Research
Search
Genes / Clones
Expression
Mutants / Tg
Antibodies
Anatomy / GO / Human Disease / Chemical
Publications
Data Mining
Downloads
Data Model
AllianceMine
BioMart
Genomics
BLAST
ZFIN
Ensembl
NCBI
UCSC
Genome Browsers
ZFIN
Ensembl
Vega
GRC
UCSC
NCBI
Resources
Zebrafish Genomics
Other Genome Databases
Resources
General
The Zebrafish Book
Protocol Wiki
Antibody Wiki
Anatomy Atlases
Resources for Students and Educators
Zebrafish Programs
ZF-Health
Husbandry Resources
More...
Resource Centers
Zebrafish International Resource Center (ZIRC)
China Zebrafish Resource Center (CZRC)
European Zebrafish Resource Center (EZRC)
Community
Announcements
News
Meetings
Jobs
Alliance Community Forum
Search
People
Labs
Companies
Societies
International Zebrafish Society (IZFS)
Zebrafish Disease Models Society (ZDMS)
Genetics Society of America (GSA)
Zebrafish Husbandry Association
Support
Nomenclature
Nomenclature Conventions
Line Designations
Wild-Type Lines
Submit a Proposed Gene Name
Submit a Proposed Mutant/Tg Line Name
Publications
Guidelines for Authors
Zebrashare
Citing ZFIN
Using ZFIN
Help & Tips
Glossary
Single Box Search Help
Submit Data
Terms of Use
About Us
About ZFIN
Contact Information
Statistics
Committees
Jobs at ZFIN
Sign In
Phenotype Figure Summary
Marker:
psenen
Conditions:
Standard or Control
Publication
Data
Fish
Anatomy
Ralser
et al.
, 2017
Fig. 3
WT + MO1-psenen
caudal fin increased pigmentation, abnormal
head decreased pigmentation, abnormal
melanocyte migration disrupted, abnormal
pigment cell decreased amount, abnormal
pigment cell morphology, abnormal
pigmentation process quality, abnormal
Fig. S6
WT + MO2-psenen
caudal fin increased pigmentation, abnormal
head decreased pigmentation, abnormal
pigment cell decreased amount, abnormal
pigmentation process quality, abnormal
Campbell
et al.
, 2006
Fig. 3
WT + MO1-psenen
head cell death increased occurrence, abnormal
head decreased size, abnormal
midbrain hindbrain boundary absent, abnormal
post-vent region decreased length, abnormal
primary motor neuron irregular spatial pattern, abnormal
spinal cord has fewer parts of type primary motor neuron, abnormal
whole organism decreased size, abnormal
Fig. 4
WT + MO1-psenen
Notch signaling pathway decreased occurrence, abnormal
presumptive neural retina molecular quality, abnormal
Fig. 5
WT + MO1-psenen
somite border amorphous, abnormal
somite shape, abnormal
somitogenesis disrupted, abnormal
Fig. 7
WT + MO1-psenen
head apoptotic process increased occurrence, abnormal
trunk apoptotic process increased occurrence, abnormal
Fig. 8
WT + MO1-psenen + MO4-tp53
, 
WT + MO1-psenen
head apoptotic process increased occurrence, abnormal
midbrain hindbrain boundary absent, abnormal
whole organism decreased size, abnormal
Fig. 9
WT + MO1-psenen + MO4-tp53
, 
WT + MO1-psenen
brain lacks parts or has fewer parts of type ventricular system, abnormal
brain primary motor neuron decreased amount, abnormal
brain primary motor neuron spatial pattern, abnormal
Rohon-Beard neuron decreased amount, abnormal
spinal cord primary motor neuron decreased amount, abnormal
spinal cord primary motor neuron spatial pattern, abnormal
Your Input Welcome
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Name:
Institution:
Email address:
Please leave blank:
Subject:
Comments:
Send your comments
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.