Busch Lab

ZMP

pcdh17

Ensembl ID:
ENSDARG00000027041
ZFIN ID:
ZDB-GENE-090608-3
Description:
Protocadherin-17 [Source:UniProtKB/TrEMBL;Acc:C4P342]
Human Orthologue:
PCDH17
Human Description:
protocadherin 17 [Source:HGNC Symbol;Acc:14267]
Mouse Orthologue:
Pcdh17
Mouse Description:
protocadherin 17 Gene [Source:MGI Symbol;Acc:MGI:2684924]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa16710 Nonsense Available for shipment Available now
sa11699 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16710
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125630 Nonsense 843 1137 2 4
Genomic Location (Zv9):
Chromosome 11 (position 33467868)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 32391916
GRCz11 11 32654728
KASP Assay ID:
2260-4482.1 (used for ordering genotyping assays)
KASP Sequence:
CACAGACAGACAATTTTCCTGCTGAGCCCAATTACATGGGTAACAGGCAG[C/T]AGTTTGTTCAAAGGTAAGGCCTATTTAACAGTTTTCTCAGCGTTATTTGT
Long Flanking Sequence:
TAAATACAATTAGCTTCTATTAAGAACAATAGTTGTGAATGGGATGCTCCCCGATGGATAGAGAAGGTTGTGTGTGTGGGTGAACGTTCAGAGCCTTTAACAACTTCAGCAAATCTTCTCATTTTCTTACACCACACACACACACACTCCCTCTTATTCGCTCCATTTTTTTTTCTTCTGCCGTGCTCCTCCACTCGTATTCGTATCTAACAGGTCATTAAGTTCACAAATGTGCAATTGAGTGTTTTGGATGTTTAATTAGCATGTTTCCTTGACTAATTAAAATGCACAAATCTACGGATTAAAGCTCCCCTCCTTTTCTCCATCTCTTCCACCACCCCCCCTCCTTTTTATGAATAATTAATCAATCTCTTTCACCAGGAGATTCTGTCGCACACCAGGACACATTTCAGTGTCGCGCAAGACGTAAACTCTTTTCCTTTTCCCCTTCACAGACAGACAATTTTCCTGCTGAGCCCAATTACATGGGTAACAGGCAG[C/T]AGTTTGTTCAAAGGTAAGGCCTATTTAACAGTTTTCTCAGCGTTATTTGTTTTTTTACACACAGACGTTCTTCAGATAAGAGCTAAGAAGCCATGCCAGGGTTAATCTGTTTGATCTTTTTTTTTTTTTTTGGTCTTGTTGTTTTTTGGACTTGTAGCAGCTCAACGTTCAAAGATCCAGAGCGTGCCAGTCTCAGAGACAGCGGACACGGGGACAGCGACCAAGCGGACAGCGATCAGGACACTAATAAAGGCTCCTGCTGTGACATGTCTGCTAAAGAAGCGCTCAAGATGAAGGCCACTGGACTCAAGCCTCAGCCACTTGAACAGGGTGAGTCCTTCAACATGAGCAACTTTAATAGTCTGTGCGCTATCACAGTCTTTTCTTTCGCCTTTTGCTCTTTGTTACTGGACGTCCTACAGTACGTGTCTGTTGCTTTATTCTAGTGTTAAGCTGTCTTCACAAGGCATGTTTCACAAATGCAGAAGACTTTTGCGTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11699
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
ENSDART00000125630 Nonsense 849 1137 3 4
Genomic Location (Zv9):
Chromosome 11 (position 33467705)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 32391753
GRCz11 11 32654565
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATCTTTTTTTTTTTTTTTGGTCTTGTTGTTTTTTGGACTTGTAGCAGCT[C/A]AACGTTCAAAGATCCAGAGCGTGCCAGTCTCAGAGACAGCGGACACGGGG
Long Flanking Sequence:
CATTTTTTTTTCTTCTGCCGTGCTCCTCCACTCGTATTCGTATCTAACAGGTCATTAAGTTCACAAATGTGCAATTGAGTGTTTTGGATGTTTAATTAGCATGTTTCCTTGACTAATTAAAATGCACAAATCTACGGATTAAAGCTCCCCTCCTTTTCTCCATCTCTTCCACCACCCCCCCTCCTTTTTATGAATAATTAATCAATCTCTTTCACCAGGAGATTCTGTCGCACACCAGGACACATTTCAGTGTCGCGCAAGACGTAAACTCTTTTCCTTTTCCCCTTCACAGACAGACAATTTTCCTGCTGAGCCCAATTACATGGGTAACAGGCAGCAGTTTGTTCAAAGGTAAGGCCTATTTAACAGTTTTCTCAGCGTTATTTGTTTTTTTACACACAGACGTTCTTCAGATAAGAGCTAAGAAGCCATGCCAGGGTTAATCTGTTTGATCTTTTTTTTTTTTTTTGGTCTTGTTGTTTTTTGGACTTGTAGCAGCT[C/A]AACGTTCAAAGATCCAGAGCGTGCCAGTCTCAGAGACAGCGGACACGGGGACAGCGACCAAGCGGACAGCGATCAGGACACTAATAAAGGCTCCTGCTGTGACATGTCTGCTAAAGAAGCGCTCAAGATGAAGGCCACTGGACTCAAGCCTCAGCCACTTGAACAGGGTGAGTCCTTCAACATGAGCAACTTTAATAGTCTGTGCGCTATCACAGTCTTTTCTTTCGCCTTTTGCTCTTTGTTACTGGACGTCCTACAGTACGTGTCTGTTGCTTTATTCTAGTGTTAAGCTGTCTTCACAAGGCATGTTTCACAAATGCAGAAGACTTTTGCGTCTCAGGCTGTTCACATAAGATAAAATCTTGATTTTGTATTAATTTCTTTTGGTCTGTTCCACCTTTTTGCCCTTCTTGACTGTTTCCAACAATTAATATCATATATGGGTCAATGACAAGGCGTCCCATTTTGGTGTCCGCATTAAATTATATTTAGAAAAGTGA
Associated Phenotype:
Not determined