Incidental Mutation 'IGL03031:Gabrg1'
| ID |
408448 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Gabrg1
|
| Ensembl Gene |
ENSMUSG00000001260 |
| Gene Name |
gamma-aminobutyric acid type A receptor subunit gamma 1 |
| Synonyms |
GabaA |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.060)
|
| Stock # |
IGL03031
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
70908390-70999960 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 70952025 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 90
(Y90*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142454
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031119]
[ENSMUST00000199705]
|
| AlphaFold |
Q9R0Y8 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000031119
AA Change: Y95*
|
| SMART Domains |
Protein: ENSMUSP00000031119
Gene: ENSMUSG00000001260
AA Change: Y95*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
low complexity region
|
40 |
46 |
N/A |
INTRINSIC |
|
Pfam:Neur_chan_LBD
|
64 |
270 |
7e-51 |
PFAM |
|
Pfam:Neur_chan_memb
|
277 |
378 |
2.3e-36 |
PFAM |
|
low complexity region
|
411 |
422 |
N/A |
INTRINSIC |
|
transmembrane domain
|
441 |
463 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197068
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000199705
AA Change: Y90*
|
| SMART Domains |
Protein: ENSMUSP00000142454
Gene: ENSMUSG00000001260
AA Change: Y90*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
35 |
41 |
N/A |
INTRINSIC |
|
Pfam:Neur_chan_LBD
|
59 |
265 |
1.7e-50 |
PFAM |
|
Pfam:Neur_chan_memb
|
272 |
304 |
9.5e-12 |
PFAM |
|
low complexity region
|
365 |
376 |
N/A |
INTRINSIC |
|
transmembrane domain
|
395 |
417 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the ligand-gated ionic channel family. It is an integral membrane protein and plays an important role in inhibiting neurotransmission by binding to the benzodiazepine receptor and opening an integral chloride channel. This gene is clustered with three other family members on chromosome 4. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca12 |
T |
C |
1: 71,353,183 (GRCm39) |
D753G |
probably benign |
Het |
| Adat2 |
T |
C |
10: 13,432,590 (GRCm39) |
|
probably benign |
Het |
| Ahsa2 |
A |
G |
11: 23,440,426 (GRCm39) |
L275S |
probably benign |
Het |
| Arhgef38 |
C |
T |
3: 132,837,828 (GRCm39) |
D118N |
possibly damaging |
Het |
| Bicra |
A |
T |
7: 15,709,726 (GRCm39) |
H1097Q |
probably benign |
Het |
| C4b |
T |
C |
17: 34,950,104 (GRCm39) |
T1389A |
possibly damaging |
Het |
| Cd180 |
A |
G |
13: 102,841,535 (GRCm39) |
S194G |
probably benign |
Het |
| Chgb |
C |
A |
2: 132,635,434 (GRCm39) |
Q459K |
probably benign |
Het |
| Clvs1 |
G |
T |
4: 9,449,385 (GRCm39) |
|
probably benign |
Het |
| Cpox |
G |
A |
16: 58,492,923 (GRCm39) |
G186R |
probably damaging |
Het |
| Cul5 |
A |
G |
9: 53,553,975 (GRCm39) |
|
probably benign |
Het |
| Epsti1 |
G |
A |
14: 78,212,021 (GRCm39) |
R249K |
probably benign |
Het |
| Gabrp |
T |
C |
11: 33,504,980 (GRCm39) |
R274G |
probably damaging |
Het |
| Gm6401 |
C |
T |
14: 41,788,851 (GRCm39) |
E73K |
possibly damaging |
Het |
| Hectd4 |
C |
T |
5: 121,486,857 (GRCm39) |
T3284M |
possibly damaging |
Het |
| Hoxc9 |
T |
C |
15: 102,892,522 (GRCm39) |
M245T |
probably damaging |
Het |
| Lpar6 |
T |
C |
14: 73,476,882 (GRCm39) |
V281A |
possibly damaging |
Het |
| Med18 |
G |
T |
4: 132,186,924 (GRCm39) |
Q192K |
possibly damaging |
Het |
| Mis18bp1 |
A |
G |
12: 65,208,704 (GRCm39) |
V3A |
probably benign |
Het |
| Mpped2 |
G |
T |
2: 106,613,968 (GRCm39) |
|
probably benign |
Het |
| Ms4a10 |
A |
G |
19: 10,946,035 (GRCm39) |
V32A |
probably benign |
Het |
| Mthfd1l |
T |
A |
10: 3,968,601 (GRCm39) |
|
probably null |
Het |
| Myh1 |
A |
T |
11: 67,097,213 (GRCm39) |
Q422L |
possibly damaging |
Het |
| Myo3b |
A |
T |
2: 70,085,721 (GRCm39) |
Q819L |
possibly damaging |
Het |
| Ncoa1 |
G |
A |
12: 4,324,818 (GRCm39) |
T921I |
possibly damaging |
Het |
| Or10d4b |
A |
G |
9: 39,534,694 (GRCm39) |
I92V |
probably damaging |
Het |
| Or6c214 |
A |
G |
10: 129,591,238 (GRCm39) |
L27P |
possibly damaging |
Het |
| Or8c16 |
A |
C |
9: 38,130,361 (GRCm39) |
T81P |
probably damaging |
Het |
| Phf3 |
A |
G |
1: 30,843,734 (GRCm39) |
S1742P |
probably benign |
Het |
| Plxdc2 |
G |
A |
2: 16,655,043 (GRCm39) |
|
probably null |
Het |
| Poc5 |
A |
G |
13: 96,538,123 (GRCm39) |
T263A |
probably benign |
Het |
| Prss41 |
T |
A |
17: 24,061,396 (GRCm39) |
I132F |
probably damaging |
Het |
| Pxylp1 |
A |
G |
9: 96,707,195 (GRCm39) |
I329T |
probably benign |
Het |
| Rbm27 |
T |
C |
18: 42,466,464 (GRCm39) |
|
probably null |
Het |
| Rnps1-ps |
T |
C |
6: 7,982,857 (GRCm39) |
|
noncoding transcript |
Het |
| Rpgrip1l |
A |
T |
8: 91,987,411 (GRCm39) |
V882E |
probably damaging |
Het |
| Sec16b |
T |
C |
1: 157,388,369 (GRCm39) |
S579P |
