CLEC12A - C-type lectin domain family 12 member A Gene

Also Known as CLL1; MICL; CD371; CLL-1; DCAL-2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 160364

About CLEC12A

Cytogenetic location: 12p13.31-p13.2 Genomic coordinates (GRCh38): 12:9,951,268-10,006,150 (from NCBI)

This gene has 7 transcripts (splice variants), 203 orthologues and 23 paralogues. Biased expression in bone marrow (RPKM 14.2), appendix (RPKM 4.4) and 7 other tissues.

Summary

This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signaling, glycoprotein turnover, and roles in inflammation and immune response. The protein encoded by this gene is a negative regulator of granulocyte and monocyte function. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. This gene is closely linked to Other CTL/CTLD superfamily members in the natural killer gene complex region on chromosome 12p13. [provided by RefSeq, May 2011]

CLEC12A Products (4)

mRNA Protein Name
NM_001207010.2 NP_001193939.1 C-type lectin domain family 12 member A isoform 3
NM_001300730.2 NP_001287659.1 C-type lectin domain family 12 member A isoform 4
NM_138337.6 NP_612210.4 C-type lectin domain family 12 member A isoform 1
NM_201623.4 NP_963917.2 C-type lectin domain family 12 member A isoform 2
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

CLEC12A Protein Structure

Lectin_C

Lectin_C: Lectin C-type domain (152 - 250)

  • 0
  • 100
  • 200
  • 265 a.a.
Protein Preferred Names Protein Names

C-type lectin domain family 12 member A

  • C-type lectin protein CLL-1

CLEC12A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CLEC12A Q5QGZ9 CLEC1A Homo sapiens Q8NC01 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CLEC12A Proteins

Cat. No. Product Name Accession Purity
HY-P76267 CLEC12A/MICL Protein, Human (HEK293, His) Q5QGZ9-1 (H75-A275) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P77631 CLEC12A/MICL Protein, Human (HEK293, Fc) Q5QGZ9-2 (H65-A265) ≥ 95%, as determined by Bis-Tris PAGE.
HY-P77633 CLEC12A/MICL Protein, Human (Biotinylated, HEK293, His-Avi) Q5QGZ9-2 (H65-A265) ≥ 95%, as determined by Bis-Tris PAGE.
HY-P77634 CLEC12A/MICL Protein, Human (Biotinylated, HEK293, Fc-Avi) Q5QGZ9-2 (H65-A265) ≥ 95%, as determined by Bis-Tris PAGE.
HY-P78653 FITC-Labeled CLEC12A/MICL Protein, Human (HEK293, His, solution) Q5QGZ9-2 (H65-A265) ≥ 95%, as determined by Bis-Tris PAGE.

CLEC12A Antibodies

Cat. No. Product Name Application Reactivity
HY-P81674 CLEC12A Antibody (YA1419) FC, ELISA Human
HY-P84631 CLEC12A Antibody (YA4328) WB, ICC/IF, FC, ELISA Human
HY-P84631A CLEC12A Antibody (YA4328)(PBS only) WB, ICC/IF, FC, ELISA Human
HY-P84992 CLEC12A Antibody (YA4684) ELISA Human

