P594 | Ensembl gene ID | ENSG00000115112 |
P704 | Ensembl transcript ID | ENST00000263707 |
ENST00000464621 | ||
P351 | Entrez Gene ID | 29842 |
P2888 | exact match | http://identifiers.org/ncbigene/29842 |
P353 | HGNC gene symbol | TFCP2L1 |
P354 | HGNC ID | 17925 |
P593 | HomoloGene ID | 8730 |
P492 | OMIM ID | 609785 |
609785 | ||
P639 | RefSeq RNA ID | NM_014553 |
XM_017003902 | ||
XM_017003903 | ||
XM_017003904 | ||
XM_017003905 | ||
XM_047444020 | ||
XM_047444021 | ||
P2892 | UMLS CUI | C1425181 |
P1057 | chromosome | human chromosome 2 | Q638893 |
P4196 | cytogenetic location | 2q14.2 | |
P688 | encodes | Transcription factor CP2 like 1 | Q21122194 |
P5572 | expressed in | rectum | Q158716 |
parotid gland | Q691653 | ||
renal medulla | Q2409399 | ||
minor salivary glands | Q3108494 | ||
right lobe of thyroid gland | Q66508047 | ||
left lobe of thyroid gland | Q66508049 | ||
skin of thigh | Q66527052 | ||
nasal epithelium | Q66559633 | ||
human kidney | Q112107043 | ||
buccal mucosa cell | Q116529247 | ||
P703 | found in taxon | Homo sapiens | Q15978631 |
P2293 | genetic association | Behçet's disease | Q911427 |
P645 | genomic end | 121285202 | |
122042783 | |||
P644 | genomic start | 121216587 | |
121974163 | |||
P684 | ortholog | Tfcp2l1 | Q18269799 |
Tfcp2l1 | Q24361492 | ||
P2548 | strand orientation | reverse strand | Q22809711 |
Q27593730 | hsa-miR-1180-5p |
Q27593105 | hsa-miR-192-5p |
Q27592906 | hsa-miR-215-5p |
Q27594239 | hsa-miR-2355-5p |
Q27594275 | hsa-miR-2467-5p |
Q27594630 | hsa-miR-302b-5p |
Q27594624 | hsa-miR-302d-5p |
Q27593076 | hsa-miR-3160-5p |
Q27593979 | hsa-miR-3188 |
Q27595177 | hsa-miR-3621 |
Q27593884 | hsa-miR-3975 |
Q27592718 | hsa-miR-4252 |
Q27594587 | hsa-miR-4274 |
Q27594944 | hsa-miR-4468 |
Q27594880 | hsa-miR-4649-3p |
Q27592935 | hsa-miR-4677-3p |
Q27593612 | hsa-miR-4717-5p |
Q27593472 | hsa-miR-485-5p |
Q27592915 | hsa-miR-5008-5p |
Q27594901 | hsa-miR-5692a |
Q27595182 | hsa-miR-6089 |
Q27593617 | hsa-miR-6768-3p |
Q27594912 | hsa-miR-6840-3p |
Q27593768 | hsa-miR-6884-5p |
Q27595224 | hsa-miR-6895-5p |
Q27595179 | hsa-miR-7114-3p |
Q27594955 | hsa-miR-7160-5p |
Q27592963 | hsa-miR-7162-3p |
Q27595080 | hsa-miR-873-5p |
Q911427 | Behçet's disease | genetic association | P2293 |
Q21122194 | Transcription factor CP2 like 1 | encoded by | P702 |
Q101404947 | human ionocyte | has marker | P8872 |
TFCP2L1 | wikipedia |
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