Sequence information
Variant position: 2 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 247 The length of the canonical sequence.
Location on the sequence:
M
T ILFLTMVISYFGCMKAAPMK
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 MT ILFLTMVISYFGCMKAAPMK
MT ILFLTMVISYFGCMKAAPMK
Chimpanzee MT ILFLTMVISYFGCMKAAPMK
Mouse MT ILFLTMVISYFGCMKAAPMK
Rat MT ILFLTMVISYFGCMKAAPMK
Pig MT ILFLTMVISYFGCMKAAPMK
Bovine MT ILFLTMVISYFGCMKAAPMK
Cat MT ILFLTMVISYFGCMKAAPMK
Horse MT ILFLTMVISYFGCMKAAPMK
Chicken MT ILFLTMVISYFSCMKAAPMK
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
Signal peptide
1 – 18
Alternative sequence
1 – 1
M -> MFHQVRRVM. In isoform 2.
Alternative sequence
1 – 1
M -> MQSREEEWFHQVRRVM. In isoform 3.
Alternative sequence
1 – 1
M -> MCGATSFLHECTRLILVTTQNAEFLQKGLQVHTCFGVYPHASVWHDCASQKKGCAVYLHVSVEFNKLIPENGFIKFHQVRRVM. In isoform 4.
Alternative sequence
1 – 1
M -> MLCAISLCARVRKLRSAGRCGKFHQVRRVM. In isoform 5.
Literature citations
Idiopathic congenital central hypoventilation syndrome: evaluation of brain-derived neurotrophic factor genomic DNA sequence variation.
Weese-Mayer D.E.; Bolk S.; Silvestri J.M.; Chakravarti A.;
Am. J. Med. Genet. 107:306-310(2002)
Cited for: VARIANT CCHS ILE-2;
Disclaimer:
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.