Incidental Mutation 'IGL01524:Ccdc175'
ID 89522
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc175
Ensembl Gene ENSMUSG00000021086
Gene Name coiled-coil domain containing 175
Synonyms 4930403N07Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL01524
Quality Score
Status
Chromosome 12
Chromosomal Location 72148074-72231803 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to A at 72177916 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000021494 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021494]
AlphaFold E9PVB3
Predicted Effect probably benign
Transcript: ENSMUST00000021494
SMART Domains Protein: ENSMUSP00000021494
Gene: ENSMUSG00000021086

DomainStartEndE-ValueType
coiled coil region 129 164 N/A INTRINSIC
coiled coil region 205 235 N/A INTRINSIC
coiled coil region 295 383 N/A INTRINSIC
low complexity region 470 490 N/A INTRINSIC
coiled coil region 517 537 N/A INTRINSIC
low complexity region 803 819 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179978
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadat A T 8: 60,969,106 (GRCm39) D117V probably damaging Het
Abca14 T C 7: 119,852,644 (GRCm39) Y870H possibly damaging Het
Ankrd36 T C 11: 5,585,092 (GRCm39) I301T probably benign Het
Atp10b T A 11: 43,150,672 (GRCm39) S1457T probably benign Het
Bltp1 A G 3: 36,996,531 (GRCm39) D1081G possibly damaging Het
Ccdc93 A G 1: 121,389,628 (GRCm39) K224E probably benign Het
Cep131 C T 11: 119,956,786 (GRCm39) A886T probably damaging Het
Clip1 A C 5: 123,717,442 (GRCm39) H1282Q probably damaging Het
Ctcfl T G 2: 172,959,177 (GRCm39) D183A probably benign Het
Cyp17a1 C T 19: 46,659,495 (GRCm39) V112I probably benign Het
Fhod3 T C 18: 25,263,659 (GRCm39) I1521T probably damaging Het
Gipc2 A G 3: 151,843,214 (GRCm39) I141T probably damaging Het
Glo1 T C 17: 30,815,393 (GRCm39) R141G possibly damaging Het
Ipmk C A 10: 71,208,631 (GRCm39) A140E probably damaging Het
Kynu A G 2: 43,561,394 (GRCm39) D310G possibly damaging Het
Myo1f T A 17: 33,798,857 (GRCm39) I174N probably damaging Het
Nat10 T A 2: 103,588,102 (GRCm39) N8Y probably damaging Het
Nhlrc2 A G 19: 56,564,587 (GRCm39) I304V probably benign Het
Pdk4 T C 6: 5,491,979 (GRCm39) H31R probably damaging Het
Sema6d T C 2: 124,505,995 (GRCm39) V644A possibly damaging Het
Slc30a4 T A 2: 122,544,308 (GRCm39) K11N possibly damaging Het
Slc6a3 T C 13: 73,686,668 (GRCm39) S12P probably benign Het
Spats2 C T 15: 99,110,127 (GRCm39) A508V probably benign Het
Tinag A G 9: 76,952,820 (GRCm39) Y55H probably damaging Het
Topbp1 T C 9: 103,188,844 (GRCm39) I172T possibly damaging Het
Trim17 A G 11: 58,861,423 (GRCm39) T279A probably damaging Het
Vmn1r216 C A 13: 23,283,519 (GRCm39) N67K probably benign Het
Washc4 T C 10: 83,411,996 (GRCm39) L709P probably benign Het
Xdh T C 17: 74,230,132 (GRCm39) probably null Het
Zfhx4 C T 3: 5,309,036 (GRCm39) P754L probably damaging Het
Zfp267 T C 3: 36,218,729 (GRCm39) Y251H possibly damaging Het
Zfp623 C A 15: 75,819,528 (GRCm39) S161R probably benign Het
Zmat3 G A 3: 32,395,827 (GRCm39) R227C possibly damaging Het
Other mutations in Ccdc175
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01805:Ccdc175 APN 12 72,176,003 (GRCm39) splice site probably benign
IGL01807:Ccdc175 APN 12 72,206,616 (GRCm39) missense probably benign 0.02
IGL01985:Ccdc175 APN 12 72,175,052 (GRCm39) nonsense probably null
