Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Phenotypes:
Affected Systems
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behavior/neurological
N
behavior/neurological phenotype
N
cellular
increased renal tubule apoptosis
craniofacial
abnormal periodontal ligament morphology
periodontal ligament hypercellularity
digestive/alimentary system
salivary gland epithelial hyperplasia
abnormal stomach mucosa morphology
endocrine/exocrine glands
salivary gland epithelial hyperplasia
enlarged thymus
thymus hyperplasia
increased T cell derived lymphoma incidence
growth/size/body
abnormal periodontal ligament morphology
periodontal ligament hypercellularity
decreased body weight
hematopoietic system
N
hematopoietic system phenotype
N
enlarged thymus
thymus hyperplasia
increased T cell derived lymphoma incidence
homeostasis/metabolism
N
homeostasis/metabolism phenotype
N
immune system
immune system phenotype
N
enlarged thymus
thymus hyperplasia
increased T cell derived lymphoma incidence
abnormal humoral immune response
tubular nephritis
decreased susceptibility to bacterial infection
integument
thin hypodermis
abnormal cutaneous collagen fibril morphology
thin dermal layer
loose skin
thin skin
decreased skin tensile strength
mortality/aging
premature death
decreased tumor-free survival time
perinatal lethality
muscle
abnormal tendon morphology
neoplasm
N
neoplasm
N
increased tumor incidence
increased T cell derived lymphoma incidence
increased hemangiosarcoma incidence
renal/urinary system
increased renal tubule apoptosis
tubular nephritis
increased glomerular capsule space
abnormal renal tubule epithelium morphology
renal interstitial fibrosis
hydronephrosis
kidney atrophy
renal tubule atrophy
dilated renal tubule
reproductive system
short gestation period
delayed parturition
early parturition
reduced female fertility
decreased litter size
male infertility
respiratory system
respiratory distress
skeleton
skeleton phenotype
N
abnormal periodontal ligament morphology
periodontal ligament hypercellularity
abnormal tendon morphology
decreased length of long bones
increased diameter of long bones
abnormal bone structure
abnormal bone collagen fibril morphology
decreased bone mineral density
decreased compact bone mass
decreased trabecular bone mass
vision/eye
N
vision/eye phenotype
N