Related Diseases

Diseases Alias
Myeloid Leukemia
  • Myeloid Leukaemia

  • Leukaemia Myelogenous

  • Leukemia Myelogenous

  • Myeloid Granulocytic Leukaemia

  • Myeloid Granulocytic Leukemia

  • Non-Lymphocytic Leukemia

  • Leukemia, Myeloid

  • Granulocytic Leukaemia

  • Myelogenous Leukaemia

  • Myeloid Leukaemia, Unspecified, Without Mention Of Remission

Mixed Phenotype Acute Leukemia, B/Myeloid
  • Doid:0081038

3mc Syndrome
  • Craniofacial-Ulnar-Renal Syndrome

  • Malpuech Facial Clefting Syndrome

  • Oculopalatoskeletal Syndrome

  • Carnevale Syndrome

  • Michels Syndrome

  • Malpuech-Michels-Mingarelli-Carnevale Syndrome

  • Carnevale-Krajewska-Fischetto Syndrome

  • Craniosynostosis With Lid Anomalies

  • Malpuech Syndrome

  • Mingarelli Syndrome

  • Oculo-Skeletal-Abdominal Syndrome

  • Osa Syndrome

  • Ptosis Of Eyelids With Diastasis Recti And Hip Dysplasia

  • Ptosis-Strabismus-Rectus Abdominis Diastasis

Langerhans Cell Histiocytosis
  • Histiocytosis X

  • Lch

  • Langerhans Cell Granulomatosis

  • Langerhans-Cell Histiocytosis

  • Letterer-Siwe Disease

  • Hashimoto-Pritzger Disease

  • Histiocytosis, Langerhans-Cell

  • Langerhan'S Cell Histiocytosis

  • Letterer-Siwe Disease Involving Intra-Abdominal Lymph Nodes

  • Letterer-Siwe Disease Involving Intrapelvic Lymph Nodes

  • Letterer-Siwe Disease Involving Intrathoracic Lymph Nodes

  • Letterer-Siwe Disease Involving Lymph Nodes Of Axilla And Upper Limb

  • Letterer-Siwe Disease Involving Lymph Nodes Of Head, Face And Neck

  • Letterer-Siwe Disease Involving Lymph Nodes Of Head, Face, And Neck

  • Letterer-Siwe Disease Involving Lymph Nodes Of Inguinal Region And Lower Limb

  • Letterer-Siwe Disease Involving Lymph Nodes Of Multiple Sites

  • Letterer-Siwe Disease Involving Spleen

  • Letterer-Siwe Disease Of Intra-Abdominal Lymph Nodes

  • Letterer-Siwe Disease Of Intrapelvic Lymph Nodes

  • Letterer-Siwe Disease Of Intrathoracic Lymph Nodes

  • Letterer-Siwe Disease Of Lymph Nodes Of Axilla And Upper Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Axilla And/Or Upper Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Head, Face And Neck

  • Letterer-Siwe Disease Of Lymph Nodes Of Head, Face And/Or Neck

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region Amd/Or Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region And Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Inguinal Region And/Or Lower Limb

  • Letterer-Siwe Disease Of Lymph Nodes Of Multiple Sites

  • Letterer-Siwe Disease Of Spleen

  • Familial Letterer-Siwe Disease

  • Langerhans-Cell Histiocytosis Nos

Human Immunodeficiency Virus Type 1
  • Aids

  • Hiv/Aids

  • Aids, Delayed/Rapid Progression To

  • Hiv-1, Susceptibility To

  • Hiv-1 Viremia, Susceptibility To

  • Human Immunodeficiency Virus Type 1, Susceptibility To

  • Hiv-1

  • Aids, Slow Progression To

  • Rapid Progression To Aids From Hiv1 Infection

  • Hiv1 Infection, Resistance To

  • Hiv1 Infection

  • Hiv-1 Viremia

  • Aids, Resistance To

  • Aids, Rapid Progression To

  • Hiv/Aids, Susceptibility To

  • Hiv-1, Resistance To

  • Hiv1, Resistance To

  • Hiv1

  • Hiv-1 Disease, Delayed Progression Of

  • Hiv-1 Disease, Rapid Progression Of

  • Hiv Infection, Resistance To

  • Hiv Type 1, Susceptibility To

  • Hiv Type 1

  • Hiv-1 Infection

  • Human Immunodeficiency Virus I Infection

  • Acquired Immunodeficiency Syndrome

  • Hiv-Infection/Aids

Immune Deficiency Disease
  • Immunodeficiency

  • Primary Immunodeficiency

  • Primary Immunodeficiency Disease

  • Immunologic Deficiency Syndromes

  • Hypoimmunity

  • Immune Deficiency Disorder

  • Immunodeficiency Syndrome

  • Immune Disorder

  • Primary Immune Deficiency Disorder

  • Immune System Diseases

  • Human Immunodeficiency Virus Infection

  • Hiv - [Human Immunodeficiency Virus Infection]

  • Hiv Positive Nos

  • Hiv Disease

  • Acquired Immune Deficiency Syndrome-Related Complex

  • Aids-Like Syndrome

  • Aids-Related Complex Nos

  • Arc - [Aids-Related Complex]

  • Immunodeficiency Due To Human Immunodeficiency Virus Infection

  • Unspecified Human Immunodeficiency Virus Disease

  • Hiv Disease Nos

  • Human Immunodeficiency Virus Positive Nos

  • Hiv Nos

  • Deficiency Of Complement Initial Pathway

  • Deficiency Of Complement Terminal Pathway

  • Cfdd - [Complement Factor D Deficiency]

  • Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

  • Nonfamilial Hypogammaglobulinaemia

  • Common Variable Immune Deficiency

  • Nonfamilial Agammaglobulinaemia

  • Common Variable Agammaglobulinaemia

  • Agammaglobulinaemia Nos

  • Agammaglobulinaemia Antibody Deficiency Syndrome

  • Hypogammaglobulinaemia Antibody Deficiency Syndrome

  • Acquired Agammaglobulinaemia Nos

  • Hypogammaglobulinaemia Nos

  • Hyper Igm

Polycystic Kidney Disease
  • Polycystic Kidney Diseases

  • Pkd

  • Polycystic Renal Disease

  • Kidney Disease, Polycystic

  • Polycystic Kidney, Autosomal Dominant

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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 CLEC12A VGNC VGNC:39325
Bos taurus CLEC12A VGNC VGNC:27423
Mus musculus CLEC12A MGD MGI:3040968
Rattus norvegicus CLEC12A RGD RGD:1592991
Macaca mulatta CLEC12A VGNC VGNC:71377
Felis catus CLEC12A VGNC VGNC:60941
Others CLEC12A NCBI