ZMP
ENSDARG00000086969
Ensembl ID:
Human Orthologues:
PCDHB1, PCDHG@, PCDHGA1, PCDHGA10, PCDHGA11, PCDHGA12, PCDHGA3, PCDHGA5, PCDHGA6, PCDHGA7, PCDHGA8
Human Descriptions:
protocadherin beta 1 [Source:HGNC Symbol;Acc:8680]
protocadherin gamma cluster [Source:HGNC Symbol;Acc:8695]
protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:8696]
protocadherin gamma subfamily A, 10 [Source:HGNC Symbol;Acc:8697]
protocadherin gamma subfamily A, 11 [Source:HGNC Symbol;Acc:8698]
protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:8699]
protocadherin gamma subfamily A, 3 [Source:HGNC Symbol;Acc:8701]
protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:8703]
protocadherin gamma subfamily A, 6 [Source:HGNC Symbol;Acc:8704]
protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:8705]
protocadherin gamma subfamily A, 8 [Source:HGNC Symbol;Acc:8706]
protocadherin gamma cluster [Source:HGNC Symbol;Acc:8695]
protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:8696]
protocadherin gamma subfamily A, 10 [Source:HGNC Symbol;Acc:8697]
protocadherin gamma subfamily A, 11 [Source:HGNC Symbol;Acc:8698]
protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:8699]
protocadherin gamma subfamily A, 3 [Source:HGNC Symbol;Acc:8701]
protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:8703]
protocadherin gamma subfamily A, 6 [Source:HGNC Symbol;Acc:8704]
protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:8705]
protocadherin gamma subfamily A, 8 [Source:HGNC Symbol;Acc:8706]
Mouse Orthologue:
Pcdhb1
Mouse Description:
protocadherin beta 1 Gene [Source:MGI Symbol;Acc:MGI:2136730]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27597 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27598 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27599 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38796 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27597
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 |
---|---|---|---|---|---|
ENSDART00000128215 | Nonsense | 99 | 782 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 21966181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 21796709 |
GRCz11 | 10 | 21754090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCAGTGTAAGTTTTGATGTGATTTTGGAGAATCCGATGGAGCTTTAT[C/T]GAGTAACAGTTGACATACAAGACATCAATGACAACAGCCCCGTCTTTCCA
Long Flanking Sequence:
