Symbol Name ID |
Smarcb1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 MGI:1328366 |
Darker colors indicate more annotations |
Human Phenotypes | Sparse scalp hair |
Thick eyebrow |
Long eyelashes |
Hirsutism |
Hypertrichosis |
Axillary freckling |
Inguinal freckling |
Hyperpigmentation of the skin |
Cafe-au-lait spot |
Neoplasm of the skin |
Neurofibroma |
Peripheral schwannoma |
Disease(s) Associated with SMARCB1 | ||||||||||||
Coffin-Siris syndrome 3 | ||||||||||||
schwannomatosis | ||||||||||||
schwannomatosis 1 | ||||||||||||
vestibular schwannomatosis |
Mouse Phenotypes | abnormal coat appearance |
abnormal skin coloration |
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Availability | Mouse Genotype | ||
Smarcb1tm1b(EUCOMM)Hmgu/Smarcb1+ |
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 04/09/2024 MGI 6.23 |
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