Incidental Mutation 'IGL03325:Ccdc198'
ID 416632
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc198
Ensembl Gene ENSMUSG00000021850
Gene Name coiled-coil domain containing 198
Synonyms 1700011H14Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL03325
Quality Score
Status
Chromosome 14
Chromosomal Location 49463815-49482902 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 49481277 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000154726 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022398] [ENSMUST00000130853] [ENSMUST00000148109] [ENSMUST00000227113] [ENSMUST00000228936]
AlphaFold Q9CPZ1
Predicted Effect probably benign
Transcript: ENSMUST00000022398
SMART Domains Protein: ENSMUSP00000022398
Gene: ENSMUSG00000021850

DomainStartEndE-ValueType
Pfam:DUF4619 1 294 1e-153 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000130853
SMART Domains Protein: ENSMUSP00000117775
Gene: ENSMUSG00000021850

DomainStartEndE-ValueType
Pfam:DUF4619 1 217 4.8e-93 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000148109
SMART Domains Protein: ENSMUSP00000114834
Gene: ENSMUSG00000021850

DomainStartEndE-ValueType
Pfam:DUF4619 1 65 3.4e-26 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000227113
Predicted Effect probably benign
Transcript: ENSMUST00000228936
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b G A 11: 109,844,422 (GRCm39) R870C possibly damaging Het
Abcf2 A T 5: 24,779,210 (GRCm39) L113I probably damaging Het
Abi1 C T 2: 22,861,240 (GRCm39) R106Q probably damaging Het
Arhgef28 A G 13: 98,036,324 (GRCm39) V1645A probably benign Het
Ceacam1 G A 7: 25,175,912 (GRCm39) A94V possibly damaging Het
Fat2 G A 11: 55,173,168 (GRCm39) T2515I probably damaging Het
Gm5800 T C 14: 51,951,983 (GRCm39) Y93C probably benign Het
Gnl1 A G 17: 36,299,548 (GRCm39) D573G probably damaging Het
Gosr1 A G 11: 76,645,229 (GRCm39) M105T probably benign Het
Gramd1c A T 16: 43,825,868 (GRCm39) Y303N probably benign Het
Heatr9 A G 11: 83,404,085 (GRCm39) probably null Het
Iigp1c T A 18: 60,378,883 (GRCm39) Y139* probably null Het
Itih2 T C 2: 10,111,546 (GRCm39) D464G probably damaging Het
Jcad T C 18: 4,673,902 (GRCm39) Y555H probably benign Het
Krtap19-3 A T 16: 88,674,609 (GRCm39) *88R probably null Het
Mrps11 T C 7: 78,440,453 (GRCm39) F114S probably damaging Het
Nat8 A T 6: 85,807,875 (GRCm39) V86E possibly damaging Het
Nek5 T C 8: 22,569,158 (GRCm39) T555A probably benign Het
Or6c3 A T 10: 129,309,474 (GRCm39) K304N probably benign Het
Pprc1 C T 19: 46,049,948 (GRCm39) T10I possibly damaging Het
Prss16 A G 13: 22,187,417 (GRCm39) V409A possibly damaging Het
Sema3d T A 5: 12,513,189 (GRCm39) L53Q probably damaging Het
Sfmbt2 T C 2: 10,582,628 (GRCm39) Y696H probably damaging Het
Sh2d3c C T 2: 32,615,270 (GRCm39) A120V probably benign Het
Smn1 A G 13: 100,264,365 (GRCm39) Y32C probably damaging Het
Sun2 C T 15: 79,622,849 (GRCm39) R110Q probably benign Het
Tcp11l2 T G 10: 84,440,764 (GRCm39) D323E possibly damaging Het
Tex55 A T 16: 38,648,355 (GRCm39) S251R probably damaging Het
Tnni3k A T 3: 154,667,451 (GRCm39) S296R probably damaging Het
Uck1 G A 2: 32,148,334 (GRCm39) R161C probably benign Het
Unc79 T A 12: 103,135,869 (GRCm39) S2435T probably damaging Het
Vmn2r114 C A 17: 23,510,652 (GRCm39) K609N probably damaging Het
Other mutations in Ccdc198
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01433:Ccdc198 APN 14 49,473,341 (GRCm39) missense probably benign 0.02
IGL02133:Ccdc198 APN 14 49,470,424 (GRCm39) missense probably benign 0.05
R1751:Ccdc198 UTSW 14 49,473,341 (GRCm39) missense probably benign 0.09
R1767:Ccdc198 UTSW 14 49,473,341 (GRCm39) missense probably benign 0.09
R1846:Ccdc198 UTSW 14 49,473,420 (GRCm39) missense probably damaging 1.00
R1908:Ccdc198 UTSW 14 49,464,032 (GRCm39) missense probably damaging 1.00
R4563:Ccdc198 UTSW 14 49,471,955 (GRCm39) missense probably benign 0.27
R4883:Ccdc198 UTSW 14 49,482,560 (GRCm39) missense probably damaging 1.00
R4915:Ccdc198 UTSW 14 49,470,351 (GRCm39) missense probably benign 0.01
R5381:Ccdc198 UTSW 14 49,470,364 (GRCm39) missense probably damaging 1.00
R5986:Ccdc198 UTSW 14 49,470,403 (GRCm39) missense probably damaging 1.00
R6379:Ccdc198 UTSW 14 49,481,191 (GRCm39) missense probably benign 0.02
R6829:Ccdc198 UTSW 14 49,464,025 (GRCm39) makesense probably null
R6841:Ccdc198 UTSW 14 49,481,270 (GRCm39) critical splice acceptor site probably null
R7337:Ccdc198 UTSW 14 49,471,948 (GRCm39) missense possibly damaging 0.94
R8327:Ccdc198 UTSW 14 49,470,356 (GRCm39) missense possibly damaging 0.76
R9154:Ccdc198 UTSW 14 49,473,367 (GRCm39) missense probably benign 0.00
Posted On 2016-08-02