hyccin 2 isoform X3 [Mus musculus]
hyccin family protein( domain architecture ID 10561132)
hyccin family protein which may have a role in the beta-catenin-Tcf/Lef signaling pathway, as well as in the process of myelination of the central and peripheral nervous system; similar to human hycinn (also known as FAM126A) and FAM126B
List of domain hits
Name | Accession | Description | Interval | E-value | ||||
Hyccin | pfam09790 | Hyccin; Members of this family of proteins may have a role in the beta-catenin-Tcf/Lef ... |
1-186 | 8.89e-86 | ||||
Hyccin; Members of this family of proteins may have a role in the beta-catenin-Tcf/Lef signaling pathway, as well as in the process of myelination of the central and peripheral nervous system. Defects in Hyccin are the cause of hypomyelination with congenital cataracts [MIM:610532]. This disorder is characterized by congenital cataracts, progressive neurologic impairment, and diffuse myelin deficiency. Affected individuals experience progressive pyramidal and cerebellar dysfunction, muscle weakness and wasting prevailing in the lower limbs. : Pssm-ID: 462903 Cd Length: 323 Bit Score: 263.12 E-value: 8.89e-86
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Name | Accession | Description | Interval | E-value | ||||
Hyccin | pfam09790 | Hyccin; Members of this family of proteins may have a role in the beta-catenin-Tcf/Lef ... |
1-186 | 8.89e-86 | ||||
Hyccin; Members of this family of proteins may have a role in the beta-catenin-Tcf/Lef signaling pathway, as well as in the process of myelination of the central and peripheral nervous system. Defects in Hyccin are the cause of hypomyelination with congenital cataracts [MIM:610532]. This disorder is characterized by congenital cataracts, progressive neurologic impairment, and diffuse myelin deficiency. Affected individuals experience progressive pyramidal and cerebellar dysfunction, muscle weakness and wasting prevailing in the lower limbs. Pssm-ID: 462903 Cd Length: 323 Bit Score: 263.12 E-value: 8.89e-86
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Name | Accession | Description | Interval | E-value | ||||
Hyccin | pfam09790 | Hyccin; Members of this family of proteins may have a role in the beta-catenin-Tcf/Lef ... |
1-186 | 8.89e-86 | ||||
Hyccin; Members of this family of proteins may have a role in the beta-catenin-Tcf/Lef signaling pathway, as well as in the process of myelination of the central and peripheral nervous system. Defects in Hyccin are the cause of hypomyelination with congenital cataracts [MIM:610532]. This disorder is characterized by congenital cataracts, progressive neurologic impairment, and diffuse myelin deficiency. Affected individuals experience progressive pyramidal and cerebellar dysfunction, muscle weakness and wasting prevailing in the lower limbs. Pssm-ID: 462903 Cd Length: 323 Bit Score: 263.12 E-value: 8.89e-86
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Blast search parameters | ||||
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