Incidental Mutation 'IGL02383:Coa8'
ID 291474
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Coa8
Ensembl Gene ENSMUSG00000037787
Gene Name cytochrome c oxidase assembly factor 8
Synonyms Apopt1, 1700081D05Rik, 2810002N01Rik, Apop-1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.119) question?
Stock # IGL02383
Quality Score
Status
Chromosome 12
Chromosomal Location 111679695-111721487 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 111690847 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131169 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040519] [ENSMUST00000159557] [ENSMUST00000162316] [ENSMUST00000163220]
AlphaFold Q9CQW7
Predicted Effect probably benign
Transcript: ENSMUST00000040519
SMART Domains Protein: ENSMUSP00000038865
Gene: ENSMUSG00000037787

DomainStartEndE-ValueType
Pfam:DUF2315 54 182 5.5e-55 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000159557
Predicted Effect noncoding transcript
Transcript: ENSMUST00000159897
Predicted Effect
SMART Domains Protein: ENSMUSP00000123929
Gene: ENSMUSG00000037787

DomainStartEndE-ValueType
Pfam:DUF2315 53 162 3.4e-48 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000162316
SMART Domains Protein: ENSMUSP00000125711
Gene: ENSMUSG00000037787

DomainStartEndE-ValueType
Pfam:DUF2315 53 130 7.5e-34 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000163220
SMART Domains Protein: ENSMUSP00000131169
Gene: ENSMUSG00000037787

DomainStartEndE-ValueType
Pfam:DUF2315 54 162 3.7e-46 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that localizes to the mitochondria, where it stimulates the release of cytochrome c, thereby promoting programmed cell death. Mutations in this gene have been found in individuals with mitochondrial complex IV deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5530400C23Rik T C 6: 133,269,205 (GRCm39) probably benign Het
Adap2 C A 11: 80,051,015 (GRCm39) A115D probably damaging Het
Ankrd1 A G 19: 36,097,165 (GRCm39) V6A probably benign Het
Apobr T A 7: 126,185,779 (GRCm39) V430E probably benign Het
Arhgap28 A G 17: 68,203,084 (GRCm39) V123A probably benign Het
Atp2b2 A G 6: 113,790,903 (GRCm39) V167A probably damaging Het
B3galnt2 A T 13: 14,171,618 (GRCm39) *505C probably null Het
Bcat2 T A 7: 45,237,431 (GRCm39) L305Q probably damaging Het
Col9a1 T C 1: 24,224,339 (GRCm39) S174P unknown Het
Ddx41 A T 13: 55,680,170 (GRCm39) D418E probably benign Het
Defa40 A G 8: 21,740,377 (GRCm39) D61G probably damaging Het
Exoc6 T C 19: 37,566,922 (GRCm39) F240L probably benign Het
Fbln7 G A 2: 128,737,477 (GRCm39) V431I probably benign Het
Gfral T A 9: 76,104,374 (GRCm39) N213Y probably damaging Het
Golgb1 A G 16: 36,706,562 (GRCm39) D22G probably benign Het
H2-M1 G A 17: 36,981,141 (GRCm39) T298I unknown Het
Haus3 A T 5: 34,323,580 (GRCm39) Y343* probably null Het
Hid1 T C 11: 115,243,446 (GRCm39) E534G probably damaging Het
Il4ra T C 7: 125,170,676 (GRCm39) V196A probably benign Het
Itm2b C A 14: 73,600,536 (GRCm39) E255* probably null Het
Kidins220 A T 12: 25,047,332 (GRCm39) probably benign Het
Klhl22 T A 16: 17,594,762 (GRCm39) F297Y possibly damaging Het
Krt9 T C 11: 100,082,041 (GRCm39) E253G probably damaging Het
Man2a2 G A 7: 80,009,388 (GRCm39) A822V probably damaging Het
Map3k6 T A 4: 132,973,932 (GRCm39) probably null Het
Med29 C A 7: 28,086,448 (GRCm39) R120L possibly damaging Het
Napa C T 7: 15,846,503 (GRCm39) probably benign Het
Ncapd3 T A 9: 26,961,624 (GRCm39) Y351N probably benign Het
Nphs1 C T 7: 30,181,060 (GRCm39) probably benign Het
Or5b94 A G 19: 12,651,899 (GRCm39) D110G probably benign Het
Prss16 T C 13: 22,193,697 (GRCm39) I33V probably benign Het
Ripk1 A G 13: 34,199,227 (GRCm39) Y193C probably damaging Het
Rph3a C T 5: 121,102,002 (GRCm39) R78H probably damaging Het
Rrp9 T A 9: 106,362,471 (GRCm39) I452N probably damaging Het
Ryr2 A T 13: 11,737,607 (GRCm39) probably benign Het
Sec23a A G 12: 59,048,813 (GRCm39) L103P probably damaging Het
Slc17a9 A C 2: 180,377,674 (GRCm39) D190A probably benign Het
Slc44a4 G A 17: 35,146,686 (GRCm39) V422I probably benign Het
Smc5 C T 19: 23,191,996 (GRCm39) probably benign Het
Tax1bp1 C T 6: 52,730,351 (GRCm39) S611F probably benign Het
Tmem38b G A 4: 53,854,345 (GRCm39) M192I probably benign Het
Unc45a G T 7: 79,989,410 (GRCm39) C34* probably null Het
Usp46 T A 5: 74,190,014 (GRCm39) M6L probably benign Het
Uspl1 G A 5: 149,150,212 (GRCm39) V471M probably damaging Het
Vmn1r35 T A 6: 66,655,875 (GRCm39) Q265L probably damaging Het
Vmn1r35 G T 6: 66,655,876 (GRCm39) Q265K probably damaging Het
Vmn1r50 A G 6: 90,084,461 (GRCm39) I69V possibly damaging Het
Vps33b A G 7: 79,935,082 (GRCm39) probably null Het
Xntrpc A C 7: 101,742,802 (GRCm39) D604A probably damaging Het
Yeats4 T A 10: 117,051,716 (GRCm39) R180S probably benign Het
Other mutations in Coa8
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0336:Coa8 UTSW 12 111,700,092 (GRCm39) intron probably benign
R2324:Coa8 UTSW 12 111,690,784 (GRCm39) missense possibly damaging 0.87
R4436:Coa8 UTSW 12 111,717,642 (GRCm39) missense probably benign 0.03
R4774:Coa8 UTSW 12 111,679,823 (GRCm39) missense possibly damaging 0.66
R5161:Coa8 UTSW 12 111,689,208 (GRCm39) missense possibly damaging 0.55
R5376:Coa8 UTSW 12 111,696,492 (GRCm39) missense probably damaging 0.96
R5864:Coa8 UTSW 12 111,717,652 (GRCm39) missense probably benign 0.03
R6802:Coa8 UTSW 12 111,717,625 (GRCm39) missense probably benign 0.00
R8095:Coa8 UTSW 12 111,689,218 (GRCm39) missense probably damaging 1.00
R9003:Coa8 UTSW 12 111,688,189 (GRCm39) makesense probably null
R9611:Coa8 UTSW 12 111,700,108 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16