probably benign |
Het |
| Senp7 |
A |
G |
16: 55,996,249 (GRCm39) |
E776G |
probably damaging |
Het |
| Smc2 |
A |
G |
4: 52,449,638 (GRCm39) |
I207V |
probably benign |
Het |
| Spata31e5 |
A |
G |
1: 28,817,664 (GRCm39) |
F123L |
probably benign |
Het |
| Spats2 |
A |
G |
15: 99,078,569 (GRCm39) |
T211A |
probably benign |
Het |
| Sphkap |
A |
T |
1: 83,254,552 (GRCm39) |
S779T |
probably damaging |
Het |
| Syt11 |
A |
T |
3: 88,656,148 (GRCm39) |
M1K |
probably null |
Het |
| Tacc2 |
A |
G |
7: 130,225,585 (GRCm39) |
T757A |
possibly damaging |
Het |
| Tecta |
A |
C |
9: 42,256,789 (GRCm39) |
M1629R |
probably benign |
Het |
| Ufsp2 |
T |
A |
8: 46,437,137 (GRCm39) |
I101N |
probably damaging |
Het |
| Unc13b |
T |
A |
4: 43,235,368 (GRCm39) |
C892S |
probably damaging |
Het |
| Ush1c |
A |
G |
7: 45,874,361 (GRCm39) |
|
probably benign |
Het |
| Vwde |
A |
T |
6: 13,208,381 (GRCm39) |
V167E |
probably benign |
Het |
| Wdfy4 |
A |
G |
14: 32,862,608 (GRCm39) |
L588P |
probably damaging |
Het |
| Zfyve1 |
T |
C |
12: 83,621,595 (GRCm39) |
T267A |
probably damaging |
Het |
|
| Other mutations in Gabrg1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00715:Gabrg1
|
APN |
5 |
70,973,298 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL00798:Gabrg1
|
APN |
5 |
70,939,626 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01012:Gabrg1
|
APN |
5 |
70,935,512 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01597:Gabrg1
|
APN |
5 |
70,939,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01637:Gabrg1
|
APN |
5 |
70,934,548 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02589:Gabrg1
|
APN |
5 |
70,999,495 (GRCm39) |
nonsense |
probably null |
|
|
IGL03346:Gabrg1
|
APN |
5 |
70,935,474 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
PIT4260001:Gabrg1
|
UTSW |
5 |
70,939,623 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0197:Gabrg1
|
UTSW |
5 |
70,931,732 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1271:Gabrg1
|
UTSW |
5 |
70,934,487 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1795:Gabrg1
|
UTSW |
5 |
70,939,596 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R1817:Gabrg1
|
UTSW |
5 |
70,911,594 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1820:Gabrg1
|
UTSW |
5 |
70,931,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2254:Gabrg1
|
UTSW |
5 |
70,939,707 (GRCm39) |
nonsense |
probably null |
|
|
R4566:Gabrg1
|
UTSW |
5 |
70,999,484 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4768:Gabrg1
|
UTSW |
5 |
70,911,516 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4976:Gabrg1
|
UTSW |
5 |
70,931,754 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5104:Gabrg1
|
UTSW |
5 |
70,931,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6062:Gabrg1
|
UTSW |
5 |
70,938,056 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6086:Gabrg1
|
UTSW |
5 |
70,911,396 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6148:Gabrg1
|
UTSW |
5 |
70,931,804 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6234:Gabrg1
|
UTSW |
5 |
70,999,484 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6724:Gabrg1
|
UTSW |
5 |
70,911,552 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R6786:Gabrg1
|
UTSW |
5 |
70,911,610 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6794:Gabrg1
|
UTSW |
5 |
70,973,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7209:Gabrg1
|
UTSW |
5 |
70,911,513 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7654:Gabrg1
|
UTSW |
5 |
70,935,504 (GRCm39) |
missense |
probably benign |
0.44 |
|
R7671:Gabrg1
|
UTSW |
5 |
70,973,323 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7844:Gabrg1
|
UTSW |
5 |
70,931,675 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7877:Gabrg1
|
UTSW |
5 |
70,973,415 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8219:Gabrg1
|
UTSW |
5 |
70,931,643 (GRCm39) |
nonsense |
probably null |
|
|
R8998:Gabrg1
|
UTSW |
5 |
70,973,378 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8999:Gabrg1
|
UTSW |
5 |
70,973,378 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9132:Gabrg1
|
UTSW |
5 |
70,939,622 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9279:Gabrg1
|
UTSW |
5 |
70,934,599 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9358:Gabrg1
|
UTSW |
5 |
70,935,422 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9483:Gabrg1
|
UTSW |
5 |
70,999,558 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R9506:Gabrg1
|
UTSW |
5 |
70,939,713 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9593:Gabrg1
|
UTSW |
5 |
70,939,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9747:Gabrg1
|
UTSW |
5 |
70,938,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0027:Gabrg1
|
UTSW |
5 |
70,911,604 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Posted On |
2016-08-02 |
Incidental Mutation