ZMP
PCDH12
Ensembl ID:
Description:
protocadherin 12 [Source:HGNC Symbol;Acc:8657]
Human Orthologue:
PCDH12
Human Description:
protocadherin 12 [Source:HGNC Symbol;Acc:8657]
Mouse Orthologue:
Pcdh12
Mouse Description:
protocadherin 12 Gene [Source:MGI Symbol;Acc:MGI:1855700]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22439 | Nonsense | Available for shipment | Available now |
sa22438 | Nonsense | Available for shipment | Available now |
sa42363 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35653 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38984 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22439
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111262 | Nonsense | 426 | 1174 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 14015254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16021401 |
GRCz11 | 14 | 16327054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATGATTGTAACCAATGGCACTCTGGATCGTGAGAAACAAATGGAATA[T/A]AACCTTACTCTTCTCGCTCAAGACAGTGGTGATCCATCTCTGTCCTGCAT
Long Flanking Sequence:
GTCTTAAATCTTCGTGCTACAGACCCCGATCAAGGTGCTAATGGGGAAGTTGAGTACTCCCTTAGTAAGCATTCCCCACTGGAAGTACAAAGACTATTTAGCATTCATCCCAAAACAGGTGCTTTGACTTTACAAGGCCCTTTAGATTTTGAAGAGAAGAATGTATATGAGGTAGACATCCAAGCTCGAGATCTAGGGCCCAATGGTATCCCATCTCACCACAAGTTGCAAATTAAATTGCAAGATATAAATGATAATGCTCCCCGCATACACATTACATGGACTCCCCCAGACTCCCCTGTTGCGACAGTCACAGAGGGAGCACCAAATGAAACTTTCCTTGCTCTTGTGATGGTATCTGATGCAGATTATGGGGCAAACGGGCAGGTACAAGTGCACATTTTGACTGGTTCTGGCCCTTTCAGACTCAAACAAATCCATGGAGACAACTACATGATTGTAACCAATGGCACTCTGGATCGTGAGAAACAAATGGAATA[T/A]AACCTTACTCTTCTCGCTCAAGACAGTGGTGATCCATCTCTGTCCTGCATTAAGCACTTGACTGTCCATGTTTTGGATGAAAATGATAACCCACCAATTTTTACCAAGAGCCACTACCGGAGTATCCTGAAAGAGAATAACACACCTGGCTTCCATTTCTTGACTGTGGAGGCACATGATGTTGACCTGGGTCTCAGTGGACAGGTATCTTTCTCCATTAGAGAGTCAAATGAACTGGGGACACCAACAGCATTTTTCTCTGTTCACCCCAGCAGTGGGGAAGTGACTGTCCAGCAATCATTAGACTATGAGGAATCCCGCGTCTACTCATTTATTGTGGAGGCTGTGGATCAAGGGTACCCACCAATGACCAGCATTGCAGCAGTGCTGGTTGAAATACAGGATGTTAATGACAATTACCCCATAATTTATGAGCCTCTACCCAAGAAGGGGATTGCATTGCTAAATGTCCCAGTGAATGTGGACAAAGGGGAGATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22438
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111262 | Nonsense | 570 | 1174 | 1 | 4 |
ENSDART00000111262 | Nonsense | 570 | 1174 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 14014822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16020969 |
GRCz11 | 14 | 16326622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTGCTGGTTGAAATACAGGATGTTAATGACAATTACCCCATAATTTA[T/G]GAGCCTCTACCCAAGAAGGGGATTGCATTGCTAAATGTCCCAGTGAATGT
Long Flanking Sequence:
