Variant position: 103 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 640 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 CVNTPGSFSCVCPEGFRLSP GLGCTDVDECAEPGLSHCHAL
Mouse CVNTPGSFKCSCQDGFRLTP ELSCTDVDECSEQGLSNCHAL
Rat CMNTLGSYECSCQDGFRLTP GLGCIDVNECTEQGLSNCHSL
Bovine CVNTLGSYTCVCPEGFLLSS ELGCEDVDECAEPGLSRCHAL
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
25 – 614 Uromodulin
25 – 587 Uromodulin, secreted form
65 – 107 EGF-like 2; calcium-binding
94 – 106
67 – 199 Missing. In isoform 2.
Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.
Hart T.C.; Gorry M.C.; Hart P.S.; Woodard A.S.; Shihabi Z.; Sandhu J.; Shirts B.; Xu L.; Zhu H.; Barmada M.M.; Bleyer A.J.;
J. Med. Genet. 39:882-892(2002)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS HNFJ1 TYR-148 AND ARG-217; VARIANT MCKD2 CYS-103;
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.