SAMD11 - sterile alpha motif domain containing 11 Gene

Also Known as MRS

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 148398

About SAMD11

Cytogenetic location: 1p36.33 Genomic coordinates (GRCh38): 1:923,923-944,574 (from NCBI)

This gene has 15 transcripts (splice variants), 199 orthologues, 18 paralogues and is associated with 1 phenotype. Ubiquitous expression in prostate (RPKM 7.4), endometrium (RPKM 5.9) and 25 other tissues.

Summary

Predicted to enable several functions, including histone binding activity; protein domain specific binding activity; and protein self-association. Predicted to be involved in negative regulation of transcription, DNA-templated. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

SAMD11 Products (3)

mRNA Protein Name
NM_001385640.1 NP_001372569.1 sterile alpha motif domain-containing protein 11 isoform 2
NM_001385641.1 NP_001372570.1 sterile alpha motif domain-containing protein 11 isoform 1
NM_152486.4 NP_689699.3 sterile alpha motif domain-containing protein 11 isoform 3
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SAMD11 Protein Structure

SAM_2

SAM_2: SAM domain (Sterile alpha motif) (543 - 597)

  • 0
  • 200
  • 400
  • 600
  • 681 a.a.
Protein Preferred Names Protein Names

sterile alpha motif domain-containing protein 11

  • SAM domain-containing protein 11

SAMD11 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SAMD11 Q96NU1 RTL8C Homo sapiens A6ZKI3 32296183
Intra
SAMD11 Q96NU1 RTL8C Homo sapiens A6ZKI3 32296183
Intra
SAMD11 Q96NU1 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
SAMD11 Q96NU1 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
SAMD11 Q96NU1 NFKBID Homo sapiens Q8NI38 32296183
Intra
SAMD11 Q96NU1 NFKBID Homo sapiens Q8NI38 32296183
Intra
SAMD11 Q96NU1 KRT34 Homo sapiens O76011 32296183
Intra
SAMD11 Q96NU1 KRT34 Homo sapiens O76011 32296183
Intra
SAMD11 Q96NU1 REL Homo sapiens Q04864-2 32296183
Intra
SAMD11 Q96NU1 REL Homo sapiens Q04864-2 32296183
Intra
SAMD11 Q96NU1 KRTAP5-7 Homo sapiens Q6L8G8 32296183
Intra
SAMD11 Q96NU1 KRTAP5-7 Homo sapiens Q6L8G8 32296183
Intra
SAMD11 Q96NU1 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
SAMD11 Q96NU1 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
SAMD11 Q96NU1 ZMYND12 Homo sapiens Q9H0C1 32296183
Intra
SAMD11 Q96NU1 PRR20D Homo sapiens P86480 32296183
Intra
SAMD11 Q96NU1 PRR20D Homo sapiens P86480 32296183
Intra
SAMD11 Q96NU1 TSC1 Homo sapiens Q86WV8 32296183
Intra
SAMD11 Q96NU1 TSC1 Homo sapiens Q86WV8 32296183
Intra
SAMD11 Q96NU1 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
SAMD11 Q96NU1 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
SAMD11 Q96NU1 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
SAMD11 Q96NU1 TRAF2 Homo sapiens Q12933 32296183
Intra
SAMD11 Q96NU1 TRAF2 Homo sapiens Q12933 32296183
Intra
SAMD11 Q96NU1 TRAF1 Homo sapiens Q13077 32296183
Intra
SAMD11 Q96NU1 TRAF1 Homo sapiens Q13077 32296183
Intra
SAMD11 Q96NU1 TRIB3 Homo sapiens Q96RU7 32296183
Intra
SAMD11 Q96NU1 TRIB3 Homo sapiens Q96RU7 32296183
Intra
SAMD11 Q96NU1 TRIB3 Homo sapiens Q96RU7 32296183
Intra
SAMD11 Q96NU1 CT55 Homo sapiens Q8WUE5 32296183
Intra
SAMD11 Q96NU1 CT55 Homo sapiens Q8WUE5 32296183
Intra
SAMD11 Q96NU1 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
SAMD11 Q96NU1 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
SAMD11 Q96NU1 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
SAMD11 Q96NU1 JMJD7 Homo sapiens P0C870 32296183
Intra
SAMD11 Q96NU1 JMJD7 Homo sapiens P0C870 32296183
Intra
SAMD11 Q96NU1 ECM1 Homo sapiens Q16610 32296183
Intra
SAMD11 Q96NU1 ECM1 Homo sapiens Q16610 32296183
Intra
SAMD11 Q96NU1 KRT31 Homo sapiens Q15323 32296183
Intra
SAMD11 Q96NU1 KRT31 Homo sapiens Q15323 32296183
Intra
SAMD11 Q96NU1 BPIFA1 Homo sapiens Q9NP55 32296183
Intra
SAMD11 Q96NU1 BPIFA1 Homo sapiens Q9NP55 32296183
Intra
SAMD11 Q96NU1 BPIFA1 Homo sapiens Q9NP55 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Chronic Intestinal Vascular Insufficiency
  • Chronic Mesenteric Ischemia

  • Cmi - Chronic Mesenteric Ischaemia

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris SAMD11 VGNC VGNC:45849
Bos taurus SAMD11 VGNC VGNC:59361
Felis catus SAMD11 VGNC VGNC:64861
Rattus norvegicus SAMD11 RGD RGD:1310271
Mus musculus SAMD11 MGD MGI:2446220
Others SAMD11 NCBI