ZMP
pcdh17
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa38852 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41877 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41876 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16710 | Nonsense | Available for shipment | Available now |
sa11699 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38852
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125630 | Nonsense | 267 | 1137 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 33534703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 32458751 |
GRCz11 | 11 | 32721563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAATAATAGATTTAAATGCTACAGATTCTGATGAAGGGATTAATGGG[C/T]AGGTTACTTATTCTTTTAGCTGTTATGTCCCAGACAGGATCAAAGAGTTG
Long Flanking Sequence:
CCAACGACAAGGAGATCTGCATGATTAAAGTTGAGATACAGGACATAAATGACAATGCACCGAGCTTTCCTTCTGAACAAATCGATATTGACATATCTGAGAATGCAGCCCCAGGCACACGTTTCCCCTTGGCTGCTGCCTACGACCCTGACACTAAGGAAAACGGCCTGAAAACATATCAGATCACTCGGGACGATTACAGTATATTTTCTTTGGATGTCAAATCCAGAGGGGATGGAACTAAATTCCCTGAACTGGTCGTTCAGAGGTCTTTGGATCGAGAGGAACGTAGCCATCATACTTTAATTATAACCGCCACAGATGGAGGGGAATACCCCAAATCAGGCACAATGCAAATCAATGTAAAAGTCACTGATTCCAATGACAACAGCCCTGTGTTTGAACAGCCCTCATATGTAGTGGAGATTCCTGAGAATGCACCGCTAGGCACAGTAATAATAGATTTAAATGCTACAGATTCTGATGAAGGGATTAATGGG[C/T]AGGTTACTTATTCTTTTAGCTGTTATGTCCCAGACAGGATCAAAGAGTTGTTTTCAATAGACCCACGAACTGGTGTCATAAAGATTCAGGGTAAAATCGACTTTGAGGAGAACCCAATTATAGAGATTGATGTTCAGGCAAAGGATCAAGGACCCAACCCAATTCCTGGCCATTGTAAAGTCACTGTTAAAGTGCTTGACAGGAATGACAACTGGCCGTCAATAGGTTTTGTAGCGGTGCGTCAGGGGGCGGTTAGTGAAGCAGCAACTCCAGGGACAGTGATTGCACTCGTGAGAGTCACAGACAAAGACTCTGGCCGCAATGGGCAGCTCCAGTGTAGGATTTTGGGCAATGTTCCTTTCAAGCTGGAGGAGAACTATGATAACTTTTACACTGTAGTGACTGACAGACCCCTGGATAGGGAGGTAAAAGATGAATATAACATCACTATTGTGGCCAAAGACAATGGCAATCCACCCCTAAACTCAACAAAGTCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41877
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125630 | Nonsense | 283 | 1137 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 33534654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 32458702 |
GRCz11 | 11 | 32721514 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGTTACTTATTCTTTTAGCTGTTATGTCCCAGACAGGATCAAAGAGT[T/A]GTTTTCAATAGACCCACGAACTGGTGTCATAAAGATTCAGGGTAAAATCG
Long Flanking Sequence:
