| GO:0008150 | biological_process |
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 |
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Synonym
AMMECR1, AMME syndrome candidate gene 1 protein, AMMERC1
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
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blood
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connective
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| EST | nodata | ||||||||||||||||||||||||||||||||||||||||
| GeneChip | cerebrum:3.94 | cerebellum:3.85 | brain stem:3.88 | corpus callosum/glia:4.10 | pineal gland:- | peripheral nerve:4.14 | spine:3.85 | retina:- | eye:- | artery/aorta:4.66 | vein:4.27 | lymphnode:6.01 | peripheral blood:- | spleen:6.42 | thymus:6.17 | bone marrow:7.08 | adipose:5.27 | bone:- | skin:6.21 | ||||||||||||||||||||||
| CAGE | cerebrum:1.82 | cerebellum:- | brain stem:1.56 | corpus callosum/glia:1.99 | pineal gland:1.39 | peripheral nerve:- | spine:1.06 | retina:- | eye:- | artery/aorta:1.68 | vein:2.37 | lymphnode:2.38 | peripheral blood:- | spleen:2.68 | thymus:2.76 | bone marrow:- | adipose:1.69 | bone:- | skin:- | ||||||||||||||||||||||
| RNA-seq | cerebrum:0.00 | cerebellum:- | brain stem:- | corpus callosum/glia:- | pineal gland:- | peripheral nerve:- | spine:- | retina:- | eye:- | artery/aorta:- | vein:- | lymphnode:0.78 | peripheral blood:- | spleen:- | thymus:- | bone marrow:- | adipose:0.99 | bone:- | skin:- | ||||||||||||||||||||||
reproductive
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muscular
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alimentary
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liver
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lung
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urinary
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endo/exo-crine
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| EST | nodata | ||||||||||||||||||||||||||||||||||||||||||||||||||||
| GeneChip | uterus:5.62 | placenta:7.12 | prostate:5.62 | ovary:6.53 | testis:4.45 | heart:4.41 | muscle:3.99 | esophagus:7.10 | stomach:5.56 | intestine:4.48 | colon:4.43 | liver/hepato:4.71 | lung:5.29 | bladder:- | kidney:5.06 | pituitary:5.53 | thyroid/parathyroid:4.88 | adrenal gland:5.49 | pancreas:4.31 | breast:5.91 | salivary:4.30 | ||||||||||||||||||||||||||||||||
| CAGE | uterus:2.32 | placenta:3.36 | prostate:2.04 | ovary:2.82 | testis:2.17 | heart:1.57 | muscle:1.65 | esophagus:2.70 | stomach:- | intestine:2.47 | colon:2.36 | liver/hepato:2.41 | lung:2.34 | bladder:2.15 | kidney:2.38 | pituitary:2.55 | thyroid/parathyroid:2.28 | adrenal gland:- | pancreas:2.34 | breast:1.36 | salivary:1.75 | ||||||||||||||||||||||||||||||||
| RNA-seq | uterus:- | placenta:- | prostate:0.08 | ovary:2.57 | testis:0.48 | heart:0.56 | muscle:0.00 | esophagus:- | stomach:- | intestine:- | colon:0.62 | liver/hepato:0.44 | lung:0.81 | bladder:- | kidney:0.29 | pituitary:- | thyroid/parathyroid:1.22 | adrenal gland:1.01 | pancreas:- | breast:0.71 | salivary:- | ||||||||||||||||||||||||||||||||
IDs
| Refseq ID | NM_015365 |
|---|---|
| Gene ID | 9949 |
| Unigene ID | - |
| Probe set ID | 204976_s_at [HG-U133_Plus_2] |
| Ensembl ID | ENSG00000101935 |
| GTEx ID | ENSG00000101935 |
Orthologous Gene
Chromosomal Region
Gene Family (Interpro ID)
| - |