1. Gene
  2. SFN - stratifin Gene

SFN - stratifin Gene

Homo sapiens

Also known as YWHAS

Gene ID: 2810 | Gene type: protein coding

About SFN

Cytogenetic location: 1p36.11 Genomic coordinates (GRCh38): 1:26,863,149-26,864,456 (from NCBI)

This gene has 1 transcript (splice variant), 120 orthologues and 6 paralogues.

Summary

This gene encodes a cell cycle checkpoint protein. The encoded protein binds to translation and initiation factors and functions as a regulator of mitotic translation. In response to DNA damage this protein plays a role in preventing DNA errors during mitosis. [provided by RefSeq, Aug 2017]

SFN Products(1)

mRNA Protein Name
NM_006142.5 NP_006133.1 2014/3/3 protein sigma
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
15778465 GOA
enables phosphoserine residue binding IDA
IDA: Inferred from direct assay
37797010 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11574543 GOA
enables protein sequestering activity IDA
IDA: Inferred from direct assay
37797010 GOA
Biological Process GO Annotation Evidence Reference Source
involved in intrinsic apoptotic signaling pathway in response to DNA damage IDA
IDA: Inferred from direct assay
11574543 GOA
involved in negative regulation of innate immune response IDA
IDA: Inferred from direct assay
37797010 GOA
involved in negative regulation of protein localization to plasma membrane IMP
IMP: Inferred from mutant phenotype
24124604 GOA
involved in positive regulation of cell adhesion IMP
IMP: Inferred from mutant phenotype
24124604 GOA
involved in positive regulation of protein localization IMP
IMP: Inferred from mutant phenotype
24124604 GOA
involved in regulation of cell-cell adhesion IMP
IMP: Inferred from mutant phenotype
29678907 GOA
involved in regulation of protein localization IMP
IMP: Inferred from mutant phenotype
29678907 GOA
involved in release of cytochrome c from mitochondria IDA
IDA: Inferred from direct assay
11574543 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
24124604 GOA
is active in cytosol IDA
IDA: Inferred from direct assay
37797010 GOA
located in cytosol IDA
IDA: Inferred from direct assay
31906564 GOA
located in nucleus IDA
IDA: Inferred from direct assay
31906564 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

SFN Protein Structure

14-3-3

14-3-3: 14-3-3 protein (4 - 237)

