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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
uterus
placenta
prostate
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_001081052 </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

Nance-Horan syndrome (human)
SynonymNhs1, Nance-Horan syndrome (human), Gm389, Xcat, Gm48, Nhs
Refseq IDNM_001081052
GeneID195727
Unigene ID-
Probe set ID-
 3Dbodymap
EST nodata
GeneChip nodata
CAGE brain:1.41  blood:1.04  connective:1.84  reproductive:1.51  muscular:-  alimentary:1.17  liver:0.64  lung:1.17  urinary:1.58  endo/exo-crine:0.76 
RNA-seq brain:0.76  blood:-  connective:-  reproductive:-  muscular:0.48  alimentary:-  liver:0.16  lung:-  urinary:-  endo/exo-crine:- 
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