Incidental Mutation 'IGL00497:Ccdc91'
ID 6318
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc91
Ensembl Gene ENSMUSG00000030301
Gene Name coiled-coil domain containing 91
Synonyms p56, 1810060J02Rik, 1700086G08Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.109) question?
Stock # IGL00497
Quality Score
Status
Chromosome 6
Chromosomal Location 147377326-147534110 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 147508485 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Lysine at position 404 (Q404K)
Ref Sequence ENSEMBL: ENSMUSP00000032441 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032441]
AlphaFold Q9D8L5
Predicted Effect unknown
Transcript: ENSMUST00000032441
AA Change: Q404K
SMART Domains Protein: ENSMUSP00000032441
Gene: ENSMUSG00000030301
AA Change: Q404K

DomainStartEndE-ValueType
coiled coil region 130 207 N/A INTRINSIC
coiled coil region 253 319 N/A INTRINSIC
low complexity region 349 365 N/A INTRINSIC
coiled coil region 376 407 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930579G24Rik G A 3: 79,538,598 (GRCm39) probably benign Het
Aatk C T 11: 119,901,012 (GRCm39) R1128Q probably benign Het
Acot6 C T 12: 84,156,212 (GRCm39) R387C probably damaging Het
Adam11 A G 11: 102,660,973 (GRCm39) E118G probably damaging Het
Adcyap1r1 G A 6: 55,449,264 (GRCm39) V73I probably damaging Het
Apol8 T C 15: 77,634,214 (GRCm39) T121A probably damaging Het
Bltp2 A G 11: 78,163,759 (GRCm39) N1076D probably damaging Het
Cpt1b T C 15: 89,306,496 (GRCm39) K294R probably benign Het
Dnah6 A C 6: 73,172,744 (GRCm39) V238G probably damaging Het
Dscaml1 T C 9: 45,663,536 (GRCm39) S1920P probably damaging Het
Gcfc2 A T 6: 81,934,951 (GRCm39) I737L probably benign Het
Gmeb1 A G 4: 131,955,296 (GRCm39) V293A probably benign Het
Gpi-ps T C 8: 5,690,563 (GRCm39) noncoding transcript Het
Hibch A G 1: 52,924,349 (GRCm39) probably benign Het
Ifnab A G 4: 88,609,419 (GRCm39) Y16H probably benign Het
Il17rc T C 6: 113,451,132 (GRCm39) V155A probably damaging Het
Lrr1 A G 12: 69,221,356 (GRCm39) H166R probably benign Het
Map4k5 G T 12: 69,892,506 (GRCm39) A141E probably damaging Het
Mettl17 A T 14: 52,126,292 (GRCm39) K233N probably damaging Het
Mon2 A G 10: 122,862,204 (GRCm39) L740S probably damaging Het
Mpdz A C 4: 81,253,979 (GRCm39) I1051S probably benign Het
Mroh8 A G 2: 157,058,834 (GRCm39) F944S probably damaging Het
Myh13 A G 11: 67,233,314 (GRCm39) Y611C probably damaging Het
Npat A G 9: 53,478,100 (GRCm39) N951D possibly damaging Het
Osmr T C 15: 6,876,547 (GRCm39) S126G probably benign Het
Parp14 T C 16: 35,655,206 (GRCm39) Y1755C probably damaging Het
Phf14 T C 6: 11,941,423 (GRCm39) probably benign Het
Prex2 T A 1: 11,256,876 (GRCm39) M1196K possibly damaging Het
Prkd1 A T 12: 50,430,264 (GRCm39) D614E probably damaging Het
Ptprm A G 17: 67,124,967 (GRCm39) L794P probably damaging Het
Rb1 C T 14: 73,502,038 (GRCm39) R449H probably damaging Het
Scfd1 A G 12: 51,474,652 (GRCm39) D469G probably benign Het
Serpinb1c T C 13: 33,067,958 (GRCm39) K213E probably damaging Het
Sgo1 A G 17: 53,984,130 (GRCm39) probably benign Het
Slc11a1 A G 1: 74,421,057 (GRCm39) probably null Het
Snw1 A G 12: 87,499,350 (GRCm39) probably null Het
Stac3 T C 10: 127,339,533 (GRCm39) I143T probably damaging Het
Tcta A T 9: 108,183,115 (GRCm39) L10Q probably damaging Het
Tha1 T C 11: 117,761,831 (GRCm39) probably benign Het
Trmt1 T C 8: 85,422,138 (GRCm39) M254T possibly damaging Het
Trps1 T A 15: 50,524,703 (GRCm39) M887L possibly damaging Het
Zfyve28 A G 5: 34,400,539 (GRCm39) V53A probably damaging Het
Other mutations in Ccdc91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:Ccdc91 APN 6 147,508,452 (GRCm39) missense unknown
IGL00795:Ccdc91 APN 6 147,409,305 (GRCm39) missense probably damaging 0.99
R1495:Ccdc91 UTSW 6 147,435,670 (GRCm39) missense possibly damaging 0.66
R1725:Ccdc91 UTSW 6 147,493,541 (GRCm39) missense unknown
R3761:Ccdc91 UTSW 6 147,464,200 (GRCm39) missense unknown
R4246:Ccdc91 UTSW 6 147,493,646 (GRCm39) missense unknown
R4591:Ccdc91 UTSW 6 147,491,963 (GRCm39) missense unknown
R4797:Ccdc91 UTSW 6 147,493,641 (GRCm39) missense unknown
R5719:Ccdc91 UTSW 6 147,477,001 (GRCm39) missense unknown
R5721:Ccdc91 UTSW 6 147,477,001 (GRCm39) missense unknown
R6092:Ccdc91 UTSW 6 147,437,114 (GRCm39) missense possibly damaging 0.66
R7156:Ccdc91 UTSW 6 147,435,676 (GRCm39) missense possibly damaging 0.83
R7393:Ccdc91 UTSW 6 147,435,527 (GRCm39) missense possibly damaging 0.92
R7411:Ccdc91 UTSW 6 147,493,696 (GRCm39) nonsense probably null
R7576:Ccdc91 UTSW 6 147,491,957 (GRCm39) missense unknown
R8165:Ccdc91 UTSW 6 147,533,086 (GRCm39) missense unknown
R8311:Ccdc91 UTSW 6 147,437,114 (GRCm39) missense possibly damaging 0.66
R8406:Ccdc91 UTSW 6 147,438,920 (GRCm39) missense possibly damaging 0.66
R8748:Ccdc91 UTSW 6 147,464,194 (GRCm39) missense unknown
R8922:Ccdc91 UTSW 6 147,412,358 (GRCm39) nonsense probably null
R9210:Ccdc91 UTSW 6 147,508,398 (GRCm39) missense unknown
R9212:Ccdc91 UTSW 6 147,508,398 (GRCm39) missense unknown
X0027:Ccdc91 UTSW 6 147,492,137 (GRCm39) critical splice donor site probably null
Posted On 2012-04-20