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Results: 13

Name/Gene IDDescriptionLocationAliasesMIM
ID: 256471
major facilitator superfamily domain containing 8 [Homo sapiens (human)]Chromosome 4, NC_000004.12 (127917805..127965984, complement)CCMD, CLN7611124
ID: 154881
potassium channel tetramerization domain containing 7 [Homo sapiens (human)]Chromosome 7, NC_000007.14 (66628881..66643229)CLN14, EPM3611725
ID: 80331
DnaJ (Hsp40) homolog, subfamily C, member 5 [Homo sapiens (human)]Chromosome 20, NC_000020.11 (63895102..63936031)CLN4, CLN4B, CSPA, NCL, mir-941-2, mir-941-3, mir-941-4, mir-941-5, DNAJC5611203
ID: 54982
ceroid-lipofuscinosis, neuronal 6, late infantile, variant [Homo sapiens (human)]Chromosome 15, NC_000015.10 (68206992..68229742, complement)CLN4A, HsT18960, nclf606725
ID: 23400
ATPase type 13A2 [Homo sapiens (human)]Chromosome 1, NC_000001.11 (16985958..17011972, complement)CLN12, HSA9947, KRPPD, PARK9610513
ID: 8722
cathepsin F [Homo sapiens (human)]Chromosome 11, NC_000011.10 (66563463..66568576, complement)CATSF, CLN13603539
ID: 5538
palmitoyl-protein thioesterase 1 [Homo sapiens (human)]Chromosome 1, NC_000001.11 (40072710..40097470, complement)CLN1, INCL, PPT600722
ID: 2896
granulin [Homo sapiens (human)]Chromosome 17, NC_000017.11 (44345086..44353106)CLN11, GEP, GP88, PCDGF, PEPI, PGRN138945
ID: 2055
ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) [Homo sapiens (human)]Chromosome 8, NC_000008.11 (1755778..1786570)C8orf61, EPMR607837
ID: 1509
cathepsin D [Homo sapiens (human)]Chromosome 11, NC_000011.10 (1752752..1763992, complement)CLN10, CPSD, HEL-S-130P116840
ID: 1203
ceroid-lipofuscinosis, neuronal 5 [Homo sapiens (human)]Chromosome 13, NC_000013.11 (76991924..77002517)NCL608102
ID: 1201
ceroid-lipofuscinosis, neuronal 3 [Homo sapiens (human)]Chromosome 16, NC_000016.10 (28466653..28492302, complement)BTS, JNCL607042
ID: 1200
tripeptidyl peptidase I [Homo sapiens (human)]Chromosome 11, NC_000011.10 (6612766..6619461, complement)CLN2, GIG1, LPIC, SCAR7, TPP-1607998

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