Incidental Mutation 'IGL00981:Or2d2b'
ID |
27946 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Or2d2b
|
Ensembl Gene |
ENSMUSG00000062987 |
Gene Name |
olfactory receptor family 2 subfamily D member 2B |
Synonyms |
EG384732, Olfr715b, Gm10081 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.125)
|
Stock # |
IGL00981
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
106705119-106706066 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
C to A
at 106705268 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Stop codon
at position 267
(E267*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000149136
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081044]
[ENSMUST00000215713]
|
AlphaFold |
E9Q725 |
Predicted Effect |
probably null
Transcript: ENSMUST00000081044
AA Change: E267*
|
SMART Domains |
Protein: ENSMUSP00000079834 Gene: ENSMUSG00000062987 AA Change: E267*
Domain | Start | End | E-Value | Type |
Pfam:7tm_4
|
31 |
306 |
7e-57 |
PFAM |
Pfam:7TM_GPCR_Srsx
|
35 |
282 |
1.8e-7 |
PFAM |
Pfam:7tm_1
|
41 |
288 |
2.5e-26 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000215713
AA Change: E267*
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
G |
A |
18: 70,586,404 (GRCm39) |
Q478* |
probably null |
Het |
Armh4 |
A |
T |
14: 50,010,447 (GRCm39) |
L420Q |
probably damaging |
Het |
Atp7b |
T |
C |
8: 22,517,543 (GRCm39) |
|
probably null |
Het |
Bcan |
T |
A |
3: 87,905,139 (GRCm39) |
I2F |
possibly damaging |
Het |
Boc |
A |
G |
16: 44,312,164 (GRCm39) |
S633P |
probably damaging |
Het |
C2cd6 |
A |
G |
1: 59,117,104 (GRCm39) |
S130P |
probably damaging |
Het |
Cacna1a |
T |
C |
8: 85,275,182 (GRCm39) |
F490L |
probably damaging |
Het |
Carm1 |
T |
A |
9: 21,498,490 (GRCm39) |
D469E |
possibly damaging |
Het |
Cdyl |
A |
T |
13: 36,000,096 (GRCm39) |
S126C |
probably damaging |
Het |
Ceacam5 |
A |
T |
7: 17,479,458 (GRCm39) |
I192F |
probably benign |
Het |
Cyp2b19 |
C |
T |
7: 26,462,886 (GRCm39) |
T256I |
possibly damaging |
Het |
Dlgap5 |
C |
T |
14: 47,635,925 (GRCm39) |
E515K |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,755,049 (GRCm39) |
D1044E |
unknown |
Het |
Eif3i |
T |
A |
4: 129,488,862 (GRCm39) |
Y125F |
probably benign |
Het |
Gnai1 |
T |
G |
5: 18,472,045 (GRCm39) |
N346T |
probably benign |
Het |
Kcnd1 |
C |
T |
X: 7,702,672 (GRCm39) |
T629I |
probably benign |
Het |
Mcc |
A |
T |
18: 44,582,416 (GRCm39) |
N578K |
probably damaging |
Het |
Ncoa6 |
C |
T |
2: 155,248,099 (GRCm39) |
R1735Q |
probably damaging |
Het |
Nlrp4d |
A |
T |
7: 10,116,021 (GRCm39) |
|
noncoding transcript |
Het |
Nsun5 |
A |
T |
5: 135,404,249 (GRCm39) |
Q352L |
possibly damaging |
Het |
Or14j6 |
G |
A |
17: 38,215,072 (GRCm39) |
V212M |
probably benign |
Het |
Or8g18 |
A |
G |
9: 39,148,901 (GRCm39) |
V276A |
probably benign |
Het |
Pkdrej |
C |
T |
15: 85,703,857 (GRCm39) |
G693D |
probably damaging |
Het |
Rpl10a-ps2 |
A |
T |
13: 8,990,566 (GRCm39) |
|
probably benign |
Het |
Spink1 |
C |
T |
18: 43,870,159 (GRCm39) |
|
probably null |
Het |
Sqle |
T |
C |
15: 59,198,468 (GRCm39) |
V464A |
probably damaging |
Het |
Trav6-4 |
A |
T |
14: 53,692,153 (GRCm39) |
T84S |
probably damaging |
Het |
Trim33 |
T |
A |
3: 103,259,311 (GRCm39) |
|
probably benign |
Het |
Txlng |
T |
C |
X: 161,567,368 (GRCm39) |
M319V |
probably benign |
Het |
Wee1 |
A |
T |
7: 109,738,876 (GRCm39) |
E582D |
probably damaging |
Het |
|
Other mutations in Or2d2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00981:Or2d2b
|
APN |
7 |
106,705,269 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01642:Or2d2b
|
APN |
7 |
106,706,029 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03174:Or2d2b
|
APN |
7 |
106,705,477 (GRCm39) |
missense |
probably benign |
0.05 |
R1724:Or2d2b
|
UTSW |
7 |
106,705,409 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:Or2d2b
|
UTSW |
7 |
106,705,643 (GRCm39) |
missense |
probably benign |
|
R2860:Or2d2b
|
UTSW |
7 |
106,705,675 (GRCm39) |
missense |
probably benign |
0.10 |
R2861:Or2d2b
|
UTSW |
7 |
106,705,675 (GRCm39) |
missense |
probably benign |
0.10 |
R2862:Or2d2b
|
UTSW |
7 |
106,705,675 (GRCm39) |
missense |
probably benign |
0.10 |
R3807:Or2d2b
|
UTSW |
7 |
106,705,670 (GRCm39) |
missense |
probably benign |
0.01 |
R4797:Or2d2b
|
UTSW |
7 |
106,705,234 (GRCm39) |
missense |
probably benign |
0.26 |
R5008:Or2d2b
|
UTSW |
7 |
106,705,288 (GRCm39) |
missense |
probably damaging |
0.99 |
R5918:Or2d2b
|
UTSW |
7 |
106,705,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6090:Or2d2b
|
UTSW |
7 |
106,705,456 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6174:Or2d2b
|
UTSW |
7 |
106,705,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R6253:Or2d2b
|
UTSW |
7 |
106,705,145 (GRCm39) |
missense |
probably benign |
0.00 |
R7408:Or2d2b
|
UTSW |
7 |
106,705,274 (GRCm39) |
missense |
probably benign |
0.05 |
R7483:Or2d2b
|
UTSW |
7 |
106,705,982 (GRCm39) |
missense |
probably benign |
0.00 |
R7750:Or2d2b
|
UTSW |
7 |
106,705,740 (GRCm39) |
nonsense |
probably null |
|
R8260:Or2d2b
|
UTSW |
7 |
106,706,062 (GRCm39) |
missense |
probably benign |
|
R8374:Or2d2b
|
UTSW |
7 |
106,706,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Or2d2b
|
UTSW |
7 |
106,705,664 (GRCm39) |
missense |
probably benign |
0.01 |
R9431:Or2d2b
|
UTSW |
7 |
106,705,336 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2013-04-17 |