P594 | Ensembl gene ID | ENSG00000104413 |
P704 | Ensembl transcript ID | ENST00000358397 |
ENST00000423620 | ||
ENST00000433389 | ||
ENST00000454170 | ||
ENST00000517556 | ||
ENST00000517610 | ||
ENST00000519505 | ||
ENST00000520385 | ||
ENST00000522756 | ||
ENST00000522920 | ||
ENST00000523347 | ||
ENST00000646773 | ||
P351 | Entrez Gene ID | 54845 |
P2888 | exact match | http://identifiers.org/ncbigene/54845 |
P2671 | Google Knowledge Graph ID | /g/11fy_q5nvz |
P353 | HGNC gene symbol | ESRP1 |
P354 | HGNC ID | 25966 |
P593 | HomoloGene ID | 9785 |
P492 | OMIM ID | 612959 |
612959 | ||
P639 | RefSeq RNA ID | NM_001034915 |
NM_001122825 | ||
NM_001122826 | ||
NM_001122827 | ||
NM_017697 | ||
XM_005250991 | ||
XM_047421916 | ||
P2892 | UMLS CUI | C1826778 |
P1057 | chromosome | human chromosome 8 | Q572848 |
P4196 | cytogenetic location | 8q22.1 | |
P688 | encodes | Epithelial splicing regulatory protein 1 | Q21132132 |
P5572 | expressed in | rectum | Q158716 |
vulva | Q2192288 | ||
corpus epididymis | Q30015794 | ||
secondary oocyte | Q66509944 | ||
mucosa of colon | Q66511131 | ||
mucosa of transverse colon | Q66511199 | ||
mucosa of sigmoid colon | Q66511227 | ||
skin of abdomen | Q66514948 | ||
skin of thigh | Q66527052 | ||
gingival epithelium | Q66558726 | ||
P703 | found in taxon | Homo sapiens | Q15978631 |
P2293 | genetic association | deafness, autosomal recessive 109 | Q55790894 |
P645 | genomic end | 94707466 | |
95719694 | |||
P644 | genomic start | 94641074 | |
95653302 | |||
P684 | ortholog | Esrp1 | Q24406584 |
Esrp1 | Q18296023 | ||
P2548 | strand orientation | forward strand | Q22809680 |
Q27593028 | hsa-miR-202-5p |
Q27594904 | hsa-miR-25-3p |
Q27595127 | hsa-miR-32-5p |
Q27593404 | hsa-miR-337-3p |
Q27595278 | hsa-miR-363-3p |
Q27594623 | hsa-miR-367-3p |
Q27593480 | hsa-miR-377-3p |
Q27595135 | hsa-miR-455-3p |
Q27594959 | hsa-miR-4659a-3p |
Q27594961 | hsa-miR-4659b-3p |
Q27593842 | hsa-miR-6516-5p |
Q27594914 | hsa-miR-6875-3p |
Q27593334 | hsa-miR-92a-3p |
Q27592842 | hsa-miR-92b-3p |
Q55790894 | deafness, autosomal recessive 109 | genetic association | P2293 |
Q21132132 | Epithelial splicing regulatory protein 1 | encoded by | P702 |
Q101405055 | human pluripotent stem cell | has marker | P8872 |
Tatar language (tt / Q25285) | ESRP1 | wikipedia |
ESRP1 | wikipedia |
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