Incidental Mutation 'IGL01909:Or8b12b'
| ID |
179741 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or8b12b
|
| Ensembl Gene |
ENSMUSG00000058628 |
| Gene Name |
olfactory receptor family 8 subfamily B member 12B |
| Synonyms |
GA_x6K02T2PVTD-31458511-31459443, Olfr875, MOR161-4 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.098)
|
| Stock # |
IGL01909
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
37683933-37684936 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 37684159 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Lysine
at position 68
(I68K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150684
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000080634]
[ENSMUST00000215128]
|
| AlphaFold |
Q7TRE5 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000080634
AA Change: I68K
PolyPhen 2
Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000079467
Gene: ENSMUSG00000058628
AA Change: I68K
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
30 |
307 |
1.1e-48 |
PFAM |
|
Pfam:7tm_1
|
40 |
289 |
1.8e-23 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000215128
AA Change: I68K
PolyPhen 2
Score 0.954 (Sensitivity: 0.79; Specificity: 0.95)
|
| 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: 35 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700111E14Rik |
A |
T |
6: 36,914,152 (GRCm39) |
|
probably benign |
Het |
| Actn2 |
A |
T |
13: 12,324,479 (GRCm39) |
|
probably null |
Het |
| Apom |
C |
T |
17: 35,350,208 (GRCm39) |
A78T |
probably benign |
Het |
| Bambi |
A |
G |
18: 3,508,229 (GRCm39) |
Y7C |
possibly damaging |
Het |
| Cdc42bpb |
T |
C |
12: 111,289,576 (GRCm39) |
M418V |
probably benign |
Het |
| Clptm1 |
T |
C |
7: 19,389,701 (GRCm39) |
N43D |
probably benign |
Het |
| Cspp1 |
T |
C |
1: 10,136,886 (GRCm39) |
V241A |
probably benign |
Het |
| Ctnna3 |
T |
A |
10: 63,339,910 (GRCm39) |
I32N |
probably benign |
Het |
| Elp2 |
A |
G |
18: 24,752,576 (GRCm39) |
|
probably benign |
Het |
| Frmd4a |
A |
G |
2: 4,608,844 (GRCm39) |
D893G |
probably benign |
Het |
| Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
| Gm21738 |
G |
A |
14: 19,416,979 (GRCm38) |
S144L |
probably benign |
Het |
| Gm5862 |
A |
C |
5: 26,227,769 (GRCm39) |
W41G |
probably benign |
Het |
| H2-M10.1 |
C |
A |
17: 36,635,971 (GRCm39) |
G154* |
probably null |
Het |
| Igdcc3 |
C |
T |
9: 65,051,819 (GRCm39) |
R141W |
probably damaging |
Het |
| Igkv14-130 |
A |
G |
6: 67,768,323 (GRCm39) |
K60E |
possibly damaging |
Het |
| Kcnmb2 |
A |
G |
3: 32,252,512 (GRCm39) |
|
probably benign |
Het |
| Lrp4 |
T |
C |
2: 91,324,529 (GRCm39) |
L1288P |
possibly damaging |
Het |
| Mavs |
T |
A |
2: 131,087,441 (GRCm39) |
M313K |
probably benign |
Het |
| Mia2 |
A |
G |
12: 59,154,731 (GRCm39) |
E148G |
possibly damaging |
Het |
| Or6c76b |
A |
T |
10: 129,692,950 (GRCm39) |
T188S |
probably damaging |
Het |
| Or8d1 |
T |
A |
9: 38,767,013 (GRCm39) |
Y218* |
probably null |
Het |
| Plekha3 |
C |
T |
2: 76,517,047 (GRCm39) |
T133M |
probably damaging |
Het |
| Plxna1 |
A |
T |
6: 89,309,066 (GRCm39) |
|
probably null |
Het |
| Septin2 |
A |
G |
1: 93,426,823 (GRCm39) |
N144S |
probably damaging |
Het |
| Slc9a4 |
T |
C |
1: 40,651,451 (GRCm39) |
|
probably benign |
Het |
| Slco1b2 |
T |
A |
6: 141,594,312 (GRCm39) |
I59K |
probably damaging |
Het |
| Sp140l2 |
A |
G |
1: 85,231,907 (GRCm39) |
|
probably benign |
Het |
| Tnrc6b |
A |
G |
15: 80,786,184 (GRCm39) |
S1243G |
possibly damaging |
Het |
| Unc13a |
T |
A |
8: 72,091,854 (GRCm39) |
|
probably benign |
Het |
| Vmn2r105 |
T |
C |
17: 20,444,918 (GRCm39) |
R525G |
probably damaging |
Het |
| Vmn2r129 |
C |
T |
4: 156,690,549 (GRCm39) |
|
noncoding transcript |
Het |
| Vmn2r37 |
T |
A |
7: 9,219,032 (GRCm39) |
K451* |
probably null |
Het |
| Vmn2r71 |
C |
T |
7: 85,270,001 (GRCm39) |
T504I |
probably benign |
Het |
| Zfp668 |
A |
T |
7: 127,465,994 (GRCm39) |
C397S |
probably damaging |
Het |
|
| Other mutations in Or8b12b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02013:Or8b12b
|
APN |
9 |
37,684,185 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02162:Or8b12b
|
APN |
9 |
37,684,227 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL02966:Or8b12b
|
APN |
9 |
37,684,882 (GRCm39) |
missense |
probably benign |
0.28 |
|
R0017:Or8b12b
|
UTSW |
9 |
37,684,274 (GRCm39) |
missense |
probably benign |
0.08 |
|
R0520:Or8b12b
|
UTSW |
9 |
37,684,849 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0553:Or8b12b
|
UTSW |
9 |
37,684,627 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0833:Or8b12b
|
UTSW |
9 |
37,684,372 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1316:Or8b12b
|
UTSW |
9 |
37,684,039 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1547:Or8b12b
|
UTSW |
9 |
37,683,960 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1888:Or8b12b
|
UTSW |
9 |
37,684,163 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1888:Or8b12b
|
UTSW |
9 |
37,684,163 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1891:Or8b12b
|
UTSW |
9 |
37,684,163 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1894:Or8b12b
|
UTSW |
9 |
37,684,163 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R3055:Or8b12b
|
UTSW |
9 |
37,684,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4816:Or8b12b
|
UTSW |
9 |
37,684,726 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R4829:Or8b12b
|
UTSW |
9 |
37,684,243 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4952:Or8b12b
|
UTSW |
9 |
37,684,360 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6111:Or8b12b
|
UTSW |
9 |
37,684,228 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6838:Or8b12b
|
UTSW |
9 |
37,684,348 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7101:Or8b12b
|
UTSW |
9 |
37,684,287 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7104:Or8b12b
|
UTSW |
9 |
37,684,437 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R7224:Or8b12b
|
UTSW |
9 |
37,684,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7334:Or8b12b
|
UTSW |
9 |
37,684,293 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7582:Or8b12b
|
UTSW |
9 |
37,684,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7909:Or8b12b
|
UTSW |
9 |
37,684,033 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8498:Or8b12b
|
UTSW |
9 |
37,684,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9158:Or8b12b
|
UTSW |
9 |
37,684,800 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2014-05-07 |
Incidental Mutation