Busch Lab

ZMP

ror1

Ensembl ID:
ENSDARG00000015176
ZFIN ID:
ZDB-GENE-030131-6104
Description:
Novel protein similar to vertebrate receptor tyrosine kinase-like orphan receptor 1 (ROR1) [Source:U
Human Orthologue:
ROR1
Human Description:
receptor tyrosine kinase-like orphan receptor 1 [Source:HGNC Symbol;Acc:10256]
Mouse Orthologue:
Ror1
Mouse Description:
receptor tyrosine kinase-like orphan receptor 1 Gene [Source:MGI Symbol;Acc:MGI:1347520]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa31514 Nonsense Available for shipment Available now
sa40718 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12160 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa31514
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
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065172 Nonsense 97 950 3 9
ENSDART00000132280 Nonsense 61 914 2 8
Genomic Location (Zv9):
Chromosome 6 (position 31515761)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 31836677
GRCz11 6 31823591
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGAGTTGCATTGCCACGTTTCGGGGACTCCATCACCCTCAGTCCGCTG[G/A]CTTAAAAACGATGCCCCTGTGGTTCAGGAGCCACGGCGGGTCTCGTACAG
Long Flanking Sequence:
GGCAAGACAGATTTTCAGGAGACAGAAGTTTCCAGAAGCTTCAAGAGTTTCTGCCGTCCCCTCTGGCGCTATCCACCCCAATGAGACAAACTAATGATTTACCACCTAGTGGCAACCGCTAAATATCATGTAAAAGATTCCTAACCGGCAGCTTAAAGGCTTGTTGCAGACTGTAAGCTCGTATGTAGTTACAAATGCACATGAACATTAGGAAAAGTCTCTTTCTGAAAAAAAAAAATAATTTTGACTTATTATGTGTCAAATAATACCTGTTTAAGGGATTAGTTCTGTCCTTATTGCACAACCTCGTCTTGTTCCAAAACCATATGATTTTTTTTGATTAAGTTAACCATATTGTATGGTTTTTAACTTTTCTGGCTTGTCTTTTCAGATCACTTCCTAAGGCTGGACGCTCCTATGAATAACATTACTACTTCCCTCGGACAGACAGCTGAGTTGCATTGCCACGTTTCGGGGACTCCATCACCCTCAGTCCGCTG[G/A]CTTAAAAACGATGCCCCTGTGGTTCAGGAGCCACGGCGGGTCTCGTACAGACCGACTCCGTACGGCTCGCGCTTGAGAATCAAAAATCTGGACACCACAGACACCGGCTACTTTCAGTGTGTGGCGACCAACAGCTATGGCACAGTGTCAACCACAGGAATCCTGTTTGTCAAGTTTGGTGAGTGATTTTTAGAACTTTAGAATGAGAAAAAAGCTTAATTAAACACATTAAACACAAGTGTCATCTTTGATAGCACAAGATGTACACTAGGATTAGGAACTTTATGATGTTTTCGGTTTAGTTTCAGTCAATGTTGTCTGCTAAATGGTGTTACAATTATTTTTGTATTATAAATACCAAGTTTCAAATGTGCTAGAATGTGTCAGCTTTTTTCTGCAAATATGAGCCAATAAAGGCTCACAAAAAAATCCATTATTGTCTTTCTACTGCATGCACATAACATCATACCTGCCAACACTCCCATTTTTCCCAGGAGTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40718
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065172 Essential Splice Site 157 950 3 9
ENSDART00000132280 Essential Splice Site 121 914 2 8
Genomic Location (Zv9):
Chromosome 6 (position 31515581)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 31836497
GRCz11 6 31823411
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGCTATGGCACAGTGTCAACCACAGGAATCCTGTTTGTCAAGTTTGG[T/G]GAGTGATTTTTAGAACTTTAGAATGAGAAAAAAGCTTAATTAAACACATT
