55 phenotypes from 2 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Prlrtm1.1Skkm/Prlrtm1.1Skkm Tg(Ins2-cre)23Herr/0 involves: C57BL/6J * CBA/J	normal endocrine/exocrine gland phenotype	J:284574
	normal homeostasis/metabolism phenotype	J:284574
Prlrtm1Cnp/Prlr+ B6.129P2-Prlrtm1Cnp/J	abnormal neuron proliferation	J:83248
Prlrtm1Cnp/Prlr+ either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	abnormal lactation	J:38093
	abnormal mammary gland development	J:38093
	abnormal maternal nurturing	J:38093
	abnormal pup retrieval	J:38093
Prlrtm1Cnp/Prlr+ involves: 129P2/OlaHsd	abnormal hair cycle	J:70207
	abnormal maternal behavior	J:83247
	abnormal pup retrieval	J:83247
	normal behavior/neurological phenotype	J:83247
	normal taste/olfaction phenotype	J:83247
Prlrtm1Cnp/Prlr+ involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	abnormal mammary gland development	J:70408
Prlrtm1Cnp/Prlrtm1Cnp either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	abnormal decidualization	J:38093
	abnormal oogenesis	J:38093
	abnormal oviduct environment	J:38093
	abnormal reproductive system physiology	J:38093
	abnormal sexual interaction	J:38093
	abnormal uterine environment	J:38093
	decreased ovulation rate	J:38093
	decreased primary ovarian follicle number	J:38093
	female infertility	J:38093
	male infertility	J:38093
	reduced male fertility	J:38093
Prlrtm1Cnp/Prlrtm1Cnp involves: 129/Sv * 129P2/OlaHsd	abnormal thyroid gland morphology	J:101609
	decreased body temperature	J:101609
	decreased thyroxine level	J:101609
	normal homeostasis/metabolism phenotype	J:85593
	increased thyroid carcinoma incidence	J:101609
	normal reproductive system phenotype	J:85593
Prlrtm1Cnp/Prlrtm1Cnp involves: 129/Sv * 129P2/OlaHsd * C57BL/6	abnormal bone mineralization	J:52026
	abnormal bone ossification	J:52026
	abnormal circulating calcium level	J:52026
	decreased bone mass	J:52026
	decreased circulating estradiol level	J:52026
	decreased circulating progesterone level	J:52026
	delayed bone ossification	J:52026
	increased circulating parathyroid hormone level	J:52026
	increased circulating prolactin level	J:52026
Prlrtm1Cnp/Prlrtm1Cnp involves: 129P2/OlaHsd	abnormal coat/ hair morphology	J:70207
	abnormal hair cycle	J:70207
	abnormal maternal behavior	J:83247
	abnormal pup retrieval	J:83247
	normal behavior/neurological phenotype	J:83247
	coarse hair	J:70207
	decreased body weight	J:95779
	decreased bone mineral density	J:95779
	slow postnatal weight gain	J:95779
	normal taste/olfaction phenotype	J:83247
Prlrtm1Cnp/Prlrtm1Cnp involves: 129P2/OlaHsd * 129S2/SvPas	abnormal Harderian gland morphology	J:66544
	abnormal Harderian gland porphyrin secretion	J:66544
	abnormal lacrimal gland morphology	J:66544
	abnormal prostate gland epithelium morphology	J:84352
	increased prostate gland ventral lobe weight	J:84352
	increased seminal vesicle weight	J:84352
	male infertility	J:84352
	reduced male fertility	J:84352
	normal vision/eye phenotype	J:66544
Prlrtm1Cnp/Prlrtm1Cnp involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	abnormal pancreatic islet morphology	J:106829
	decreased abdominal fat pad weight	J:67354
	decreased body weight	J:67354
	decreased circulating leptin level	J:67354
	decreased insulin secretion	J:106829
	decreased pancreatic beta cell mass	J:106829
	impaired glucose tolerance	J:106829
	slow postnatal weight gain	J:67354
	small pancreatic islets	J:106829