Busch Lab

ZMP

ENSDARG00000058941

Ensembl ID:
ENSDARG00000058941
Human Orthologues:
PCDHGC4, PCDHGC5
Human Descriptions:
protocadherin gamma subfamily C, 4 [Source:HGNC Symbol;Acc:8717]
protocadherin gamma subfamily C, 5 [Source:HGNC Symbol;Acc:8718]
Mouse Orthologue:
Pcdhga11
Mouse Description:
protocadherin gamma subfamily A, 11 Gene [Source:MGI Symbol;Acc:MGI:1935228]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa12288 Nonsense Available for shipment Available now
sa31970 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12288
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
ENSDART00000081912 Nonsense 278 888 1 3
Genomic Location (Zv9):
Chromosome 14 (position 3026407)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 2007652
GRCz11 14 1926003
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGTGGACTCTGGYGTAAACGGGAAGATATCCTACTCATTCAGTAAGTA[C/A]ACTCCAGAGAGAAWACTGAAGATGTTCAGCGTCGATTCTAAAKCGGGGGA
Long Flanking Sequence:
AGAGTTCTTATTCAGATTGATGATGTGAACGACAACGCGCCGCAGTTCCCAAACGCGAATTCATCACTTGAGATATCCGAGGCGGCCGCTCCGGGAACGCGGTTCCGCTTGGAGAGCGCGCGCGATCCCGATGTGGGCATTAACTCGCTGCGCACGTACAGCCTCTCCGCGAGCGACTACTTTGTTTTACACGTGGAGACCAAAAGCGACGGCAGCAAATTTCCAGAGCTGACTCTGGAGAAGGCTTTGGATCGCGAGACGATTTCCGCGTTTCAACTCCTGCTCACGGCTGTGGACGGAGGACAGCCGGAGAAATCCGGGACCACCCTTCTGCTCATTAAGATCCTGGACGTGAATGACAACGCGCCTGTGTTTGATGAGCCGGTCAAAAGGGTTAGCCTTTTGGAGAACTCTCCTCCGGGGACACTCGTGACCAAACTAAACACCACCGATGTGGACTCTGGTGTAAACGGGAAGATATCCTACTCATTCAGTAAGTA[C/A]ACTCCAGAGAGAATACTGAAGATGTTCAGCGTCGATTCTAAATCGGGGGAAATCCGTGTTGTGGGGGATGTGGACTATGAGGAAGCAAATGTGTATGACATCACTGTTCAGGCCAGGGATGGAGGCTCTCCCGCCATGGAGGGCTCATGCAACATCAAAGTGGAAATAATCGATGTGAACGATAACACTCCGGAGGTGACATTAACCTCTCTGACCAGCCCCATCCGGGAGGATGCTGACAGCGGGACTGTTATAGCACTGATCAGTGCGAAGGACTTAGATTCAGGGGATAACGGGAAAGTGACACTTAAAGTGTCCCAAGGACTTCCGTTTAAGCTCAAGTCAGCTTTTGGAGAACACTACACGCTTGTGACGGACGGACGTCTGGACAGAGAAGCCATTGATGAGTACACTGTTGTTGTCACGGCGACTGACTCCGGCTCGCCTCAGCTGTCCTCTGAGAAGCGCTTTGCGGTGCGTCTGTCAGACGTTAACGATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31970
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081912 Nonsense 668 888 1 3
Genomic Location (Zv9):
Chromosome 14 (position 3027575)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 2006484
GRCz11 14 1924835
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGATCCAGCTTTGTCCACTAGTGTTATGGTCACAGTTACCATCGAGGAG[A/T]AAACCCCAGACAAATCGACAGACTTTCGCATGACTCCTCGCAAAGCGACT
Long Flanking Sequence:
ACGTCTACATCAACCCAGAGAACGGAAACATCTTCACCATGCGCTCTCTGGATTATGAGCAGATGAATGCGTTCAGGATCGAAGTGCAGGTGCGTGATGCTGGCGTGCCGCCGCAGGCATCCAATGTCACCGTGCACGTTTTTGTAGTTGACAAGAACGATAACCCACCGGTTATCCTGTACCCGGCGCACTCTGAAGAGACGGGGCTCCAGCTGACAGTCCCGCATGGAGTTCCAGTGGGCCATCGTGTCAATAAAATAGTCGCGGTTGATTCGGACAGCGGCCACAATGCTTGGCTCTTCTACACCATTGCTCCCGGAGACGATTCGTCACTGTTTCACATTGAACTGCACACTGGCGAGCTGCGGACTGCACAGAAACTCATGGACGACGAACAGGGTGGTAAAACCCACCCAGCATACAACTTCGTTGTGAATGTGCGAGACAATGGCGATCCAGCTTTGTCCACTAGTGTTATGGTCACAGTTACCATCGAGGAG[A/T]AAACCCCAGACAAATCGACAGACTTTCGCATGACTCCTCGCAAAGCGACTGGAATGACTGACGTCACACTATACCTCATAATCTCGCTGGGTTGTGTGACTTTGGTGTCGCTGTTAACAATGGCGATACTCTTGGTACGGTGCATCAGGCACAAGGGCGGATCTACATGCTGCTACTCCAGATCGGGATTGCGTTCTCGCCATGCTTACCAGCAGAGAGCAAACAAAGACCTTCACCTCCAGCTGAACACTGACGGACCCATCAGGTACATGGAGGTGGTCGGAGGCCCTCAGGAGCCTCACACCAGGACGTACAGGCCCTGCTACTCGACGCTCTCCAGCAGGAGCGACTTTGTGTTCGTCAAGACTCCCATTTTGAGTCACAACAACACGCTTAACATGACTTTAACTAGGAAGCACTTAATGAACTCAACCAATGAGGTGAGAGCACGCTCATCCCCACAGCCAATCAAATGCTTTGCTGCCACTAATGGATTTTCT
Associated Phenotype:
Not determined