Gene HUMAN100192 (RPGR_HUMAN)

E Homo sapiens | X-linked retinitis pigmentosa GTPase regulator [RPGR]

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General Information

Descriptionretinitis pigmentosa GTPase regulator [Source:HGNC Symbol;Acc:HGNC:10295]; transcript_id=ENST00000645032.1
Organism HUMAN - Homo sapiens
Locus[ Chromosome X ]: 38285540 ... 38327367
Number of exons15
Exonsjoin(complement(38327340..38327367), complement(38323399..38323524), complement(38322853..38322945), complement(38321027..38321089), complement(38318829..38318987), complement(38317316..38317465), complement(38310615..38310773), complement(38304635..38304790), complement(38301247..38301371), complement(38298956..38299141), complement(38297284..38297452), complement(38291393..38291484), complement(38290959..38291024), complement(38287861..38288041), complement(38285540..38287245))

IDs and Cross-references

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