Description: | teratocarcinoma-derived growth factor 1 [Source:MGI Symbol;Acc:MGI:98658] |
Synonyms: | CR1, cripto |
Other ID(s): | MGI:98658, ENSMUSG00000032494 |
Protein Accession Numbers: | XP_017168764, NP_035692 |
Statistics: | ClinVar(9) COSMIC(68) |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000296145 You are here now!
ENST00000542931
NP_001167607
NP_003203 You are here now!
Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
---|---|---|---|---|---|
Arhinencephaly | Musculoskeletal Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Holoprosencephaly | Musculoskeletal Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Asplenia Syndrome | Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Polysplenia Syndrome | Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Situs ambiguus | Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Lobar Holoprosencephaly | Musculoskeletal Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Alobar Holoprosencephaly | Musculoskeletal Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Semilobar Holoprosencephaly | Musculoskeletal Diseases ; Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Heterotaxy Syndrome | Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Right Atrial Isomerism | Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
Left Atrial Isomerism | Cardiovascular Diseases ; Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.6 | 0.552 | ||
NO RESULT FOUND |