Incidental Mutation 'IGL02351:Cbwd1'
ID289502
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cbwd1
Ensembl Gene ENSMUSG00000024878
Gene NameCOBW domain containing 1
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.132) question?
Stock #IGL02351
Quality Score
Status
Chromosome19
Chromosomal Location24919916-24961616 bp(-) (GRCm38)
Type of Mutationcritical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to T at 24931662 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000025815 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025815]
Predicted Effect probably null
Transcript: ENSMUST00000025815
SMART Domains Protein: ENSMUSP00000025815
Gene: ENSMUSG00000024878

DomainStartEndE-ValueType
low complexity region 9 16 N/A INTRINSIC
Pfam:cobW 41 229 7.1e-51 PFAM
CobW_C 271 374 5.34e-1 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abi3bp A G 16: 56,654,055 T448A possibly damaging Het
Adamtsl1 T A 4: 86,156,873 probably null Het
Adgra3 A G 5: 50,058,558 V73A probably benign Het
Aggf1 T C 13: 95,352,850 probably benign Het
Aktip C T 8: 91,126,892 V96I possibly damaging Het
Atm A G 9: 53,522,176 I258T probably benign Het
Baz1b C T 5: 135,244,306 T1428I probably damaging Het
C3ar1 A T 6: 122,849,975 Y428N probably damaging Het
C87499 A T 4: 88,627,890 I405N probably damaging Het
Cadps A G 14: 12,597,380 S437P probably damaging Het
Car4 C T 11: 84,965,767 P294S probably damaging Het
Cenpq A G 17: 40,924,332 L213P probably damaging Het
Cept1 A G 3: 106,539,188 probably null Het
Cln6 A G 9: 62,847,125 I150V probably benign Het
Cyb5r3 T C 15: 83,160,935 T94A probably benign Het
Cyp2c67 A G 19: 39,617,417 M345T probably damaging Het
Dapk2 T A 9: 66,246,523 I187N probably damaging Het
Dkk2 A G 3: 132,177,912 D191G probably benign Het
Dnah8 T A 17: 30,767,811 F3145I probably damaging Het
Dock1 A C 7: 135,108,819 D1190A possibly damaging Het
Ehhadh T A 16: 21,762,870 L457F probably damaging Het
Ercc6l2 T C 13: 63,853,683 L552P probably damaging Het
Ghrhr T G 6: 55,384,153 I284S probably damaging Het
Gm10288 A T 3: 146,839,199 noncoding transcript Het
Gp6 T G 7: 4,394,508 I19L probably benign Het
Gria4 G A 9: 4,456,206 S698L possibly damaging Het
Ifng A T 10: 118,442,505 I53F possibly damaging Het
Kazn A C 4: 142,147,016 probably null Het
Khk A T 5: 30,928,504 I136F probably damaging Het
Lnx1 T A 5: 74,627,366 N98Y probably damaging Het
Lsp1 T C 7: 142,488,942 probably null Het
Lta4h A T 10: 93,478,467 N467I probably benign Het
Mcmbp C A 7: 128,709,781 probably null Het
Me2 A T 18: 73,797,967 I85K probably benign Het
Muc4 C T 16: 32,750,986 T288I possibly damaging Het
Nadsyn1 A T 7: 143,799,912 Y525N probably damaging Het
Nt5e G A 9: 88,327,893 V70M probably damaging Het
Olfr677 G A 7: 105,056,975 G243D probably damaging Het
Olfr827 T G 10: 130,210,734 Y132S probably damaging Het
Olfr883 A T 9: 38,026,036 I77L possibly damaging Het
Pkd1l3 A G 8: 109,646,497 probably benign Het
Ppm1d A T 11: 85,345,715 E440V probably damaging Het
Ripor2 A T 13: 24,731,589 E1047D probably damaging Het
Rwdd2b G A 16: 87,437,448 A18V probably benign Het
Serpina5 G T 12: 104,102,125 K148N probably damaging Het
Setx A G 2: 29,146,964 K1154E probably benign Het
Skap1 T A 11: 96,708,556 probably null Het
Spcs2 T C 7: 99,849,034 K81R probably damaging Het
Stt3b T A 9: 115,250,907 M646L possibly damaging Het
Suco T C 1: 161,818,626 T1169A probably benign Het
Susd1 A T 4: 59,427,985 Y66* probably null Het
Trim34a T A 7: 104,261,234 C414* probably null Het
Trim58 G A 11: 58,651,350 G379S probably damaging Het
Vmn2r50 T A 7: 10,053,075 Q35L probably benign Het
Zfp418 T C 7: 7,174,691 probably benign Het
Zfp57 G A 17: 37,010,027 V258I probably benign Het
Other mutations in Cbwd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00720:Cbwd1 APN 19 24921131 missense probably benign 0.01
IGL01618:Cbwd1 APN 19 24940776 missense possibly damaging 0.83
IGL02358:Cbwd1 APN 19 24931662 critical splice donor site probably null
IGL02628:Cbwd1 APN 19 24957905 missense probably damaging 1.00
IGL03001:Cbwd1 APN 19 24922638 missense probably benign 0.01
IGL03053:Cbwd1 APN 19 24955377 missense probably damaging 1.00
IGL03409:Cbwd1 APN 19 24922766 missense probably benign 0.01
R0544:Cbwd1 UTSW 19 24949211 missense possibly damaging 0.79
R0655:Cbwd1 UTSW 19 24953320 missense possibly damaging 0.90
R0833:Cbwd1 UTSW 19 24940839 splice site probably benign
R1296:Cbwd1 UTSW 19 24942675 splice site probably benign
R1723:Cbwd1 UTSW 19 24948094 missense possibly damaging 0.89
R1888:Cbwd1 UTSW 19 24955405 missense probably damaging 1.00
R1888:Cbwd1 UTSW 19 24955405 missense probably damaging 1.00
R4526:Cbwd1 UTSW 19 24957964 missense probably benign 0.20
R5092:Cbwd1 UTSW 19 24921019 critical splice donor site probably null
R5238:Cbwd1 UTSW 19 24920630 missense probably damaging 0.99
R5852:Cbwd1 UTSW 19 24955405 missense possibly damaging 0.89
R7248:Cbwd1 UTSW 19 24921141 missense probably damaging 0.99
R7699:Cbwd1 UTSW 19 24942681 critical splice donor site probably null
R7700:Cbwd1 UTSW 19 24942681 critical splice donor site probably null
R7733:Cbwd1 UTSW 19 24940794 missense probably damaging 1.00
R8363:Cbwd1 UTSW 19 24942727 missense probably benign 0.01
Posted On2015-04-16