Incidental Mutation 'IGL02726:Got1'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Got1
Ensembl Gene ENSMUSG00000025190
Gene Nameglutamic-oxaloacetic transaminase 1, soluble
Synonymscytosolic aspartate aminotransferase, cAspAT, Got-1
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.672) question?
Stock #IGL02726
Quality Score
Chromosomal Location43499752-43524605 bp(-) (GRCm38)
Type of Mutationunclassified (3202 bp from exon)
DNA Base Change (assembly) G to A at 43500412 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131830 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026196] [ENSMUST00000165311]
Predicted Effect probably benign
Transcript: ENSMUST00000026196
SMART Domains Protein: ENSMUSP00000026196
Gene: ENSMUSG00000025190

Pfam:Aminotran_1_2 31 405 1.4e-94 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132504
Predicted Effect probably benign
Transcript: ENSMUST00000133325
SMART Domains Protein: ENSMUSP00000117986
Gene: ENSMUSG00000025190

Pfam:Aminotran_1_2 1 181 7.2e-39 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000165311
SMART Domains Protein: ENSMUSP00000131830
Gene: ENSMUSG00000025189

low complexity region 25 32 N/A INTRINSIC
low complexity region 78 95 N/A INTRINSIC
low complexity region 112 120 N/A INTRINSIC
low complexity region 165 183 N/A INTRINSIC
low complexity region 193 202 N/A INTRINSIC
Pfam:DUF21 224 414 1.8e-27 PFAM
Blast:CBS 438 489 2e-12 BLAST
CBS 505 561 5.02e0 SMART
Blast:cNMP 634 802 2e-44 BLAST
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933417A18Rik A G 13: 34,952,960 probably benign Het
Anapc1 A T 2: 128,659,785 M779K probably benign Het
Art1 G A 7: 102,110,748 V85M probably damaging Het
Atad2b G T 12: 4,974,003 E43* probably null Het
Clec4a4 A T 6: 122,990,379 I5F probably damaging Het
Cr1l A T 1: 195,129,880 I45N probably damaging Het
Dmbt1 T A 7: 131,074,410 probably benign Het
Dnajb3 A T 1: 88,205,650 V10E probably damaging Het
Dnajc22 A T 15: 99,101,000 H22L probably damaging Het
Dnal4 A G 15: 79,763,544 V40A probably damaging Het
Dsg1b G A 18: 20,399,485 V529I probably benign Het
Fam131c T A 4: 141,382,802 D170E probably benign Het
Gm13088 G T 4: 143,655,385 P247H probably damaging Het
Herc1 T A 9: 66,441,988 V2043E probably benign Het
Hmcn1 A T 1: 150,656,694 Y3147* probably null Het
Ifi44 T C 3: 151,749,596 probably benign Het
Ikbkap T A 4: 56,767,878 probably null Het
Il1b A T 2: 129,367,322 D129E probably damaging Het
Ino80 A T 2: 119,442,483 I504N probably damaging Het
Itpr2 A G 6: 146,375,921 I655T probably benign Het
Kcnk4 A G 19: 6,927,089 probably null Het
Mrgprb2 T A 7: 48,552,870 R36W probably damaging Het
Mslnl T C 17: 25,744,103 probably null Het
Olfr1008 G T 2: 85,690,210 L260F possibly damaging Het
Olfr1338 T A 4: 118,753,764 Y260F probably benign Het
Olfr393 T C 11: 73,847,865 S87G probably benign Het
Olfr694 A C 7: 106,689,370 Y120* probably null Het
Pcnx4 G T 12: 72,574,212 M935I probably benign Het
Pdgfra C T 5: 75,194,957 Q1043* probably null Het
Pf4 T C 5: 90,772,664 V28A probably benign Het
Piezo1 A G 8: 122,487,155 L1689P probably damaging Het
Ppa2 A G 3: 133,370,461 S284G possibly damaging Het
Psd2 T C 18: 35,987,302 probably null Het
Rbm25 G T 12: 83,672,852 G549W probably damaging Het
Ryr2 T C 13: 11,738,320 D1705G probably damaging Het
Shf A T 2: 122,359,488 D96E probably damaging Het
Slc1a1 G A 19: 28,911,769 V481M probably benign Het
Slc4a9 T C 18: 36,539,617 V807A probably benign Het
Syne2 T A 12: 76,015,582 I4226N probably damaging Het
Tkfc A T 19: 10,596,212 V254E possibly damaging Het
Ubr2 A C 17: 46,972,921 Y601D probably damaging Het
Ubr5 A C 15: 38,000,562 probably benign Het
Vmn1r27 A T 6: 58,215,869 I50K possibly damaging Het
Wdr55 A G 18: 36,763,382 E375G probably benign Het
Other mutations in Got1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01402:Got1 APN 19 43504609 missense possibly damaging 0.72
IGL01404:Got1 APN 19 43504609 missense possibly damaging 0.72
IGL01431:Got1 APN 19 43503049 nonsense probably null
IGL01476:Got1 APN 19 43524409 missense probably damaging 1.00
IGL01688:Got1 APN 19 43524336 critical splice donor site probably null
IGL01977:Got1 APN 19 43515845 missense probably benign 0.00
IGL02353:Got1 APN 19 43524443 missense probably damaging 1.00
IGL02360:Got1 APN 19 43524443 missense probably damaging 1.00
F5770:Got1 UTSW 19 43500561 unclassified probably benign
R0128:Got1 UTSW 19 43524377 missense probably benign
R0245:Got1 UTSW 19 43504507 splice site probably benign
R0578:Got1 UTSW 19 43515783 missense probably benign 0.01
R1116:Got1 UTSW 19 43502974 nonsense probably null
R1927:Got1 UTSW 19 43515680 critical splice donor site probably null
R4516:Got1 UTSW 19 43504841 missense probably damaging 1.00
R4774:Got1 UTSW 19 43502906 critical splice donor site probably null
R4785:Got1 UTSW 19 43502937 missense possibly damaging 0.80
R5463:Got1 UTSW 19 43504597 missense probably benign 0.03
R6612:Got1 UTSW 19 43504803 missense probably damaging 1.00
Posted On2015-04-16