TCHP - trichoplein keratin filament binding Gene

Also Known as TpMs

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84260

About TCHP

Cytogenetic location: 12q24.11 Genomic coordinates (GRCh38): 12:109,880,667-109,918,069 (from NCBI)

This gene has 10 transcripts (splice variants) and 27 orthologues. Ubiquitous expression in skin (RPKM 11.4), testis (RPKM 6.8) and 25 other tissues.

Summary

Involved in apoptotic process; negative regulation of cell growth; and negative regulation of cilium assembly. Located in several cellular components, including apical cortex; cytoskeleton; and mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

TCHP Products (2)

mRNA Protein Name
NM_001143852.2 NP_001137324.1 trichoplein keratin filament-binding protein
NM_032300.5 NP_115676.1 trichoplein keratin filament-binding protein
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
15731013 GOA
Biological Process GO Annotation Evidence References Source
involved in apoptotic process IDA
IDA: Inferred from direct assay
18931701 GOA
involved in negative regulation of cell growth IDA
IDA: Inferred from direct assay
18931701 GOA
involved in negative regulation of cilium assembly IMP
IMP: Inferred from mutant phenotype
25270598 GOA
Cellular Component GO Annotation Evidence References Source
located in apical cortex IDA
IDA: Inferred from direct assay
15731013 GOA
located in centrosome IDA
IDA: Inferred from direct assay
21399614 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
18931701 GOA
located in keratin filament IDA
IDA: Inferred from direct assay
15731013 GOA
located in mitochondrion IDA
IDA: Inferred from direct assay
18931701 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
18931701 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

TCHP Protein Structure

TPH

TPH: Trichohyalin-plectin-homology domain (146 - 479)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 498 a.a.
Protein Preferred Names Protein Names

