Incidental Mutation 'R6782:Tada1'
ID 531440
Institutional Source Beutler Lab
Gene Symbol Tada1
Ensembl Gene ENSMUSG00000026563
Gene Name transcriptional adaptor 1
Synonyms Tada1l, 2900026B15Rik
MMRRC Submission 044896-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6782 (G1)
Quality Score 225.009
Status Not validated
Chromosome 1
Chromosomal Location 166206736-166221190 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 166217541 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 226 (N226S)
Ref Sequence ENSEMBL: ENSMUSP00000027846 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000027846] [ENSMUST00000131487] [ENSMUST00000135673] [ENSMUST00000169324]
AlphaFold Q99LM9
Predicted Effect probably benign
Transcript: ENSMUST00000027846
AA Change: N226S

PolyPhen 2 Score 0.253 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000027846
Gene: ENSMUSG00000026563
AA Change: N226S

DomainStartEndE-ValueType
Pfam:SAGA-Tad1 6 131 3.2e-18 PFAM
Pfam:SAGA-Tad1 116 194 4.8e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000131487
SMART Domains Protein: ENSMUSP00000116477
Gene: ENSMUSG00000040596

DomainStartEndE-ValueType
low complexity region 12 27 N/A INTRINSIC
KRAB 47 107 1.53e-19 SMART
Pfam:BrkDBD 195 247 2.1e-29 PFAM
CENPB 256 323 3.93e-21 SMART
Pfam:DDE_1 355 567 1.4e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000135673
SMART Domains Protein: ENSMUSP00000120352
Gene: ENSMUSG00000040596

DomainStartEndE-ValueType
low complexity region 12 27 N/A INTRINSIC
KRAB 47 107 1.53e-19 SMART
Pfam:BrkDBD 195 247 2.1e-29 PFAM
CENPB 256 323 3.93e-21 SMART
Pfam:DDE_1 355 567 1.4e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000169324
SMART Domains Protein: ENSMUSP00000127395
Gene: ENSMUSG00000040596

