Variant position: 73 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 970 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 ITTFRHHVQCRCSWHRFLRC VLTIFPFLEWMCMYRLKDWLL
Mouse ITTFKHHVQCGCSWHKFLRC MLTVFPFLEWICLYRFKDWLL
Bovine ISTVSHHVQCRCSWHKFRRC LLTVFPFLEWMCFYRFKDWLL
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 – 970 Testis anion transporter 1
1 – 95 Cytoplasmic
2 – 419 Missing. In isoform 3.
Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling.
Toure A.; Morin L.; Pineau C.; Becq F.; Dorseuil O.; Gacon G.;
J. Biol. Chem. 276:20309-20315(2001)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); FUNCTION; INTERACTION WITH RACGAP1; SUBCELLULAR LOCATION; TISSUE SPECIFICITY; INDUCTION; GLYCOSYLATION; VARIANT MET-73;
Cloning of human SLC26A8, a new member of the sulphate transporter gene family of anion transporter/exchangers.
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); VARIANTS MET-73; VAL-148; ASN-230 AND VAL-639;
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2); VARIANTS MET-73 AND VAL-639;
Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure.
Makela S.; Eklund R.; Lahdetie J.; Mikkola M.; Hovatta O.; Kere J.;
Mol. Hum. Reprod. 11:129-132(2005)
Cited for: VARIANTS MET-73; VAL-148; ASN-230 AND VAL-639; MUTAGENESIS OF PRO-914;
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