Version 5.4
| Homo sapiens Gene: KHDC3L | |||||
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| Summary | |||||
| InnateDB Gene | IDBG-92327.7 | ||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||
| Gene Symbol | KHDC3L | ||||
| Gene Name | KH domain containing 3-like, subcortical maternal complex member | ||||
| Synonyms | |||||
| Species | Homo sapiens | ||||
| Ensembl Gene | ENSG00000203908 | ||||
| Encoded Proteins |
chromosome 6 open reading frame 221
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| Protein Structure |
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| Useful resources | Stemformatics EHFPI ImmGen | ||||
| Entrez Gene | |||||
| Summary |
The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole. [provided by RefSeq, Dec 2011] |
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| Gene Information | |||||
| Type | Protein coding | ||||
| Genomic Location | Chromosome 6:73362677-73364171 | ||||
| Strand | Forward strand | ||||
| Band | q13 | ||||
| Transcripts |
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| Interactions | |||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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| Gene Ontology | |||||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Orthologs | |||||
| No orthologs found for this gene | |||||
| Cross-References | |||||
| SwissProt | Q587J8 | ||||
| TrEMBL | |||||
| UniProt Splice Variant | |||||
| Entrez Gene | 154288 | ||||
| UniGene | Hs.128326 | ||||
| RefSeq | NM_001017361 | ||||
| HUGO | HGNC:33699 | ||||
| OMIM | 611687 | ||||
| CCDS | CCDS34484 | ||||
| HPRD | |||||
| IMGT | |||||
| EMBL | AB211062 BC132844 BC137160 | ||||
| GenPept | AAI32845 AAI37161 BAD95489 | ||||
| RNA Seq Atlas | 154288 | ||||