Name

MSL3P1 Gene

male-specific lethal 3 homolog (Drosophila) pseudogene 1

Predicted to be involved in chromatin organization and regulation of DNA-templated transcription. Predicted to be located in nucleus. Predicted to be part of MSL complex and NuA4 histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025]

MGCT Gene

male germ cell tumor

MSL2 Gene

male-specific lethal 2 homolog (Drosophila)

Enables histone H2B ubiquitin ligase activity. Involved in DNA damage response and protein monoubiquitination. Part of MSL complex and nucleus. Is active in chromatin. [provided by Alliance of Genome Resources, Mar 2025]

MSL3 Gene

male-specific lethal 3 homolog (Drosophila)

This gene encodes a nuclear protein that is similar to the product of the Drosophila male-specific lethal-3 gene. The Drosophila protein plays a critical role in a dosage-compensation pathway, which equalizes X-linked gene expression in males and females. Thus, the human protein is thought to play a similar function in chromatin remodeling and transcriptional regulation, and it has been found as part of a complex that is responsible for histone H4 lysine-16 acetylation. This gene can undergo X inactivation. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2, 7 and 8. [provided by RefSeq, Jul 2010]

DEL15Q15.3 Gene

Deafness and male infertility

MSL1 Gene

male-specific lethal 1 homolog (Drosophila)

Enables protein-macromolecule adaptor activity. Involved in positive regulation of DNA-templated transcription. Located in nucleoplasm. Part of MSL complex. [provided by Alliance of Genome Resources, Mar 2025]

MEA1 Gene

male-enhanced antigen 1

Predicted to be involved in male gonad development and spermatogenesis. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

LOC100499192 Gene

male-specific lethal 3 homolog (Drosophila) pseudogene

MAK Gene

male germ cell-associated kinase

The product of this gene is a serine/threonine protein kinase related to kinases involved in cell cycle regulation. Studies of the mouse and rat homologs have localized the kinase to the chromosomes during meiosis in spermatogenesis, specifically to the synaptonemal complex that exists while homologous chromosomes are paired. Mutations in this gene have been associated with ciliary defects resulting in retinitis pigmentosa 62. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

LOC100499191 Gene

male-specific lethal 3 homolog (Drosophila) pseudogene

SSD Gene

Speech-sound disorder

OHDS Gene

Orthostatic hypotensive disorder of Streeten

MAFD9 Gene

Major affective disorder-9, susceptibility to

MAFD8 Gene

Major affective disorder-8, susceptibility to

MAFD5 Gene

Major affective disorder 5

MAFD1 Gene

major affective disorder 1

MAFD3 Gene

Major affective disorder 3, early onset

MDD2 Gene

Major depressive disorder 2

MDD1 Gene

Major depressive disorder

MAFD2 Gene

major affective disorder 2

MAFD4 Gene

Major affective disorder 4

MAFD6 Gene

Major affective disorder 6

ADHD2 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

HDL3 Gene

Huntington-like neurodegenerative disorder 2

PAND1 Gene

Panic disorder 1

PAND2 Gene

panic disorder 2

PAND3 Gene

panic disorder 3

BDET Gene

Bleeding disorder, east Texas type

ADHD4 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 4

ADHD5 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 5

ADHD6 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 6

ADHD1 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 1

ADHD3 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

SCZD8 Gene

schizophrenia disorder 8

SCZD7 Gene

schizophrenia disorder 7

SCZD6 Gene

schizophrenia disorder 6

SCZD1 Gene

schizophrenia disorder 1

SCZD3 Gene

schizophrenia disorder 3

SCZD10 Gene

schizophrenia disorder 10 (periodic catatonia)

NDNC9 Gene

Nail disorder, nonsyndromic congenital, 9

CLA3 Gene

cerebellar ataxia 3 (cerebellar parenchyma disorder 1)

SCZD2 Gene

schizophrenia disorder 2

PDR Gene

pigment disorder, reticulate