Incidental Mutation 'R5102:BC035044'
ID392419
Institutional Source Beutler Lab
Gene Symbol BC035044
Ensembl Gene ENSMUSG00000090164
Gene NamecDNA sequence BC035044
Synonyms
MMRRC Submission 042690-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.228) question?
Stock #R5102 (G1)
Quality Score225
Status Not validated
Chromosome6
Chromosomal Location128849090-128891126 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 128884986 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032519] [ENSMUST00000159866] [ENSMUST00000160290] [ENSMUST00000160867] [ENSMUST00000162666] [ENSMUST00000178918]
Predicted Effect probably benign
Transcript: ENSMUST00000032519
SMART Domains Protein: ENSMUSP00000032519
Gene: ENSMUSG00000030365

DomainStartEndE-ValueType
transmembrane domain 54 76 N/A INTRINSIC
CLECT 92 203 3.78e-20 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159080
Predicted Effect probably benign
Transcript: ENSMUST00000159866
SMART Domains Protein: ENSMUSP00000123804
Gene: ENSMUSG00000030365

DomainStartEndE-ValueType
transmembrane domain 58 80 N/A INTRINSIC
CLECT 96 207 3.78e-20 SMART
Predicted Effect unknown
Transcript: ENSMUST00000160290
AA Change: E82G
Predicted Effect probably benign
Transcript: ENSMUST00000160867
SMART Domains Protein: ENSMUSP00000145115
Gene: ENSMUSG00000030365

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
CLECT 31 142 1.9e-22 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000162666
SMART Domains Protein: ENSMUSP00000124910
Gene: ENSMUSG00000030365

DomainStartEndE-ValueType
transmembrane domain 83 105 N/A INTRINSIC
CLECT 121 232 3.78e-20 SMART
Predicted Effect unknown
Transcript: ENSMUST00000178918
AA Change: E82G
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203621
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.0%
  • 20x: 91.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810006K23Rik A G 5: 124,338,891 N83D probably damaging Het
Aox4 C T 1: 58,240,778 R518C probably damaging Het
Apbb2 A T 5: 66,312,249 probably null Het
Arhgap45 C T 10: 80,021,428 P254S probably benign Het
Arl4c T C 1: 88,701,600 D22G probably damaging Het
Asxl1 A G 2: 153,400,955 T1142A probably benign Het
Bmp4 T C 14: 46,384,001 N362S probably damaging Het
Cbll1 G T 12: 31,487,913 T280N probably damaging Het
Cdh10 A T 15: 18,986,885 T401S probably benign Het
Cps1 A T 1: 67,206,793 M1148L probably benign Het
Crybg1 T C 10: 43,997,836 D1092G probably damaging Het
Cyth2 A G 7: 45,810,702 S173P probably damaging Het
D3Ertd254e G A 3: 36,162,665 C55Y possibly damaging Het
D6Ertd527e A T 6: 87,111,811 I319F unknown Het
Dchs1 A T 7: 105,772,177 H345Q probably benign Het
Ddx50 A T 10: 62,640,861 V211E probably damaging Het
Dlx6 AGG AG 6: 6,865,180 probably null Het
Dnajb5 G A 4: 42,956,639 D109N possibly damaging Het
Dner A T 1: 84,405,970 N564K probably damaging Het
Fam234b T C 6: 135,209,284 S97P probably benign Het
Fam53b G A 7: 132,715,955 R60* probably null Het
Fmo3 T G 1: 162,963,977 K244Q probably benign Het
Gm12800 T C 4: 101,909,239 F40S probably damaging Het
Golim4 A G 3: 75,903,272 I192T possibly damaging Het
Gpr1 A G 1: 63,183,167 V303A probably damaging Het
Gprin1 T C 13: 54,739,763 M233V probably benign Het
Gtf2f1 A T 17: 57,003,626 V443D probably damaging Het
H2afy C G 13: 56,096,123 probably null Het
Hmgcs2 T C 3: 98,280,470 probably benign Het
Ide T A 19: 37,314,984 I271L unknown Het
Kat8 G A 7: 127,924,816 E343K probably damaging Het
Kif14 A G 1: 136,516,403 I1378V probably benign Het
Lhx3 TCCTACGGGCCGGCCC TCC 2: 26,201,423 probably null Het
Lhx6 T C 2: 36,094,210 probably null Het
Lrp2 C T 2: 69,489,158 G2007D probably damaging Het
Lrp5 T C 19: 3,659,304 K142R probably damaging Het
Mrpl2 G A 17: 46,650,038 R286Q probably benign Het
Nacad T A 11: 6,598,528 D1402V probably damaging Het
Ndfip2 T C 14: 105,298,105 I275T possibly damaging Het
Neb A C 2: 52,226,570 V4131G possibly damaging Het
Nfe2l1 G A 11: 96,822,108 A83V probably damaging Het
Nos3 A G 5: 24,371,627 D418G probably damaging Het
Olfr1126 A T 2: 87,457,794 M210L probably benign Het
Olfr353 T A 2: 36,890,044 K268M possibly damaging Het
Plcd4 A G 1: 74,565,154 T764A probably damaging Het
Plppr3 G T 10: 79,865,386 P541T possibly damaging Het
Polr2a A G 11: 69,746,945 I191T possibly damaging Het
Rab11fip1 T C 8: 27,156,374 K225E probably damaging Het
Rara A T 11: 98,966,359 Q64L possibly damaging Het
Rtkn G A 6: 83,149,773 V305M probably damaging Het
Sh2b1 A C 7: 126,471,236 F399V probably benign Het
Slc7a4 T C 16: 17,575,618 T106A probably damaging Het
Srcap G A 7: 127,530,623 G539D probably damaging Het
Stab1 C T 14: 31,148,017 probably null Het
Other mutations in BC035044
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1406:BC035044 UTSW 6 128885084 splice site probably null
R1406:BC035044 UTSW 6 128885084 splice site probably null
R1543:BC035044 UTSW 6 128890985 start gained probably benign
R2147:BC035044 UTSW 6 128890904 intron probably benign
R3727:BC035044 UTSW 6 128890859 nonsense probably null
R4115:BC035044 UTSW 6 128890850 intron probably benign
R5431:BC035044 UTSW 6 128885007 unclassified probably benign
R6180:BC035044 UTSW 6 128885034 unclassified probably benign
R6273:BC035044 UTSW 6 128890889 intron probably benign
R6467:BC035044 UTSW 6 128890892 intron probably benign
X0025:BC035044 UTSW 6 128890841 intron probably benign
X0028:BC035044 UTSW 6 128890864 intron probably benign
Predicted Primers PCR Primer
(F):5'- ATTACTTGGGAAGGGTCTGAATTC -3'
(R):5'- CCAAGGCTTATTTATTTCTGGGC -3'

Sequencing Primer
(F):5'- GGAAGGGTCTGAATTCTCTATTTTTG -3'
(R):5'- TGTTCATGCTAAGCACATGACC -3'
Posted On2016-06-15