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AIFM1

AIFM1

Protein-coding gene in humans

Apoptosis-inducing factor 1, mitochondrial is a protein that in humans is encoded by the AIFM1 gene on the X chromosome. This protein localizes to the mitochondria, as

AIFM1

Apoptosis-inducing factor

Protein family

genes encoding apoptosis inducing factor isozymes include:[citation needed] AIFM1 AIFM2 AIFM3 The apoptotic function of AIFs has been shown in organisms belonging

Apoptosis-inducing factor

Apoptosis-inducing_factor

List of human protein-coding genes 1

HGNC:25761; Q96BJ3 471 AIF1 HGNC:352; P55008 472 AIF1L HGNC:28904; Q9BQI0 473 AIFM1 HGNC:8768; O95831 474 AIFM2 HGNC:21411; Q9BRQ8 475 AIFM3 HGNC:26398; Q96NN9

List of human protein-coding genes 1

List_of_human_protein-coding_genes_1

Charcot–Marie–Tooth disease classifications

Peripheral nervous system disorders

X-linked recessive CMTX3 302802 CMTX3 Xq26 X-linked recessive CMTX4 310490 AIFM1 Xq24–q26.1 X-linked recessive Also known as Cowchock syndrome CMTX5 311070

Charcot–Marie–Tooth disease classifications

Charcot–Marie–Tooth_disease_classifications

FAM162A

Protein-coding gene in the species Homo sapiens

In neuronal cells, it additionally stimulates mitochondrial release of AIFM1, which then translocates to the nucleus to effect apoptosis, which indicates

FAM162A

AIFM2

Protein-coding gene in the species Homo sapiens

determined. The phylogenetic studies indicates that the divergence of the AIFM1 and other AIFs occurred before the divergence of eukaryotes. AIFM2 is shown

AIFM2

HSPA1A

Protein-coding gene in the species Homo sapiens

Hsp72 is also involved in caspase-independent apoptosis, as it also binds AIFM1. The Hsp70 member proteins are important apoptotic constituents. During

HSPA1A

List of OMIM disorder codes

611719; MRPS22 Combined oxidative phosphorylation deficiency 6; 300816; AIFM1 Combined SAP deficiency; 611721; PSAP Complement component 4, partial deficiency

List of OMIM disorder codes

List_of_OMIM_disorder_codes

X-linked Charcot–Marie–Tooth disease

Medical condition

2: Xp22.2 Type 3: Rearragement of chromosome 8q24.3 and Xq27.1. Type 4: AIFM1, located in Xq26.1 Type 5: PRPS1, located in Xq22.3 Type 6: PDK3, located

X-linked Charcot–Marie–Tooth disease

X-linked_Charcot–Marie–Tooth_disease

COA6

Protein-coding gene in humans

protein interacts with COA1, SCO1, COX16, TTC19, DTX2, NADSYN1, GABARAP, AIFM1, COX4I1, CD81, COX14, SFXN1, and PLGRKT. GRCh38: Ensembl release 89: ENSG00000168275

COA6