GCGATGCGTAACTGATCACCAAATCGCCTTTCAGATTCGACTACAGGTTCTGTAATCTAGAGGGAAAGACAATTTGTTGGAAACATACAGAATACAATTCATTGTGCCTTTTGCTTTAAATGCATCCTCTTCATCTTTGTTGATCAAAAATGGAGTCGGGAGGAAAAGGCTGGAGATATGGCTCACTATTCTATGCGTTATGCGCAATGGCTTTATTTTCTCCTCGCGTGAGCGGGCAGATCCGTTATTCGATACCCGAGGAAATGCAGGTGGGCTCATTTGTTGGAAATATTGCCTTGGACCTAGGGATTGAGCCGAAGAGATTGGTTTCAGGAAAAGCGCGTGTTTTCACCGCGGACAGCAGGGAGTACATTGGCCTGGACAAGGAAAACGGACATCTGGTTATCAAGAATAAAATAAACAGAGAAGAGCTTTGTGGAGAGATTTCTGCCTGCAGTGTAAGTTTTGATGTGATTTTGGAGAATCCGATGGAGCTTTAT[C/T]GAGTAACAGTTGACATACAAGACATCAATGACAACAGCCCCGTCTTTCCAAAAGCTAAAATTGAACAAGAAATAAGCGAATTAGCGGTTGTAGGTGCGCGATTTCCATTAGAGAGCGCGGTAGATCCAGACGTGGGAGTGAACGCGCTACAAAAATACACTCTTCAACCCACCGACCATTTTAAGCTTAATGTTCAGAGTGGTGATGATGGGAGTAAAAATATCGAGATGGTTCTTAATTCACCACTCGATAGAGAAAAGAAAAAGCATCATAGTTTGATTCTTACAGCATTCGATGGTGGAAGACCTCAAAGATCTGCGACTGTGCATATTAACATTATTGTCCTTGATGGAAATGACAACGCACCTGTGTTTAGTCAGTCATCTTACAAAACATCAGTTATTGAAAACGTTGCTAAAGGCACACTCGTTACTAAAGTCAGTGCTACCGATGCTGACGAGTCTAGTCACGGCATTCAGTATTATTTTGAGCACGCGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27598
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 |
---|---|---|---|---|---|
ENSDART00000128215 | Nonsense | 149 | 782 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 21966331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 21796859 |
GRCz11 | 10 | 21754240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTCCATTAGAGAGCGCGGTAGATCCAGACGTGGGAGTGAACGCGCTA[C/T]AAAAATACACTCTTCAACCCACCGACCATTTTAAGCTTAATGTTCAGAGT
Long Flanking Sequence:
TGGAGTCGGGAGGAAAAGGCTGGAGATATGGCTCACTATTCTATGCGTTATGCGCAATGGCTTTATTTTCTCCTCGCGTGAGCGGGCAGATCCGTTATTCGATACCCGAGGAAATGCAGGTGGGCTCATTTGTTGGAAATATTGCCTTGGACCTAGGGATTGAGCCGAAGAGATTGGTTTCAGGAAAAGCGCGTGTTTTCACCGCGGACAGCAGGGAGTACATTGGCCTGGACAAGGAAAACGGACATCTGGTTATCAAGAATAAAATAAACAGAGAAGAGCTTTGTGGAGAGATTTCTGCCTGCAGTGTAAGTTTTGATGTGATTTTGGAGAATCCGATGGAGCTTTATCGAGTAACAGTTGACATACAAGACATCAATGACAACAGCCCCGTCTTTCCAAAAGCTAAAATTGAACAAGAAATAAGCGAATTAGCGGTTGTAGGTGCGCGATTTCCATTAGAGAGCGCGGTAGATCCAGACGTGGGAGTGAACGCGCTA[C/T]AAAAATACACTCTTCAACCCACCGACCATTTTAAGCTTAATGTTCAGAGTGGTGATGATGGGAGTAAAAATATCGAGATGGTTCTTAATTCACCACTCGATAGAGAAAAGAAAAAGCATCATAGTTTGATTCTTACAGCATTCGATGGTGGAAGACCTCAAAGATCTGCGACTGTGCATATTAACATTATTGTCCTTGATGGAAATGACAACGCACCTGTGTTTAGTCAGTCATCTTACAAAACATCAGTTATTGAAAACGTTGCTAAAGGCACACTCGTTACTAAAGTCAGTGCTACCGATGCTGACGAGTCTAGTCACGGCATTCAGTATTATTTTGAGCACGCGACACCCACAGTAAAAGCTTTGTTCTCCATCGATGCGGATTCTGGAGAGGTTATAGTCATAGGCGGAATAGATTATGAAAAACACAAGCAGTTTAAAATTAAAGTTAAAGCCAAAGATCATGGCGATCTCACAGACTTAAGTGAGATAATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27599
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128215 | Nonsense | 457 | 782 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 21967255)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 21797783 |
GRCz11 | 10 | 21755164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAGCTGAAAATAACCCACCATCTACGACTATTCTGACTGTCAAAGCA[G/T]AAGACATGGACTGGGGGCCGAATGCAAAGGTCTCATACTTTCTTATCGAT
