lumbar vertebral transformation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description homeotic transformation of any lumbar vertebrae to adopt the fate of another vertebrae (Mammalian Phenotype Ontology, MP_0004616)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004616
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Genes

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

Symbol Name
ACVR2B activin A receptor, type IIB
ASXL2 additional sex combs like transcriptional regulator 2
CBX5 chromobox homolog 5
COMMD3-BMI1 COMMD3-BMI1 readthrough
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
E2F6 E2F transcription factor 6
ESCO1 establishment of sister chromatid cohesion N-acetyltransferase 1
FGFR1 fibroblast growth factor receptor 1
GDF11 growth differentiation factor 11
HOXA10 homeobox A10
HOXA5 homeobox A5
HOXA9 homeobox A9
HOXC10 homeobox C10
HOXC8 homeobox C8
HOXC9 homeobox C9
HOXD8 homeobox D8
HOXD9 homeobox D9
KAT2A K(lysine) acetyltransferase 2A
KMT2A lysine (K)-specific methyltransferase 2A
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
PGAP1 post-GPI attachment to proteins 1
PHC1 polyhomeotic homolog 1 (Drosophila)
PHC2 polyhomeotic homolog 2 (Drosophila)
PNN pinin, desmosome associated protein
PSIP1 PC4 and SFRS1 interacting protein 1
RARA retinoic acid receptor, alpha
RPL38 ribosomal protein L38
RPS7 ribosomal protein S7
SF3B1 splicing factor 3b, subunit 1, 155kDa
SLC44A5 solute carrier family 44, member 5
SUZ12 SUZ12 polycomb repressive complex 2 subunit
TAPT1 transmembrane anterior posterior transformation 1
TASP1 taspase, threonine aspartase, 1
TERT telomerase reverse transcriptase
WNT3A wingless-type MMTV integration site family, member 3A
ZBTB16 zinc finger and BTB domain containing 16