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XB-GENEPAGE-483454
bmpr1b bone morphogenetic protein receptor type 1B
Anatomical Phenotypes
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increased pigmentation in the head (4 sources), abnormally incomplete structure of head (3 sources), decreased pigmentation in the eye (3 sources), abnormal branchial arch morphology (2 sources), abnormal cartilage element morphology (2 sources), abnormal ceratohyal morphology (2 sources), abnormal ventral tail fin morphology (2 sources), abnormally localised dorsal fin (2 sources), abnormally localised melanophore in dorsal fin (2 sources), absent branchial arch (2 sources), absent cartilage element in the branchial arch (2 sources), absent ceratohyal (2 sources), absent intercanthal region (2 sources), decreased size of the branchial arch (2 sources), decreased width of the cartilage element in head (2 sources), decreased width of the head (2 sources), abnormal cell migration in neural crest (1 source), wholly anteriorized tadpole (1 source), wholly dorsalized embryo (1 source) |
Expression Phenotypes
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Manual annotations: bmpr1b manipulated (5 sources) |
Computed annotations: bmpr1b assayed (9 sources) |
Experiments (Reagents)
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Xla Wt + bmpr1b MO (7 sources), Xla Wt + bmpr1b MO (4 sources), Xla Wt + bmpr1b MO (2 sources), Xla Wt + bmpr1a MO + bmpr1b MO (1 source), Xla Wt + bmpr1b MO (1 source) |
Monarch Ortholog Phenotypes
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Human (90 sources): 2-3 toe syndactyly, Abnormal epiphysis morphology, Abnormal hip bone morphology, Abnormal thumb morphology, Abnormality of the radius, Abnormality of the ulna, Abnormality of tibia morphology, Acromesomelia, Aplasia of the middle phalanges of the toes, Aplasia of the proximal phalanges of the hand, [+] |
Mouse (19 sources): abnormal axon guidance, abnormal cartilage development, abnormal chondrocyte differentiation, abnormal digit development, abnormal endometrial gland development, abnormal metacarpal bone morphology, abnormal phalanx morphology, abnormal retina ganglion cell morphology, absent cumulus expansion, absent endometrial glands, [+] |
View all ortholog results at Monarch |