trichoplein keratin filament-binding protein

  • mitochondrial protein with oncostatic activity

TCHP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TCHP Q9BT92 KRT40 Homo sapiens Q6A162 25416956
Intra
TCHP Q9BT92 KRT40 Homo sapiens Q6A162 25416956
Intra
TCHP Q9BT92 NDOR1 Homo sapiens Q9UHB4 31515488
Intra
TCHP Q9BT92 NDOR1 Homo sapiens Q9UHB4 25416956
Intra
TCHP Q9BT92 NDOR1 Homo sapiens Q9UHB4 32296183
Intra
TCHP Q9BT92 NDOR1 Homo sapiens Q9UHB4 25416956
Intra
TCHP Q9BT92 KRT32 Homo sapiens Q14532 32296183
Intra
TCHP Q9BT92 KRT32 Homo sapiens Q14532 32296183
Intra
TCHP Q9BT92 KRT34 Homo sapiens O76011 32296183
Intra
TCHP Q9BT92 KRT34 Homo sapiens O76011 32296183
Intra
TCHP Q9BT92 BCAS2 Homo sapiens O75934 32296183
Intra
TCHP Q9BT92 BCAS2 Homo sapiens O75934 32296183
Intra
TCHP Q9BT92 KRT35 Homo sapiens Q92764 32296183
Intra
TCHP Q9BT92 KRT35 Homo sapiens Q92764 32296183
Intra
TCHP Q9BT92 CCDC13 Homo sapiens Q8IYE1 32296183
Intra
TCHP Q9BT92 CCDC13 Homo sapiens Q8IYE1 32296183
Intra
TCHP Q9BT92 HOOK2 Homo sapiens Q96ED9-2 32296183
Intra
TCHP Q9BT92 HOOK2 Homo sapiens Q96ED9-2 32296183
Intra
TCHP Q9BT92 CDR2L Homo sapiens Q86X02 32296183
Intra
TCHP Q9BT92 CDR2L Homo sapiens Q86X02 32296183
Intra
TCHP Q9BT92 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
TCHP Q9BT92 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
TCHP Q9BT92 CBY2 Homo sapiens Q8NA61-2 32296183
Intra
TCHP Q9BT92 CBY2 Homo sapiens Q8NA61-2 32296183
Intra
TCHP Q9BT92 CDR2 Homo sapiens Q01850 32296183
Intra
TCHP Q9BT92 CDR2 Homo sapiens Q01850 25416956
Intra
TCHP Q9BT92 CDR2 Homo sapiens Q01850 32296183
Intra
TCHP Q9BT92 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
TCHP Q9BT92 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
TCHP Q9BT92 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
TCHP Q9BT92 CCDC125 Homo sapiens Q86Z20 32296183
Intra
TCHP Q9BT92 CCDC125 Homo sapiens Q86Z20 32296183
Intra
TCHP Q9BT92 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
TCHP Q9BT92 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
TCHP Q9BT92 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
TCHP Q9BT92 EURL Homo sapiens Q9NYK6-3 32296183
Intra
TCHP Q9BT92 EURL Homo sapiens Q9NYK6-3 32296183
Intra
TCHP Q9BT92 RABGEF1 Homo sapiens Q9UJ41-4 32296183
Intra
TCHP Q9BT92 RABGEF1 Homo sapiens Q9UJ41-4 32296183
Intra
TCHP Q9BT92 RABGEF1 Homo sapiens Q9UJ41-4 32296183
Intra
TCHP Q9BT92 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TCHP Q9BT92 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TCHP Q9BT92 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
TCHP Q9BT92 MKRN3 Homo sapiens Q13064 25416956
Intra
TCHP Q9BT92 MKRN3 Homo sapiens Q13064 32296183
Intra
TCHP Q9BT92 MKRN3 Homo sapiens Q13064 25416956
Intra
TCHP Q9BT92 MKRN3 Homo sapiens Q13064 32296183
Intra
TCHP Q9BT92 MIPOL1 Homo sapiens Q8TD10 25416956
Intra
TCHP Q9BT92 CCDC172 Homo sapiens P0C7W6 32296183
Intra
TCHP Q9BT92 CCDC172 Homo sapiens P0C7W6 31515488
Intra
TCHP Q9BT92 CCDC172 Homo sapiens P0C7W6 25416956
Intra
TCHP Q9BT92 CCDC172 Homo sapiens P0C7W6 32296183
Intra
TCHP Q9BT92 MIIP Homo sapiens Q5JXC2 32296183
Intra
TCHP Q9BT92 MIIP Homo sapiens Q5JXC2 32296183
Intra
TCHP Q9BT92 KIAA0753 Homo sapiens Q2KHM9 32296183
Intra
