ZMP
ENSDARG00000037682
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 is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17703 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17703
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054881 | Nonsense | 381 | 802 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 3004659)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 2029246 |
GRCz11 | 14 | 1947597 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCCCAGAGGACTCTRTTCYAGACACGGTGATTGCGATGCTTAATATT[A/T]AAGATATAGACTCTGGTAAAAAYGGACAATTTAGATGCTTTGTTAGTTCA
Long Flanking Sequence:
ATGAAGAATTGAAATTAACCCTTACTGCATTTGATGGAGGAAACCCTCAAAAATCCGGAACGGTTAAAATAATTGTCACAGTAATTGATGCAAACGACAACACCCCCGCGTTCAGCCAGTCAGTGTACAGAGTTTCTTTAGCAGAAAATGCACCGATAGGTACAGTAGTGGTTATTGTACTTGCTACAGACAAAGACAAAGGATCAAATGGCGAGGTGATATATTCGTTTTCACAAAGCTCTGGAAAGGATTTAGACCTTTTTAGAATTGATCAGGAGACTGGGAAAATAACCGTAAATGGCTTATTAGATTATGAAAAATCAAAGCAATATGAACTAAATATTGAGGCAATGGATAAGGGAGGATTAACCGACAACAGTAAAGTGTTCATTGAACTGACTGACGTTAATGATAATGCACCTGTAATAAGTGTTATCTCTTTTTCCAATCACATCCCAGAGGACTCTGTTCTAGACACGGTGATTGCGATGCTTAATATT[A/T]AAGATATAGACTCTGGTAAAAACGGACAATTTAGATGCTTTGTTAGTTCAGATTTGCCATTTCGCATTAAACCGTCGTCCTCAAATTTTTACACTTTAGTCACTGATCAGATTTTAGATCGTGAACAGATATCTGAATACAATATCACAGTAACCGCTACTGATGAGGGCTCTCCATCCTTCTCCACTAATAAAACACTGACTCTGAAAATCTCCGATGTGAATGACAACGCCCCTGTGTTTGAGCGTCAGTCATACACCGCATTTATCATGGAGAATAATTCTCCAGGAGTCTCTGTTTTATCTGTTAAAGCGCACGACAGAGACTCTGGCAATAACGCGCGTATCTCCTATTTTCTAGAGGATGTTGTTGTGAATGGCGTCTCTGCCTCGACCTTTATTTCAGTCCATGCAGAGAGCGGAGAGATTCTTGCTGCTCGCTCTTTTGATTACGAGCAAACAAAAGATTTTAGCATCCGCGTAAAAGCGCAGGACGGAGGC
Associated Phenotype:
Not determined