Incidental Mutation 'R1157:Or7c19'
| ID |
101809 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or7c19
|
| Ensembl Gene |
ENSMUSG00000051952 |
| Gene Name |
olfactory receptor family 7 subfamily C member 19 |
| Synonyms |
MOR141-3, Olfr371, GA_x6K02T2NUPS-13298842-13299780 |
| MMRRC Submission |
039230-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.067)
|
| Stock # |
R1157 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
85957126-85958064 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 85957889 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Cysteine to Phenylalanine
at position 255
(C255F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151714
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000070849]
[ENSMUST00000218663]
|
| AlphaFold |
Q8VGB8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000070849
AA Change: C255F
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000077921
Gene: ENSMUSG00000051952
AA Change: C255F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
308 |
9.1e-55 |
PFAM |
|
Pfam:7TM_GPCR_Srx
|
32 |
305 |
2.2e-6 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
305 |
3.2e-8 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
9.2e-27 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000218663
AA Change: C255F
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.7%
|
| 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: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamtsl4 |
C |
A |
3: 95,590,971 (GRCm39) |
S332I |
possibly damaging |
Het |
| Alpl |
A |
G |
4: 137,481,331 (GRCm39) |
V107A |
probably damaging |
Het |
| Baz1a |
A |
T |
12: 54,976,349 (GRCm39) |
F442L |
probably damaging |
Het |
| Cachd1 |
T |
A |
4: 100,832,037 (GRCm39) |
M733K |
possibly damaging |
Het |
| Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
| Cenpf |
A |
T |
1: 189,390,650 (GRCm39) |
C1061S |
probably benign |
Het |
| Crispld1 |
G |
A |
1: 17,815,587 (GRCm39) |
V90M |
possibly damaging |
Het |
| Ergic1 |
T |
A |
17: 26,833,369 (GRCm39) |
L41Q |
probably damaging |
Het |
| Fhod3 |
C |
T |
18: 25,118,293 (GRCm39) |
A210V |
probably damaging |
Het |
| Gas2l2 |
G |
A |
11: 83,314,154 (GRCm39) |
P386L |
probably benign |
Het |
| Gm21726 |
T |
C |
13: 90,731,724 (GRCm39) |
|
noncoding transcript |
Het |
| Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
| Hoxa13 |
CCG |
CCGCG |
6: 52,237,618 (GRCm39) |
|
probably null |
Het |
| Iqsec1 |
A |
G |
6: 90,646,366 (GRCm39) |
V771A |
possibly damaging |
Het |
| Klhl29 |
T |
C |
12: 5,140,650 (GRCm39) |
N664S |
possibly damaging |
Het |
| Krit1 |
T |
C |
5: 3,882,176 (GRCm39) |
Y659H |
probably damaging |
Het |
| Lap3 |
T |
A |
5: 45,664,490 (GRCm39) |
D373E |
probably damaging |
Het |
| Lrrc7 |
A |
G |
3: 157,865,892 (GRCm39) |
I1283T |
probably damaging |
Het |
| Lrrk1 |
T |
C |
7: 65,912,031 (GRCm39) |
Y1843C |
probably benign |
Het |
| Mapre1 |
T |
A |
2: 153,599,937 (GRCm39) |
D120E |
probably benign |
Het |
| Mgp |
A |
T |
6: 136,850,204 (GRCm39) |
M44K |
possibly damaging |
Het |
| Mrps25 |
A |
T |
6: 92,160,947 (GRCm39) |
M3K |
probably damaging |
Het |
| Myo3a |
G |
T |
2: 22,434,456 (GRCm39) |
|
probably null |
Het |
| Nedd9 |
C |
T |
13: 41,467,979 (GRCm39) |
|
probably null |
Het |
| Or52e4 |
A |
G |
7: 104,706,091 (GRCm39) |
I213V |
probably benign |
Het |
| Or6c8b |
T |
G |
10: 128,882,027 (GRCm39) |
T302P |
probably benign |
Het |
| Pate12 |
G |
A |
9: 36,344,143 (GRCm39) |
C42Y |
probably benign |
Het |
| Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
| Pigs |
T |
C |
11: 78,219,820 (GRCm39) |
V65A |
possibly damaging |
Het |
| Pip5k1a |
G |
A |
3: 94,985,423 (GRCm39) |
T60I |
probably benign |
Het |
| Rp9 |
A |
T |
9: 22,370,036 (GRCm39) |
Y44N |
probably damaging |
Het |
| Tcea1 |
T |
A |
1: 4,959,670 (GRCm39) |
|
probably null |
Het |
| Trim33 |
C |
T |
3: 103,261,146 (GRCm39) |
T1098I |
probably damaging |
Het |
| Vmn2r114 |
T |
A |
17: 23,529,314 (GRCm39) |
I263F |
possibly damaging |
Het |
| Wdr12 |
A |
T |
1: 60,117,389 (GRCm39) |
S402R |
probably damaging |
Het |
| Zfp619 |
A |
G |
7: 39,186,282 (GRCm39) |
S771G |
probably damaging |
Het |
|
| Other mutations in Or7c19 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01104:Or7c19
|
APN |
8 |
85,957,813 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL01380:Or7c19
|
APN |
8 |
85,957,775 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01380:Or7c19
|
APN |
8 |
85,957,958 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01680:Or7c19
|
APN |
8 |
85,957,308 (GRCm39) |
missense |
probably benign |
|
|
IGL01880:Or7c19
|
APN |
8 |
85,957,712 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02194:Or7c19
|
APN |
8 |
85,957,262 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02416:Or7c19
|
APN |
8 |
85,957,662 (GRCm39) |
nonsense |
probably null |
|
|
IGL02494:Or7c19
|
APN |
8 |
85,957,312 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03072:Or7c19
|
APN |
8 |
85,957,139 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL03130:Or7c19
|
APN |
8 |
85,957,258 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0017:Or7c19
|
UTSW |
8 |
85,957,706 (GRCm39) |
missense |
probably benign |
0.25 |
|
R1165:Or7c19
|
UTSW |
8 |
85,957,400 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1730:Or7c19
|
UTSW |
8 |
85,957,477 (GRCm39) |
missense |
probably benign |
0.16 |
|
R2017:Or7c19
|
UTSW |
8 |
85,957,373 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2426:Or7c19
|
UTSW |
8 |
85,957,693 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4447:Or7c19
|
UTSW |
8 |
85,957,995 (GRCm39) |
nonsense |
probably null |
|
|
R4703:Or7c19
|
UTSW |
8 |
85,957,237 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4797:Or7c19
|
UTSW |
8 |
85,957,567 (GRCm39) |
missense |
probably benign |
|
|
R5029:Or7c19
|
UTSW |
8 |
85,957,835 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5173:Or7c19
|
UTSW |
8 |
85,957,205 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6349:Or7c19
|
UTSW |
8 |
85,957,787 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7754:Or7c19
|
UTSW |
8 |
85,957,427 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8955:Or7c19
|
UTSW |
8 |
85,957,913 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
|
| Posted On |
2014-01-15 |
Incidental Mutation