TCHP Q9BT92 KIAA0753 Homo sapiens Q2KHM9 32296183
Intra
TCHP Q9BT92 KRT75 Homo sapiens O95678 32296183
Intra
TCHP Q9BT92 KRT75 Homo sapiens O95678 32296183
Intra
TCHP Q9BT92 KRT24 Homo sapiens Q2M2I5 32296183
Intra
TCHP Q9BT92 KRT24 Homo sapiens Q2M2I5 32296183
Intra
TCHP Q9BT92 EIF4ENIF1 Homo sapiens Q9NRA8 32296183
Intra
TCHP Q9BT92 EIF4ENIF1 Homo sapiens Q9NRA8 32296183
Intra
TCHP Q9BT92 EIF4ENIF1 Homo sapiens Q9NRA8 32296183
Intra
TCHP Q9BT92 KRT16 Homo sapiens P08779 32296183
Intra
TCHP Q9BT92 KRT16 Homo sapiens P08779 32296183
Intra
TCHP Q9BT92 PSMB5 Homo sapiens P28074 32296183
Intra
TCHP Q9BT92 PSMB5 Homo sapiens P28074 32296183
Intra
TCHP Q9BT92 DMAP1 Homo sapiens Q9NPF5 32296183
Intra
TCHP Q9BT92 DMAP1 Homo sapiens Q9NPF5 32296183
Intra
TCHP Q9BT92 DMAP1 Homo sapiens Q9NPF5 32296183
Intra
TCHP Q9BT92 RUSC1 Homo sapiens Q9BVN2 32296183
Intra
TCHP Q9BT92 RUSC1 Homo sapiens Q9BVN2 32296183
Intra
TCHP Q9BT92 RUSC1 Homo sapiens Q9BVN2 32296183
Intra
TCHP Q9BT92 ID2 Homo sapiens Q02363 32296183
Intra
TCHP Q9BT92 ID2 Homo sapiens Q02363 32296183
Intra
TCHP Q9BT92 TRIM27 Homo sapiens P14373 25416956
Intra
TCHP Q9BT92 TRIM27 Homo sapiens P14373 25416956
Intra
TCHP Q9BT92 TRIM27 Homo sapiens P14373 25416956
Intra
TCHP Q9BT92 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
TCHP Q9BT92 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
TCHP Q9BT92 HMG20A Homo sapiens Q9NP66 32296183
Intra
TCHP Q9BT92 HMG20A Homo sapiens Q9NP66 32296183
Intra
TCHP Q9BT92 HMG20A Homo sapiens Q9NP66 32296183
Intra
TCHP Q9BT92 DYDC1 Homo sapiens Q8WWB3 25416956
Intra
TCHP Q9BT92 DYDC1 Homo sapiens Q8WWB3 32296183
Intra
TCHP Q9BT92 DYDC1 Homo sapiens Q8WWB3 25416956
Intra
TCHP Q9BT92 DYDC1 Homo sapiens Q8WWB3 32296183
Intra
TCHP Q9BT92 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
TCHP Q9BT92 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
TCHP Q9BT92 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
TCHP Q9BT92 NUP54 Homo sapiens Q7Z3B4 32296183
Intra
TCHP Q9BT92 BEGAIN Homo sapiens Q9BUH8 32296183
Intra
TCHP Q9BT92 BEGAIN Homo sapiens Q9BUH8 32296183
Intra
TCHP Q9BT92 BEGAIN Homo sapiens Q9BUH8 32296183
Intra
TCHP Q9BT92 KRT19 Homo sapiens P08727 32296183
Intra
TCHP Q9BT92 KRT19 Homo sapiens P08727 32296183
Intra
TCHP Q9BT92 NME7 Homo sapiens Q9Y5B8 32296183
Intra
TCHP Q9BT92 NME7 Homo sapiens Q9Y5B8 32296183
Intra
TCHP Q9BT92 NME7 Homo sapiens Q9Y5B8 25416956
Intra
TCHP Q9BT92 NME7 Homo sapiens Q9Y5B8 32296183
Intra
TCHP Q9BT92 STN1 Homo sapiens Q9H668 32296183
Intra
TCHP Q9BT92 STN1 Homo sapiens Q9H668 32296183
Intra
TCHP Q9BT92 STN1 Homo sapiens Q9H668 32296183
Intra
TCHP Q9BT92 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TCHP Q9BT92 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TCHP Q9BT92 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TCHP Q9BT92 ZMAT5 Homo sapiens Q9UDW3 32296183
Intra
TCHP Q9BT92 ZMAT5 Homo sapiens Q9UDW3 32296183
Intra
TCHP Q9BT92 ZMAT5 Homo sapiens Q9UDW3 32296183
Intra
TCHP Q9BT92 NAB2 Homo sapiens Q15742 25416956
Intra
TCHP Q9BT92 NAB2 Homo sapiens Q15742 25416956
Intra
TCHP Q9BT92 NAB2 Homo sapiens Q15742 32296183
Intra
TCHP Q9BT92 NAB2 Homo sapiens Q15742 32296183
Intra
TCHP Q9BT92 NAB2 Homo sapiens Q15742 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

