Variant position: 1034 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1219 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human QQLDPQEHLNQGRPHLSPRP PPTGDPGSQPQWGSGVPRAGK
Mouse RQLDPGQHLNQGQPHLSAHP TSKGHTSHCTKVGCAV---EK
Rat RQLDPGEHLNQGWPHLSTHL TSKGDTSNCPKVGCVG---EK
Bovine RQLDPCEQLNQGRPHLASGP FPAGDLNCSLHKGSRAPGAEK
Zebrafish EQLNSSRLLNQGGSHLGTIQ LNGGEVNVRSE--EQKPQTSI
Caenorhabditis elegans RNTLPDEY------------ ---------------------
Drosophila VEPSSSQ------------- -------------------AK
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 1219 Regulator of telomere elongation helicase 1
998 – 1219 GRTAPDPKLTVSTAAAQQLDPQEHLNQGRPHLSPRPPPTGDPGSQPQWGSGVPRAGKQGQHAVSAYLADARRALGSAGCSQLLAALTAYKQDDDLDKVLAVLAALTTAKPEDFPLLHRFSMFVRPHHKQRFSQTCTDLTGRPYPGMEPPGPQEERLAVPPVLTHRAPQPGPSRSEKTGKTQSKISSFLRQRPAGTVGAGGEDAGPSQSSGPPHGPAASEWGL -> ERRRIPS. In isoform 8.
1024 – 1219 Missing. In isoform 4.
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in dyskeratosis congenita.
Ballew B.J.; Yeager M.; Jacobs K.; Giri N.; Boland J.; Burdett L.; Alter B.P.; Savage S.A.;
Hum. Genet. 132:473-480(2013)
Cited for: VARIANT DKCB5 ASP-591; VARIANT DKCA4 THR-621; VARIANTS SER-124; GLN-684; PRO-829; ASP-849; THR-929; HIS-1034; HIS-1042 AND THR-1059;
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.