abnormal cervical atlas morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the first (topmost, C1) cervical vertebra which supports the globe of the head (Mammalian Phenotype Ontology, MP_0004607)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004607
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41 gene mutations causing the abnormal cervical atlas morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CBX2 chromobox homolog 2
CDX1 caudal type homeobox 1
CHRD chordin
CTGF connective tissue growth factor
FGFR1 fibroblast growth factor receptor 1
FGFRL1 fibroblast growth factor receptor-like 1
FOXC1 forkhead box C1
FSTL1 follistatin-like 1
HOXB2 homeobox B2
HOXB3 homeobox B3
HOXD1 homeobox D1
HOXD3 homeobox D3
HOXD4 homeobox D4
HYAL2 hyaluronoglucosaminidase 2
KAT6A K(lysine) acetyltransferase 6A
KMT2A lysine (K)-specific methyltransferase 2A
MBTD1 mbt domain containing 1
MLLT3 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3
NKX3-2 NK3 homeobox 2
NPR2 natriuretic peptide receptor 2
PAX1 paired box 1
PDS5A PDS5 cohesin associated factor A
PHC2 polyhomeotic homolog 2 (Drosophila)
PKDCC protein kinase domain containing, cytoplasmic
PSIP1 PC4 and SFRS1 interacting protein 1
RAI1 retinoic acid induced 1
RARA retinoic acid receptor, alpha
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma
RING1 ring finger protein 1
RPL38 ribosomal protein L38
SHH sonic hedgehog
SKI SKI proto-oncogene
SP3 Sp3 transcription factor
T T, brachyury homolog (mouse)
TASP1 taspase, threonine aspartase, 1
TBX1 T-box 1
TBX15 T-box 15
TBX6 T-box 6
TSHZ1 teashirt zinc finger homeobox 1
WNT9A wingless-type MMTV integration site family, member 9A