Incidental Mutation 'R0057:Or5m10b'
| ID |
64368 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Or5m10b
|
| Ensembl Gene |
ENSMUSG00000057761 |
| Gene Name |
olfactory receptor family 5 subfamily M member 10B |
| Synonyms |
GA_x6K02T2Q125-47347069-47348016, Olfr1022, MOR196-1 |
| MMRRC Submission |
038351-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.057)
|
| Stock # |
R0057 (G1)
|
| Quality Score |
167 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
85698938-85699885 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to A
at 85699597 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 220
(Y220*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000059312
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054736]
[ENSMUST00000121914]
|
| AlphaFold |
L7MTT3 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000054736
AA Change: Y220*
|
| SMART Domains |
Protein: ENSMUSP00000059312
Gene: ENSMUSG00000057761
AA Change: Y220*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
31 |
312 |
4.8e-51 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
35 |
304 |
8e-6 |
PFAM |
|
Pfam:7tm_1
|
41 |
290 |
9.8e-22 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000121914
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.9%
- 10x: 97.7%
- 20x: 95.9%
|
| Validation Efficiency |
100% (50/50) |
| 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: 28 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam23 |
T |
A |
1: 63,610,078 (GRCm39) |
H693Q |
probably damaging |
Het |
| Ap5z1 |
T |
C |
5: 142,456,144 (GRCm39) |
|
probably benign |
Het |
| Bloc1s6 |
T |
A |
2: 122,586,141 (GRCm39) |
|
probably benign |
Het |
| Caskin1 |
A |
G |
17: 24,723,870 (GRCm39) |
N886S |
probably damaging |
Het |
| Ctse |
G |
T |
1: 131,591,109 (GRCm39) |
D97Y |
probably damaging |
Het |
| Dcaf11 |
T |
C |
14: 55,806,767 (GRCm39) |
V490A |
probably benign |
Het |
| Dctn1 |
A |
G |
6: 83,156,874 (GRCm39) |
H7R |
probably benign |
Het |
| Dscam |
A |
C |
16: 96,474,936 (GRCm39) |
W1209G |
probably damaging |
Het |
| Fcsk |
C |
T |
8: 111,620,400 (GRCm39) |
|
probably benign |
Het |
| Gna11 |
A |
G |
10: 81,366,774 (GRCm39) |
M312T |
probably benign |
Het |
| Hacd2 |
T |
A |
16: 34,895,997 (GRCm39) |
V105D |
probably damaging |
Het |
| Htra4 |
C |
A |
8: 25,528,824 (GRCm39) |
V23L |
probably benign |
Het |
| Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
| Msh4 |
C |
T |
3: 153,575,318 (GRCm39) |
A686T |
probably benign |
Het |
| Nbas |
T |
A |
12: 13,440,958 (GRCm39) |
M1096K |
probably benign |
Het |
| Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
| Prlr |
A |
G |
15: 10,328,509 (GRCm39) |
Y328C |
probably damaging |
Het |
| Ros1 |
C |
T |
10: 52,056,287 (GRCm39) |
V68I |
probably benign |
Het |
| Shmt2 |
G |
A |
10: 127,356,917 (GRCm39) |
T31M |
possibly damaging |
Het |
| Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
| Tas2r135 |
A |
G |
6: 42,383,354 (GRCm39) |
T298A |
probably benign |
Het |
| Tmem175 |
C |
T |
5: 108,787,428 (GRCm39) |
H92Y |
probably damaging |
Het |
| Top3a |
C |
T |
11: 60,631,510 (GRCm39) |
A951T |
probably benign |
Het |
| Trpc4ap |
T |
C |
2: 155,482,406 (GRCm39) |
E528G |
possibly damaging |
Het |
| Trpm6 |
T |
C |
19: 18,764,119 (GRCm39) |
C242R |
probably benign |
Het |
| Vwa7 |
G |
A |
17: 35,243,523 (GRCm39) |
S710N |
possibly damaging |
Het |
| Zfa-ps |
A |
T |
10: 52,421,202 (GRCm39) |
|
noncoding transcript |
Het |
| Zfp770 |
T |
A |
2: 114,027,713 (GRCm39) |
R119* |
probably null |
Het |
|
| Other mutations in Or5m10b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02701:Or5m10b
|
APN |
2 |
85,699,802 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL03265:Or5m10b
|
APN |
2 |
85,699,494 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
PIT4366001:Or5m10b
|
UTSW |
2 |
85,699,226 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0057:Or5m10b
|
UTSW |
2 |
85,699,597 (GRCm39) |
nonsense |
probably null |
|
|
R0554:Or5m10b
|
UTSW |
2 |
85,699,863 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3873:Or5m10b
|
UTSW |
2 |
85,699,306 (GRCm39) |
nonsense |
probably null |
|
|
R3913:Or5m10b
|
UTSW |
2 |
85,699,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4698:Or5m10b
|
UTSW |
2 |
85,699,596 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5628:Or5m10b
|
UTSW |
2 |
85,699,149 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6467:Or5m10b
|
UTSW |
2 |
85,699,714 (GRCm39) |
nonsense |
probably null |
|
|
R6947:Or5m10b
|
UTSW |
2 |
85,699,271 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7092:Or5m10b
|
UTSW |
2 |
85,698,951 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7351:Or5m10b
|
UTSW |
2 |
85,694,415 (GRCm39) |
unclassified |
probably benign |
|
|
R7574:Or5m10b
|
UTSW |
2 |
85,699,350 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8430:Or5m10b
|
UTSW |
2 |
85,699,526 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8771:Or5m10b
|
UTSW |
2 |
85,699,712 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8969:Or5m10b
|
UTSW |
2 |
85,699,832 (GRCm39) |
missense |
probably benign |
0.19 |
|
R9101:Or5m10b
|
UTSW |
2 |
85,694,523 (GRCm39) |
unclassified |
probably benign |
|
|
R9630:Or5m10b
|
UTSW |
2 |
85,699,493 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9649:Or5m10b
|
UTSW |
2 |
85,699,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9649:Or5m10b
|
UTSW |
2 |
85,699,278 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGCAGCCCCTTGCATTACAGTACC -3'
(R):5'- CTGACAGAAATTCCCCTTGATCACCTG -3'
Sequencing Primer
(F):5'- CCTTGCATTACAGTACCAGGATG -3'
(R):5'- CTTAGGCTATAGATCAAAGGGTTCAG -3'
|
| Posted On |
2013-08-06 |
Incidental Mutation