Incidental Mutation 'IGL00903:Hacd3'
ID 28127
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Hacd3
Ensembl Gene ENSMUSG00000033629
Gene Name 3-hydroxyacyl-CoA dehydratase 3
Synonyms B-ind1, Ptplad1, Hspc121
Accession Numbers
Essential gene? Probably non essential (E-score: 0.125) question?
Stock # IGL00903
Quality Score
Status
Chromosome 9
Chromosomal Location 64894265-64928975 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 64911535 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000044955 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036615]
AlphaFold Q8K2C9
Predicted Effect probably benign
Transcript: ENSMUST00000036615
SMART Domains Protein: ENSMUSP00000044955
Gene: ENSMUSG00000033629

DomainStartEndE-ValueType
Pfam:CS 8 84 2.3e-7 PFAM
low complexity region 119 136 N/A INTRINSIC
transmembrane domain 153 175 N/A INTRINSIC
Pfam:PTPLA 195 356 1.5e-46 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arsk A G 13: 76,246,487 (GRCm39) probably null Het
As3mt A G 19: 46,700,673 (GRCm39) I159V probably benign Het
Atpsckmt T C 15: 31,606,261 (GRCm39) V73A possibly damaging Het
Ctsll3 C A 13: 60,948,075 (GRCm39) V201L probably benign Het
Dapk1 T C 13: 60,909,211 (GRCm39) Y1275H probably damaging Het
Erap1 G A 13: 74,821,826 (GRCm39) R727H probably benign Het
Fcrl6 T A 1: 172,426,674 (GRCm39) T91S probably benign Het
Gvin1 T C 7: 105,757,377 (GRCm39) E2364G probably benign Het
Hcls1 T A 16: 36,776,383 (GRCm39) probably null Het
Igf2r C T 17: 12,902,754 (GRCm39) R2432H possibly damaging Het
Kif27 C A 13: 58,492,486 (GRCm39) V218F possibly damaging Het
Klhl20 T C 1: 160,918,076 (GRCm39) Y70C probably benign Het
Krt86 C T 15: 101,371,741 (GRCm39) H104Y probably benign Het
Lcn12 G T 2: 25,383,332 (GRCm39) N15K possibly damaging Het
Mrgpra1 T C 7: 46,985,326 (GRCm39) M118V probably benign Het
Nacad G T 11: 6,550,632 (GRCm39) T853K probably damaging Het
Nos3 A T 5: 24,574,860 (GRCm39) Q293L probably damaging Het
Prkca C T 11: 107,874,800 (GRCm39) V381M probably damaging Het
Ptcd3 A G 6: 71,884,828 (GRCm39) F37S possibly damaging Het
Ptgs2 A G 1: 149,980,175 (GRCm39) Y371C probably damaging Het
Pygl T C 12: 70,254,516 (GRCm39) Y143C probably damaging Het
Samhd1 A G 2: 156,949,343 (GRCm39) probably benign Het
Scube1 T A 15: 83,587,702 (GRCm39) H89L probably damaging Het
Tmem59l G A 8: 70,938,315 (GRCm39) probably benign Het
Vmn2r108 A G 17: 20,682,774 (GRCm39) V810A probably damaging Het
Vmn2r61 T G 7: 41,949,935 (GRCm39) F785C probably damaging Het
Zfas1 G T 2: 166,907,406 (GRCm39) probably benign Het
Other mutations in Hacd3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01323:Hacd3 APN 9 64,905,587 (GRCm39) missense probably damaging 1.00
IGL02943:Hacd3 APN 9 64,897,718 (GRCm39) missense probably damaging 0.99
R0145:Hacd3 UTSW 9 64,911,524 (GRCm39) splice site probably benign
R0390:Hacd3 UTSW 9 64,908,304 (GRCm39) missense possibly damaging 0.89
R2403:Hacd3 UTSW 9 64,908,311 (GRCm39) missense probably damaging 1.00
R3117:Hacd3 UTSW 9 64,905,591 (GRCm39) missense probably damaging 1.00
R3740:Hacd3 UTSW 9 64,928,755 (GRCm39) missense possibly damaging 0.58
R4972:Hacd3 UTSW 9 64,897,718 (GRCm39) missense probably damaging 0.99
R6174:Hacd3 UTSW 9 64,912,909 (GRCm39) missense probably damaging 1.00
R7085:Hacd3 UTSW 9 64,905,525 (GRCm39) missense probably damaging 1.00
R9131:Hacd3 UTSW 9 64,908,286 (GRCm39) missense probably damaging 0.99
Posted On 2013-04-17