|Institutional Source||Beutler Lab|
|Gene Name||cadherin, EGF LAG seven-pass G-type receptor 3|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R1657 (G1)|
|Chromosomal Location||108826320-108852969 bp(+) (GRCm38)|
|Type of Mutation||nonsense|
|DNA Base Change (assembly)||T to A at 108842952 bp (GRCm38)|
|Amino Acid Change||Cysteine to Stop codon at position 2512 (C2512*)|
|Ref Sequence||ENSEMBL: ENSMUSP00000150759 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000024238] [ENSMUST00000194079] [ENSMUST00000213524]|
|AlphaFold||no structure available at present|
AA Change: C2505*
AA Change: C2505*
AA Change: C2512*
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the flamingo subfamily, which is included in the cadherin superfamily. The flamingo cadherins consist of nonclassic-type cadherins that do not interact with catenins. They are plasma membrane proteins containing seven epidermal growth factor-like repeats, nine cadherin domains and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic feature of their subfamily. The encoded protein may be involved in the regulation of contact-dependent neurite growth and may play a role in tumor formation. [provided by RefSeq, Jun 2013]
PHENOTYPE: Mice homozygous for a null allele exhibit neonatal lethality, abnormal neurvous system development, and abnormal respiratory system development. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Celsr3||
(F):5'- ACAAATCCCTGCCTGCAATGGGAC -3'
(R):5'- ACGCACATTGGACTTGAGGCTG -3'
(F):5'- CACGTCCTGGGCAGAAAG -3'
(R):5'- TCAGTACTAGCGCCGTTACAG -3'