Entity Details

Primary name MAMLD1
Entity type gene
Source Source Link

Details

PrimaryID10046
RefseqGeneNG_017093
SymbolMAMLD1
Namemastermind like domain containing 1
ChromosomeX
LocationXq28
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-08-23
ModificationDate2021-06-13

Ontological Relatives

UniProt IDsMAMD1_HUMAN

GO terms

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GOName
GO:0005654 nucleoplasm
GO:0005794 Golgi apparatus
GO:0005813 centrosome
GO:0006357 regulation of transcription by RNA polymerase II
GO:0008584 male gonad development
GO:0016604 nuclear body

Diseases

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Disease IDSourceNameDescription
300758 OMIMHypospadias 2, X-linked (HYSP2)A common malformation in which the urethra opens on the ventral side of the penis, due to developmental arrest of urethral fusion. The opening can be located glandular, penile, or even more posterior in the scrotum or perineum. Hypospadias is a feature of several syndromic disorders, including the androgen insensitivity syndrome and Opitz syndrome. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
MAMLD1MTNR1ABioGRID, IntAct26514267 details
MAMLD1VIRMABioGRID29507755 details