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

14-3-3 protein sigma

epithelial cell marker protein 1

SFN Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SFN P31947 CCDC102B Homo sapiens Q68D86 25416956
Intra
SFN P31947 FAM9B Homo sapiens Q8IZU0 25416956
Intra
SFN P31947 FAM9B Homo sapiens Q8IZU0 25416956
Intra
SFN P31947 FAM9B Homo sapiens Q8IZU0 25416956
Intra
SFN P31947 MPRIP Homo sapiens Q6WCQ1 36931259
Intra
SFN P31947 MYCBP2 Homo sapiens O75592
TAP
15778465
Intra
SFN P31947 MYCBP2 Homo sapiens O75592 36931259
Intra
SFN P31947 PPFIBP1 Homo sapiens Q86W92
TAP
15778465
Intra
SFN P31947 PPFIBP1 Homo sapiens Q86W92 36931259
Intra
SFN P31947 PPFIBP1 Homo sapiens Q86W92 36931259
Intra
SFN P31947 ISCU Homo sapiens Q9H1K1 36931259
Intra
SFN P31947 ISCU Homo sapiens Q9H1K1
TAP
15778465
Intra
SFN P31947 SAMD4A Homo sapiens Q9UPU9 36931259
Intra
SFN P31947 SAMD4A Homo sapiens Q9UPU9 36931259
Intra
SFN P31947 ANKS1A Homo sapiens Q92625
TAP
15778465
Intra
SFN P31947 ANKS1A Homo sapiens Q92625 36931259
Intra
SFN P31947 IRS2 Homo sapiens Q9Y4H2 36931259
Intra
SFN P31947 IRS2 Homo sapiens Q9Y4H2
TAP
15778465
Intra
SFN P31947 RALGPS2 Homo sapiens Q86X27 36931259
Intra
SFN P31947 USP8 Homo sapiens P40818
TAP
15778465
Intra
SFN P31947 USP8 Homo sapiens P40818 36931259
Intra
SFN P31947 USP8 Homo sapiens P40818 36931259
Intra
SFN P31947 CDC25B Homo sapiens P30305 16672277
Intra
SFN P31947 CDC25B Homo sapiens P30305 15173315
Intra
SFN P31947 CDC25B Homo sapiens P30305 36931259
Intra
SFN P31947 EPB41L2 Homo sapiens O43491 36931259
Intra
SFN P31947 EPB41L2 Homo sapiens O43491 36931259
Intra
SFN P31947 LARP1 Homo sapiens Q6PKG0 36931259
Intra
SFN P31947 LARP1 Homo sapiens Q6PKG0 36931259
Intra
SFN P31947 KIAA0930 Homo sapiens Q6ICG6 36931259
Intra
SFN P31947 ARHGEF16 Homo sapiens Q5VV41 36931259
Intra
SFN P31947 ARHGEF16 Homo sapiens Q5VV41
TAP
15778465
Intra
SFN P31947 ARHGEF16 Homo sapiens Q5VV41 36931259
Intra
SFN P31947 COP1 Homo sapiens Q8NHY2 20843328
Intra
SFN P31947 COP1 Homo sapiens Q8NHY2 21625211
Intra
SFN P31947 COP1 Homo sapiens Q8NHY2
GMS
21625211
Intra
SFN P31947 COP1 Homo sapiens Q8NHY2 20843328
Intra
SFN P31947 NUAK2 Homo sapiens Q9H093 36931259
Intra
SFN P31947 CCDC125 Homo sapiens Q86Z20 32296183
Intra
SFN P31947 CCDC125 Homo sapiens Q86Z20 32296183
Intra
SFN P31947 PAX9 Homo sapiens P55771 32296183
Intra
SFN P31947 PAX9 Homo sapiens P55771 32296183
Intra
SFN P31947 PAX9 Homo sapiens P55771 32296183
Intra
SFN P31947 MAP3K6 Homo sapiens O95382 36931259
Intra
SFN P31947 TNK1 Homo sapiens Q13470 36931259
Intra
SFN P31947 RICTOR Homo sapiens Q6R327 36931259
Intra
SFN P31947 ARHGAP21 Homo sapiens Q5T5U3 36931259
Intra
SFN P31947 ZFP36L2 Homo sapiens P47974 36931259
Intra
SFN P31947 ZFP36L2 Homo sapiens P47974 36931259
Intra
SFN P31947 FOXO3 Homo sapiens O43524 36931259
Intra
SFN P31947 FOXO3 Homo sapiens O43524 36931259
Intra
SFN P31947 FAM53C Homo sapiens Q9NYF3 25416956
Intra
SFN P31947 FAM53C Homo sapiens Q9NYF3 25416956
Intra
SFN P31947 SASH1 Homo sapiens O94885 36931259
Intra
SFN P31947 PLEKHA7 Homo sapiens Q6IQ23 36931259
Intra
SFN P31947 PLEKHA7 Homo sapiens Q6IQ23 36931259
Intra
SFN P31947 MINK1 Homo sapiens Q8N4C8 36931259
Intra
SFN P31947 MINK1 Homo sapiens Q8N4C8 36931259
Intra
SFN P31947 MKRN3 Homo sapiens Q13064 25416956
Intra
SFN P31947 LONRF1 Homo sapiens Q17RB8 25416956
Intra
SFN P31947 SIPA1L3 Homo sapiens O60292 36931259
Intra
SFN P31947 SIPA1L3 Homo sapiens O60292
TAP
15778465
Intra
SFN P31947 PDGFRA Homo sapiens P16234 36931259
Intra
SFN P31947 ERRFI1 Homo sapiens Q9UJM3
IF
15778465
Intra
SFN P31947 ERRFI1 Homo sapiens Q9UJM3
TAP
15778465
