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MACROD1 (Mono-ADP Ribosylhydrolase 1) is a Protein Coding gene. Diseases associated with MACROD1 include Hypercholesterolemia, Familial, 4 and Endometrial Cancer. Gene Ontology (GO) annotations related to this gene include hydrolase activity, acting on glycosyl bonds and deacetylase activity. An important paralog of this gene is MACROD2.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005515 | protein binding | IPI | 17914104 |
GO:0016787 | hydrolase activity | IEA | -- |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | IDA | 23474712 |
GO:0019213 | deacetylase activity | IDA | 21257746 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IEA,IDA | 23474712 |
GO:0005654 | nucleoplasm | IBA,IDA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006974 | cellular response to DNA damage stimulus | IBA,IMP | 23474712 |
GO:0042278 | purine nucleoside metabolic process | IBA,IDA | 21257746 |
GO:0051725 | protein de-ADP-ribosylation | IDA | 23474712 |
ExUns: | 1a | · | 1b | ^ | 2 | ^ | 3 | ^ | 4 | ^ | 5a | · | 5b | ^ | 6 | ^ | 7 | ^ | 8 | ^ | 9 | ^ | 10 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | ||||||||||||||||||||||
SP2: | - |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | MACROD1 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | MACROD1 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | MACROD1 30 31 |
|
OneToOne | |
Mouse (Mus musculus) |
Mammalia | Macrod1 30 17 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Macrod1 30 |
|
||
Platypus (Ornithorhynchus anatinus) |
Mammalia | MACROD1 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | MACROD1 31 |
|
OneToOne | |
African clawed frog (Xenopus laevis) |
Amphibia | MGC68697 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | macrod1 30 31 |
|
OneToMany | |
zgc65960 30 |
|
||||
Rainbow Trout (Oncorhynchus mykiss) |
Actinopterygii | Omy.8510 30 |
|
||
Worm (Caenorhabditis elegans) |
Secernentea | B0035.3 31 |
|
OneToMany | |
Sea Squirt (Ciona savignyi) |
Ascidiacea | -- 31 |
|
OneToMany | |
Sea Vase (Ciona intestinalis) |
Ascidiacea | Cin.8148 30 |
|
SNP ID | Clinical significance and condition | Chr 11 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
835656 | Uncertain Significance: Peripheral neuropathy | 64,117,913(-) |
C/T NM_014067.4(MACROD1):c.517+33326G>A |
MISSENSE_VARIANT,INTRON | |
840095 | Uncertain Significance: Peripheral neuropathy | 64,118,059(-) |
G/A NM_014067.4(MACROD1):c.517+33180C>T |
MISSENSE_VARIANT,INTRON | |
842634 | Uncertain Significance: Peripheral neuropathy | 64,116,738(-) |
C/A NM_014067.4(MACROD1):c.517+34501G>T |
MISSENSE_VARIANT,INTRON | |
845837 | Uncertain Significance: Peripheral neuropathy | 64,118,042(-) |
G/A NM_014067.4(MACROD1):c.517+33197C>T |
MISSENSE_VARIANT,INTRON | |
857225 | Uncertain Significance: Peripheral neuropathy | 64,116,518(-) |
C/T NM_014067.4(MACROD1):c.517+34721G>A |
MISSENSE_VARIANT,INTRON |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv15n68 | CNV | loss | 17160897 |
esv2666053 | CNV | deletion | 23128226 |
esv2669519 | CNV | deletion | 23128226 |
esv2744613 | CNV | deletion | 23290073 |
esv29993 | CNV | loss | 17803354 |
esv3431264 | CNV | duplication | 20981092 |
esv3626656 | CNV | loss | 21293372 |
esv996910 | CNV | loss | 20482838 |
nsv1042075 | CNV | loss | 25217958 |
nsv1078325 | CNV | duplication | 25765185 |
nsv1134139 | CNV | deletion | 24896259 |
nsv1141196 | CNV | duplication | 24896259 |
nsv1143685 | CNV | deletion | 24896259 |
nsv1159904 | CNV | deletion | 26073780 |
nsv354 | CNV | insertion | 18451855 |
nsv356 | CNV | deletion | 18451855 |
nsv469961 | CNV | loss | 18288195 |
nsv473286 | CNV | novel sequence insertion | 20440878 |
nsv555181 | CNV | loss | 21841781 |
nsv555182 | CNV | loss | 21841781 |
nsv555183 | CNV | loss | 21841781 |
nsv555184 | CNV | loss | 21841781 |
nsv951010 | CNV | deletion | 24416366 |
Disorder | Aliases | PubMed IDs |
---|---|---|
hypercholesterolemia, familial, 4 |
|
|
endometrial cancer |
|
|
cardiomyopathy, dilated, 1e |
|
|
familial hypercholesterolemia |
|
|
hereditary spastic paraplegia |
|
|