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Tissue Specificity
Source datasetGeneChip RNA-seq

cerebrum
cerebellum
brain stem
corpus callosum/glia
pineal gland
peripheral nerve
spine
retina
eye
artery/aorta
vein
lymphnode
peripheral blood
spleen
thymus
bone marrow
adipose
bone
skin
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ovary
testis
heart
muscle
esophagus
stomach
intestine
colon
liver/hepato
lung
bladder
kidney
pituitary
thyroid/parathyroid
adrenal gland
pancreas
breast
salivary

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<ul id="tissue40_ex"> </ul>
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<input type="hidden" name="idkind" value="3">Refseq ID<br/><textarea name="ids" rows="4" cols="17" style="width:140px">NM_178719 </textarea><input type="hidden" name="lang" value="en"/> <input type="hidden" name="db" value="mouse"/>

Included Dataset

ALL
EST
GeneChip
CAGE
RNA-seq

Gene Name

3D Maps

Relative Value
brain blood connective reproductive muscular alimentary liver lung urinary endo/exo-crine

Smith-Magenis syndrome chromosome region, candidate 7-like (human)
SynonymAI452372, Smcr7l, A230016E22
Refseq IDNM_178719
GeneID239555
Unigene IDMm.307163
Probe set ID-
 3Dbodymap
EST brain:49.90  blood:121.20  connective:61.70  reproductive:31.40  muscular:207.50  alimentary:8.70  liver:9.10  lung:-  urinary:86.20  endo/exo-crine:69.20 
GeneChip nodata
CAGE brain:2.83  blood:3.29  connective:3.25  reproductive:3.01  muscular:-  alimentary:3.10  liver:3.24  lung:2.84  urinary:3.02  endo/exo-crine:3.00 
RNA-seq brain:1.95  blood:-  connective:-  reproductive:-  muscular:1.67  alimentary:-  liver:1.98  lung:-  urinary:-  endo/exo-crine:- 
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