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Gene

Genes and mapped phenotypes

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 119467 CLRN3 ID: 119467	clarin 3 [Homo sapiens (human)]	Chromosome 10, NC_000010.11 (127877841..127892941, complement)	TMEM12, USH3AL1	620256
Select item 3052 HCCS ID: 3052	holocytochrome c synthase [Homo sapiens (human)]	Chromosome X, NC_000023.11 (11111332..11123086)	CCHL, LSDMCA1, MCOPS7, MLS	300056
Select item 23390 ZDHHC17 ID: 23390	zinc finger DHHC-type palmitoyltransferase 17 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (76764115..76853701)	DHHC-17, DHHC17, HIP14, HIP3, HSPC294, HYPH	607799
Select item 10190 TXNDC9 ID: 10190	thioredoxin domain containing 9 [Homo sapiens (human)]	Chromosome 2, NC_000002.12 (99306184..99336333, complement)	APACD, PHLP3	612564
Select item 124808 CCDC43 ID: 124808	coiled-coil domain containing 43 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (44677440..44689776, complement)
Select item 283458 NME2P1 ID: 283458	NME2 pseudogene 1 [Homo sapiens (human)]	Chromosome 12, NC_000012.12 (120282218..120282856)