Details for: FEM1C
Associated with
Other Information
Genular Protein ID: 446551078
Symbol: FEM1C_HUMAN
Name: FEM1-gamma
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 11733146
Title: Identification of human FEM1A, the ortholog of a C. elegans sex-differentiation gene.
PubMed ID: 11733146
PubMed ID: 14527725
Title: The Fem1c genes: conserved members of the Fem1 gene family in vertebrates.
PubMed ID: 14527725
PubMed ID: 11347906
Title: Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
PubMed ID: 11347906
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 17974005
Title: The full-ORF clone resource of the German cDNA consortium.
PubMed ID: 17974005
PubMed ID: 22814378
Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
PubMed ID: 22814378
PubMed ID: 16959974
Title: The consensus coding sequences of human breast and colorectal cancers.
PubMed ID: 16959974
PubMed ID: 26138980
Title: SELENOPROTEINS. CRL2 aids elimination of truncated selenoproteins produced by failed UGA/Sec decoding.
PubMed ID: 26138980
PubMed ID: 28118078
Title: FEM1 proteins are ancient regulators of SLBP degradation.
PubMed ID: 28118078
PubMed ID: 29779948
Title: The eukaryotic proteome is shaped by E3 ubiquitin ligases targeting C-terminal degrons.
PubMed ID: 29779948
PubMed ID: 29775578
Title: C-terminal end-directed protein elimination by CRL2 ubiquitin ligases.
PubMed ID: 29775578
PubMed ID: 33398168
Title: Molecular basis for arginine C-terminal degron recognition by Cul2FEM1 E3 ligase.
PubMed ID: 33398168
PubMed ID: 33398170
Title: Molecular basis for ubiquitin ligase CRL2FEM1C-mediated recognition of C-degron.
PubMed ID: 33398170
PubMed ID: 36336956
Title: A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs, and limb ataxia.
PubMed ID: 36336956
DOI: 10.1093/hmg/ddac276
Sequence Information:
- Length: 617
- Mass: 68673
- Checksum: 6218B3963C486369
- Sequence:
MDLKTAVFNA ARDGKLRLLT KLLASKSKEE VSSLISEKTN GATPLLMAAR YGHLDMVEFL LEQCSASIEV GGSVNFDGET IEGAPPLWAA SAAGHLKVVQ SLLNHGASVN NTTLTNSTPL RAACFDGHLE IVKYLVEHKA DLEVSNRHGH TCLMISCYKG HKEIAQYLLE KGADVNRKSV KGNTALHDCA ESGSLDIMKM LLMYCAKMEK DGYGMTPLLS ASVTGHTNIV DFLTHHAQTS KTERINALEL LGATFVDKKR DLLGALKYWK KAMNMRYSDR TNIISKPVPQ TLIMAYDYAK EVNSAEELEG LIADPDEMRM QALLIRERIL GPSHPDTSYY IRYRGAVYAD SGNFKRCINL WKYALDMQQS NLDPLSPMTA SSLLSFAELF SFMLQDRAKG LLGTTVTFDD LMGILCKSVL EIERAIKQTQ CPADPLQLNK ALSIILHLIC LLEKVPCTLE QDHFKKQTIY RFLKLHPRGK NNFSPLHLAV DKNTTCVGRY PVCKFPSLQV TAILIECGAD VNVRDSDDNS PLHIAALNNH PDIMNLLIKS GAHFDATNLH KQTASDLLDE KEIAKNLIQP INHTTLQCLA ARVIVNHRIY YKGHIPEKLE TFVSLHR
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.