ENSG00000141497
Homo sapiens | |
Features
| Gene ID: | ENSG00000141497 | | | | | Biological name : | ZMYND15 | | | | | Synonyms : | Q9H091 / zinc finger MYND-type containing 15 / ZMYND15 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | 17 | | Strand: | 1 | | Band: | p13.2 | | Gene start: | 4740015 | | Gene end: | 4746119 | | | | | Corresponding Affymetrix probe sets: | 223683_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000269289
Ensembl peptide - ENSP00000391742
Ensembl peptide - ENSP00000459501
Ensembl peptide - ENSP00000465435
NCBI entrez gene - 84225
See in Manteia.
OMIM - 614312
RefSeq - XM_017025218
RefSeq - NM_001136046
RefSeq - NM_001267822
RefSeq - NM_032265
RefSeq Peptide - NP_001254751
RefSeq Peptide - NP_115641
RefSeq Peptide - NP_001129518
swissprot - Q9H091
Ensembl - ENSG00000141497
| | | | | Related genetic diseases (OMIM): | 615842 - ?Spermatogenic failure 14, 615842 |
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed
Ortholog prediction (from Ensembl)
Paralog prediction (from Ensembl)
No match
Protein motifs (from Interpro)
Gene Ontology (GO)
Pathways (from Reactome)
No match
Phenotype (from MGI, Zfin or HPO)
| HP:0000007 | Autosomal recessive inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators] |
Show
| | HP:0000027 | Azoospermia | |
Show
| | HP:0000837 | Elevated gonadotropins | |
Show
| | HP:0008734 | Decreased testicular size | |
Show
| | HP:0011961 | Non-obstructive azoospermia | "Absence of any measurable level of sperm in his semen, resulting from a defect in the production of spermatozoa in the testes. Can be differentiated from obstructive azoospermia on the basis of testicular biopsy." [HPO:probinson, pmid:20514278] |
Show
| | HP:0011962 | Obstructive azoospermia | "Absence of any measurable level of sperm in his semen, resulting from post-testicular obstruction or retrograde ejaculation. Can be differentiated from obstructive azoospermia on the basis of testicular biopsy." [HPO:probinson, pmid:20514278] |
Show
|
Interacting proteins (from Reactome)
No match
0 s.
|
