Incidental Mutation 'IGL00497:Ccdc91'
ID6318
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc91
Ensembl Gene ENSMUSG00000030301
Gene Namecoiled-coil domain containing 91
Synonyms1810060J02Rik, p56, 1700086G08Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.101) question?
Stock #IGL00497
Quality Score
Status
Chromosome6
Chromosomal Location147475828-147632612 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 147606987 bp
ZygosityHeterozygous
Amino Acid Change Glutamine to Lysine at position 404 (Q404K)
Ref Sequence ENSEMBL: ENSMUSP00000032441 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032441]
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
2610507B11Rik A G 11: 78,272,933 N1076D probably damaging Het
4930579G24Rik G A 3: 79,631,291 probably benign Het
Aatk C T 11: 120,010,186 R1128Q probably benign Het
Acot6 C T 12: 84,109,438 R387C probably damaging Het
Adam11 A G 11: 102,770,147 E118G probably damaging Het
Adcyap1r1 G A 6: 55,472,279 V73I probably damaging Het
Apol8 T C 15: 77,750,014 T121A probably damaging Het
Cpt1b T C 15: 89,422,293 K294R probably benign Het
Dnah6 A C 6: 73,195,761 V238G probably damaging Het
Dscaml1 T C 9: 45,752,238 S1920P probably damaging Het
Gcfc2 A T 6: 81,957,970 I737L probably benign Het
Gm1840 T C 8: 5,640,563 noncoding transcript Het
Gmeb1 A G 4: 132,227,985 V293A probably benign Het
Hibch A G 1: 52,885,190 probably benign Het
Ifnab A G 4: 88,691,182 Y16H probably benign Het
Il17rc T C 6: 113,474,171 V155A probably damaging Het
Lrr1 A G 12: 69,174,582 H166R probably benign Het
Map4k5 G T 12: 69,845,732 A141E probably damaging Het
Mettl17 A T 14: 51,888,835 K233N probably damaging Het
Mon2 A G 10: 123,026,299 L740S probably damaging Het
Mpdz A C 4: 81,335,742 I1051S probably benign Het
Mroh8 A G 2: 157,216,914 F944S probably damaging Het
Myh13 A G 11: 67,342,488 Y611C probably damaging Het
Npat A G 9: 53,566,800 N951D possibly damaging Het
Osmr T C 15: 6,847,066 S126G probably benign Het
Parp14 T C 16: 35,834,836 Y1755C probably damaging Het
Phf14 T C 6: 11,941,424 probably benign Het
Prex2 T A 1: 11,186,652 M1196K possibly damaging Het
Prkd1 A T 12: 50,383,481 D614E probably damaging Het
Ptprm A G 17: 66,817,972 L794P probably damaging Het
Rb1 C T 14: 73,264,598 R449H probably damaging Het
Scfd1 A G 12: 51,427,869 D469G probably benign Het
Serpinb1c T C 13: 32,883,975 K213E probably damaging Het
Sgo1 A G 17: 53,677,102 probably benign Het
Slc11a1 A G 1: 74,381,898 probably null Het
Snw1 A G 12: 87,452,580 probably null Het
Stac3 T C 10: 127,503,664 I143T probably damaging Het
Tcta A T 9: 108,305,916 L10Q probably damaging Het
Tha1 T C 11: 117,871,005 probably benign Het
Trmt1 T C 8: 84,695,509 M254T possibly damaging Het
Trps1 T A 15: 50,661,307 M887L possibly damaging Het
Zfyve28 A G 5: 34,243,195 V53A probably damaging Het
Other mutations in Ccdc91
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00428:Ccdc91 APN 6 147606954 missense unknown
IGL00795:Ccdc91 APN 6 147507807 missense probably damaging 0.99
R1495:Ccdc91 UTSW 6 147534172 missense possibly damaging 0.66
R1725:Ccdc91 UTSW 6 147592043 missense unknown
R3761:Ccdc91 UTSW 6 147562702 missense unknown
R4246:Ccdc91 UTSW 6 147592148 missense unknown
R4591:Ccdc91 UTSW 6 147590465 missense unknown
R4797:Ccdc91 UTSW 6 147592143 missense unknown
R5719:Ccdc91 UTSW 6 147575503 missense unknown
R5721:Ccdc91 UTSW 6 147575503 missense unknown
R6092:Ccdc91 UTSW 6 147535616 missense possibly damaging 0.66
R7156:Ccdc91 UTSW 6 147534178 missense possibly damaging 0.83
R7393:Ccdc91 UTSW 6 147534029 missense possibly damaging 0.92
R7411:Ccdc91 UTSW 6 147592198 nonsense probably null
R7576:Ccdc91 UTSW 6 147590459 missense unknown
R8165:Ccdc91 UTSW 6 147631588 missense unknown
R8311:Ccdc91 UTSW 6 147535616 missense possibly damaging 0.66
X0027:Ccdc91 UTSW 6 147590639 critical splice donor site probably null
Posted On2012-04-20