRCm39) |
|
probably null |
Het |
| Or51l4 |
G |
A |
7: 103,404,462 (GRCm39) |
S110F |
probably damaging |
Het |
| Pdcd1 |
C |
T |
1: 93,967,092 (GRCm39) |
D269N |
probably benign |
Het |
| Pira12 |
A |
G |
7: 3,897,256 (GRCm39) |
S527P |
probably damaging |
Het |
| Plbd2 |
A |
G |
5: 120,637,121 (GRCm39) |
Y114H |
probably damaging |
Het |
| Plch1 |
A |
G |
3: 63,618,391 (GRCm39) |
C715R |
probably damaging |
Het |
| Plin4 |
G |
A |
17: 56,411,010 (GRCm39) |
A1007V |
probably benign |
Het |
| Ptprs |
G |
T |
17: 56,742,946 (GRCm39) |
P399T |
probably damaging |
Het |
| Pum1 |
T |
A |
4: 130,507,186 (GRCm39) |
I1181N |
possibly damaging |
Het |
| Qrich1 |
A |
G |
9: 108,436,502 (GRCm39) |
|
probably benign |
Het |
| Rbm12 |
T |
C |
2: 155,938,841 (GRCm39) |
E477G |
probably damaging |
Het |
| Rpl7 |
T |
C |
1: 16,173,753 (GRCm39) |
K57R |
probably benign |
Het |
| Spata31h1 |
G |
A |
10: 82,123,476 (GRCm39) |
A3178V |
probably benign |
Het |
| Stab2 |
C |
T |
10: 86,832,728 (GRCm39) |
C99Y |
probably damaging |
Het |
| Tas1r1 |
T |
A |
4: 152,113,047 (GRCm39) |
T669S |
probably benign |
Het |
| Tle5 |
A |
T |
10: 81,400,534 (GRCm39) |
I73F |
probably benign |
Het |
| Tm2d2 |
T |
C |
8: 25,507,443 (GRCm39) |
L20P |
possibly damaging |
Het |
| Tmem158 |
G |
T |
9: 123,089,132 (GRCm39) |
A160E |
possibly damaging |
Het |
| Tpst2 |
T |
A |
5: 112,457,714 (GRCm39) |
Y347* |
probably null |
Het |
| Trpm3 |
T |
C |
19: 22,887,493 (GRCm39) |
I876T |
probably damaging |
Het |
| Ttc6 |
T |
C |
12: 57,751,199 (GRCm39) |
F1364L |
probably damaging |
Het |
| Ttc6 |
T |
A |
12: 57,776,194 (GRCm39) |
S1713T |
possibly damaging |
Het |
| Vmn2r85 |
A |
G |
10: 130,254,171 (GRCm39) |
S838P |
probably damaging |
Het |
| Zc2hc1c |
T |
C |
12: 85,336,549 (GRCm39) |
S69P |
possibly damaging |
Het |
| Zfp982 |
C |
A |
4: 147,595,320 (GRCm39) |
N47K |
probably benign |
Het |
|
| Other mutations in Or52h7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01311:Or52h7
|
APN |
7 |
104,214,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01620:Or52h7
|
APN |
7 |
104,214,220 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01712:Or52h7
|
APN |
7 |
104,214,226 (GRCm39) |
missense |
probably benign |
|
|
IGL02211:Or52h7
|
APN |
7 |
104,214,333 (GRCm39) |
nonsense |
probably null |
|
|
IGL03328:Or52h7
|
APN |
7 |
104,213,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
K7894:Or52h7
|
UTSW |
7 |
104,213,739 (GRCm39) |
missense |
probably benign |
0.12 |
|
R0138:Or52h7
|
UTSW |
7 |
104,214,210 (GRCm39) |
missense |
probably benign |
|
|
R0632:Or52h7
|
UTSW |
7 |
104,213,544 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1457:Or52h7
|
UTSW |
7 |
104,214,278 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1494:Or52h7
|
UTSW |
7 |
104,214,038 (GRCm39) |
nonsense |
probably null |
|
|
R1879:Or52h7
|
UTSW |
7 |
104,214,118 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R2188:Or52h7
|
UTSW |
7 |
104,213,883 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2323:Or52h7
|
UTSW |
7 |
104,213,826 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3862:Or52h7
|
UTSW |
7 |
104,214,145 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3908:Or52h7
|
UTSW |
7 |
104,213,848 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4942:Or52h7
|
UTSW |
7 |
104,214,212 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5443:Or52h7
|
UTSW |
7 |
104,213,583 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5572:Or52h7
|
UTSW |
7 |
104,214,201 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6045:Or52h7
|
UTSW |
7 |
104,213,974 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6973:Or52h7
|
UTSW |
7 |
104,214,183 (GRCm39) |
missense |
probably benign |
0.42 |
|
R7147:Or52h7
|
UTSW |
7 |
104,213,273 (GRCm39) |
start gained |
probably benign |
|
|
R7349:Or52h7
|
UTSW |
7 |
104,213,857 (GRCm39) |
missense |
probably benign |
|
|
R7968:Or52h7
|
UTSW |
7 |
104,213,857 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8031:Or52h7
|
UTSW |
7 |
104,214,316 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8129:Or52h7
|
UTSW |
7 |
104,213,584 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8198:Or52h7
|
UTSW |
7 |
104,214,140 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8296:Or52h7
|
UTSW |
7 |
104,213,593 (GRCm39) |
missense |
probably benign |
|
|
R8345:Or52h7
|
UTSW |
7 |
104,213,431 (GRCm39) |
start codon destroyed |
probably null |
0.08 |
|
R8475:Or52h7
|
UTSW |
7 |
104,214,066 (GRCm39) |
missense |
probably benign |
|
|
R8881:Or52h7
|
UTSW |
7 |
104,213,619 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R8927:Or52h7
|
UTSW |
7 |
104,214,229 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8928:Or52h7
|
UTSW |
7 |
104,214,229 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0024:Or52h7
|
UTSW |
7 |
104,213,457 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGCTACATTCAACCTCAGCAG -3'
(R):5'- ATGGTGGTATATCTTAAGGGGAAGC -3'
Sequencing Primer
(F):5'- TCAGCAGCTTCAATCCAGG -3'
(R):5'- GCAGATAGCAACATAGCGATC -3'
|
| Posted On |
2021-07-15 |
Incidental Mutation