Busch Lab

ZMP

ror2

Ensembl ID:
ENSDARG00000076227
ZFIN ID:
ZDB-GENE-060427-5
Human Orthologue:
ROR2
Human Description:
receptor tyrosine kinase-like orphan receptor 2 [Source:HGNC Symbol;Acc:10257]
Mouse Orthologue:
Ror2
Mouse Description:
receptor tyrosine kinase-like orphan receptor 2 Gene [Source:MGI Symbol;Acc:MGI:1347521]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41584 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17931 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa41584
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114491 Essential Splice Site 396 939 7 9
Genomic Location (Zv9):
Chromosome 10 (position 5408158)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 5404452
GRCz11 10 5404756
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTGGACCCGAATGTTCGAGTGGATCTCTGTGACATTCCGCCCTGCAG[T/C]AAGTAGTAGAGCATTAATAATCAGACCCTCCATTTTGAGCAAATGTATTG
Long Flanking Sequence:
AGGAAAAGTACCGACACAGCACTTAAAATGGTGAAAGTAAAAGCGCACATTTTAAAACTAATTAGTAAATTACAATTCCTGAGAAAAACTACTCGCAGTAATTTGGGTATTTGTAATTTGTTACTTTACTTCTGCTTTTCATTTTTTCTTTTTCACTGCTTGTCATTTCACTTAATTAATTTCACTGTTTGACTTCATGTTTTGCGAGAAAATCCTGAACAATTTTCCATCCTTCTTAAAGATTCACCCCCAGATCACAGCTGTTACAACGAAAGCGGTGGCAACTACAAAGGCACAGTCAGCGTCACCAAATCCGGCTTCCAGTGTCAGCCCTGGAGCGCGCAGTATCCGCACAGCCATCACTTGAGCCCTATCGAGTACCCCCAACTCAGAGGAGGACACAACTTCTGCAGGAACCCTGGAGGGCAAATGGAGAGCCCGTGGTGCTTCACGTTGGACCCGAATGTTCGAGTGGATCTCTGTGACATTCCGCCCTGCAG[T/C]AAGTAGTAGAGCATTAATAATCAGACCCTCCATTTTGAGCAAATGTATTGACTTTTTCTGTATGCTTTGGTCACCAGATCCTCCGGAGAAAATGAAAAAGGAGCTCCTGTACATCTTAATCCCCAGTGTAGCCACTCCTCTGGTTTTTGCCTGCTTGTTCTTCTTGATCTGCATGTGCCGCAACAAACAGAAGGAGTCTGTTGACACTCCAACACGCAGACAGCTCACGGCCTCGCCGAGTCAGGAGATGGAGCTGCCGCTGCTTAATCAGCACAAACATCAGGTAATCTTGCATTGTATTAGGTTATAAAATTGTTAAACATCATAATTCTTTCTGAAAAGGTGGGGCTGGGCGATAATTCGATAACGATAATTATCACGATATATAATTAACAAACAGATTACATCTGATGAGTAACAAGACACTTTGCCTTTTAAACTGATCAAAACAAATTTAAAACACCTTATTTTCTTTCATTTCTAGGCAAAGTTACGAGAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17931
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114491 Nonsense 830 939 9 9
Genomic Location (Zv9):
Chromosome 10 (position 5409740)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 5406034
GRCz11 10 5406338
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACCTCAACTCTACATCCCAGTCAATGGCTATCAGCCAATGCCRGCTTA[C/A]CCGTATCTCCAGAACTTCTACCCCATGCAGATCCCCATGCAKATGCCACM
Long Flanking Sequence:
GAAGCCATCCTATACGGGAAGTTCTCAACCGATTCCGACATCTGGTCCTACGGCGTGGTGCTTTGGGAGATCTTCAGCTACGGCCTTCAGCCTTACTGTGGCTACTCGAATCAAGATGTGATCGAGATGGTACGCAACAGACAAGTGCTGTCCTGCCCAGACGACTGTCCAGCCTGGATATACACGATGATGCTAGAGTGCTGGAACGAGTTTCCCTCAAGAAGACCACGGTTTAAAGACATCCACGCACGATTGCGCACATGGGAGAGCTTATCCAACTACAACAGCTCCGCTCAGACATCAGGAGCAAGCAACACCACTCAAACCAGCTCCCTCAGCACGAGTCCCGTCAGTAATATCAGCAATGCCCGCTATGTTAGTCCCAAGAAGTCATCACCCTTTCCTCAGCCTCAGTTTGTGTCCATGAAAGGCCAGATGCGGCCAATGGTGCCACCTCAACTCTACATCCCAGTCAATGGCTATCAGCCAATGCCGGCTTA[C/A]CCGTATCTCCAGAACTTCTACCCCATGCAGATCCCCATGCAGATGCCACCTCAACAGATGCACCCGCAGATGGTGGCTAAGGCTGGGTCGCACCATAGCGGCAGCGGCTCCACCAGCACTGGATACGTGACCACAGCACCATCTAATGGATCAGGCACAGATAAGGTCGCCCTCATGAATGAAGACCTGAAGGCAACGGAGGATGATTTCGCAGATGGGGCGTCTCAGAAAGGCCTACACCACGAGGACCTGTCGGTTCCAGAGACTGAGCTCCTGGGGGACAATGACAGCCCGCACACAGAGGACAATGAAATCAACTCTGACGCATAAGACGATCTTATTTTTTTAGCCAGATGAGAAGAATGGTTCTCTGCTATGTAATGTTTGGATGTTTTTCTCTGATGTACAGGTTTAAAAAGTGAAGGGAAACCAGTAAGTGACACGTGGATGTTGTGTTATTTATGAGGTTTTATTTGTGTTATCGGCAGCCACTGATGGAT
Associated Phenotype:
Not determined