Mus musculus Gene: Tssc4 | |||||||
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Summary | |||||||
InnateDB Gene | IDBG-212680.6 | ||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
Gene Symbol | Tssc4 | ||||||
Gene Name | tumor-suppressing subchromosomal transferable fragment 4 | ||||||
Synonyms | AA241958; ESTM671070 | ||||||
Species | Mus musculus | ||||||
Ensembl Gene | ENSMUSG00000045752 | ||||||
Encoded Proteins |
tumor-suppressing subchromosomal transferable fragment 4
tumor-suppressing subchromosomal transferable fragment 4
tumor-suppressing subchromosomal transferable fragment 4
tumor-suppressing subchromosomal transferable fragment 4
tumor-suppressing subchromosomal transferable fragment 4
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Protein Structure | |||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||
Entrez Gene | |||||||
Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000184281:
This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is located among several imprinted genes; however, this gene, as well as the pan-hematopoietic expression gene (PHEMX), escapes imprinting. This gene may play a role in malignancies and disease that involve this region. [provided by RefSeq, Jul 2008] This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is located among several imprinted genes; however, this gene, as well as the pan-hematopoietic expression gene (PHEMX), escapes imprinting. This gene may play a role in malignancies and disease that involve this region. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014] |
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Gene Information | |||||||
Type | Protein coding | ||||||
Genomic Location | Chromosome 7:143069249-143071093 | ||||||
Strand | Forward strand | ||||||
Band | F5 | ||||||
Transcripts | |||||||
Interactions | |||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
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Gene Ontology | |||||||
Molecular Function |
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Biological Process |
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Orthologs | |||||||
Species
Homo sapiens
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||
SwissProt | |||||||
TrEMBL | |||||||
UniProt Splice Variant | |||||||
Entrez Gene | |||||||
UniGene | |||||||
RefSeq | NM_001115085 NM_020285 NM_138631 | ||||||
OMIM | |||||||
CCDS | CCDS40195 CCDS40196 | ||||||
HPRD | |||||||
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GenPept | |||||||
RNA Seq Atlas | |||||||