Type |
Details |
Score |
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
frog, western clawed |
|
•
•
•
•
•
|
Gene |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
dog, domestic |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chimpanzee |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
cattle |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
chicken |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
zebrafish |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
The Fanconi Anemia (FA) pathway is responsible for interstrand crosslink DNA repair []. The name originates the recessive syndrome known as Fanconi anemia, which causes developmental problems and cancer predisposition []. In this pathway, the FANCI-FANCD2 (ID) complex is ubiquitinated by the FA core complex and then travels to sites of damage to coordinate repair [, ]. FA pathway activation seems to trigger dissociation of FANCD2 from FANCI, coinciding with FANCD2 monoubiquitination which precedes monoubiquitination of FANCI []. This suggests a functional separation for FANCD2 from FANCI [].Monoubiquitinated FANCD2 functions to recruit DNA repair factors FAN1 (Fanconi-associated nuclease 1) []and SLX4 [], suggesting that chromatin-bound FANCD2Ub is a docking platform for certain DNA repair nucleases. FANCD2 has also a role in replication fork recovery []. |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Publication |
First Author: |
Sareen A |
Year: |
2012 |
Journal: |
Nucleic Acids Res |
Title: |
Fanconi anemia proteins FANCD2 and FANCI exhibit different DNA damage responses during S-phase. |
Volume: |
40 |
Issue: |
17 |
Pages: |
8425-39 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chaudhury I |
Year: |
2013 |
Journal: |
Nucleic Acids Res |
Title: |
FANCD2 regulates BLM complex functions independently of FANCI to promote replication fork recovery. |
Volume: |
41 |
Issue: |
13 |
Pages: |
6444-59 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1450
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1450
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1429
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1144
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1437
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
84
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
1450
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Yao CJ |
Year: |
2013 |
Journal: |
Pharmazie |
Title: |
Fanconi anemia pathway--the way of DNA interstrand cross-link repair. |
Volume: |
68 |
Issue: |
1 |
Pages: |
5-11 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yamashita T |
Year: |
2001 |
Journal: |
Int J Hematol |
Title: |
Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes. |
Volume: |
74 |
Issue: |
1 |
Pages: |
33-41 |
|
•
•
•
•
•
|
Publication |
First Author: |
Smogorzewska A |
Year: |
2010 |
Journal: |
Mol Cell |
Title: |
A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair. |
Volume: |
39 |
Issue: |
1 |
Pages: |
36-47 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kratz K |
Year: |
2010 |
Journal: |
Cell |
Title: |
Deficiency of FANCD2-associated nuclease KIAA1018/FAN1 sensitizes cells to interstrand crosslinking agents. |
Volume: |
142 |
Issue: |
1 |
Pages: |
77-88 |
|
•
•
•
•
•
|
Publication |
First Author: |
MacKay C |
Year: |
2010 |
Journal: |
Cell |
Title: |
Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2. |
Volume: |
142 |
Issue: |
1 |
Pages: |
65-76 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yamamoto KN |
Year: |
2011 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway. |
Volume: |
108 |
Issue: |
16 |
Pages: |
6492-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yeo JE |
Year: |
2014 |
Journal: |
Hum Mol Genet |
Title: |
CtIP mediates replication fork recovery in a FANCD2-regulated manner. |
Volume: |
23 |
Issue: |
14 |
Pages: |
3695-705 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
246
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Park E |
Year: |
2013 |
Journal: |
Mol Cell |
Title: |
FANCD2 activates transcription of TAp63 and suppresses tumorigenesis. |
Volume: |
50 |
Issue: |
6 |
Pages: |
908-18 |
