QuickView for Txnl6 (gene)

Gene Symbol:

NXNL1 Homo sapiens

Full name:

nucleoredoxin like 1

Synonyms:

RDCVF, TXNL6, nucleoredoxin-like protein 1, rod-derived cone viability factor, thioredoxin-like 6, thioredoxin-like protein 6

Genomic Location:

Chr 19: 17427234-17432725

Description:

Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP.

Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Gallus gallus ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

Cytogenetic Map:

19p13.11

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