Intra
SFN P31947 EGFR Homo sapiens P00533 24658140
Intra
SFN P31947 ARHGEF2 Homo sapiens Q92974 36931259
Intra
SFN P31947 ARHGEF2 Homo sapiens Q92974 36931259
Intra
SFN P31947 KIF23 Homo sapiens Q02241 36931259
Intra
SFN P31947 KIF23 Homo sapiens Q02241
TAP
15778465
Intra
SFN P31947 NAV1 Homo sapiens Q8NEY1 36931259
Intra
SFN P31947 NAV1 Homo sapiens Q8NEY1 36931259
Intra
SFN P31947 HDAC4 Homo sapiens P56524 36931259
Intra
SFN P31947 HDAC4 Homo sapiens P56524 36931259
Intra
SFN P31947 ARHGAP32 Homo sapiens A7KAX9 36931259
Intra
SFN P31947 SIPA1L1 Homo sapiens O43166 36931259
Intra
SFN P31947 SORBS2 Homo sapiens O94875 36931259
Intra
SFN P31947 SORBS2 Homo sapiens O94875
TAP
15778465
Intra
SFN P31947 SH3RF1 Homo sapiens Q7Z6J0 36931259
Intra
SFN P31947 SH3RF1 Homo sapiens Q7Z6J0 36931259
Intra
SFN P31947 YWHAZ Homo sapiens P63104 33961781
Intra
SFN P31947 YWHAZ Homo sapiens P63104 15161933
Intra
SFN P31947 YWHAZ Homo sapiens P63104 36931259
Intra
SFN P31947 LUZP1 Homo sapiens Q86V48 36931259
Intra
SFN P31947 LUZP1 Homo sapiens Q86V48 36931259
Intra
SFN P31947 SRSF10 Homo sapiens O75494 36931259
Intra
SFN P31947 SRSF10 Homo sapiens O75494 36931259
Intra
SFN P31947 YWHAE Homo sapiens P62258 36931259
Intra
SFN P31947 YWHAE Homo sapiens P62258 36931259
Intra
SFN P31947 IRS4 Homo sapiens O14654 36931259
Intra
SFN P31947 IRS4 Homo sapiens O14654 36931259
Intra
SFN P31947 DNAJB1 Homo sapiens P25685 36931259
Intra
SFN P31947 DNAJB1 Homo sapiens P25685 36931259
Intra
SFN P31947 MAP3K2 Homo sapiens Q9Y2U5 36931259
Intra
SFN P31947 YWHAG Homo sapiens P61981
TAP
15778465
Intra
SFN P31947 YWHAG Homo sapiens P61981 33961781
Intra
SFN P31947 ARAF Homo sapiens P10398 36931259
Intra
SFN P31947 ARAF Homo sapiens P10398
TAP
15778465
Intra
SFN P31947 BRAF Homo sapiens P15056 36931259
Intra
SFN P31947 BRAF Homo sapiens P15056 36931259
Intra
SFN P31947 RAF1 Homo sapiens P04049
FPS
35044719
Intra
SFN P31947 RAF1 Homo sapiens P04049
TAP
15778465
Intra
SFN P31947 RAF1 Homo sapiens P04049 11697890
Intra
SFN P31947 RAF1 Homo sapiens P04049 36931259
Intra
SFN P31947 TP53 Homo sapiens P04637
ITC
20206173
Intra
SFN P31947 TP53 Homo sapiens P04637 20206173
Intra
SFN P31947 TP53 Homo sapiens P04637 21625211
Intra
SFN P31947 TP53 Homo sapiens P04637 36931259
Intra
SFN P31947 INA Homo sapiens Q16352 36931259
Intra
SFN P31947 INA Homo sapiens Q16352 36931259
Intra
SFN P31947 ABL1 Homo sapiens P00519 36931259
Intra
SFN P31947 ABL1 Homo sapiens P00519 36931259
Intra
SFN P31947 FAM117B Homo sapiens Q6P1L5 36931259
Intra
SFN P31947 NTRK3 Homo sapiens Q16288 36931259
Intra
SFN P31947 MDM4 Homo sapiens O15151 36931259
Intra
SFN P31947 MDM4 Homo sapiens O15151 16511572
Intra
SFN P31947 HNRNPD Homo sapiens Q14103-4 16902409
Intra
SFN P31947 HNRNPD Homo sapiens Q14103-4 16902409
Intra
SFN P31947 FOXO4 Homo sapiens P98177 36931259
Intra
SFN P31947 FOXO4 Homo sapiens P98177 25416956
Intra
SFN P31947 FOXO4 Homo sapiens P98177 25416956
Intra
SFN P31947 WNK1 Homo sapiens Q9H4A3 36931259
Intra
SFN P31947 WNK1 Homo sapiens Q9H4A3 36931259
Intra
SFN P31947 KIF1B Homo sapiens O60333 36931259
Intra
SFN P31947 KIF1B Homo sapiens O60333 36931259
Intra
SFN P31947 BAD Homo sapiens Q92934 21988832
Intra
SFN P31947 BAD Homo sapiens Q92934 36931259
Intra
SFN P31947 BAD Homo sapiens Q92934 20005908
Intra
SFN P31947 BAD Homo sapiens Q92934 36931259
Intra
SFN P31947 COPS6 Homo sapiens Q7L5N1 21625211
Intra
SFN P31947 COPS6 Homo sapiens Q7L5N1
GMS
21625211
Intra
SFN P31947 ABLIM1 Homo sapiens O14639 36931259
Intra
SFN P31947 ABLIM1 Homo sapiens O14639 36931259
Intra
SFN P31947 IRS1 Homo sapiens P35568 36931259
Intra