|
•
•
•
•
•
|
Publication |
First Author: |
Du W |
Year: |
2014 |
Journal: |
Blood |
Title: |
Deletion of Fanca or Fancd2 dysregulates Treg in mice. |
Volume: |
123 |
Issue: |
12 |
Pages: |
1938-47 |
|
•
•
•
•
•
|
Publication |
First Author: |
Song X |
Year: |
2016 |
Journal: |
Biochem Biophys Res Commun |
Title: |
FANCD2 protects against bone marrow injury from ferroptosis. |
Volume: |
480 |
Issue: |
3 |
Pages: |
443-449 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yang Q |
Year: |
2019 |
Journal: |
Biochem Biophys Res Commun |
Title: |
Severe Fanconi Anemia phenotypes in Fancd2 depletion mice. |
Volume: |
514 |
Issue: |
3 |
Pages: |
713-719 |
|
•
•
•
•
•
|
Publication |
First Author: |
Nie Y |
Year: |
2020 |
Journal: |
Reproduction |
Title: |
FANCD2 is required for the repression of germline transposable elements. |
Volume: |
159 |
Issue: |
6 |
Pages: |
659-668 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lachaud C |
Year: |
2016 |
Journal: |
Science |
Title: |
Ubiquitinated Fancd2 recruits Fan1 to stalled replication forks to prevent genome instability. |
Volume: |
351 |
Issue: |
6275 |
Pages: |
846-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Parmar K |
Year: |
2010 |
Journal: |
Stem Cells |
Title: |
Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1. |
Volume: |
28 |
Issue: |
7 |
Pages: |
1186-95 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bogliolo M |
Year: |
2007 |
Journal: |
EMBO J |
Title: |
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability. |
Volume: |
26 |
Issue: |
5 |
Pages: |
1340-51 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hays LE |
Year: |
2008 |
Journal: |
Br J Cancer |
Title: |
Cigarette smoke induces genetic instability in airway epithelial cells by suppressing FANCD2 expression. |
Volume: |
98 |
Issue: |
10 |
Pages: |
1653-61 |
|
•
•
•
•
•
|
Publication |
First Author: |
Houghtaling S |
Year: |
2005 |
Journal: |
Hum Mol Genet |
Title: |
Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joining. |
Volume: |
14 |
Issue: |
20 |
Pages: |
3027-33 |
|
•
•
•
•
•
|
Publication |
First Author: |
Li X |
Year: |
2015 |
Journal: |
J Biol Chem |
Title: |
Fancd2 is required for nuclear retention of Foxo3a in hematopoietic stem cell maintenance. |
Volume: |
290 |
Issue: |
5 |
Pages: |
2715-27 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ho GP |
Year: |
2006 |
Journal: |
Mol Cell Biol |
Title: |
Phosphorylation of FANCD2 on two novel sites is required for mitomycin C resistance. |
Volume: |
26 |
Issue: |
18 |
Pages: |
7005-15 |
|
•
•
•
•
•
|
Publication |
First Author: |
Reliene R |
Year: |
2010 |
Journal: |
Cancer Res |
Title: |
Genomic instability in mice is greater in Fanconi anemia caused by deficiency of Fancd2 than Fancg. |
Volume: |
70 |
Issue: |
23 |
Pages: |
9703-10 |
|
•
•
•
•
•
|
Publication |
First Author: |
van de Vrugt HJ |
Year: |
2009 |
Journal: |
Cancer Res |
Title: |
Embryonic lethality after combined inactivation of Fancd2 and Mlh1 in mice. |
Volume: |
69 |
Issue: |
24 |
Pages: |
9431-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu L |
Year: |
2021 |
Journal: |
Br J Haematol |
Title: |
FANCD2 and HES1 suppress inflammation-induced PPARÉ£ to prevent haematopoietic stem cell exhaustion. |
Volume: |
192 |
Issue: |
3 |
Pages: |
652-663 |
|
•
•
•
•
•
|
Publication |
First Author: |
Langevin F |
Year: |
2011 |
Journal: |
Nature |
Title: |
Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice. |
Volume: |
475 |
Issue: |
7354 |
Pages: |
53-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhao S |
Year: |
2023 |
Journal: |
J Biol Chem |
Title: |
DNA repair protein FANCD2 has both ubiquitination-dependent and ubiquitination-independent functions during germ cell development. |
Volume: |
299 |
Issue: |
3 |
Pages: |
102905 |
|
•
•
•
•
•
|
Publication |
First Author: |
Li X |
Year: |
2014 |
Journal: |
Antioxid Redox Signal |
Title: |
Concomitant inactivation of foxo3a and fancc or fancd2 reveals a two-tier protection from oxidative stress-induced hydrocephalus. |
Volume: |
21 |
Issue: |
12 |
Pages: |
1675-92 |
|
•
•
•
•
•
|
Publication |
First Author: |
Balcerek J |
Year: |
2018 |
