vertebral transformation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description homeotic transformation of a specific vertebrae to adopt the fate of another (Mammalian Phenotype Ontology, MP_0003036)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003036
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Genes

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

Symbol Name
ACVR2B activin A receptor, type IIB
ARL4D ADP-ribosylation factor-like 4D
ARPC2 actin related protein 2/3 complex, subunit 2, 34kDa
ASXL1 additional sex combs like transcriptional regulator 1
ASXL2 additional sex combs like transcriptional regulator 2
BMPER BMP binding endothelial regulator
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
BRDT bromodomain, testis-specific
BTG2 BTG family, member 2
CBX2 chromobox homolog 2
CBX5 chromobox homolog 5
CDX1 caudal type homeobox 1
CDX2 caudal type homeobox 2
CDX4 caudal type homeobox 4
CENPJ centromere protein J
COMMD3-BMI1 COMMD3-BMI1 readthrough
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
DSCC1 DNA replication and sister chromatid cohesion 1
DUSP4 dual specificity phosphatase 4
E2F6 E2F transcription factor 6
EFNA1 ephrin-A1
ESCO1 establishment of sister chromatid cohesion N-acetyltransferase 1
FGFR1 fibroblast growth factor receptor 1
GDF11 growth differentiation factor 11
GSC goosecoid homeobox
HOXA10 homeobox A10
HOXA11 homeobox A11
HOXA4 homeobox A4
HOXA5 homeobox A5
HOXA6 homeobox A6
HOXA9 homeobox A9
HOXB2 homeobox B2
HOXB4 homeobox B4
HOXB5 homeobox B5
HOXB6 homeobox B6
HOXB8 homeobox B8
HOXB9 homeobox B9
HOXC10 homeobox C10
HOXC13 homeobox C13
HOXC4 homeobox C4
HOXC6 homeobox C6
HOXC8 homeobox C8
HOXC9 homeobox C9
HOXD11 homeobox D11
HOXD4 homeobox D4
HOXD8 homeobox D8
HOXD9 homeobox D9
JMJD1C jumonji domain containing 1C
KAT2A K(lysine) acetyltransferase 2A
KAT6A K(lysine) acetyltransferase 6A
KMT2A lysine (K)-specific methyltransferase 2A
MLLT3 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
MTA1 metastasis associated 1
MTF2 metal response element binding transcription factor 2
NACC1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
NDRG2 NDRG family member 2
PCGF2 polycomb group ring finger 2
PDS5A PDS5 cohesin associated factor A
PEX3 peroxisomal biogenesis factor 3
PGAP1 post-GPI attachment to proteins 1
PHC1 polyhomeotic homolog 1 (Drosophila)
PHC2 polyhomeotic homolog 2 (Drosophila)
PNN pinin, desmosome associated protein
PPP5C protein phosphatase 5, catalytic subunit
PSIP1 PC4 and SFRS1 interacting protein 1
RARA retinoic acid receptor, alpha
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma
RING1 ring finger protein 1
RNF2 ring finger protein 2
RPL38 ribosomal protein L38
RPS7 ribosomal protein S7
SCMH1 sex comb on midleg homolog 1 (Drosophila)
SF3B1 splicing factor 3b, subunit 1, 155kDa
SKI SKI proto-oncogene
SLC44A5 solute carrier family 44, member 5
SUZ12 SUZ12 polycomb repressive complex 2 subunit
SYTL1 synaptotagmin-like 1
TAPT1 transmembrane anterior posterior transformation 1
TASP1 taspase, threonine aspartase, 1
TERT telomerase reverse transcriptase
TM9SF4 transmembrane 9 superfamily protein member 4
TSHZ1 teashirt zinc finger homeobox 1
UBA2 ubiquitin-like modifier activating enzyme 2
WFIKKN1 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
WNT3A wingless-type MMTV integration site family, member 3A
ZBTB16 zinc finger and BTB domain containing 16
ZC3HC1 zinc finger, C3HC-type containing 1
ZIC3 Zic family member 3