| Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YLR404W | FLD1 | SGDID:S000004396 | BSCL2 |
Seipin (Bernardinelli-Seip congenital lipodystrophy type 2 protein) |
Homo sapiens | Paraplegia,Lipodystrophy, Congenital Generalized, Type 3,Spastic Paraplegia 42, Autosomal Dominant,Complete Generalized Lipodystrophy,Acquired Generalized Lipodystrophy,Adiposis Dolorosa,Diabetes Mellitus,Monogenic Diabetes,Neuromuscular Disease,Lipodystrophy, Congenital Generalized, Type 2,Lipodystrophy, Congenital Generalized, Type 1,Lipodystrophy, Familial Partial, Type 1,Neuronopathy, Distal Hereditary Motor, Type Vc,Spinal Muscular Atrophy,Charcot-Marie-Tooth Disease, Axonal, Type 2d,Motor Neuron Disease,Muscular Atrophy,Charcot-Marie-Tooth Disease, Axonal, Type 2l,Spastic Paraplegia 17, Autosomal Dominant,Autosomal Dominant Distal Hereditary Motor Neuronopathy,Distal Hereditary Motor Neuronopathy Type 2,Hereditary Spastic Paraplegia,Motor Peripheral Neuropathy,Bscl2-Related Neurologic Disorders/Seipinopathy,Berardinelli-Seip Congenital Lipodystrophy,Acquired Lipodystrophy,Pigmentation Disease,Spastic Paraplegia 17,Lipodystrophy, Familial Partial, Type 5,Charcot-Marie-Tooth Disease,Lipodystrophy, Congenital Generalized, Type 4,Spastic Paraplegia 20, Autosomal Recessive,Nemaline Myopathy 1,Thoracic Outlet Syndrome,Tooth Disease,Charcot-Marie-Tooth Disease And Deafness,Spastic Paraplegia 8, Autosomal Dominant,Spastic Paraplegia 31, Autosomal Dominant,Spastic Paraplegia 10, Autosomal Dominant,Type 2 Diabetes Mellitus,Lipodystrophy, Familial Partial, Type 3,Encephalopathy, Progressive, With Or Without Lipodystrophy,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Spastic Paraplegia 4, Autosomal Dominant,Familial Partial Lipodystrophy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2,Congenital Generalized Lipodystrophy,Autosomal Recessive Disease,Charcot-Marie-Tooth Disease, Axonal, Type 2f,Spinocerebellar Ataxia, Autosomal Recessive 20,Donohue Syndrome,Charcot-Marie-Tooth Disease, X-Linked Recessive, 2,Masa Syndrome,Spastic Paraplegia 19, Autosomal Dominant,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Lipodystrophy, Familial Partial, Type 2,Umbilical Hernia,Spastic Paraplegia 6, Autosomal Dominant,Neuronopathy, Distal Hereditary Motor, Type Va |
6ds5_j | Q96G97 | ENSG00000168000 | BSCL2 | 100.00 | 1.30E-43 | 1.00E-47 | 340.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YLR404W | FLD1 | SGDID:S000004396 | Seipin CG9904 |
Seipin |
Drosophila melanogaster | 6mlu_a | Q9V3X4 | 100.00 | 3.10E-47 | 2.50E-51 | 363.80 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
| YLR404W | FLD1 | SGDID:S000004396 | Seipin |
Putative adipose-regulatory protein (Seipin) |
pfam Family | PF06775 | 100.00 | 8.00E-40 | 7.30E-44 | 283.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |