Incidental Mutation 'R3691:Btbd19'
ID 268771
Institutional Source Beutler Lab
Gene Symbol Btbd19
Ensembl Gene ENSMUSG00000073771
Gene Name BTB domain containing 19
Synonyms 9530048O09Rik
MMRRC Submission 040686-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.114) question?
Stock # R3691 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 116976416-116982922 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to T at 116977789 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000138230 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000143213] [ENSMUST00000153257] [ENSMUST00000183310]
AlphaFold S4R1I0
Predicted Effect noncoding transcript
Transcript: ENSMUST00000097915
SMART Domains Protein: ENSMUSP00000095528
Gene: ENSMUSG00000073771

DomainStartEndE-ValueType
low complexity region 28 43 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123226
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123346
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125896
Predicted Effect probably benign
Transcript: ENSMUST00000143213
Predicted Effect probably benign
Transcript: ENSMUST00000153257
SMART Domains Protein: ENSMUSP00000121768
Gene: ENSMUSG00000073771

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Blast:BACK 33 84 5e-16 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153303
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153924
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181979
Predicted Effect probably benign
Transcript: ENSMUST00000183310
SMART Domains Protein: ENSMUSP00000138230
Gene: ENSMUSG00000073771

DomainStartEndE-ValueType
BTB 29 124 1.82e-18 SMART
BACK 129 233 4.17e-8 SMART
low complexity region 260 280 N/A INTRINSIC
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 100% (34/34)
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afdn A G 17: 14,108,671 (GRCm39) E1398G probably damaging Het
Avl9 C T 6: 56,713,812 (GRCm39) H357Y probably benign Het
Best2 A G 8: 85,737,883 (GRCm39) F171L probably benign Het
Cap1 A G 4: 122,758,419 (GRCm39) S254P probably damaging Het
Cfap43 G A 19: 47,885,512 (GRCm39) L368F probably benign Het
Clasrp C A 7: 19,319,165 (GRCm39) probably benign Het
Cog3 T C 14: 75,991,878 (GRCm39) M1V probably null Het
Drosha G A 15: 12,834,724 (GRCm39) R276H unknown Het
Efr3b T A 12: 4,032,059 (GRCm39) D183V possibly damaging Het
Epha1 T C 6: 42,338,064 (GRCm39) T794A probably damaging Het
Fbxo17 G A 7: 28,436,887 (GRCm39) V281I probably damaging Het
Flii T C 11: 60,610,583 (GRCm39) Y571C probably benign Het
Flywch1 G A 17: 23,982,186 (GRCm39) P6L probably damaging Het
Foxj3 T C 4: 119,473,839 (GRCm39) probably benign Het
Fras1 C T 5: 96,929,371 (GRCm39) T3925I probably benign Het
Gk5 T C 9: 96,011,149 (GRCm39) probably null Het
Gm12588 T G 11: 121,796,751 (GRCm39) Q366P possibly damaging Het
Gm3248 A G 14: 5,943,068 (GRCm38) I161T probably damaging Het
Gzmg T A 14: 56,395,134 (GRCm39) probably benign Het
Lrrc69 A T 4: 14,795,980 (GRCm39) N22K possibly damaging Het
Med13l A G 5: 118,859,562 (GRCm39) R250G probably benign Het
Mideas C T 12: 84,203,245 (GRCm39) G886S probably benign Het
Mxi1 T C 19: 53,358,062 (GRCm39) L73P probably damaging Het
Myo9b G A 8: 71,786,981 (GRCm39) R721Q probably benign Het
Napb T C 2: 148,544,977 (GRCm39) probably null Het
Nsun2 A G 13: 69,760,456 (GRCm39) N45D probably damaging Het
Or10ag2 T C 2: 87,248,514 (GRCm39) F39L probably benign Het
Oxct1 A G 15: 4,076,999 (GRCm39) M111V probably benign Het
Pcnx4 A G 12: 72,620,493 (GRCm39) D771G probably damaging Het
Serpina6 T C 12: 103,620,668 (GRCm39) D27G probably benign Het
Tecpr1 A G 5: 144,146,797 (GRCm39) F523S probably benign Het
Zan A G 5: 137,418,281 (GRCm39) I2939T unknown Het
Zfc3h1 A G 10: 115,256,595 (GRCm39) T1522A probably benign Het
Other mutations in Btbd19
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3690:Btbd19 UTSW 4 116,977,789 (GRCm39) utr 3 prime probably benign
R4907:Btbd19 UTSW 4 116,977,764 (GRCm39) utr 3 prime probably benign
R5052:Btbd19 UTSW 4 116,979,454 (GRCm39) missense possibly damaging 0.60
R5163:Btbd19 UTSW 4 116,978,628 (GRCm39) missense probably damaging 1.00
R5396:Btbd19 UTSW 4 116,980,957 (GRCm39) missense probably damaging 1.00
R5398:Btbd19 UTSW 4 116,980,957 (GRCm39) missense probably damaging 1.00
R5399:Btbd19 UTSW 4 116,980,957 (GRCm39) missense probably damaging 1.00
R5998:Btbd19 UTSW 4 116,978,196 (GRCm39) missense probably benign 0.39
R7313:Btbd19 UTSW 4 116,978,616 (GRCm39) missense probably damaging 1.00
R9105:Btbd19 UTSW 4 116,977,961 (GRCm39) missense probably damaging 0.98
RF020:Btbd19 UTSW 4 116,979,472 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGAGAAGCTCGAATTTGCGC -3'
(R):5'- GGGATCACCATCGCTTTCTG -3'

Sequencing Primer
(F):5'- GATGAGCTACATAGAGATCGCGTC -3'
(R):5'- GGACCTTCGTTTCAAATGATCCAC -3'
Posted On 2015-02-19