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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Pkdcc
protein kinase domain containing, cytoplasmic
MGI:2147077
67 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Pkdccem1(IMPC)Mbp/Pkdcc+
C57BL/6N-Pkdccem1(IMPC)Mbp/MbpMmucd 		abnormal kidney morphology J:211773
abnormal liver morphology J:211773
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
no spontaneous movement J:211773
small kidney J:211773
small liver J:211773
Pkdccem1(IMPC)Mbp/Pkdccem1(IMPC)Mbp
C57BL/6N-Pkdccem1(IMPC)Mbp/MbpMmucd 		abnormal craniofacial morphology J:211773
abnormal facial morphology J:211773
abnormal head shape J:211773
abnormal heart morphology J:211773
abnormal hindbrain development J:211773
abnormal neural tube morphology J:211773
abnormal pericardium morphology J:211773
abnormal placenta morphology J:211773
abnormal placenta vasculature J:211773
edema J:211773
embryonic growth retardation J:211773
no spontaneous movement J:211773
preweaning lethality, complete penetrance J:211773
Pkdcctm1.1Mask/Pkdcctm1.1Mask
involves: C57BL/6 * CBA * FVB/N 		abnormal craniofacial bone morphology J:158147
abnormal craniofacial morphology J:158147
abnormal limb morphology J:158147
abnormal long bone morphology J:158147
abnormal lung morphology J:158147
abnormal nasal capsule morphology J:158147
abnormal palatal shelf elevation J:158147
abnormal pulmonary alveolus morphology J:158147
absent gastric milk in neonates J:158147
cleft palate J:158147
cyanosis J:158147
decreased birth body size J:158147
delayed bone ossification J:158147
delayed chondrocyte differentiation J:158147
impaired lung alveolus development J:158147
increased diameter of humerus J:158147
increased diameter of radius J:158147
increased diameter of ulna J:158147
neonatal lethality, complete penetrance J:158147
respiratory failure J:158147
short humerus J:158147
short limbs J:158147
short maxilla J:158147
short radius J:158147
short ulna J:158147
small maxilla J:158147
thick pulmonary interalveolar septum J:158147
Pkdcctm1.2Azun/Pkdcctm1.2Azun
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal cartilage development J:199462
cleft secondary palate J:199462
decreased birth body size J:199462
decreased length of long bones J:199462
delayed endochondral bone ossification J:199462
neonatal lethality, complete penetrance J:199462
respiratory failure J:199462
short humerus J:199462
short tibia J:199462
Pkdcctm1Belo/Pkdcctm1Belo
involves: C57BL/6 		abnormal bone mineralization J:173403
abnormal hindlimb morphology J:173403
decreased birth body size J:173403
short limbs J:173403
short radius J:173403
short tibia J:173403
short ulna J:173403
Pkdcctm1Hssk/Pkdcc+
involves: C57BL/6 * CBA 		no abnormal phenotype detected J:140470
Pkdcctm1Hssk/Pkdcctm1Hssk
involves: C57BL/6 * CBA 		abnormal bone mineralization J:140470
abnormal caudal vertebrae morphology J:140470
abnormal cervical atlas morphology J:140470
abnormal cervical axis morphology J:140470
abnormal cervical vertebrae morphology J:140470
abnormal intestine morphology J:140470
abnormal long bone hypertrophic chondrocyte zone J:140470
abnormal maxilla morphology J:140470
abnormal palatine bone morphology J:140470
abnormal sternum morphology J:140470
abnormal xiphoid process morphology J:140470
basisphenoid bone foramen J:140470
bowed tibia J:140470
cleft secondary palate J:140470
cyanosis J:140470
decreased birth body size J:140470
decreased birth weight J:140470
decreased length of long bones J:140470
decreased pulmonary ventilation J:140470
normal embryo phenotype J:140470
median cleft palate J:140470
neonatal lethality, complete penetrance J:140470
short limbs J:140470
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory