transmembrane 6 superfamily member 1 isoform X3 [Mus musculus]
DUF2781 domain-containing protein( domain architecture ID 15340014)
DUF2781 domain-containing protein similar to Homo sapiens sigma intracellular receptor 2 (also known as transmembrane protein 97, TMEM97) that corresponds to the sigma-2 receptor, which is thought to play important role in regulating cell survival, morphology and differentiation
List of domain hits
Name | Accession | Description | Interval | E-value | ||||
TM6SF1-like | cd21106 | transmembrane 6 superfamily member 1, member 2, and similar proteins; This family includes ... |
1-213 | 4.03e-111 | ||||
transmembrane 6 superfamily member 1, member 2, and similar proteins; This family includes transmembrane 6 superfamily members 1 (TM6SF1) and 2 (TM6SF2), and similar proteins. TM6SF1 is a widely expressed lysosomal transmembrane protein that may be suitable as a lysosomal marker. Polymorphism of its paralog, TM6SF2, has been associated with the risk for hepatocellular carcinoma, and a variant of the gene has been found to impact the processing of lipids in the liver and the small intestine, causing non-alcoholic fatty liver disease (NAFLD). : Pssm-ID: 411047 Cd Length: 356 Bit Score: 322.21 E-value: 4.03e-111
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Name | Accession | Description | Interval | E-value | ||||
TM6SF1-like | cd21106 | transmembrane 6 superfamily member 1, member 2, and similar proteins; This family includes ... |
1-213 | 4.03e-111 | ||||
transmembrane 6 superfamily member 1, member 2, and similar proteins; This family includes transmembrane 6 superfamily members 1 (TM6SF1) and 2 (TM6SF2), and similar proteins. TM6SF1 is a widely expressed lysosomal transmembrane protein that may be suitable as a lysosomal marker. Polymorphism of its paralog, TM6SF2, has been associated with the risk for hepatocellular carcinoma, and a variant of the gene has been found to impact the processing of lipids in the liver and the small intestine, causing non-alcoholic fatty liver disease (NAFLD). Pssm-ID: 411047 Cd Length: 356 Bit Score: 322.21 E-value: 4.03e-111
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EBP | pfam05241 | EXPERA (EXPanded EBP superfamily); The EXPERA (EXPanded EBP superfamily) domain is conserved ... |
110-205 | 7.44e-06 | ||||
EXPERA (EXPanded EBP superfamily); The EXPERA (EXPanded EBP superfamily) domain is conserved among the following protein families: TM6SF1 (Transmembrane 6 Superfamily Member 1), TM6SF2 (Transmembrane 6 Superfamily Member 2), MAC30 (Meningioma-associated protein 30 also known as TMEM97, or Transmembrane protein 97), and EBP (Emopamil binding protein). EBP is an enzyme with a D8, D7 sterol isomerase activity that catalyzes the transposition of a double bond from C8=C9 to C7=C8 in the sterol B-ring. Mutations of EBP are known to cause the genetic disorder of X-linked dominant chondrodysplasia punctata (CDPX2). This syndrome of humans is lethal in most males, and affected females display asymmetric hyperkeratotic skin and skeletal abnormalities. Pssm-ID: 461600 Cd Length: 112 Bit Score: 43.68 E-value: 7.44e-06
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Name | Accession | Description | Interval | E-value | ||||
TM6SF1-like | cd21106 | transmembrane 6 superfamily member 1, member 2, and similar proteins; This family includes ... |
1-213 | 4.03e-111 | ||||
transmembrane 6 superfamily member 1, member 2, and similar proteins; This family includes transmembrane 6 superfamily members 1 (TM6SF1) and 2 (TM6SF2), and similar proteins. TM6SF1 is a widely expressed lysosomal transmembrane protein that may be suitable as a lysosomal marker. Polymorphism of its paralog, TM6SF2, has been associated with the risk for hepatocellular carcinoma, and a variant of the gene has been found to impact the processing of lipids in the liver and the small intestine, causing non-alcoholic fatty liver disease (NAFLD). Pssm-ID: 411047 Cd Length: 356 Bit Score: 322.21 E-value: 4.03e-111
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EBP | pfam05241 | EXPERA (EXPanded EBP superfamily); The EXPERA (EXPanded EBP superfamily) domain is conserved ... |
110-205 | 7.44e-06 | ||||
EXPERA (EXPanded EBP superfamily); The EXPERA (EXPanded EBP superfamily) domain is conserved among the following protein families: TM6SF1 (Transmembrane 6 Superfamily Member 1), TM6SF2 (Transmembrane 6 Superfamily Member 2), MAC30 (Meningioma-associated protein 30 also known as TMEM97, or Transmembrane protein 97), and EBP (Emopamil binding protein). EBP is an enzyme with a D8, D7 sterol isomerase activity that catalyzes the transposition of a double bond from C8=C9 to C7=C8 in the sterol B-ring. Mutations of EBP are known to cause the genetic disorder of X-linked dominant chondrodysplasia punctata (CDPX2). This syndrome of humans is lethal in most males, and affected females display asymmetric hyperkeratotic skin and skeletal abnormalities. Pssm-ID: 461600 Cd Length: 112 Bit Score: 43.68 E-value: 7.44e-06
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Blast search parameters | ||||
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