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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
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liver/hepato
lung
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kidney
pituitary
thyroid/parathyroid
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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_080458 </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

Bartter syndrome, infantile, with sensorineural deafness (Barttin)
SynonymMGC47291, Bsnd, Barttin
Refseq IDNM_080458
GeneID140475
Unigene IDMm.135448
Probe set ID1421482_at
 3Dbodymap
EST brain:4.40  blood:2.30  connective:-  reproductive:-  muscular:-  alimentary:-  liver:-  lung:-  urinary:86.20  endo/exo-crine:- 
GeneChip brain:5.27  blood:5.28  connective:5.43  reproductive:5.42  muscular:5.71  alimentary:5.49  liver:5.68  lung:5.43  urinary:6.52  endo/exo-crine:5.90 
CAGE brain:0.04  blood:0.00  connective:0.00  reproductive:0.04  muscular:-  alimentary:0.00  liver:0.00  lung:0.00  urinary:0.00  endo/exo-crine:0.00 
RNA-seq nodata
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