abnormal tail pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the coloration of the tail due to changes in the amount, shape, or distribution of cells producing pigment (Mammalian Phenotype Ontology, MP_0005174)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005174
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Genes

27 gene mutations causing the abnormal tail pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AEBP2 AE binding protein 2
AP3B1 adaptor-related protein complex 3, beta 1 subunit
BLOC1S3 biogenesis of lysosomal organelles complex-1, subunit 3
CBL Cbl proto-oncogene, E3 ubiquitin protein ligase
DOCK7 dedicator of cytokinesis 7
EDNRB endothelin receptor type B
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
HPS1 Hermansky-Pudlak syndrome 1
HPS5 Hermansky-Pudlak syndrome 5
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
KRT2 keratin 2, type II
LYST lysosomal trafficking regulator
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
MCOLN3 mucolipin 3
MITF microphthalmia-associated transcription factor
MYO10 myosin X
MYO5A myosin VA (heavy chain 12, myoxin)
OCA2 oculocutaneous albinism II
PAX3 paired box 3
RECQL4 RecQ protein-like 4
RPL27A ribosomal protein L27a
RPS19 ribosomal protein S19
SOX10 SRY (sex determining region Y)-box 10
TP53 tumor protein p53
TTC7A tetratricopeptide repeat domain 7A