split hand/foot malformation (ectrodactyly) type 1

Synonym

26 proteasome complex subunit DSS1, Deleted in split hand/split foot protein 1 homolog, split hand/foot malformation (ectrodactyly) type 1, Shfdg1, Split hand/foot deleted protein 1 homolog, Shfg, Dss1, Shfm1, DSS1

normal 40 tissues
developmental tissues and primary cells（FANTOM5 CAGE）

Choropleth map on BodyParts3D

Choropleth maps on 3D human body images were generated by the relative gene expression values measured by GeneChip.

Classification in 40 Organs

brain

blood

connective

EST

cerebrum:6.90

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:-

GeneChip

cerebrum:10.49

cerebellum:10.31

brain stem:-

corpus callosum/glia:-

pineal gland:-

peripheral nerve:11.32

spine:10.39

retina:9.48

eye:10.19

artery/aorta:-

vein:11.72

lymphnode:11.32

peripheral blood:-

spleen:11.22

thymus:-

bone marrow:11.80

adipose:11.21

bone:12.05

skin:11.59

CAGE

cerebrum:4.86

cerebellum:-

brain stem:4.95

corpus callosum/glia:-

pineal gland:-

peripheral nerve:-

spine:4.90

retina:-

eye:-

artery/aorta:4.93

vein:-

lymphnode:4.77

peripheral blood:-

spleen:5.28

thymus:5.35

bone marrow:-

adipose:-

bone:5.64

skin:5.24

RNA-seq

cerebrum:28.13

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:-

reproductive

muscular

alimentary

liver

lung

urinary

endo/exo-crine

EST

uterus:-

placenta:-

prostate:-

ovary:-

testis:-

heart:-

muscle:-

esophagus:-

stomach:-

intestine:-

colon:-

liver/hepato:-

lung:-

bladder:-

kidney:-

pituitary:103.30

thyroid/parathyroid:-

adrenal gland:-

pancreas:-

breast:-

salivary:-

GeneChip

uterus:11.89

placenta:11.04

prostate:11.50

ovary:11.71

testis:10.64

heart:11.71

muscle:11.66

esophagus:-

stomach:11.43

intestine:11.54

colon:-

liver/hepato:11.03

lung:11.48

bladder:11.45

kidney:10.90

pituitary:11.26

thyroid/parathyroid:-

adrenal gland:11.26

pancreas:11.04

breast:11.44

salivary:11.21

CAGE

uterus:5.46

placenta:5.34

prostate:5.35

ovary:5.19

testis:6.20

heart:-

muscle:-

esophagus:-

stomach:5.81

intestine:5.61

colon:5.42

liver/hepato:5.40

lung:5.37

bladder:5.23

kidney:-

pituitary:4.99

thyroid/parathyroid:-

adrenal gland:4.94

pancreas:5.40

breast:5.20

salivary:-

RNA-seq

uterus:-

placenta:-

prostate:-

ovary:-

testis:-

heart:-

muscle:32.49

esophagus:-

stomach:-

intestine:-

colon:-

liver/hepato:33.57

lung:-

bladder:-

kidney:-

pituitary:-

thyroid/parathyroid:-

adrenal gland:-

pancreas:-

breast:-

salivary:-

IDs

Refseq ID	NM_009169
Gene ID	20422
Unigene ID	Mm.246905
Probe set ID	1418575_at [Mouse430_2]
Ensembl ID	ENSMUSG00000042541

Orthologous Gene

Human[1]	NM_001201450, NM_006304
Rat[1]	NM_001126090, NM_006304

Chromosomal Region

Gene Family (Interpro ID)

Link to Pubmed (Pubmed ID)

Gene Ontology (GO ID)

Biological Process

GO:0000724	double-strand break repair via homologous recombination
GO:0006508	proteolysis

Cellular Component

GO:0032039	integrator complex
GO:0000502	proteasome complex

Molecular Function

GO:0008233	peptidase activity
GO:0005515	protein binding

split hand/foot malformation (ectrodactyly) type 1

Synonym

Expression Pattern

Choropleth map on BodyParts3D

Classification in 40 Organs

Gene Information

IDs

Orthologous Gene

Chromosomal Region

Gene Family (Interpro ID)

Link to Pubmed (Pubmed ID)

Gene Ontology (GO ID)

Biological Process

Cellular Component

Molecular Function