TCHP Antibodies

Cat. No. Product Name Application Reactivity
HY-P89675 trichoplein Antibody (YA9019) WB, ICC/IF, IF-Tissue, IP, ELISA human

Related Diseases

Diseases Alias
Neurofibromatosis, Type Ii
  • Neurofibromatosis 2

  • Neurofibromatosis, Type 2

  • NF2

  • Neurofibromatosis Type Ii

  • Bilateral Acoustic Neurofibromatosis

  • Banf

  • Acn

  • Central Neurofibromatosis

  • Neurofibromatosis, Central Type

  • Acoustic Schwannomas, Bilateral

  • Acoustic Neurinoma, Bilateral

  • Bilateral Acoustic Neurinoma

  • Bilateral Acoustic Schwannomas

  • Familial Acoustic Neuromas

External Ear Squamous Cell Carcinoma
  • Epidermoid Carcinoma Of The External Ear

  • Squamous Cell Carcinoma Of External Ear

Retinal Cancer
  • Malignant Neoplasm Of Retina

  • Retinal Neoplasms

  • Malignant Retinal Neoplasm

  • Malignant Tumor Of Retina

  • Neoplasm Of Retina

  • Retinal Tumor

  • Retinal Neoplasm

  • Cancer Of The Retina

  • Malignant Retinal Tumour

  • Malignant Tumour Of Retina

  • Primary Malignant Neoplasm Of Retina

Cecal Benign Neoplasm
  • Cecal Neoplasms

  • Cecum Neoplasm

  • Neoplasm Of Caecum

  • Cecal Neoplasm

  • Cecum Carcinoma

  • Malignant Neoplasm Of Cecum

Cecum Adenoma
  • Caecum Adenoma

Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

Breast Hemangioma
  • Angioma Of The Breast

  • Hemangioma Of Breast

  • Haemangioma Of Breast

X-Linked Intellectual Disability-Cardiomegaly-Congestive Heart Failure Syndrome
  • Mental Retardation, X-Linked, Syndromic 32

