Incidental Mutation 'IGL03382:Ccdc159'
ID 420756
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc159
Ensembl Gene ENSMUSG00000006241
Gene Name coiled-coil domain containing 159
Synonyms 2510048L02Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03382
Quality Score
Status
Chromosome 9
Chromosomal Location 21838767-21847168 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 21842992 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148950 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000006403] [ENSMUST00000046831] [ENSMUST00000170304] [ENSMUST00000213698] [ENSMUST00000214569] [ENSMUST00000214734] [ENSMUST00000216710]
AlphaFold Q8C963
Predicted Effect probably null
Transcript: ENSMUST00000006403
SMART Domains Protein: ENSMUSP00000006403
Gene: ENSMUSG00000006241

DomainStartEndE-ValueType
low complexity region 42 52 N/A INTRINSIC
coiled coil region 152 172 N/A INTRINSIC
low complexity region 217 227 N/A INTRINSIC
coiled coil region 261 288 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000046831
SMART Domains Protein: ENSMUSP00000048832
Gene: ENSMUSG00000040883

DomainStartEndE-ValueType
Pfam:DUF4149 17 119 1.2e-27 PFAM
transmembrane domain 164 186 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000170304
SMART Domains Protein: ENSMUSP00000126474
Gene: ENSMUSG00000006241

DomainStartEndE-ValueType
low complexity region 50 60 N/A INTRINSIC
coiled coil region 160 180 N/A INTRINSIC
low complexity region 225 235 N/A INTRINSIC
coiled coil region 269 296 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000213698
Predicted Effect probably benign
Transcript: ENSMUST00000214569
Predicted Effect probably benign
Transcript: ENSMUST00000214734
Predicted Effect probably null
Transcript: ENSMUST00000216710
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215650
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217589
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aff1 A G 5: 103,988,926 (GRCm39) D831G possibly damaging Het
Amer2 A G 14: 60,617,331 (GRCm39) K509E possibly damaging Het
Ankrd6 T C 4: 32,808,771 (GRCm39) K449E probably damaging Het
Atp8b2 G A 3: 89,855,828 (GRCm39) P459L probably benign Het
Atr C T 9: 95,802,875 (GRCm39) R1846* probably null Het
Brd10 C T 19: 29,694,676 (GRCm39) G1606R probably damaging Het
Ccna1 A C 3: 54,954,698 (GRCm39) Y338D probably damaging Het
Cpq A T 15: 33,213,089 (GRCm39) E36V probably damaging Het
Cyp2c23 A G 19: 44,003,371 (GRCm39) I268T probably damaging Het
Dctn2 G T 10: 127,114,057 (GRCm39) Q332H probably damaging Het
Dnah17 T A 11: 117,972,769 (GRCm39) I2055F probably damaging Het
Dnmt3b A G 2: 153,528,279 (GRCm39) H764R probably damaging Het
Gphn T A 12: 78,528,087 (GRCm39) I135K probably damaging Het
Hnrnpul1 A G 7: 25,450,409 (GRCm39) M1T probably null Het
Htra4 T C 8: 25,519,714 (GRCm39) D406G probably benign Het
Klk10 G T 7: 43,433,883 (GRCm39) probably benign Het
Lilrb4a T A 10: 51,367,616 (GRCm39) W53R probably benign Het
Magel2 T C 7: 62,028,461 (GRCm39) V455A probably benign Het
Mrgprb5 T C 7: 47,818,442 (GRCm39) T98A probably benign Het
Mrps35 T A 6: 146,951,373 (GRCm39) C76* probably null Het
Myh7b C T 2: 155,465,399 (GRCm39) R701C probably damaging Het
Nbeal1 G A 1: 60,300,745 (GRCm39) probably null Het
Neb T A 2: 52,215,720 (GRCm39) M196L probably benign Het
Nmd3 A G 3: 69,642,421 (GRCm39) K207R probably damaging Het
Plxna4 C T 6: 32,179,129 (GRCm39) R962Q probably benign Het
Pom121 T C 5: 135,421,261 (GRCm39) K230E unknown Het
Psme4 A G 11: 30,757,788 (GRCm39) D307G possibly damaging Het
Rnf41 T G 10: 128,274,149 (GRCm39) M267R possibly damaging Het
Sis T C 3: 72,836,052 (GRCm39) N846D probably benign Het
Slc22a19 T A 19: 7,659,227 (GRCm39) I463L probably benign Het
Slc25a39 A T 11: 102,297,030 (GRCm39) probably null Het
Slc35b2 C T 17: 45,877,571 (GRCm39) R233C probably damaging Het
Slc4a4 T C 5: 89,376,695 (GRCm39) L983P probably damaging Het
Sp110 A C 1: 85,505,050 (GRCm39) F434C probably benign Het
Tbc1d10a A G 11: 4,159,984 (GRCm39) Y123C probably damaging Het
Thbs4 A C 13: 92,906,056 (GRCm39) I395S probably benign Het
Triml2 A G 8: 43,646,776 (GRCm39) T422A probably benign Het
Ubn2 T C 6: 38,417,382 (GRCm39) probably benign Het
Vmn1r15 T A 6: 57,235,555 (GRCm39) M141K probably benign Het
Vmn2r80 A G 10: 79,005,362 (GRCm39) E333G probably damaging Het
Zfp169 T C 13: 48,644,639 (GRCm39) probably benign Het
Zfp942 G A 17: 22,148,083 (GRCm39) P182L probably benign Het
Other mutations in Ccdc159
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00425:Ccdc159 APN 9 21,840,765 (GRCm39) missense possibly damaging 0.83
IGL02322:Ccdc159 APN 9 21,840,669 (GRCm39) missense possibly damaging 0.46
IGL03156:Ccdc159 APN 9 21,840,771 (GRCm39) missense probably benign
R1622:Ccdc159 UTSW 9 21,840,666 (GRCm39) missense possibly damaging 0.66
R2076:Ccdc159 UTSW 9 21,840,802 (GRCm39) splice site probably null
R3905:Ccdc159 UTSW 9 21,845,815 (GRCm39) critical splice donor site probably null
R4083:Ccdc159 UTSW 9 21,840,699 (GRCm39) missense possibly damaging 0.83
R4625:Ccdc159 UTSW 9 21,840,762 (GRCm39) missense probably benign
R4700:Ccdc159 UTSW 9 21,839,027 (GRCm39) splice site probably null
R5004:Ccdc159 UTSW 9 21,844,241 (GRCm39) missense probably damaging 1.00
R5743:Ccdc159 UTSW 9 21,840,686 (GRCm39) missense probably benign 0.19
R6245:Ccdc159 UTSW 9 21,846,864 (GRCm39) missense probably damaging 0.99
R7263:Ccdc159 UTSW 9 21,843,007 (GRCm39) missense probably benign 0.04
R8171:Ccdc159 UTSW 9 21,845,007 (GRCm39) missense possibly damaging 0.82
R8477:Ccdc159 UTSW 9 21,844,223 (GRCm39) missense probably damaging 1.00
R8712:Ccdc159 UTSW 9 21,845,051 (GRCm39) missense probably benign 0.27
R9649:Ccdc159 UTSW 9 21,840,672 (GRCm39) missense possibly damaging 0.66
Posted On 2016-08-02