DomainStartEndE-ValueType
low complexity region 6 18 N/A INTRINSIC
low complexity region 31 46 N/A INTRINSIC
KRAB 66 126 1.53e-19 SMART
Pfam:BrkDBD 214 266 8.7e-29 PFAM
CENPB 275 342 3.93e-21 SMART
Pfam:DDE_1 414 586 1.5e-48 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.4%
  • 20x: 95.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] TADA1L is a protein subunit of the human STAGA complex (SPT3; (MIM 602947)/TAF9 (MIM 600822)/GCN5 (MIM 602301) acetyltransferase complex), which is a chromatin-modifying multiprotein complex (Martinez et al., 2001 [PubMed 11564863]).[supplied by OMIM, Apr 2009]
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca14 C T 7: 119,847,308 (GRCm39) A724V probably damaging Het
Abcc3 A T 11: 94,249,776 (GRCm39) F1055L probably damaging Het
Akt3 A T 1: 176,877,756 (GRCm39) Y337* probably null Het
Ankrd17 T C 5: 90,402,597 (GRCm39) K1488R possibly damaging Het
Ano1 G A 7: 144,175,424 (GRCm39) T498I probably damaging Het
Arhgap42 T A 9: 9,115,721 (GRCm39) K118N probably damaging Het
Arl5b A G 2: 15,077,993 (GRCm39) E106G probably damaging Het
Atp5mc3 C T 2: 73,739,672 (GRCm39) R56Q probably benign Het
Bbx T C 16: 50,020,928 (GRCm39) R749G probably benign Het
Cacna1g A G 11: 94,350,376 (GRCm39) S490P probably damaging Het
Ccdc63 A T 5: 122,249,077 (GRCm39) Y417* probably null Het
Cep162 A T 9: 87,093,737 (GRCm39) N880K probably benign Het
Chd2 G A 7: 73,125,127 (GRCm39) Q77* probably null Het
Cntrl T G 2: 35,060,658 (GRCm39) M1397R possibly damaging Het
Dcaf7 A G 11: 105,945,581 (GRCm39) Y310C probably damaging Het
Dnah5 T A 15: 28,449,302 (GRCm39) S4235T possibly damaging Het
Dot1l C T 10: 80,625,224 (GRCm39) P1157L probably damaging Het
Esco2 T C 14: 66,057,465 (GRCm39) T577A probably benign Het
Foxp1 T C 6: 98,907,106 (GRCm39) D624G probably damaging Het
Gfi1 A T 5: 107,873,819 (GRCm39) probably null Het
Gm10985 TTCTCTCTCTCTCTCTCT TTCTCTCTCTCTCTCT 3: 53,752,626 (GRCm39) probably null Het
Gm5113 G A 7: 29,878,178 (GRCm39) V89I probably benign Het
Gtf3c2 A C 5: 31,327,180 (GRCm39) L382R probably benign Het
H3c2 T C 13: 23,936,393 (GRCm39) S11P probably benign Het
Hhip T C 8: 80,778,233 (GRCm39) N99S probably damaging Het
Htr5b T C 1: 121,438,227 (GRCm39) I335V probably benign Het
Ifi206 A G 1: 173,308,923 (GRCm39) S358P unknown Het
Loxhd1 T A 18: 77,518,873 (GRCm39) V1893D probably damaging Het
Mical2 A G 7: 111,945,968 (GRCm39) R11G probably damaging Het
Mrc1 T C 2: 14,266,148 (GRCm39) probably null Het
Npr1 T C 3: 90,363,560 (GRCm39) N821S probably benign Het
Or4g16 A G 2: 111,137,090 (GRCm39) D180G probably damaging Het
Or52a24 A G 7: 103,381,549 (GRCm39) T139A possibly damaging Het
Or5p63 T C 7: 107,811,670 (GRCm39) D22G probably benign Het
Or5p70 T G 7: 107,994,744 (GRCm39) M139R probably damaging Het
Pi4ka T A 16: 17,143,852 (GRCm39) D739V probably damaging Het
Pi4ka A G 16: 17,194,846 (GRCm39) L184P possibly damaging Het
Ptprd T C 4: 76,243,377 (GRCm39) probably null Het
Ralgapb G A 2: 158,278,486 (GRCm39) G5R probably damaging Het
Ric8b T C 10: 84,783,391 (GRCm39) V83A probably damaging Het
Sdc2 C A 15: 33,028,281 (GRCm39) T133K probably damaging Het
Slc12a7 T A 13: 73,947,088 (GRCm39) V592D probably damaging Het
Sorcs1 G T 19: 50,164,560 (GRCm39) Y990* probably null Het
Spata13 G T 14: 60,928,912 (GRCm39) G157W probably damaging Het
Tenm3 A G 8: 49,099,291 (GRCm39) probably null Het
Tll1 A G 8: 64,524,315 (GRCm39) V457A probably benign Het
Tmem232 T C 17: 65,807,119 (GRCm39) K25E possibly damaging Het
Tnrc18 T C 5: 142,773,063 (GRCm39) S406G unknown Het
Ush2a A G 1: 188,089,031 (GRCm39) M329V probably benign Het
Vmn2r107 T C 17: 20,577,141 (GRCm39) S380P probably damaging Het
Vmn2r73 A G 7: 85,519,563 (GRCm39) M465T probably benign Het
Wwc2 A G 8: 48,353,826 (GRCm39) Y103H possibly damaging Het
Zfp217 T C 2: 169,958,178 (GRCm39) D463G probably damaging Het
Zfp345 T C 2: 150,315,274 (GRCm39) S88G probably damaging Het
Zfp975 A C 7: 42,311,454 (GRCm39) N386K probably benign Het
Other mutations in Tada1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01462:Tada1 APN 1 166,216,294 (GRCm39) missense probably damaging 1.00
IGL02458:Tada1 APN 1 166,220,203 (GRCm39) missense probably damaging 0.99
R0959:Tada1 UTSW 1 166,216,198 (GRCm39) missense probably benign 0.13
R1442:Tada1 UTSW 1 166,214,319 (GRCm39) missense possibly damaging 0.90
R1586:Tada1 UTSW 1 166,214,319 (GRCm39) missense possibly damaging 0.90
R4790:Tada1 UTSW 1 166,219,523 (GRCm39) missense possibly damaging 0.87
R5344:Tada1 UTSW 1 166,207,081 (GRCm39) intron probably benign
R7254:Tada1 UTSW 1 166,216,217 (GRCm39) nonsense probably null
R7679:Tada1 UTSW 1 166,219,540 (GRCm39) missense probably benign
R7733:Tada1 UTSW 1 166,217,511 (GRCm39) missense probably damaging 0.99
R7831:Tada1 UTSW 1 166,217,442 (GRCm39) missense probably damaging 1.00
R9140:Tada1 UTSW 1 166,216,177 (GRCm39) missense probably benign 0.38
R9175:Tada1 UTSW 1 166,210,005 (GRCm39) missense probably damaging 0.98
R9657:Tada1 UTSW 1 166,214,312 (GRCm39) missense possibly damaging 0.69
Predicted Primers PCR Primer
(F):5'- GCACTTGACGGTGGAACTTC -3'
(R):5'- CTTCAGGAAGTGAGAAGCAATC -3'

Sequencing Primer
(F):5'- CACTTGACGGTGGAACTTCTATGC -3'
(R):5'- GCACTGAGGTCCTGAGTTCAAATC -3'
Posted On 2018-08-29