Journal: |
Nat Commun |
Title: |
Lnk/Sh2b3 deficiency restores hematopoietic stem cell function and genome integrity in Fancd2 deficient Fanconi anemia. |
Volume: |
9 |
Issue: |
1 |
Pages: |
3915 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang J |
Year: |
2010 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
CCAAT/enhancer binding protein delta (C/EBPdelta, CEBPD)-mediated nuclear import of FANCD2 by IPO4 augments cellular response to DNA damage. |
Volume: |
107 |
Issue: |
37 |
Pages: |
16131-6 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
178
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
178
 |
Fragment?: |
false |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:7544970 |
Assay Type: |
Immunohistochemistry |
Annotation Date: |
2023-11-01 |
Strength: |
Present |
Sex: |
Female |
Emaps: |
EMAPS:1657819 |
Pattern: |
Not Specified |
Stage: |
TS19 |
Assay Id: |
MGI:7545022 |
Age: |
embryonic day 11.5 |
|
Note: |
The proportion of Fancd2 positive cells was significantly decreased compared with the wild-type (quantified in Fig 7B). |
Specimen Label: |
7A E11.5 -/- |
Detected: |
true |
Specimen Num: |
2 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:7544970 |
Assay Type: |
Immunohistochemistry |
Annotation Date: |
2023-11-01 |
Strength: |
Present |
Sex: |
Female |
Emaps: |
EMAPS:1657820 |
Pattern: |
Not Specified |
Stage: |
TS20 |
Assay Id: |
MGI:7545022 |
Age: |
embryonic day 12.5 |
|
Note: |
The proportion of Fancd2 positive cells was significantly decreased compared with the wild-type (quantified in Fig 7B). |
Specimen Label: |
7A E12.5 -/- |
Detected: |
true |
Specimen Num: |
4 |
|
•
•
•
•
•
|
Gene |
Type: |
gene |
Organism: |
human |
|
•
•
•
•
•
|
Publication |
First Author: |
GarcÃa-Rubio ML |
Year: |
2015 |
Journal: |
PLoS Genet |
Title: |
The Fanconi Anemia Pathway Protects Genome Integrity from R-loops. |
Volume: |
11 |
Issue: |
11 |
Pages: |
e1005674 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kim JM |
Year: |
2009 |
Journal: |
Dev Cell |
Title: |
Inactivation of murine Usp1 results in genomic instability and a Fanconi anemia phenotype. |
Volume: |
16 |
Issue: |
2 |
Pages: |
314-20 |
|
•
•
•
•
•
|
Publication |
First Author: |
Moore ES |
Year: |
2019 |
Journal: |
J Biol Chem |
Title: |
Sex-specific hepatic lipid and bile acid metabolism alterations in Fancd2-deficient mice following dietary challenge. |
Volume: |
294 |
Issue: |
43 |
Pages: |
15623-15637 |
|
•
•
•
•
•
|
Publication |
First Author: |
Park JW |
Year: |
2010 |
Journal: |
Cancer Res |
Title: |
Deficiencies in the Fanconi anemia DNA damage response pathway increase sensitivity to HPV-associated head and neck cancer. |
Volume: |
70 |
Issue: |
23 |
Pages: |
9959-68 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sabol M |
Year: |
2020 |
Journal: |
DNA Repair (Amst) |
Title: |
Novel TALEN-generated mCitrine-FANCD2 fusion reporter mouse model for in vivo research of DNA damage response. |
Volume: |
94 |
|
Pages: |
102936 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhang QS |
Year: |
2010 |
Journal: |
Blood |
Title: |
Fancd2-/- mice have hematopoietic defects that can be partially corrected by resveratrol. |
Volume: |
116 |
Issue: |
24 |
Pages: |
5140-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Houghtaling S |
Year: |
2003 |
Journal: |
Genes Dev |
Title: |
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice. |
Volume: |
17 |
Issue: |
16 |
Pages: |
2021-35 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kim M |
Year: |
2016 |
Journal: |
FEBS Lett |
Title: |
The role of USP1 autocleavage in DNA interstrand crosslink repair. |
Volume: |
590 |
Issue: |
3 |
Pages: |
340-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hemphill AW |
Year: |
2008 |
Journal: |
Mol Genet Metab |
Title: |
Mammalian SNM1 is required for genome stability. |
Volume: |
94 |
Issue: |
1 |
Pages: |
38-45 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jiang Q |
Year: |
2015 |
Journal: |
Genes Dev |
Title: |
MERIT40 cooperates with BRCA2 to resolve DNA interstrand cross-links. |
Volume: |
29 |
Issue: |
18 |
Pages: |
1955-68 |
|
•
•
•
•
•
|
Publication |
First Author: |
