OMIM Links for GEO Profiles (Select 77916929) - OMIM - NCBI

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Links from GEO Profiles

Items: 4

Select item 3010451.

#301045 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIr; CDG2R

Cytogenetic locations: 29127204

OMIM:: 301045

Gene summaries Genetic tests Medical literature

Select item 3009112.

#300911 - PARKINSONISM WITH SPASTICITY, X-LINKED; XPDS

Cytogenetic locations: 20629132

OMIM:: 300911

Gene summaries Genetic tests Medical literature

Select item 3005563.

*300556 - ATPase, H+ TRANSPORTING, LYSOSOMAL, ACCESSORY PROTEIN 2; ATP6AP2

Cytogenetic locations: 29127204

OMIM:: 300556

Gene summaries Genetic tests Medical literature

Select item 3004234.

#300423 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH

Cytogenetic locations: 15746149

OMIM:: 300423

Gene summaries Genetic tests Medical literature

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OMIM Links for GEO Profiles (Select 77916929) (4)
OMIM
NSUN3 NOP2/Sun RNA methyltransferase 3 [Homo sapiens]
NSUN3 NOP2/Sun RNA methyltransferase 3 [Homo sapiens]
Gene ID:63899

Gene
Gene Links for GEO Profiles (Select 6116337) (1)
Gene
Gene Links for GEO Profiles (Select 6134697) (1)
Gene
CMSS1 cms1 ribosomal small subunit homolog [Homo sapiens]
CMSS1 cms1 ribosomal small subunit homolog [Homo sapiens]
Gene ID:84319

Gene

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