CAAATCCATGGAGACAACTACATGATTGTAACCAATGGCACTCTGGATCGTGAGAAACAAATGGAATATAACCTTACTCTTCTCGCTCAAGACAGTGGTGATCCATCTCTGTCCTGCATTAAGCACTTGACTGTCCATGTTTTGGATGAAAATGATAACCCACCAATTTTTACCAAGAGCCACTACCGGAGTATCCTGAAAGAGAATAACACACCTGGCTTCCATTTCTTGACTGTGGAGGCACATGATGTTGACCTGGGTCTCAGTGGACAGGTATCTTTCTCCATTAGAGAGTCAAATGAACTGGGGACACCAACAGCATTTTTCTCTGTTCACCCCAGCAGTGGGGAAGTGACTGTCCAGCAATCATTAGACTATGAGGAATCCCGCGTCTACTCATTTATTGTGGAGGCTGTGGATCAAGGGTACCCACCAATGACCAGCATTGCAGCAGTGCTGGTTGAAATACAGGATGTTAATGACAATTACCCCATAATTTA[T/A]GAGCCTCTACCCAAGAAGGGGATTGCATTGCTAAATGTCCCAGTGAATGTGGACAAAGGGGAGATTGTGACTGAACTTGGAGATAAAGCAATGGAGGATAATTTCCACAAACATAGAAATTACTCTTCCCTCAACAAACCTGAAGGATTTCTGGCCACCACAATTAGGGCCAGTGATCCAGATTCTGGTCTCAATGGAAGACTCAATTTTGGAATAACAGGCGGCAACCCTTCTAATATATTTTTTCTGGACAAAACATCTGGGGAGTTCTATGTTAACACAACTAATGCCACAGAACTTATTGGGAGAACATTTAAACTGGGAATTGAAGTATCTGATATGGGAACTCCAATACTAAGCACAAGAACCACTTTGGAAGTGACTTTCATTAATTTTCGTGACCATCTGAAGAACTTGTCTCATGATAACCAGGCCCAGTATAGCTTTACAATGCTTTTGGCCATCTGCCTTGGATCTACCTGTCTGGTATTATTTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42363
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111262 | Nonsense | 570 | 1174 | 1 | 4 |
ENSDART00000111262 | Nonsense | 570 | 1174 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 14014822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16020969 |
GRCz11 | 14 | 16326622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTGCTGGTTGAAATACAGGATGTTAATGACAATTACCCCATAATTTA[T/G]GAGCCTCTACCCAAGAAGGGGATTGCATTGCTAAATGTCCCAGTGAATGT
Long Flanking Sequence:
CAAATCCATGGAGACAACTACATGATTGTAACCAATGGCACTCTGGATCGTGAGAAACAAATGGAATATAACCTTACTCTTCTCGCTCAAGACAGTGGTGATCCATCTCTGTCCTGCATTAAGCACTTGACTGTCCATGTTTTGGATGAAAATGATAACCCACCAATTTTTACCAAGAGCCACTACCGGAGTATCCTGAAAGAGAATAACACACCTGGCTTCCATTTCTTGACTGTGGAGGCACATGATGTTGACCTGGGTCTCAGTGGACAGGTATCTTTCTCCATTAGAGAGTCAAATGAACTGGGGACACCAACAGCATTTTTCTCTGTTCACCCCAGCAGTGGGGAAGTGACTGTCCAGCAATCATTAGACTATGAGGAATCCCGCGTCTACTCATTTATTGTGGAGGCTGTGGATCAAGGGTACCCACCAATGACCAGCATTGCAGCAGTGCTGGTTGAAATACAGGATGTTAATGACAATTACCCCATAATTTA[T/G]GAGCCTCTACCCAAGAAGGGGATTGCATTGCTAAATGTCCCAGTGAATGTGGACAAAGGGGAGATTGTGACTGAACTTGGAGATAAAGCAATGGAGGATAATTTCCACAAACATAGAAATTACTCTTCCCTCAACAAACCTGAAGGATTTCTGGCCACCACAATTAGGGCCAGTGATCCAGATTCTGGTCTCAATGGAAGACTCAATTTTGGAATAACAGGCGGCAACCCTTCTAATATATTTTTTCTGGACAAAACATCTGGGGAGTTCTATGTTAACACAACTAATGCCACAGAACTTATTGGGAGAACATTTAAACTGGGAATTGAAGTATCTGATATGGGAACTCCAATACTAAGCACAAGAACCACTTTGGAAGTGACTTTCATTAATTTTCGTGACCATCTGAAGAACTTGTCTCATGATAACCAGGCCCAGTATAGCTTTACAATGCTTTTGGCCATCTGCCTTGGATCTACCTGTCTGGTATTATTTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35653
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 |
---|---|---|---|---|---|
ENSDART00000111262 | Nonsense | 731 | 1174 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 14014339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16020486 |
