OMIM Links for Gene (Select 59341) - OMIM - NCBI

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Links from Gene

Items: 12

Select item 6173831.

#617383 - AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2; ANFH2

OMIM:: 617383

Gene summaries Genetic tests Medical literature

Select item 6135082.

#613508 - SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1; SSQTL1

HYPONATREMIA, INCLUDED

OMIM:: 613508

Gene summaries Genetic tests Medical literature

Select item 6068353.

#606835 - DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB

Cytogenetic locations: 21964574

OMIM:: 606835

Gene summaries Genetic tests Medical literature

Select item 6060714.

#606071 - HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C

OMIM:: 606071

Gene summaries Genetic tests Medical literature

Select item 6054275.

*605427 - TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY V, MEMBER 4; TRPV4

Cytogenetic locations: 11094154

OMIM:: 605427

Gene summaries Genetic tests Medical literature

Select item 6001756.

#600175 - NEURONOPATHY, DISTAL HEREDITARY MOTOR, AUTOSOMAL DOMINANT 8; HMND8

Cytogenetic locations: 19781046

OMIM:: 600175

Gene summaries Genetic tests Medical literature

Select item 1842527.

#184252 - SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE; SMDK

Cytogenetic locations: 14661491

OMIM:: 184252

Gene summaries Genetic tests Medical literature

Select item 1840958.

#184095 - SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE

OMIM:: 184095

Gene summaries Genetic tests Medical literature

Select item 1814059.

#181405 - SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA

OMIM:: 181405

Gene summaries Genetic tests Medical literature

Select item 16840010.

#168400 - PARASTREMMATIC DWARFISM

OMIM:: 168400

Gene summaries Genetic tests Medical literature

Select item 15653011.

#156530 - METATROPIC DYSPLASIA; MTD

OMIM:: 156530

Gene summaries Genetic tests Medical literature

Select item 11350012.

#113500 - BRACHYOLMIA TYPE 3; BCYM3

OMIM:: 113500

Gene summaries Genetic tests Medical literature

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OMIM Links for Gene (Select 59341) (12)
OMIM
transient receptor potential cation channel subfamily V member 4 isoform X11 [Ho...
transient receptor potential cation channel subfamily V member 4 isoform X11 [Homo sapiens]
gi|2217290371|ref|XP_047285252.1|

Protein
PREDICTED: Homo sapiens transient receptor potential cation channel subfamily V ...
PREDICTED: Homo sapiens transient receptor potential cation channel subfamily V member 4 (TRPV4), transcript variant X11, mRNA
gi|2217290370|ref|XM_047429296.1|

Nucleotide
RecName: Full=Transient receptor potential cation channel subfamily V member 4; ...
RecName: Full=Transient receptor potential cation channel subfamily V member 4; Short=TrpV4; AltName: Full=Osm-9-like TRP channel 4; Short=OTRPC4; AltName: Full=Transient receptor potential protein 12; Short=TRP12; AltName: Full=Vanilloid receptor-like channel 2; AltName: Full=Vanilloid receptor-like protein 2; Short=VRL-2; AltName: Full=Vanilloid receptor-related osmotically-activated channel; Short=VR-OAC
gi|62901470|sp|Q9HBA0.2|TRPV4_HUMAN

Protein

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