ZMP

ENSDARG00000004722

Ensembl ID:

ENSDARG00000004722

Human Orthologue:

DDR2

Human Description:

discoidin domain receptor tyrosine kinase 2 [Source:HGNC Symbol;Acc:2731]

Mouse Orthologue:

Ddr2

Mouse Description:

discoidin domain receptor family, member 2 Gene [Source:MGI Symbol;Acc:MGI:1345277]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa13982	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa13982

Status:

Available for shipment
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Availability:

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Mutation:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000049466	Nonsense	716	740	13	13

Genomic Location (Zv9):

Chromosome 5 (position 10378118)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	9195429
GRCz11	5	9700067

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCTCCGCCGCTCTGCCCATCCTCCCTMTTMAAGYTGATGAWGCGCTGCTG[G/A]AGTCGTGACATCACAGACCGGCCATYGTTTAACAAATTGCATCAGGCCCT

Long Flanking Sequence:

TCGCTGGTTTGAGTCCTGGCTGGGCCAGTTGGCTTTTCTATGTGGAGTTTGCATGTTCTCCCCGTGTTGGTGTGGGTTTTCTCTGGGTGCTCTGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGTGAATTGGACAAGCTAAACTGGTCATGGTGTATGAATATGAGTGTGTACTGGGTTGCAGCTGGAAGGCATCCACTGTGTAAACATAGTTTTCATATTAACATCTAAAAAAGTGGTTCTTAACCATGTTCCACCACCAGCACTGCATGTTTTGGATGTCTTCCTTATCATTTCAGTCTCTGCTACTGTGCTGATGATCTGAATCAGGCGTTTGGTTAAGGAGACATGGAAAATGTGCAGAACTGGTGATCCTCCAGCAACGTGGTTGAGAAAAAAAGTCTTCTTATTGTTCACCTTTTCTCTTCTCTACAGATCTTTCTCTCCGCTCCGCCGCTCTGCCCATCCTCCCTCTTCAAGCTGATGATGCGCTGCTG[G/A]AGTCGTGACATCACAGACCGGCCATCGTTTAACAAATTGCATCAGGCCCTGCGAACTTTTGCACCCCATTCGTGACTGACATCTGCTCTACTAAAGCAACCTGGAGGAAAACTGCTATAAACATAGAGCGGGAACATTTTAGCCACAATGTAGCGTCATCACGGCATCGTAAATCCAGAAGAGAGATCTAGAGGTGATGAGGTTTCACAGAAAAAGGCATTCACTAGCTCACTAAACATTCATCTCTATTGAGACTCTTTTAAAAAAAAAATCCACTTGAGACACTTGAGATTTTTTTTTTTTTGTACTTTTTATTGTTGTTACTTCCTTTCAAGTACAGTTAGCTTTCTCTCTCTCTCATAAATGTATTTCTGTTCGTCGTTTTCCCAGAAAAACAGCGAGTCTTGAGCCTACTGTGTATTCTAGGCGGAACTGGACGAATGTCTTTGTCAAAGCTGTGGTTTGTGTATCGTTAAGCACTGCTGTCTTTTGGTTTTATT

Associated Phenotype:

Not determined