TGACAATGCACCGAGCTTTCCTTCTGAACAAATCGATATTGACATATCTGAGAATGCAGCCCCAGGCACACGTTTCCCCTTGGCTGCTGCCTACGACCCTGACACTAAGGAAAACGGCCTGAAAACATATCAGATCACTCGGGACGATTACAGTATATTTTCTTTGGATGTCAAATCCAGAGGGGATGGAACTAAATTCCCTGAACTGGTCGTTCAGAGGTCTTTGGATCGAGAGGAACGTAGCCATCATACTTTAATTATAACCGCCACAGATGGAGGGGAATACCCCAAATCAGGCACAATGCAAATCAATGTAAAAGTCACTGATTCCAATGACAACAGCCCTGTGTTTGAACAGCCCTCATATGTAGTGGAGATTCCTGAGAATGCACCGCTAGGCACAGTAATAATAGATTTAAATGCTACAGATTCTGATGAAGGGATTAATGGGCAGGTTACTTATTCTTTTAGCTGTTATGTCCCAGACAGGATCAAAGAGT[T/A]GTTTTCAATAGACCCACGAACTGGTGTCATAAAGATTCAGGGTAAAATCGACTTTGAGGAGAACCCAATTATAGAGATTGATGTTCAGGCAAAGGATCAAGGACCCAACCCAATTCCTGGCCATTGTAAAGTCACTGTTAAAGTGCTTGACAGGAATGACAACTGGCCGTCAATAGGTTTTGTAGCGGTGCGTCAGGGGGCGGTTAGTGAAGCAGCAACTCCAGGGACAGTGATTGCACTCGTGAGAGTCACAGACAAAGACTCTGGCCGCAATGGGCAGCTCCAGTGTAGGATTTTGGGCAATGTTCCTTTCAAGCTGGAGGAGAACTATGATAACTTTTACACTGTAGTGACTGACAGACCCCTGGATAGGGAGGTAAAAGATGAATATAACATCACTATTGTGGCCAAAGACAATGGCAATCCACCCCTAAACTCAACAAAGTCTTTCACTGTAAAGATTTTAGATGAAAACGACAACGCACCACGCTTCACAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41876
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125630 | Nonsense | 842 | 1137 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 33467871)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 32391919 |
GRCz11 | 11 | 32654731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCACAGACAGACAATTTTCCTGCTGAGCCCAATTACATGGGTAACAGG[C/T]AGCAGTTTGTTCAAAGGTAAGGCCTATTTAACAGTTTTCTCAGCGTTATT
Long Flanking Sequence:
AAATAAATACAATTAGCTTCTATTAAGAACAATAGTTGTGAATGGGATGCTCCCCGATGGATAGAGAAGGTTGTGTGTGTGGGTGAACGTTCAGAGCCTTTAACAACTTCAGCAAATCTTCTCATTTTCTTACACCACACACACACACACTCCCTCTTATTCGCTCCATTTTTTTTTCTTCTGCCGTGCTCCTCCACTCGTATTCGTATCTAACAGGTCATTAAGTTCACAAATGTGCAATTGAGTGTTTTGGATGTTTAATTAGCATGTTTCCTTGACTAATTAAAATGCACAAATCTACGGATTAAAGCTCCCCTCCTTTTCTCCATCTCTTCCACCACCCCCCCTCCTTTTTATGAATAATTAATCAATCTCTTTCACCAGGAGATTCTGTCGCACACCAGGACACATTTCAGTGTCGCGCAAGACGTAAACTCTTTTCCTTTTCCCCTTCACAGACAGACAATTTTCCTGCTGAGCCCAATTACATGGGTAACAGG[C/T]AGCAGTTTGTTCAAAGGTAAGGCCTATTTAACAGTTTTCTCAGCGTTATTTGTTTTTTTACACACAGACGTTCTTCAGATAAGAGCTAAGAAGCCATGCCAGGGTTAATCTGTTTGATCTTTTTTTTTTTTTTTGGTCTTGTTGTTTTTTGGACTTGTAGCAGCTCAACGTTCAAAGATCCAGAGCGTGCCAGTCTCAGAGACAGCGGACACGGGGACAGCGACCAAGCGGACAGCGATCAGGACACTAATAAAGGCTCCTGCTGTGACATGTCTGCTAAAGAAGCGCTCAAGATGAAGGCCACTGGACTCAAGCCTCAGCCACTTGAACAGGGTGAGTCCTTCAACATGAGCAACTTTAATAGTCTGTGCGCTATCACAGTCTTTTCTTTCGCCTTTTGCTCTTTGTTACTGGACGTCCTACAGTACGTGTCTGTTGCTTTATTCTAGTGTTAAGCTGTCTTCACAAGGCATGTTTCACAAATGCAGAAGACTTTTGCG
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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