Incidental Mutation 'IGL01686:Gabrp'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gabrp
Ensembl Gene ENSMUSG00000020159
Gene Namegamma-aminobutyric acid (GABA) A receptor, pi
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #IGL01686
Quality Score
Chromosomal Location33550781-33578959 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to T at 33552826 bp
Amino Acid Change Serine to Stop codon at position 346 (S346*)
Ref Sequence ENSEMBL: ENSMUSP00000020366 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020366]
Predicted Effect probably null
Transcript: ENSMUST00000020366
AA Change: S346*
SMART Domains Protein: ENSMUSP00000020366
Gene: ENSMUSG00000020159
AA Change: S346*

signal peptide 1 23 N/A INTRINSIC
Pfam:Neur_chan_LBD 40 242 1.3e-49 PFAM
Pfam:Neur_chan_memb 249 353 5.2e-23 PFAM
transmembrane domain 420 437 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 gamma-aminobutyric acid (GABA) A receptor is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. The subunit encoded by this gene is expressed in several non-neuronal tissues including the uterus and ovaries. This subunit can assemble with known GABA A receptor subunits, and the presence of this subunit alters the sensitivity of recombinant receptors to modulatory agents such as pregnanolone. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]
PHENOTYPE: Homozygous mutation of this gene does not appear to result in a phenotype. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 A G 6: 142,603,075 V1316A possibly damaging Het
Ada T G 2: 163,730,316 K254N probably benign Het
Adamts17 A G 7: 66,840,289 R40G probably benign Het
Akr1d1 C T 6: 37,530,243 probably benign Het
Aldh1l1 T A 6: 90,559,233 probably benign Het
Bbox1 T A 2: 110,265,486 I378F probably benign Het
BC028528 T C 3: 95,888,900 N50S probably damaging Het
Casp8ap2 T A 4: 32,641,294 S783T possibly damaging Het
Cmpk2 C T 12: 26,477,178 R389W probably damaging Het
Cplx1 C T 5: 108,548,527 probably null Het
Crim1 T C 17: 78,344,434 L529P probably benign Het
Ctps A G 4: 120,553,986 S278P probably benign Het
Defb21 C A 2: 152,574,901 probably benign Het
Ecm1 T A 3: 95,736,064 N308I probably benign Het
Flg2 T C 3: 93,202,284 S540P unknown Het
Gli2 C A 1: 118,848,435 C419F probably damaging Het
Grid2 T A 6: 64,320,196 F514L probably benign Het
Hormad1 T G 3: 95,578,269 M256R probably benign Het
Itsn2 T G 12: 4,636,693 probably benign Het
Klhl38 A T 15: 58,323,311 D7E probably benign Het
Map3k1 G A 13: 111,754,662 T1248I possibly damaging Het
Mki67 A T 7: 135,707,813 V303E probably benign Het
Mterf4 A T 1: 93,304,721 L136* probably null Het
Mtmr14 A G 6: 113,240,430 D61G possibly damaging Het
Nf2 A T 11: 4,818,613 D85E probably benign Het
Nmnat2 G T 1: 153,076,997 probably benign Het
Olfm3 T A 3: 115,122,848 D476E probably benign Het
Olfr297 T C 7: 86,526,778 V7A probably benign Het
Olfr920 T A 9: 38,756,254 C189S probably damaging Het
Pdia6 T C 12: 17,283,957 probably benign Het
Prrg1 G A X: 78,483,782 A47V probably damaging Het
Rgs22 A T 15: 36,103,835 I160K probably benign Het
Sardh T C 2: 27,189,613 Y889C probably damaging Het
Syne2 C A 12: 75,909,336 D605E probably benign Het
Other mutations in Gabrp
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00558:Gabrp APN 11 33552644 missense possibly damaging 0.91
IGL01299:Gabrp APN 11 33554476 missense probably damaging 1.00
IGL01305:Gabrp APN 11 33555055 missense probably damaging 1.00
IGL01729:Gabrp APN 11 33552689 missense probably damaging 1.00
IGL03031:Gabrp APN 11 33554980 missense probably damaging 1.00
IGL03172:Gabrp APN 11 33554388 missense probably damaging 1.00
IGL03280:Gabrp APN 11 33552616 missense probably benign 0.12
ANU22:Gabrp UTSW 11 33555055 missense probably damaging 1.00
R0265:Gabrp UTSW 11 33552614 missense probably damaging 1.00
R0326:Gabrp UTSW 11 33554362 missense probably damaging 0.99
R1744:Gabrp UTSW 11 33572462 missense probably benign 0.03
R4174:Gabrp UTSW 11 33568092 missense probably damaging 1.00
R5043:Gabrp UTSW 11 33568072 missense probably benign 0.00
R5213:Gabrp UTSW 11 33567211 critical splice donor site probably null
R5290:Gabrp UTSW 11 33567310 missense probably damaging 0.99
R5665:Gabrp UTSW 11 33554308 missense possibly damaging 0.56
R6698:Gabrp UTSW 11 33557017 missense probably damaging 1.00
Z1176:Gabrp UTSW 11 33552673 missense probably benign 0.06
Posted On2014-01-21