SFN P31947 CBL Homo sapiens P22681 36931259
Intra
SFN P31947 TBC1D4 Homo sapiens O60343 36931259
Intra
SFN P31947 TBC1D4 Homo sapiens O60343 36931259
Intra
SFN P31947 BAIAP2 Homo sapiens Q9UQB8 36931259
Intra
SFN P31947 BAIAP2 Homo sapiens Q9UQB8 36931259
Intra
SFN P31947 ARHGEF5 Homo sapiens Q12774 36931259
Intra
SFN P31947 MAP3K20 Homo sapiens Q9NYL2 36931259
Intra
SFN P31947 MAP3K20 Homo sapiens Q9NYL2
TAP
15778465
Intra
SFN P31947 PIK3C2B Homo sapiens O00750 36931259
Intra
SFN P31947 PKP2 Homo sapiens Q99959
TAP
15778465
Intra
SFN P31947 PKP2 Homo sapiens Q99959 36931259
Intra
SFN P31947 PKP2 Homo sapiens Q99959 36931259
Intra
SFN P31947 PRKCE Homo sapiens Q02156 36931259
Intra
SFN P31947 REPS2 Homo sapiens Q8NFH8 18647389
Intra
SFN P31947 REPS2 Homo sapiens Q8NFH8 18647389
Intra
SFN P31947 MARK3 Homo sapiens P27448 36931259
Intra
SFN P31947 MARK3 Homo sapiens P27448 16189514
Intra
SFN P31947 MARK3 Homo sapiens P27448 36931259
Intra
SFN P31947 PAK4 Homo sapiens O96013 36931259
Intra
SFN P31947 WDR62 Homo sapiens O43379 36931259
Intra
SFN P31947 WDR62 Homo sapiens O43379 36931259
Intra
SFN P31947 HDAC5 Homo sapiens Q9UQL6
Y2H
15923258
Intra
SFN P31947 PRAG1 Homo sapiens Q86YV5
TAP
15778465
Intra
SFN P31947 PRAG1 Homo sapiens Q86YV5 36931259
Intra
SFN P31947 KLC2 Homo sapiens Q9H0B6 36931259
Intra
SFN P31947 KLC2 Homo sapiens Q9H0B6 36931259
Intra
SFN P31947 GPRIN2 Homo sapiens O60269
TAP
15778465
Intra
SFN P31947 GPRIN2 Homo sapiens O60269 16189514
Intra
SFN P31947 ZC2HC1C Homo sapiens Q53FD0 25416956
Intra
SFN P31947 MAGEA1 Homo sapiens P43355 25416956
Intra
SFN P31947 MAGEA1 Homo sapiens P43355 25416956
Intra
SFN P31947 NTAQ1 Homo sapiens Q96HA8 16189514
Intra
SFN P31947 NTAQ1 Homo sapiens Q96HA8 32296183
Intra
SFN P31947 CCNH Homo sapiens P51946 31515488
Intra
SFN P31947 CCNH Homo sapiens P51946 25416956
Intra
SFN P31947 CCNH Homo sapiens P51946 25416956
Intra
SFN P31947 PLK4 Homo sapiens O00444 36931259
Intra
SFN P31947 PLK4 Homo sapiens O00444 16189514
Intra
SFN P31947 RAB3IP Homo sapiens Q96QF0 25416956
Intra
SFN P31947 RAB3IP Homo sapiens Q96QF0 25416956
Intra
SFN P31947 RAB3IP Homo sapiens Q96QF0 25416956
Intra
SFN P31947 REEP4 Homo sapiens Q9H6H4 36931259
Intra
SFN P31947 REEP3 Homo sapiens Q6NUK4
TAP
15778465
Intra
SFN P31947 REEP3 Homo sapiens Q6NUK4 36931259
Intra
SFN P31947 GAN Homo sapiens Q9H2C0 36931259
Intra
SFN P31947 GAN Homo sapiens Q9H2C0 36931259
Intra
SFN P31947 GAN Homo sapiens Q9H2C0
TAP
15778465
Intra
SFN P31947 CGN Homo sapiens Q9P2M7 36931259
Intra
SFN P31947 GRB10 Homo sapiens Q13322 36931259
Intra
SFN P31947 PARD3 Homo sapiens Q8TEW0 36931259
Intra
SFN P31947 PARD3 Homo sapiens Q8TEW0
TAP
15778465
Intra
SFN P31947 CLASP1 Homo sapiens Q7Z460 36931259
Intra
SFN P31947 CLASP1 Homo sapiens Q7Z460 36931259
Intra
SFN P31947 CLASP2 Homo sapiens O75122 36931259
Intra
SFN P31947 CLASP2 Homo sapiens O75122 36931259
Intra
SFN P31947 WEE1 Homo sapiens P30291 36931259
Intra
SFN P31947 WEE1 Homo sapiens P30291 36931259
Intra
SFN P31947 WEE1 Homo sapiens P30291
TAP
15778465
Intra
SFN P31947 WEE1 Homo sapiens P30291 36931259
Intra
SFN P31947 PUM1 Homo sapiens Q14671 36931259
Intra
SFN P31947 PUM1 Homo sapiens Q14671 36931259
Intra
SFN P31947 KLC4 Homo sapiens Q9NSK0 36931259
Intra
SFN P31947 KLC4 Homo sapiens Q9NSK0 36931259
Intra
SFN P31947 AJUBA Homo sapiens Q96IF1
TAP
15778465
Intra
SFN P31947 AJUBA Homo sapiens Q96IF1 15778465
Intra
SFN P31947 ITK Homo sapiens Q08881 36931259
Intra
SFN P31947 EDC3 Homo sapiens Q96F86 36931259
Intra
SFN P31947 EDC3 Homo sapiens Q96F86
TAP
15778465
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SFN Proteins