IGL02719:Ccdc175 APN 12 72,221,899 (GRCm39) missense probably damaging 0.97
IGL02944:Ccdc175 APN 12 72,164,667 (GRCm39) missense probably benign 0.02
IGL03113:Ccdc175 APN 12 72,191,557 (GRCm39) missense probably benign 0.00
IGL03143:Ccdc175 APN 12 72,182,832 (GRCm39) missense probably benign 0.03
IGL03356:Ccdc175 APN 12 72,186,667 (GRCm39) splice site probably null
R0009:Ccdc175 UTSW 12 72,182,739 (GRCm39) missense possibly damaging 0.87
R0233:Ccdc175 UTSW 12 72,152,650 (GRCm39) missense probably benign 0.00
R0233:Ccdc175 UTSW 12 72,152,650 (GRCm39) missense probably benign 0.00
R0609:Ccdc175 UTSW 12 72,204,281 (GRCm39) missense probably benign 0.07
R0706:Ccdc175 UTSW 12 72,186,722 (GRCm39) missense probably benign 0.04
R0948:Ccdc175 UTSW 12 72,177,897 (GRCm39) missense probably damaging 1.00
R1054:Ccdc175 UTSW 12 72,225,318 (GRCm39) missense possibly damaging 0.85
R1166:Ccdc175 UTSW 12 72,152,706 (GRCm39) missense probably damaging 1.00
R1481:Ccdc175 UTSW 12 72,148,722 (GRCm39) unclassified probably benign
R1860:Ccdc175 UTSW 12 72,152,700 (GRCm39) missense probably benign
R2077:Ccdc175 UTSW 12 72,186,794 (GRCm39) missense possibly damaging 0.54
R3806:Ccdc175 UTSW 12 72,227,598 (GRCm39) missense possibly damaging 0.72
R3879:Ccdc175 UTSW 12 72,182,792 (GRCm39) missense probably damaging 1.00
R3887:Ccdc175 UTSW 12 72,182,822 (GRCm39) missense possibly damaging 0.65
R4557:Ccdc175 UTSW 12 72,175,080 (GRCm39) missense probably benign 0.08
R4585:Ccdc175 UTSW 12 72,221,953 (GRCm39) missense possibly damaging 0.65
R4686:Ccdc175 UTSW 12 72,159,052 (GRCm39) missense probably damaging 1.00
R4766:Ccdc175 UTSW 12 72,158,979 (GRCm39) missense probably benign 0.00
R4773:Ccdc175 UTSW 12 72,182,822 (GRCm39) missense probably damaging 0.99
R4909:Ccdc175 UTSW 12 72,206,527 (GRCm39) missense probably damaging 1.00
R4964:Ccdc175 UTSW 12 72,227,619 (GRCm39) missense probably damaging 1.00
R5338:Ccdc175 UTSW 12 72,231,745 (GRCm39) missense probably damaging 0.99
R5539:Ccdc175 UTSW 12 72,191,587 (GRCm39) missense probably benign 0.00
R5897:Ccdc175 UTSW 12 72,206,578 (GRCm39) missense probably benign 0.06
R6128:Ccdc175 UTSW 12 72,175,933 (GRCm39) missense probably benign 0.07
R6520:Ccdc175 UTSW 12 72,186,804 (GRCm39) missense probably damaging 0.98
R6523:Ccdc175 UTSW 12 72,191,565 (GRCm39) missense probably benign 0.01
R6917:Ccdc175 UTSW 12 72,231,679 (GRCm39) missense probably damaging 1.00
R7035:Ccdc175 UTSW 12 72,202,419 (GRCm39) missense probably benign 0.01
R7097:Ccdc175 UTSW 12 72,175,183 (GRCm39) splice site probably null
R7339:Ccdc175 UTSW 12 72,182,815 (GRCm39) missense probably damaging 1.00
R7450:Ccdc175 UTSW 12 72,202,447 (GRCm39) missense possibly damaging 0.93
R7481:Ccdc175 UTSW 12 72,202,398 (GRCm39) missense probably benign 0.00
R7676:Ccdc175 UTSW 12 72,148,821 (GRCm39) missense possibly damaging 0.57
R8045:Ccdc175 UTSW 12 72,202,676 (GRCm39) intron probably benign
R8383:Ccdc175 UTSW 12 72,155,952 (GRCm39) missense possibly damaging 0.95
R8470:Ccdc175 UTSW 12 72,202,392 (GRCm39) missense probably damaging 0.97
R9211:Ccdc175 UTSW 12 72,153,458 (GRCm39) missense probably damaging 1.00
R9739:Ccdc175 UTSW 12 72,186,792 (GRCm39) missense probably benign 0.00
Z1088:Ccdc175 UTSW 12 72,175,153 (GRCm39) missense probably benign 0.01
Z1176:Ccdc175 UTSW 12 72,159,082 (GRCm39) missense possibly damaging 0.90
Posted On 2013-12-03