cervical vertebral transformation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description homeotic transformation of any cervical vertebrae to adopt the fate of another vertebrae (Mammalian Phenotype Ontology, MP_0004615)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004615
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Genes

37 gene mutations causing the cervical vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BTG2 BTG family, member 2
CDX1 caudal type homeobox 1
CDX2 caudal type homeobox 2
COMMD3-BMI1 COMMD3-BMI1 readthrough
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
E2F6 E2F transcription factor 6
FGFR1 fibroblast growth factor receptor 1
GDF11 growth differentiation factor 11
GSC goosecoid homeobox
HOXA4 homeobox A4
HOXA5 homeobox A5
HOXB2 homeobox B2
HOXB4 homeobox B4
HOXB5 homeobox B5
HOXB6 homeobox B6
HOXB8 homeobox B8
HOXC8 homeobox C8
HOXD4 homeobox D4
KMT2A lysine (K)-specific methyltransferase 2A
MLLT3 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
MTF2 metal response element binding transcription factor 2
PCGF2 polycomb group ring finger 2
PDS5A PDS5 cohesin associated factor A
PGAP1 post-GPI attachment to proteins 1
PHC1 polyhomeotic homolog 1 (Drosophila)
PHC2 polyhomeotic homolog 2 (Drosophila)
PSIP1 PC4 and SFRS1 interacting protein 1
RARA retinoic acid receptor, alpha
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma
RNF2 ring finger protein 2
RPS7 ribosomal protein S7
SCMH1 sex comb on midleg homolog 1 (Drosophila)
SF3B1 splicing factor 3b, subunit 1, 155kDa
SUZ12 SUZ12 polycomb repressive complex 2 subunit
TASP1 taspase, threonine aspartase, 1
WNT3A wingless-type MMTV integration site family, member 3A