Cat. No. Product Name Accession Purity
HY-P71339 Stratifin Protein, Human P31947-1 (M1-S248) ≥95%
HY-P700308 Stratifin Protein, Human (N-His, C-Myc) P31947-1 (M1-S248) ≥95%

SFN Antibodies

Cat. No. Product Name Application Reactivity
HY-P82909 14-3-3 sigma Antibody (YA2654) WB, IHC-P Human, Rat

Related Diseases

Diseases Alias
Benign Breast Adenomyoepithelioma

Benign Adenomyoepithelioma Of The Breast

Fetal Encasement Syndrome

Cocoon Syndrome

COCOS

Fetal Diseases

Microphthalmia, Isolated 1

Isolated Microphthalmia 1

MCOP1

Mcop

Anophthalmia, Clinical, Isolated

Microphthalmos, Autosomal Recessive

Popliteal Pterygium Syndrome

PPS

Faciogenitopopliteal Syndrome

Facio-Genito-Popliteal Syndrome

Popliteal Web Syndrome

Autosomal Dominant Popliteal Pterygium Syndrome

Cleft Lip/Palate, Paramedian Mucous Cysts Of The Lower Lip, Popliteal Pterygium, Digital And Genital Anomalies

Popliteal Pterygium Syndrome 1

Cleft Lip/Palate Paramedian Mucous Cysts Of The Lower Lip Popliteal Pterygium Digital And Genital Anomalies

Popliteal Pterygium

Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

Fraser Syndrome 1

Fraser Syndrome

Cryptophthalmos With Other Malformations

Cryptophthalmos Syndrome

FRASRS1

Cryptophthalmos-Syndactyly Syndrome

Fraser-Francois Syndrome

Cyclopism

Meyer-Schwickerath'S Syndrome

Ulrich-Feichtiger Syndrome

Cryptophthalmos Syndactyly Syndrome

Fraser'S Syndrome

Meyer-Schwickerath Syndrome

Ullrich-Feichtiger Syndrome

Salivary Gland Adenoid Cystic Carcinoma

Cylindroma

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

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 SFN VGNC VGNC:34517
Macaca mulatta SFN VGNC VGNC:77183
Canis familiaris SFN VGNC VGNC:46078
Mus musculus SFN MGD MGI:1891831
Rattus norvegicus SFN RGD RGD:1304729
Others SFN NCBI