domain-containing protein 3 is a protein that in humans is encoded by the WDFY3 gene. This gene encodes a protein which contains WD repeats and an FYVE...
6 KB (651 words) - 03:45, 28 October 2022
MTMR4, PIKFYVE, PLEKHF1, PLEKHF2 RUFY1, RUFY2, RUFY3, RUFY4, WDFY1, WDFY2, WDFY3, ZFYVE1, ZFYVE9, ZFYVE16, ZFYVE19, ZFYVE20, ZFYVE21, ZFYVE26, ZFYVE27, ZFYVE28...
4 KB (445 words) - 22:57, 18 March 2023
TRAF7, TSSC1, TULP4, TUWD12, UTP15, UTP18, WAIT1, WDF3, WDFY1, WDFY2, WDFY3, WDFY4, WDHD1, WDR1, WDR10, WDR11, WDR12, WDR13, WDR16, WDR17, WDR18, WDR19...
13 KB (958 words) - 04:46, 26 August 2024
Q9H6R7 18230 WDFY1 HGNC:20451 Q8IWB7 18231 WDFY2 HGNC:20482 Q96P53 18232 WDFY3 HGNC:20751 Q8IZQ1 18233 WDFY4 HGNC:29323 Q6ZS81 18234 WDHD1 HGNC:23170 O75717...
242 KB (17 words) - 18:43, 6 October 2024
GeneCards, NBEAL1 has a few paralogs: NBEAL2, WDFY3, NBEA, LRBA, Lysosomal trafficking regulator (LYST), and WDFY3. The table below summarizes the paralogs...
15 KB (1,439 words) - 20:44, 22 January 2024
intellectual disability, dyskinesia, dysmorphism. Microcephaly caused by WDFY3 (ALFY) mutation – delineating novel pathway controlling Wnt signaling. CCDC174-associated...
36 KB (3,396 words) - 18:05, 24 January 2025