Incidental Mutation 'IGL01084:Gata3os'
ID 50452
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gata3os
Ensembl Gene ENSMUSG00000025783
Gene Name GATA binding protein 3 opposite strand
Synonyms Gm10853, Gata3as, 4930412O13Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.109) question?
Stock # IGL01084
Quality Score
Status
Chromosome 2
Chromosomal Location 9886063-9888732 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to G at 9887884 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000119730 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026889] [ENSMUST00000102976] [ENSMUST00000114915] [ENSMUST00000114919] [ENSMUST00000130615]
AlphaFold Q9D5M9
Predicted Effect unknown
Transcript: ENSMUST00000026889
AA Change: T48A
Predicted Effect probably benign
Transcript: ENSMUST00000102976
SMART Domains Protein: ENSMUSP00000100041
Gene: ENSMUSG00000015619

DomainStartEndE-ValueType
low complexity region 128 149 N/A INTRINSIC
low complexity region 153 165 N/A INTRINSIC
low complexity region 229 247 N/A INTRINSIC
ZnF_GATA 257 307 3.65e-20 SMART
ZnF_GATA 311 361 2.9e-23 SMART
low complexity region 367 377 N/A INTRINSIC
low complexity region 399 425 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114915
Predicted Effect unknown
Transcript: ENSMUST00000114919
AA Change: T48A
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125091
Predicted Effect probably benign
Transcript: ENSMUST00000130615
SMART Domains Protein: ENSMUSP00000119730
Gene: ENSMUSG00000015619

DomainStartEndE-ValueType
low complexity region 93 114 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131297
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142305
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147533
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aagab C A 9: 63,546,901 (GRCm39) Q284K probably damaging Het
Adgrd1 A T 5: 129,216,656 (GRCm39) N341I probably benign Het
Arhgap40 T C 2: 158,385,138 (GRCm39) F457S probably damaging Het
Cacng5 C T 11: 107,772,531 (GRCm39) V106I probably benign Het
Catsper1 G A 19: 5,387,800 (GRCm39) V360M probably damaging Het
Cdc42bpa T A 1: 179,969,839 (GRCm39) probably benign Het
Cep250 C T 2: 155,840,313 (GRCm39) H2424Y probably benign Het
Cln3 T C 7: 126,174,426 (GRCm39) E304G probably damaging Het
Eml2 T A 7: 18,924,663 (GRCm39) C177* probably null Het
Epha5 G A 5: 84,218,946 (GRCm39) R917* probably null Het
Gabra2 A G 5: 71,163,576 (GRCm39) F244L probably damaging Het
Gars1 C A 6: 55,032,812 (GRCm39) D261E probably benign Het
Keg1 A G 19: 12,691,976 (GRCm39) K98E probably damaging Het
Kif13a A G 13: 46,904,110 (GRCm39) probably benign Het
Matn1 A G 4: 130,679,245 (GRCm39) K300E probably benign Het
Mesp1 A G 7: 79,442,831 (GRCm39) S149P probably benign Het
Mmp10 T C 9: 7,505,651 (GRCm39) V305A possibly damaging Het
Muc5b T C 7: 141,397,186 (GRCm39) probably benign Het
Myof T C 19: 37,924,884 (GRCm39) T1181A probably damaging Het
Or1r1 A T 11: 73,875,353 (GRCm39) L27Q probably damaging Het
Or5d35 T C 2: 87,855,347 (GRCm39) S94P probably benign Het
Or9i16 G T 19: 13,864,866 (GRCm39) T236N probably damaging Het
Osbpl11 T C 16: 33,047,221 (GRCm39) probably benign Het
Prune2 T C 19: 17,095,573 (GRCm39) V359A probably benign Het
Ptch1 T A 13: 63,691,451 (GRCm39) E267D probably damaging Het
Rbl2 A G 8: 91,848,941 (GRCm39) E1049G probably damaging Het
Ruvbl2 A T 7: 45,071,947 (GRCm39) probably null Het
Sec23b A G 2: 144,406,509 (GRCm39) I101M possibly damaging Het
Srms A C 2: 180,848,177 (GRCm39) probably null Het
Svep1 T A 4: 58,111,419 (GRCm39) T1067S possibly damaging Het
Tedc1 C T 12: 113,126,808 (GRCm39) R357* probably null Het
Tmem127 T C 2: 127,099,006 (GRCm39) V180A probably damaging Het
Trpm7 A G 2: 126,687,992 (GRCm39) probably null Het
Trpv3 G A 11: 73,184,826 (GRCm39) probably null Het
Tti1 C T 2: 157,824,379 (GRCm39) V1025I probably damaging Het
Vmn2r80 A G 10: 79,030,433 (GRCm39) Y753C probably damaging Het
Vps13d A G 4: 144,881,525 (GRCm39) L1350S probably benign Het
Zfp287 G T 11: 62,604,716 (GRCm39) Y730* probably null Het
Zfp583 A G 7: 6,320,184 (GRCm39) F276S probably damaging Het
Zfp638 T C 6: 83,921,780 (GRCm39) Y636H probably benign Het
Other mutations in Gata3os
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03189:Gata3os APN 2 9,888,634 (GRCm39) intron probably benign
R6005:Gata3os UTSW 2 9,887,638 (GRCm39) intron probably benign
R7909:Gata3os UTSW 2 9,888,668 (GRCm39) missense unknown
R8332:Gata3os UTSW 2 9,887,650 (GRCm39) missense unknown
R9021:Gata3os UTSW 2 9,887,345 (GRCm39) intron probably benign
R9526:Gata3os UTSW 2 9,887,634 (GRCm39) missense unknown
Posted On 2013-06-21