IMP: Integrative Multi-species Prediction

19 genes annotated in human

paraplegia

DOID:607

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Known genes in the process in humanInclude functional analogs

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Show only novel predictionsShow only unknown genesHighlight genes with functional analogs involved in "paraplegia" (in gray)

Name	Description	Probability
HSPE1	heat shock 10kDa protein 1 (chaperonin 10)	0.015
SPG20	spastic paraplegia 20 (Troyer syndrome)	0.003
ZFYVE27	zinc finger, FYVE domain containing 27	0.003
SPG11	spastic paraplegia 11 (autosomal recessive)	0.003
PLP1	proteolipid protein 1	0.003
ATL1	atlastin GTPase 1	0.002
KIAA0196	KIAA0196	0.002
ZFYVE26	zinc finger, FYVE domain containing 26	0.002
REEP1	receptor accessory protein 1	0.002
NIPA1	non imprinted in Prader-Willi/Angelman syndrome 1	0.002
CYP7B1	cytochrome P450, family 7, subfamily B, polypeptide 1	0.002
SPG7	spastic paraplegia 7 (pure and complicated autosomal recessive)	0.002
KIAA0415	KIAA0415	0.002
BSCL2	Berardinelli-Seip congenital lipodystrophy 2 (seipin)	0.002
SLC33A1	solute carrier family 33 (acetyl-CoA transporter), member 1	0.002
PNPLA6	patatin-like phospholipase domain containing 6	0.002
KIF5A	kinesin family member 5A	0.002
GJC2	gap junction protein, gamma 2, 47kDa	0.002
SPAST	spastin	0.001
HSPD1	heat shock 60kDa protein 1 (chaperonin)	0.001