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PKHD1 gene

PKHD1 ciliary IPT domain containing fibrocystin/polyductin

Key facts

Official symbol
PKHD1
Full name
PKHD1
Chromosome
6
Map location
6p12.3-p12.2
Organism
Homo sapiens
NCBI Gene ID
5314
Also known as
ARPKD, FCYT, FPC, PCYT, PKD4, TIGM1

Function summary

The protein encoded by this gene is predicted to have a single transmembrane (TM)-spanning domain and multiple copies of an immunoglobulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have been described, but the full length sequences have not been determined. Several of these transcripts are predicted to encode truncated products which lack the TM and may be secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney and hepatic disease-1. [provided by RefSeq, Jul 2008].

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Data source: NCBI Gene · alsesAI Gene Library