Houghtaling S |
Year: |
2005 |
Journal: |
Cancer Res |
Title: |
Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice. |
Volume: |
65 |
Issue: |
1 |
Pages: |
85-91 |
|
•
•
•
•
•
|
Publication |
First Author: |
Vinciguerra P |
Year: |
2010 |
Journal: |
J Clin Invest |
Title: |
Cytokinesis failure occurs in Fanconi anemia pathway-deficient murine and human bone marrow hematopoietic cells. |
Volume: |
120 |
Issue: |
11 |
Pages: |
3834-42 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bunting SF |
Year: |
2012 |
Journal: |
Mol Cell |
Title: |
BRCA1 functions independently of homologous recombination in DNA interstrand crosslink repair. |
Volume: |
46 |
Issue: |
2 |
Pages: |
125-35 |
|
•
•
•
•
•
|
Publication |
First Author: |
Dubois EL |
Year: |
2019 |
Journal: |
Nucleic Acids Res |
Title: |
A Fanci knockout mouse model reveals common and distinct functions for FANCI and FANCD2. |
Volume: |
47 |
Issue: |
14 |
Pages: |
7532-7547 |
|
•
•
•
•
•
|
Publication |
First Author: |
Park JW |
Year: |
2013 |
Journal: |
PLoS One |
Title: |
High incidence of HPV-associated head and neck cancers in FA deficient mice is associated with E7's induction of DNA damage through its inactivation of pocket proteins. |
Volume: |
8 |
Issue: |
9 |
Pages: |
e75056 |
|
•
•
•
•
•
|
Publication |
First Author: |
Park E |
Year: |
2013 |
Journal: |
Mol Cell Biol |
Title: |
Inactivation of Uaf1 causes defective homologous recombination and early embryonic lethality in mice. |
Volume: |
33 |
Issue: |
22 |
Pages: |
4360-70 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chatla S |
Year: |
2019 |
Journal: |
Stem Cell Res |
Title: |
Fancd2-deficient hematopoietic stem and progenitor cells depend on augmented mitochondrial translation for survival and proliferation. |
Volume: |
40 |
|
Pages: |
101550 |
|
•
•
•
•
•
|
Publication |
First Author: |
Alavattam KG |
Year: |
2016 |
Journal: |
Cell Rep |
Title: |
Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications. |
Volume: |
17 |
Issue: |
4 |
Pages: |
1141-1157 |
|
•
•
•
•
•
|
Publication |
First Author: |
Jamsai D |
Year: |
2013 |
Journal: |
PLoS One |
Title: |
Loss of GGN leads to pre-implantation embryonic lethality and compromised male meiotic DNA double strand break repair in the mouse. |
Volume: |
8 |
Issue: |
2 |
Pages: |
e56955 |
|
•
•
•
•
•
|
Publication |
First Author: |
Freie BW |
Year: |
2004 |
Journal: |
J Biol Chem |
Title: |
A role for the Fanconi anemia C protein in maintaining the DNA damage-induced G2 checkpoint. |
Volume: |
279 |
Issue: |
49 |
Pages: |
50986-93 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wong JC |
Year: |
2003 |
Journal: |
Hum Mol Genet |
Title: |
Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. |
Volume: |
12 |
Issue: |
16 |
Pages: |
2063-76 |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus caroli |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
mouse, laboratory |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus pahari |
|
•
•
•
•
•
|
Protein Coding Gene |
Type: |
protein_coding_gene |
Organism: |
Mus spretus |
|
•
•
•
•
•
|
Publication |
First Author: |
Sczelecki S |
Year: |
2023 |
Journal: |
Cancers (Basel) |
Title: |
The Validation of a Precursor Lesion of Epithelial Ovarian Cancer in Fancd2-KO Mice. |
Volume: |
15 |
Issue: |
9 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Ruiz-Torres S |
Year: |
2021 |
Journal: |
Cell Stem Cell |
Title: |
Inherited DNA Repair Defects Disrupt the Structure and Function of Human Skin. |
Volume: |
28 |
Issue: |
3 |
Pages: |
424-435.e6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhang X |
Year: |
2016 |
Journal: |
Oncotarget |
Title: |
Evolution of malignant plasmacytoma cell lines from K14E7 Fancd2-/- mouse long-term bone marrow cultures. |
Volume: |
7 |
Issue: |
42 |
Pages: |
68449-68472 |
|
•
•
•
•
•
|
GXD Expression |
Probe: |
MGI:6287134 |
Assay Type: |
RT-PCR |
Annotation Date: |
2019-04-12 |
Strength: |
Present |
Sex: |
Not Specified |
Emaps: |
EMAPS:160404 |
|
Stage: |
TS04 |
Assay Id: |
MGI:6287212 |
Age: |
embryonic day 3.0 |
Image: |
4 |
|
Specimen Label: |
fx/fx |
Detected: |
true |
Specimen Num: |
1 |
|
•
•
•
•
•
|