Long Flanking Sequence:
GTATGTAGTTACAAATGCACATGAACATTAGGAAAAGTCTCTTTCTGAAAAAAAAAAATAATTTTGACTTATTATGTGTCAAATAATACCTGTTTAAGGGATTAGTTCTGTCCTTATTGCACAACCTCGTCTTGTTCCAAAACCATATGATTTTTTTTGATTAAGTTAACCATATTGTATGGTTTTTAACTTTTCTGGCTTGTCTTTTCAGATCACTTCCTAAGGCTGGACGCTCCTATGAATAACATTACTACTTCCCTCGGACAGACAGCTGAGTTGCATTGCCACGTTTCGGGGACTCCATCACCCTCAGTCCGCTGGCTTAAAAACGATGCCCCTGTGGTTCAGGAGCCACGGCGGGTCTCGTACAGACCGACTCCGTACGGCTCGCGCTTGAGAATCAAAAATCTGGACACCACAGACACCGGCTACTTTCAGTGTGTGGCGACCAACAGCTATGGCACAGTGTCAACCACAGGAATCCTGTTTGTCAAGTTTGG[T/G]GAGTGATTTTTAGAACTTTAGAATGAGAAAAAAGCTTAATTAAACACATTAAACACAAGTGTCATCTTTGATAGCACAAGATGTACACTAGGATTAGGAACTTTATGATGTTTTCGGTTTAGTTTCAGTCAATGTTGTCTGCTAAATGGTGTTACAATTATTTTTGTATTATAAATACCAAGTTTCAAATGTGCTAGAATGTGTCAGCTTTTTTCTGCAAATATGAGCCAATAAAGGCTCACAAAAAAATCCATTATTGTCTTTCTACTGCATGCACATAACATCATACCTGCCAACACTCCCATTTTTCCCAGGAGTCTCCTGTATTTCAGACCCATCTCCCGCTACCCTCCCATTTTATTATTTCTCCCTGTAAACTACCGTAATTTCACCCGCCCCCAGTCCTCGTCATTTTGGTACAGTCTGTAACAACCCCGGGTTACCAACTTTGGTATCTTATCCGATCGCAGCGACCCCTCCCACCACAACATCCCAACCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12160
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065172 Nonsense 675 950 9 9
ENSDART00000132280 Nonsense 639 914 8 8
Genomic Location (Zv9):
Chromosome 6 (position 31466745)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 31787661
GRCz11 6 31774575
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCAACACCCTCCTCCCTATTCGCTGGATGCCACCAGAGGCCATAGTTTA[T/A]GGGAAATACAGCACAGATTCTGACGTTTGGGCGTTTGGTGTGGTTTTATG
Long Flanking Sequence:
GCTCAACTTGTGGCCATAAAAACCCTGAAGGACATCTCCAGTGCACAACACTGGGGCGATTTCCAGCAGGAAGCATCCGTCTTGGCAGAACTTCACCACCCTAATGTGGTTTGTCTCCTGGGTGTAGTGACCCAAGAGCAGCCCGTCTGCATGCTCTTCGAGTTCCTGGCCCAAGGCGACCTCCACGAGTTCCTCATCATGCGCTCTCCACATTCAGATGTGGGCTGCAGCAGCGACGAAGACGGCACTGTCAAGTCCAGCCTCGACCACGGAGACTTCCTTCACCTGGCCATTCAGGTGGCGGCTGGAATGGAATACCTGGCCAGCCATTTTTTCATCCACAAAGATCTTGCAGCCCGTAACATCCTAGTTGGCGAACAACTGCACATCAAAATCTCCGACCTTGGGTTGTCTAGAGAAATCTACTCCTCTGATTATTACAGAGTCCAACCCAACACCCTCCTCCCTATTCGCTGGATGCCACCAGAGGCCATAGTTTA[T/A]GGGAAATACAGCACAGATTCTGACGTTTGGGCGTTTGGTGTGGTTTTATGGGAGATCTTCAGCTTTGGTTTGCAGCCTTATTATGGCTTCAGCAATCAGGAGGTGATGGAGATGGTACGAAAGAGGCAGCTGTTGCCCTGTCCAGAGGATTGCCCTCCTCGCATGTATGCCCTGATGACTGAGTGTTGGCAAGAAGGTCCTGCTCGCCGGCCGAGATTTAAAGACATCCATACACGTCTACGGGCTTGGGAGGGTCTGTCCTCTCATGCCAGCTCCAGCACACCATCTGGAGGCAACGCCACCACCCAGACTACCTCTCTGAGCGCAAGTCCTGTCAGCAACCTCAGCAGCCCACGCTATGCCGGCTACATCTATGGGGCTCCACAGAGCCTTCAACCTGGACAGATTACAGGCTTCATGGCGGCACCAATGCCACAAAGCCAACGTTTTATACCTGTGAATGGATACCCTATTCCTACGGGATACGCCGCATTTCCTGC
Associated Phenotype:
Not determined