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Gene

Genes and mapped phenotypes

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 6424 SFRP4 ID: 6424	secreted frizzled related protein 4 [Homo sapiens (human)]	Chromosome 7, NC_000007.14 (37905932..37916817, complement)	FRP-4, FRPHE, FRZB-2, PYL, sFRP-4	606570
Select item 1436 CSF1R ID: 1436	colony stimulating factor 1 receptor [Homo sapiens (human)]	Chromosome 5, NC_000005.10 (150053295..150113365, complement)	BANDDOS, C-FMS, CD115, CSF-1R, CSFR, FIM2, FMS, GPSC, HDLS, HDLS1, M-CSF-R	164770

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Pyle AND (alive[prop]) (2)
Gene
MIR135-2 [Sus scrofa]
MIR135-2 [Sus scrofa]
Gene ID:100316549

Gene
Acromegaly
Acromegaly
A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET...<br/>

MeSH
Digitorenocerebral Syndrome [Supplementary Concept]
Digitorenocerebral Syndrome [Supplementary Concept]
A rare hereditary disorder associated with mutations in the TBC1D24 gene and characterized by MICROCEPHALY and facial abnormalities, SENSORINEURAL DEAFNESS, blindness and eye ...<br/>Date introduced: November 5, 2012<br/>

MeSH
4930589L23Rik RIKEN cDNA 4930589L23 gene [Mus musculus]
4930589L23Rik RIKEN cDNA 4930589L23 gene [Mus musculus]
Gene ID:75879

Gene

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