Mammalian Phenotype (MP): decreased insulin secretion

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children)	MP term [MP ID] <#Children>	(#SF|#FA)	#Supra-domain (Single|Duplex|Triple)
+ + + + + + + 7:	mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:	endocrine/exocrine gland phenotype [MP:0005379] <2>	(51|81)	(55|36|12)
+ + + + + 5:	abnormal gland physiology [MP:0002164] <4>	(9|19)	(11|11|5)
+ + + + 4:	abnormal pancreas physiology [MP:0002693] <8>	(5|12)	(5|7|3)
+ + + + 4:	abnormal endocrine gland physiology [MP:0013561] <6>	(4|10)	(4|6|2)
+ + + + 4:	homeostasis/metabolism phenotype [MP:0005376] <7>	(140|174)	(149|96|44)
+ + + 3:	abnormal homeostasis [MP:0001764] <27>	(103|129)	(113|73|31)
+ + + 3:	abnormal pancreas secretion [MP:0002694] <2>	(5|10)	(5|7|3)
+ + + 3:	abnormal endocrine pancreas physiology [MP:0010147] <6>	(3|7)	(3|5|2)
+ + 2:	abnormal endocrine pancreas secretion [MP:0014195] <6>	(3|8)	(3|5|2)
+ + 2:	abnormal pancreatic beta cell physiology [MP:0003562] <4>	(3|7)	(3|5|2)
+ + 2:	abnormal glucose homeostasis [MP:0002078] <14>	(15|22)	(17|17|8)
+ 1:	abnormal insulin secretion [MP:0003564] <2>	(1|4)	(1|1|0)
0:	decreased insulin secretion [MP:0003059]	(0|1)	(0|0|0)

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Family

Family domains annotated to this MP term (Not in SDMP)
Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
FYVE, a phosphatidylinositol-3-phosphate binding domain	0.000525	DIRECT

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