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Symbol
Name
ID
Ift140
intraflagellar transport 140
MGI:2146906
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Craniosynostosis
Scaphocephaly
Trigonocephaly
Micrognathia
Microcephaly
Prominent metopic ridge
Wide anterior fontanel
Short neck
Absent middle phalanx of 2nd finger
Clinodactyly of the 2nd finger
Absent middle phalanx of 5th finger
Clinodactyly of the 5th finger
Postaxial hand polydactyly
Cone-shaped epiphyses of the phalanges of the hand
Short middle phalanx of finger
Short phalanx of finger
Short toe
Hypoplasia of the capital femoral epiphysis
Short femoral neck
Short metatarsal
Broad metacarpals
Rhizomelia
Phalangeal cone-shaped epiphyses
Short ribs
Short thorax
Thoracic hypoplasia
Narrow chest
Osteopenia
Disease(s) Associated with IFT140
short-rib thoracic dysplasia 9 with or without polydactyly

Mouse Phenotypes
abnormal exoccipital bone morphology
fusion of atlas and occipital bones
absent alisphenoid bone
absent neurocranium
abnormal maxilla morphology
premaxilla hypoplasia
maxilla hypoplasia
absent palatine bone
absent facial bone
facial bone hypoplasia
abnormal costovertebral joint morphology
abnormal rib morphology
rib bifurcation
cervical vertebral fusion
exostosis
Availability Mouse Genotype
Ift140cauli/Ift140cauli

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
03/19/2024
MGI 6.23
The Jackson Laboratory