GRCz11 | 14 | 16326139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCAGTATAGCTTTACAATGCTTTTGGCCATCTGCCTTGGATCTACCTG[T/A]CTGGTATTATTTTTAATCATTGCTTTAGCCAAGACATTCTGTCACCCTAA
Long Flanking Sequence:
AATTACCCCATAATTTATGAGCCTCTACCCAAGAAGGGGATTGCATTGCTAAATGTCCCAGTGAATGTGGACAAAGGGGAGATTGTGACTGAACTTGGAGATAAAGCAATGGAGGATAATTTCCACAAACATAGAAATTACTCTTCCCTCAACAAACCTGAAGGATTTCTGGCCACCACAATTAGGGCCAGTGATCCAGATTCTGGTCTCAATGGAAGACTCAATTTTGGAATAACAGGCGGCAACCCTTCTAATATATTTTTTCTGGACAAAACATCTGGGGAGTTCTATGTTAACACAACTAATGCCACAGAACTTATTGGGAGAACATTTAAACTGGGAATTGAAGTATCTGATATGGGAACTCCAATACTAAGCACAAGAACCACTTTGGAAGTGACTTTCATTAATTTTCGTGACCATCTGAAGAACTTGTCTCATGATAACCAGGCCCAGTATAGCTTTACAATGCTTTTGGCCATCTGCCTTGGATCTACCTG[T/A]CTGGTATTATTTTTAATCATTGCTTTAGCCAAGACATTCTGTCACCCTAACAAACGGGACAACCGTGCTTACAACTGTAGACAAGCTGAGTCCACGTACACTCGCCACCCACGACGGCCTCAGAAGCACATTCAAAAGACTGACATCCAGCTGGTGCCAGTGCTTCGGGGTCGTAGAGAAACGTCTCAAGAAGATGAAGCTGAGGCATTATCATCTACATCACCCTTAGTGGAAAAAGCACATTCACAGAGCCAGTTTACCTTTACACCAACACTTGCTCGCATGACTCAAAATCAAGCTCATACAGAAATGGATGGGAACCTGCCACTCACTCAAAGCAAGATACTCAAAAAGCCTGGGAGCATAGAGTGGAATGGAACACTTCCATATACCTCAGGAACCCCATGCCGGACCCTGCAAAAGACAAGAAATTCTTCCTCATCATCATTTGCAAACTCACAGGCTAGTACGCTCAGACGAAATAAAATTGAAGAATCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38984
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 |
---|---|---|---|---|---|
ENSDART00000111262 | Nonsense | 966 | 1174 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 14013636)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16019783 |
GRCz11 | 14 | 16325436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTGCAGAAAACGGTTCTTTTGAACTATCTTCTGCCTCACCTGAAGTG[C/T]AAGTATGAAAACTTTCCATTTTTACTTATAGCTTATTAATTTACAATTTC
Long Flanking Sequence:
AGGCATTATCATCTACATCACCCTTAGTGGAAAAAGCACATTCACAGAGCCAGTTTACCTTTACACCAACACTTGCTCGCATGACTCAAAATCAAGCTCATACAGAAATGGATGGGAACCTGCCACTCACTCAAAGCAAGATACTCAAAAAGCCTGGGAGCATAGAGTGGAATGGAACACTTCCATATACCTCAGGAACCCCATGCCGGACCCTGCAAAAGACAAGAAATTCTTCCTCATCATCATTTGCAAACTCACAGGCTAGTACGCTCAGACGAAATAAAATTGAAGAATCCAAGCCCACTAGCATGGACACCTCACAAACTGTGACTTCAGTTTCTAGTAATCAGGCAACATTGCGGAGACAAAAGACCACAGAAAAAAGAGGAAGGATGGAAGAATCAGACCAAAGGCAGATCCTGAGGAACCTTGTTAGACTCTCTATGGCAGCCTTTGCAGAAAACGGTTCTTTTGAACTATCTTCTGCCTCACCTGAAGTG[C/T]AAGTATGAAAACTTTCCATTTTTACTTATAGCTTATTAATTTACAATTTCCCATATAAAAACAAGATATCAACAGAGATACTTTAAAGGTTCTTGGCTTCAATTTCAAGGCACATCAGTTCATATAAGCTCAAGTATATGATAGTTTTCCCACTCTAGTTTTACTGCAGGATTGGCCCATATCTGTATGTCCCCTAAGGGGACAGCTGACAGATGATGAAGGCACTGAAGTGTATTTAGTGTCACACAGTAACTTAAACCTTCAGTAAGCCTCAGGAGAAAACTTTGCCAATCCTCAATATTATCATATTACACAGTCAAACTAAATATGAGGGGAAAAATTCATTCCATTGTTGTCTTTAGAGAGGGGTGACTATTAAAGCAAGTATAGATATTTCTAAACAGTAGCCTAATAGTTTTCAAACATGTATGGGCGGGGAACAAATTGCTTGTACTGATATAATTTTCTTTAATTTAAAAAAGGAAGAAAAAAAGAAAAGT
Associated Phenotype:
Not determined