  • Mrxs32

Ocular Cancer
  • Eye Neoplasm

  • Eye Carcinoma

  • Eye Cancer

  • Eye Neoplasms

  • Malignant Eye Neoplasm

  • Neoplasm Of Eye

  • Neoplasm Of Eye Proper

  • Ocular Tumor

  • Carcinoma Of Eye

  • Ocular Carcinoma

  • Malignant Tumor Of Eye

External Ear Carcinoma
  • Carcinoma Of External Ear

  • Carcinoma Of The External Ear

Cowden Syndrome 1
  • Bannayan-Riley-Ruvalcaba Syndrome

  • Pten Hamartoma Tumor Syndrome

  • Lhermitte-Duclos Disease

  • Bannayan-Zonana Syndrome

  • Phts

  • Riley-Smith Syndrome

  • Bzs

  • Ruvalcaba-Myhre-Smith Syndrome

  • Multiple Hamartoma Syndrome

  • Rmss

  • Brrs

  • Dysplastic Gangliocytoma Of The Cerebellum

  • CWS1

  • Cs

  • Cd

  • Mham

  • Pten Hamartoma Tumor Syndrome With Granular Cell Tumor

  • Macrocephaly Multiple Lipomas And Hemangiomata

  • Bannayan-Ruvalcaba-Riley Syndrome

  • Myhre-Riley-Smith Syndrome

  • LDD

  • Cerebelloparenchymal Disorder Vi

  • Hamartoma Syndrome, Multiple

  • Bbrs

  • Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata

  • Macrocephaly, Multiple Lipomas, And Hemangiomata

  • Macrocephaly Pseudopapilledema And Multiple Hemangiomas

  • Ruvalcaba -Myhre-Smith Syndrome

  • Ruvalcaba-Myhre Syndrome

  • Cowden Disease

  • Macrocephaly Pseudopapilledema And Multiple Hemangiomata

  • Cerebellar Granule Cell Hypertrophy And Megalencephaly

  • Cpd6

  • Pten Hamartoma Tumor Syndromes

  • Cowden Syndrome, Type 1

Thrombophilia, X-Linked, Due To Factor Ix Defect
  • THPH8

  • Deep Venous Thrombosis, Protection Against

  • X-Linked Thrombophilia Due To Factor Ix Defect

  • Thrombophilia, X-Linked, Due To Factor 9 Defect

  • Thrombophilia 8, X-Linked, Due To Factor Ix Defect

Retinal Disease
  • Retinal Diseases

  • Retinal Disorder

  • Retinal Disorders

Bile Duct Cystadenoma
  • Cystadenoma Of The Bile Duct

Li-Fraumeni Syndrome
  • Sarcoma Family Syndrome Of Li And Fraumeni

  • Sbla Syndrome

  • LFS

  • Li-Fraumeni Familiar Cancer Susceptibility Syndrome

  • Sarcoma, Breast, Leukaemia And Adrenal Gland Syndrome

  • Lfs1

  • Li Fraumeni Syndrome

  • Sarcoma, Breast, Leukemia, And Adrenal Gland Syndrome

  • Lfl

  • Sbla Syndrome Li-Fraumeni-Like Syndrome

  • Li-Fraumeni Syndrome 1

Myopathy, Lactic Acidosis, And Sideroblastic Anemia 3
  • MLASA3

Retinitis Pigmentosa 61
  • RP61

  • Retinitis Pigmentosa, Type 61

Petrous Apex Meningioma
  • Meningioma Of The Petrous Ridge

Vallecula Cancer
  • Malignant Tumor Of Vallecula

Eye Disease
  • Eye Diseases

  • Abnormality Of The Eye

  • Toxoplasma Oculopathy

Cowden Syndrome
  • Cowden Disease

  • Multiple Hamartoma Syndrome

  • Cowden'S Disease

  • Lhermitte-Duclos Disease

  • Cd

  • Cs

  • Mham

  • Dysplastic Gangliocytoma Of Cerebellum

  • Cowden'S Syndrome

  • Hamartoma Syndrome, Multiple

Melanoma, Cutaneous Malignant 1
  • Familial Melanoma

  • Melanoma, Cutaneous Malignant, Susceptibility To, 1

  • Melanoma, Malignant

  • CMM1

  • Melanoma, Cutaneous Malignant

  • Cmm

  • Familial Atypical Mole-Malignant Melanoma Syndrome

  • Fammm

  • Melanoma, Familial

  • Mlm

  • Dysplastic Nevus Syndrome, Hereditary

  • Dns

  • B-K Mole Syndrome

  • Melanoma, Cutaneous Malignant, 1

  • Malignant Melanoma, Cutaneous

  • Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1

  • Dysplastic Nevus Syndrome

  • Cutaneous Melanoma

  • Familial Atypical Mole Melanoma Syndrome

  • Hereditary Melanoma

Breast Adenocarcinoma
  • Mammary Adenocarcinoma

  • Adenocarcinoma Of Breast

Meningioma, Familial
  • Meningioma

  • Familial Meningioma

  • Meningioma, Familial, Susceptibility To

  • Meningeal Neoplasm

  • Meningeal Neoplasms

  • Meningiomas

  • Meningioma, Nf2-Related, Somatic

  • Meningioma, Sis-Related

  • Meningothelial Cell Tumor

  • Neoplasm Of The Meninges

  • Primary Meningeal Tumor

  • Familial Multiple Meningioma

  • MNGMA

  • Meningioma, Benign, No Icd-O Subtype

  • Intracranial Meningioma

  • Meningothelial Cell Neoplasm

  • Supratentorial Meningioma

  • Primary Neoplasm Of Spinal Meninges

  • Benign Intracranial Meningioma

  • Benign Meningioma

  • Meningeal Tumours

  • Meningeal Sarcoma Of Unspecified Site

  • Meningothelial Sarcoma Of Unspecified Site

Hereditary Breast Ovarian Cancer Syndrome
  • Hereditary Breast And Ovarian Cancer Syndrome

  • Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer

  • Breast And/Or Ovarian Cancer

  • Breast And Ovarian Cancer Syndrome

  • Hboc Syndrome

  • Hereditary Breast And Ovarian Cancer

  • Brca1- Brca2-Associated Hboc

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

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
Bos taurus TCHP VGNC VGNC:35697
Felis catus TCHP VGNC VGNC:80498
Mus musculus TCHP MGD MGI:1925082
Rattus norvegicus TCHP RGD RGD:1310813
Canis familiaris TCHP VGNC VGNC:47202
Others TCHP NCBI