Incidental Mutation 'IGL00886:Or13g1'
| ID |
27748 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or13g1
|
| Ensembl Gene |
ENSMUSG00000054054 |
| Gene Name |
olfactory receptor family 13 subfamily G member 1 |
| Synonyms |
MOR251-4P, GA_x6K02T2NHDJ-9801340-9802266, Olfr309 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.058)
|
| Stock # |
IGL00886
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
85955393-85956319 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 85956259 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Phenylalanine
at position 21
(L21F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134377
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055690]
[ENSMUST00000174158]
|
| AlphaFold |
Q7TS01 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000055690
AA Change: L21F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000061929
Gene: ENSMUSG00000054054
AA Change: L21F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7TM_GPCR_Srsx
|
33 |
303 |
4.5e-11 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
1.5e-26 |
PFAM |
|
Pfam:7tm_4
|
137 |
281 |
7.9e-44 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000174158
AA Change: L21F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000134377
Gene: ENSMUSG00000054054
AA Change: L21F
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
29 |
305 |
1.6e-55 |
PFAM |
|
Pfam:7TM_GPCR_Srsx
|
33 |
303 |
4.5e-11 |
PFAM |
|
Pfam:7tm_1
|
39 |
288 |
2.4e-18 |
PFAM |
|
| Coding Region Coverage |
|
| 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: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca9 |
C |
T |
11: 110,054,101 (GRCm39) |
R67H |
possibly damaging |
Het |
| Ak4 |
G |
T |
4: 101,304,386 (GRCm39) |
E59* |
probably null |
Het |
| Ano10 |
T |
C |
9: 122,100,390 (GRCm39) |
N116S |
probably benign |
Het |
| Arid1b |
T |
A |
17: 5,177,254 (GRCm39) |
H658Q |
probably damaging |
Het |
| Atf2 |
G |
A |
2: 73,675,847 (GRCm39) |
T208I |
possibly damaging |
Het |
| Bco1 |
T |
C |
8: 117,857,376 (GRCm39) |
W448R |
probably damaging |
Het |
| Cel |
A |
T |
2: 28,449,397 (GRCm39) |
C277S |
probably damaging |
Het |
| Chd5 |
T |
A |
4: 152,444,156 (GRCm39) |
D296E |
probably benign |
Het |
| Crygd |
C |
T |
1: 65,101,250 (GRCm39) |
R115Q |
probably benign |
Het |
| Fmo9 |
T |
C |
1: 166,507,714 (GRCm39) |
|
probably null |
Het |
| Gdpgp1 |
T |
G |
7: 79,889,100 (GRCm39) |
L377R |
probably damaging |
Het |
| Gm26938 |
T |
A |
5: 139,812,091 (GRCm39) |
D3V |
probably damaging |
Het |
| Gpld1 |
T |
A |
13: 25,146,336 (GRCm39) |
Y193* |
probably null |
Het |
| Gtf2h4 |
T |
C |
17: 35,980,874 (GRCm39) |
H265R |
probably damaging |
Het |
| Hadh |
G |
T |
3: 131,043,465 (GRCm39) |
T83K |
probably benign |
Het |
| Hao1 |
T |
C |
2: 134,365,079 (GRCm39) |
M183V |
probably benign |
Het |
| Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
| Ift88 |
T |
C |
14: 57,715,525 (GRCm39) |
Y523H |
probably damaging |
Het |
| Il23r |
G |
T |
6: 67,450,874 (GRCm39) |
Q202K |
possibly damaging |
Het |
| Iyd |
T |
C |
10: 3,540,444 (GRCm38) |
D50A |
probably benign |
Het |
| Katnal2 |
A |
T |
18: 77,090,450 (GRCm39) |
L248Q |
probably damaging |
Het |
| Krtap26-1 |
A |
T |
16: 88,444,267 (GRCm39) |
V118E |
possibly damaging |
Het |
| Lzic |
T |
C |
4: 149,577,753 (GRCm39) |
|
probably null |
Het |
| Meak7 |
T |
C |
8: 120,500,007 (GRCm39) |
|
probably benign |
Het |
| Mical2 |
T |
A |
7: 111,914,279 (GRCm39) |
N316K |
probably benign |
Het |
| Ndufc2 |
T |
A |
7: 97,049,397 (GRCm39) |
M1K |
probably null |
Het |
| Net1 |
A |
G |
13: 3,943,391 (GRCm39) |
|
probably benign |
Het |
| Pde1c |
A |
G |
6: 56,150,659 (GRCm39) |
Y287H |
probably damaging |
Het |
| Pitpnm1 |
T |
C |
19: 4,160,665 (GRCm39) |
|
probably null |
Het |
| Pla2r1 |
T |
A |
2: 60,254,668 (GRCm39) |
E1300V |
probably damaging |
Het |
| Polr3g |
T |
C |
13: 81,842,796 (GRCm39) |
Y73C |
probably damaging |
Het |
| Ryr1 |
T |
A |
7: 28,723,654 (GRCm39) |
E4137V |
probably damaging |
Het |
| Scrib |
T |
C |
15: 75,920,643 (GRCm39) |
D1425G |
possibly damaging |
Het |
| Slc25a12 |
A |
G |
2: 71,174,376 (GRCm39) |
Y23H |
possibly damaging |
Het |
| Spef2 |
C |
A |
15: 9,663,181 (GRCm39) |
G867W |
probably damaging |
Het |
| Strn3 |
A |
T |
12: 51,656,933 (GRCm39) |
Y698N |
probably damaging |
Het |
| Ube3a |
T |
A |
7: 58,934,485 (GRCm39) |
F533I |
probably damaging |
Het |
|
| Other mutations in Or13g1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
R0370:Or13g1
|
UTSW |
7 |
85,956,057 (GRCm39) |
missense |
probably benign |
0.42 |
|
R1869:Or13g1
|
UTSW |
7 |
85,955,875 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R2047:Or13g1
|
UTSW |
7 |
85,956,012 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3939:Or13g1
|
UTSW |
7 |
85,955,437 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4562:Or13g1
|
UTSW |
7 |
85,956,360 (GRCm39) |
start gained |
probably benign |
|
|
R4640:Or13g1
|
UTSW |
7 |
85,956,274 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4811:Or13g1
|
UTSW |
7 |
85,956,166 (GRCm39) |
missense |
probably benign |
0.41 |
|
R4867:Or13g1
|
UTSW |
7 |
85,955,491 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4954:Or13g1
|
UTSW |
7 |
85,955,809 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5784:Or13g1
|
UTSW |
7 |
85,955,743 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6043:Or13g1
|
UTSW |
7 |
85,955,547 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6498:Or13g1
|
UTSW |
7 |
85,956,226 (GRCm39) |
missense |
probably benign |
|
|
R6849:Or13g1
|
UTSW |
7 |
85,956,248 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R7238:Or13g1
|
UTSW |
7 |
85,955,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7811:Or13g1
|
UTSW |
7 |
85,955,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7917:Or13g1
|
UTSW |
7 |
85,955,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8010:Or13g1
|
UTSW |
7 |
85,956,260 (GRCm39) |
missense |
probably benign |
0.24 |
|
R8271:Or13g1
|
UTSW |
7 |
85,955,962 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9017:Or13g1
|
UTSW |
7 |
85,955,957 (GRCm39) |
nonsense |
probably null |
|
|
R9150:Or13g1
|
UTSW |
7 |
85,955,942 (GRCm39) |
missense |
probably damaging |
0.96 |
|
T0975:Or13g1
|
UTSW |
7 |
85,955,492 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2013-04-17 |
Incidental Mutation