ID: ENSBTAT00000133993
DBxRefs: refseq:XM_005201603 refseq:XP_005201660
Gene: ENSBTAG00000016457 FMR1 autosomal homolog 1 [Source:VGNC Symbol;Acc:VGNC:56218]
Polypeptide: ENSBTAT00000133993
1:86047793..86120958 -1
Ontology | ID | Term |
---|---|---|
molecular_function | GO:0003676 | nucleic acid binding |
molecular_function | GO:0003723 | RNA binding |
molecular_function | GO:0003729 | mRNA binding |
biological_process | GO:0006417 | regulation of translation |
Protein database | Protein domain |
---|---|
FUNFAM | G3DSA:2.30.30.140:FF:000001 null |
FUNFAM | G3DSA:3.30.1370.10:FF:000004 null |
FUNFAM | G3DSA:2.30.30.140:FF:000002 null |
FUNFAM | G3DSA:3.30.1370.10:FF:000017 null |
SMART | SM00322 kh_6 |
GENE3D | G3DSA:2.30.30.140 |
PFAM | PF00013 KH_1 |
PFAM | PF12235 FXMRP1_C_core |
PFAM | PF05641 Agenet |
GENE3D | G3DSA:3.30.1370.10 K Homology domain, type 1 |
PFAM | PF17904 KH_9 |
PFAM | PF18336 Tudor_FRX1 |
PFAM | PF16096 FXR_C1 |
MOBIDB_LITE | mobidb-lite disorder_prediction |
PANTHER | PTHR10603 FRAGILE X MENTAL RETARDATION SYNDROME-RELATED PROTEIN |
PROSITE_PROFILES | PS50084 KH_TYPE_1 |
PROSITE_PROFILES | PS51641 AGENET_LIKE |
CDD | cd22504 KH_I_FXR1_rpt1 |
CDD | cd20472 Tudor_Agenet_FXR1_rpt1 |
CDD | cd20475 Tudor_Agenet_FXR1_rpt2 |
CDD | cd22510 KH_I_FXR1_rpt3 |
CDD | cd22507 KH_I_FXR1_rpt2 |
SUPERFAMILY | SSF54791 Eukaryotic type KH-domain (KH-domain type I) |