QuickView for RP1;jsessionid=C8C5C2E947B1BE0036412B0A8746258D;jsessionid=11DF44EA96B9ADAAA7F55A6D3BD16FB8;jsessionid=F8EBF6CB2D8C9EC1D6E865FED23CC75A (gene)

Gene Symbol:

Rp1 Rattus norvegicus

Full name:

RP1, axonemal microtubule associated

Synonyms:

Rp1h, oxygen-regulated protein 1, rCG30348-like, retinitis pigmentosa 1 (autosomal dominant), retinitis pigmentosa 1 homolog

Genomic Location:

Chr 5: 15391827-15402293

Description:

This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 prote...

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This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa.

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Orthologs:

Homo sapiens ,  Mus musculus ,  C. elegans ,  Macaca mulatta ,  Bos taurus ,  Canis lupus familiaris ,  Pan troglodytes ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

FREAC7_01 ,  POU3F2_02 ,  FOXO4_01 ,  PITX2_Q2 ,  TGCTGAY_UNKNOWN ,  TTGTTT_FOXO4_01 ,  RTAAACA_FREAC2_01 ,  GGATTA_PITX2_Q2

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