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Symbol
Name
ID
Chd7
chromodomain helicase DNA binding protein 7
MGI:2444748
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Feeding difficulties in infancy
Autism
Compulsive behaviors
Attention deficit hyperactivity disorder
Self-mutilation
Disease(s) Associated with CHD7
CHARGE syndrome

Mouse Phenotypes
behavior/neurological phenotype
abnormal behavior
abnormal suckling behavior
abnormal response to stress-induced hyperthermia
abnormal motor capabilities/coordination/movement
impaired righting response
decreased startle reflex
abnormal motor coordination/balance
abnormal placing response
impaired coordination
impaired swimming
decreased grip strength
trunk curl
abnormal stationary movement
head bobbing
head shaking
head tilt
head tossing
increased locomotor activity
hyperactivity
circling
bidirectional circling
increased thermal nociceptive threshold
abnormal maternal nurturing
behavioral developmental delay
Availability Mouse Genotype
Chd7tm1.2Dmm/Chd7tm1.2Dmm
Chd7Coa1/Chd7+
Chd7Cycn/Chd7+
Chd7Dz/Chd7+
Chd7Edy/Chd7+
Chd7Flo/Chd7+
Chd7Gt(RRR136)Byg/Chd7+
Chd7Gt(S20-7E1)Sor/Chd7+
Chd7Gt(XK403)Byg/Chd7+
Chd7Lda/Chd7+
Chd7Looper/Chd7+
Chd7Mt/Chd7+
Chd7Obt/Chd7+
Chd7Ome/Chd7+
Chd7tm2a(EUCOMM)Wtsi/Chd7+ *
Chd7Todo/Chd7+
Chd7Trooper/Chd7+
Chd7Whi/Chd7+
Chd7tm2c(EUCOMM)Wtsi/Chd7tm2c(EUCOMM)Wtsi
Tg(Atoh1-cre)1Bfri/0  (conditional)
*
Chd7Gt(S20-7E1)Sor/Chd7tm1.1Dmm
Foxg1tm1(cre)Skm/Foxg1+  (conditional)

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory