Incidental Mutation 'IGL00163:Ccdc77'
ID 1558
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ccdc77
Ensembl Gene ENSMUSG00000030177
Gene Name coiled-coil domain containing 77
Synonyms 2700091N06Rik, 2400002C23Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00163
Quality Score
Status
Chromosome 6
Chromosomal Location 120301283-120341330 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 120306045 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000127096 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032283] [ENSMUST00000112703] [ENSMUST00000127146] [ENSMUST00000144131]
AlphaFold Q9CZH8
Predicted Effect probably benign
Transcript: ENSMUST00000032283
SMART Domains Protein: ENSMUSP00000032283
Gene: ENSMUSG00000030177

DomainStartEndE-ValueType
coiled coil region 57 120 N/A INTRINSIC
low complexity region 221 235 N/A INTRINSIC
coiled coil region 346 380 N/A INTRINSIC
coiled coil region 414 445 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000112703
SMART Domains Protein: ENSMUSP00000108323
Gene: ENSMUSG00000030177

DomainStartEndE-ValueType
coiled coil region 39 102 N/A INTRINSIC
low complexity region 203 217 N/A INTRINSIC
internal_repeat_1 258 283 9.62e-5 PROSPERO
internal_repeat_1 321 348 9.62e-5 PROSPERO
low complexity region 352 369 N/A INTRINSIC
coiled coil region 396 427 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000127146
SMART Domains Protein: ENSMUSP00000120896
Gene: ENSMUSG00000030177

DomainStartEndE-ValueType
coiled coil region 39 102 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000144131
SMART Domains Protein: ENSMUSP00000127096
Gene: ENSMUSG00000030177

DomainStartEndE-ValueType
coiled coil region 39 102 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930553M12Rik G A 4: 88,786,310 (GRCm39) Q103* probably null Het
4933406P04Rik C A 10: 20,186,970 (GRCm39) probably benign Het
Adgrg6 T C 10: 14,343,194 (GRCm39) E251G probably damaging Het
Ago2 T C 15: 72,998,302 (GRCm39) H292R probably benign Het
Akr1c6 T C 13: 4,498,977 (GRCm39) probably benign Het
Arhgap24 T A 5: 103,008,265 (GRCm39) M62K possibly damaging Het
Bicd1 A G 6: 149,451,888 (GRCm39) H834R possibly damaging Het
Cdadc1 G T 14: 59,818,818 (GRCm39) H337N probably damaging Het
Cep192 A G 18: 68,013,871 (GRCm39) T2424A possibly damaging Het
Cep78 T C 19: 15,946,504 (GRCm39) T443A probably benign Het
Chrna1 T A 2: 73,400,986 (GRCm39) E181D probably benign Het
Dmxl1 G A 18: 49,984,534 (GRCm39) D177N probably damaging Het
Eif3h T A 15: 51,650,195 (GRCm39) I330F probably damaging Het
Fam184b T C 5: 45,697,091 (GRCm39) E691G probably benign Het
Fastkd1 T A 2: 69,537,893 (GRCm39) S230C probably benign Het
Gipc2 T C 3: 151,843,215 (GRCm39) I141V probably damaging Het
Hsd17b2 A T 8: 118,485,410 (GRCm39) D291V probably damaging Het
Itpr2 G A 6: 146,292,334 (GRCm39) A420V possibly damaging Het
Jag1 C T 2: 136,927,952 (GRCm39) probably null Het
Minar1 A T 9: 89,473,150 (GRCm39) probably benign Het
Mmp1b T A 9: 7,387,946 (GRCm39) Y16F probably benign Het
Muc4 G T 16: 32,754,090 (GRCm38) R1322M probably benign Het
Myo9b T C 8: 71,801,379 (GRCm39) I1179T probably benign Het
Nos1ap A G 1: 170,342,175 (GRCm39) probably benign Het
Npc1l1 A T 11: 6,174,199 (GRCm39) V702E probably damaging Het
Or13d1 G A 4: 52,971,058 (GRCm39) V146M possibly damaging Het
Or1j21 A G 2: 36,684,012 (GRCm39) I255V probably benign Het
Or2ag17 T A 7: 106,389,796 (GRCm39) R137S probably benign Het
Or2y10 A C 11: 49,454,747 (GRCm39) probably benign Het
Or4c31 A T 2: 88,291,696 (GRCm39) Y4F probably benign Het
Or4f7 A C 2: 111,644,126 (GRCm39) probably benign Het
Osmr A T 15: 6,873,926 (GRCm39) L157* probably null Het
Pdzph1 T C 17: 59,281,791 (GRCm39) T164A possibly damaging Het
Ptn T C 6: 36,720,424 (GRCm39) K43E probably benign Het
Rbm45 T C 2: 76,209,051 (GRCm39) V340A probably damaging Het
Rnf5 C T 17: 34,821,083 (GRCm39) G83E probably damaging Het
Scin G T 12: 40,126,971 (GRCm39) Q459K probably benign Het
Serpina5 C A 12: 104,071,479 (GRCm39) A362D probably damaging Het
Tex47 T A 5: 7,355,468 (GRCm39) Y216* probably null Het
Tll1 A T 8: 64,469,170 (GRCm39) H984Q probably benign Het
Tmem259 A G 10: 79,815,568 (GRCm39) V81A probably benign Het
Tns3 A T 11: 8,401,066 (GRCm39) S1077R probably benign Het
Trgv3 G A 13: 19,427,381 (GRCm39) S88N probably benign Het
Ttc17 A G 2: 94,153,428 (GRCm39) probably benign Het
Tubgcp2 T C 7: 139,610,935 (GRCm39) T149A possibly damaging Het
Ulk1 G A 5: 110,935,738 (GRCm39) A25V probably damaging Het
Vps13d T C 4: 144,895,110 (GRCm39) E378G probably damaging Het
Vsig10 A G 5: 117,476,479 (GRCm39) N311S probably benign Het
Zfp511 T C 7: 139,617,429 (GRCm39) Y144H possibly damaging Het
Other mutations in Ccdc77
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01323:Ccdc77 APN 6 120,311,757 (GRCm39) missense probably benign 0.25
IGL02086:Ccdc77 APN 6 120,316,119 (GRCm39) missense possibly damaging 0.89
IGL02388:Ccdc77 APN 6 120,308,858 (GRCm39) missense probably benign
R0576:Ccdc77 UTSW 6 120,308,809 (GRCm39) missense probably benign 0.00
R1485:Ccdc77 UTSW 6 120,315,101 (GRCm39) nonsense probably null
R2422:Ccdc77 UTSW 6 120,316,120 (GRCm39) missense probably benign 0.01
R2497:Ccdc77 UTSW 6 120,302,433 (GRCm39) missense possibly damaging 0.62
R4906:Ccdc77 UTSW 6 120,311,796 (GRCm39) missense probably damaging 0.98
R5104:Ccdc77 UTSW 6 120,325,346 (GRCm39) splice site probably null
R6467:Ccdc77 UTSW 6 120,327,242 (GRCm39) missense probably damaging 0.99
R7165:Ccdc77 UTSW 6 120,327,193 (GRCm39) missense probably damaging 1.00
R7783:Ccdc77 UTSW 6 120,327,334 (GRCm39) missense probably damaging 0.97
R8296:Ccdc77 UTSW 6 120,308,870 (GRCm39) missense possibly damaging 0.53
R8695:Ccdc77 UTSW 6 120,318,962 (GRCm39) missense probably damaging 0.99
Posted On 2011-07-12