Long Flanking Sequence:
AAAAACACAAGCAGTTTAAAATTAAAGTTAAAGCCAAAGATCATGGCGATCTCACAGACTTAAGTGAGATAATTATTGACGTCATTGATGTGAACGACAACAAGCCCAAAATCACTATAATGTCTTTTTCCAGCGCAGTATCTGAAGACGCTGCACCAGGAACTGTTATAGCCATGATTAATGTTCAAGATCTCGATTCAGGTGACAACAGCAAGATTACATGTTCTATTGATCTGAACTCTCCATTTAAAATCATTTCTTCATTAACTAATTATTACAACCTGGTGACAGACTCAGAACTAGACAGGGAACAGACAGCAGAGTATAATATCACTATAACTGCAGTAGATGGAGGAAACCCACCTCTTTCTATTAAAGAGATTTTAAACTTAAAGATATCAGATGTGAATGATCACGCACCTCAGTTTGTGCAGGAATCATATAATGCCTTTATAGCTGAAAATAACCCACCATCTACGACTATTCTGACTGTCAAAGCA[G/T]AAGACATGGACTGGGGGCCGAATGCAAAGGTCTCATACTTTCTTATCGATGCAGATTTAAACGGAGCACCTCTTGCATCTTATATTTCTATAAATTCAGAGAGTGGAGTAGTTTATGCAGAAAAATCTTTTGATTATGAACAACTCAAATCATTCAAAATGCAAGTCAAAGCTCAAGATGGAGGCTCGCCTCCTTTATCCAGTAATGTGACTCTAAACATCATCATTCAAGACCAGAATGACAACGCTCCTCAGGTTCTGTATCCAGTACAGACTGGCGCTTCAGTGGTGGCTGAGATTGTGCCTCGTGCTGCAGATGTTGGATATCTGGTCACTAAAGTTGTGGCTGTTGATGTGGACTCTGGTCAGAATGCCTGGCTCTCCTATAAACTACAGAAAGCTGCAGACAGAGCGCTGTTTGAAGTGGGTTTACAGAATGGAGAAATAAGAACTGTGCGACAAGTGACTGATAAAGATGCTGTCAAACAAAAACTCACTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38796
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128215 | Nonsense | 750 | 782 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 21968136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 21798664 |
GRCz11 | 10 | 21756045 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGGACCACAGACTCAAGGATGAGTGACGTAAAGTTTGTCAGGCCCTA[C/A]AGTCAGAACACACTGGTCAGCCAGAGTCGTTTGGGGACAGTTCAGAGAGA
Long Flanking Sequence:
TCCTATAAACTACAGAAAGCTGCAGACAGAGCGCTGTTTGAAGTGGGTTTACAGAATGGAGAAATAAGAACTGTGCGACAAGTGACTGATAAAGATGCTGTCAAACAAAAACTCACTGTTGTTGTGGAGGATAACGGACAGCCCTCTCGCTCAGCTGTGGTCTCCATTAATGTGGCTGTGGCTGACAGCTTTCCTGAAGTGCTGTCAGAGTTCACAGACTTTACGCATGAGAAAAAATATAACGACAGCTTAACTTTTTATTTAGTTCTGGCTCTTGCAGTGGTTTCCCTGCTCTTCATAGTCTCCATTATTTCCATCATTTCAGTCAAAATCTACAGATGGAGGCAGAATAAGTTGTTTTATAAATCAGGAGCAAATCTACCTGTAATTCCATATTATCCTCCGGTCTACGCAGACGGAACATTACAGCACGTTTATAATTATGAAATGTGTGGGACCACAGACTCAAGGATGAGTGACGTAAAGTTTGTCAGGCCCTA[C/A]AGTCAGAACACACTGGTCAGCCAGAGTCGTTTGGGGACAGTTCAGAGAGAAAAGAAGGAGCAGGAGGTTGATGAGCTGATTTTAGAGGTGAGAGTCTTCCACATACTGTATGTCCTCACAGCAGCAGCAGGTGTTTAAAGCTTAAAGTACTGTACTTCTCATAGAGAATTTGTAAGACATTAAGCTTTATCTGTATGTGTTAGCAGATGTTGTATGTCTTGTTTTGAGAAAATGGACTACATGTTTAGTGTCTTAAGTGCAAAGTTAGAGCATAGAAAACTCAATTGCCCCCACACACACCTACAGTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAATCATGTCTGTGTTGTAAATTCTAAATATATTCCATTGGTGTAATTATTTTTATATTATACAAATTGTATTTGCTATCACCTTACATACAACACTACTTATATGAAAACTGCATTTTTACCTTTTC
Associated Phenotype:
Not determined