Chst14 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Chst14
carbohydrate sulfotransferase 14
MGI:1919386

41 phenotypes from 5 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Chst14^em1(IMPC)Tcp/Chst14⁺ C57BL/6NCrl-Chst14^em1(IMPC)Tcp/Tcp	decreased exploration in new environment	J:211773
Chst14^em1(IMPC)Tcp/Chst14^em1(IMPC)Tcp C57BL/6NCrl-Chst14^em1(IMPC)Tcp/Tcp	preweaning lethality, complete penetrance	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Chst14^em1Taok/Chst14^em1Taok Not Specified	abnormal dermal layer morphology	J:328985
	abnormal glycosaminoglycan level	J:328985
	abnormal skeletal muscle fiber morphology	J:328985
	decreased grip strength	J:328985
	decreased skeletal muscle fiber diameter	J:328985
	decreased skin tensile strength	J:328985
	kyphosis	J:328985
	postnatal growth retardation	J:328985
	prenatal lethality, incomplete penetrance	J:328985
	thin skin	J:328985
Chst14^em2Taok/Chst14^em2Taok involves: C3H/He * C57BL/6J	abnormal dermal layer morphology	J:328985
	abnormal skeletal muscle fiber morphology	J:328985
	abnormal skeletal muscle fiber type ratio	J:328985
	abnormal urine glycosaminoglycan level	J:328985
	decreased aerobic running capacity	J:328985
	decreased grip strength	J:328985
	decreased skeletal muscle fiber diameter	J:328985
	decreased skeletal muscle mass	J:328985
	decreased skin tensile strength	J:328985
	kyphosis	J:328985
Chst14^tm1.1Msch/Chst14^tm1.1Msch B6.129-Chst14^tm1.1Msch	perinatal lethality, complete penetrance	J:203583
Chst14^tm1.1Msch/Chst14^tm1.1Msch involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal axon extension	J:203583
	abnormal fertility/fecundity	J:203583
	abnormal neurite morphology	J:203583
	abnormal response to injury	J:203583
	abnormal Schwann cell morphology	J:203583
	abnormal tibia morphology	J:203583
	abnormal tooth development	J:203583
	decreased birth weight	J:203583
	decreased body weight	J:203583
	decreased heart weight	J:203583
	decreased kidney weight	J:203583
	decreased liver weight	J:203583
	decreased skin tensile strength	J:203583
	increased Schwann cell proliferation	J:203583
	kinked tail	J:203583
	lethality throughout fetal growth and development, incomplete penetrance	J:203583
	normal nervous system phenotype	J:203583
	postnatal lethality, incomplete penetrance	J:203583
Chst14^tm1Lex/Chst14^tm1Lex B6;129S5-Chst14^tm1Lex/Mmucd	abnormal muscle morphology	J:328985
	abnormal skeletal muscle fiber morphology	J:328985
	abnormal urine glycosaminoglycan level	J:328985
	decreased aerobic running capacity	J:328985
	decreased anxiety-related response	J:171883
	decreased body length	J:171883
	decreased grip strength	J:328985
	decreased skeletal muscle fiber diameter	J:328985
	decreased skeletal muscle mass	J:328985
	enhanced sensorimotor gating	J:171883
	normal homeostasis/metabolism phenotype	J:328985
	kyphosis	J:328985
	perinatal lethality, incomplete penetrance	J:328985
	postnatal growth retardation	J:328985

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 06/09/2026 MGI 6.24