ENSG00000197779
Homo sapiens | |
Features
| Gene ID: | ENSG00000197779 | | | | | Biological name : | ZNF81 | | | | | Synonyms : | P51508 / zinc finger protein 81 / ZNF81 | | | | | Possible biological names infered from orthology : | | | | | | Species: | Homo sapiens | | | | | Chr. number: | X | | Strand: | 1 | | Band: | p11.23 | | Gene start: | 47836902 | | Gene end: | 48002561 | | | | | Corresponding Affymetrix probe sets: | 1561038_at (Human Genome U133 Plus 2.0 Array) 1561039_a_at (Human Genome U133 Plus 2.0 Array) 215901_at (Human Genome U133 Plus 2.0 Array) 240079_at (Human Genome U133 Plus 2.0 Array) 242083_at (Human Genome U133 Plus 2.0 Array) | | | | | Cross references: | Ensembl peptide - ENSP00000366149
Ensembl peptide - ENSP00000366153
Ensembl peptide - ENSP00000334641
Ensembl peptide - ENSP00000341151
NCBI entrez gene - 347344
See in Manteia.
OMIM - 314998
RefSeq - XM_017029487
RefSeq - XM_005272600
RefSeq - XM_011543899
RefSeq - XM_011543900
RefSeq - XM_017029486
RefSeq - NM_007137
RefSeq Peptide - NP_009068
swissprot - B1AJV2
swissprot - B1AJV1
swissprot - P51508
Ensembl - ENSG00000197779
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This gene has been taged as a transcription factor by TFT
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)
Protein motifs (from Interpro)
Gene Ontology (GO)
Pathways (from Reactome)
No match
Phenotype (from MGI, Zfin or HPO)
| HP:0000218 | High palate | "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428] |
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| | HP:0000400 | Large ears | |
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| | HP:0000411 | Protruding ears | |
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| | HP:0000426 | Prominent nasal bridge | |
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| | HP:0001249 | Mental retardation | |
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| | HP:0001419 | X-linked recessive inheritance | "A mode of inheritance that is observed for recessive traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked recessive disorders manifest in males (who have one copy of the X chromosome and are thus hemizygotes), but generally not in female heterozygotes who have one mutant and one normal allele." [HPO:curators] |
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| | HP:0004322 | Decreased body height | "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators] |
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Interacting proteins (from Reactome)
No match
0 s.
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