Busch Lab

ZMP

pcdh1a4

Ensembl ID:
ENSDARG00000093215
ZFIN ID:
ZDB-GENE-050202-4
Description:
protocadherin 1 alpha 4 [Source:RefSeq peptide;Acc:NP_001019270]
Human Orthologues:
PCDHA1, PCDHA10, PCDHA11, PCDHA12, PCDHA13, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
Human Descriptions:
protocadherin alpha 1 [Source:HGNC Symbol;Acc:8663]
protocadherin alpha 10 [Source:HGNC Symbol;Acc:8664]
protocadherin alpha 11 [Source:HGNC Symbol;Acc:8665]
protocadherin alpha 12 [Source:HGNC Symbol;Acc:8666]
protocadherin alpha 13 [Source:HGNC Symbol;Acc:8667]
protocadherin alpha 2 [Source:HGNC Symbol;Acc:8668]
protocadherin alpha 3 [Source:HGNC Symbol;Acc:8669]
protocadherin alpha 4 [Source:HGNC Symbol;Acc:8670]
protocadherin alpha 5 [Source:HGNC Symbol;Acc:8671]
protocadherin alpha 6 [Source:HGNC Symbol;Acc:8672]
protocadherin alpha 7 [Source:HGNC Symbol;Acc:8673]
protocadherin alpha 8 [Source:HGNC Symbol;Acc:8674]
protocadherin alpha 9 [Source:HGNC Symbol;Acc:8675]
Mouse Orthologue:
AC020968.2
Mouse Description:
protocadherin alpha-3 [Source:RefSeq peptide;Acc:NP_619603]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa21717 Nonsense Available for shipment Available now
sa21718 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa21717
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100600 Nonsense 258 789 1 4
Genomic Location (Zv9):
Chromosome 10 (position 21646064)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21607478
GRCz11 10 21564859
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTAAAGTGAAGGAAAACACGCCAGTTGGAACTAAAATAATCTCTGTAT[C/A]AGCCAGAGATTTGGATGAGGGCATTAACAGCGAAATTCAATATTCATTTC
Long Flanking Sequence:
CGTTAATCAGAAATGTGCACTGAATTTAGAGGCTCTTGCTCAGAATCCTCACAGACTTTATCGACTTGAAATTGTAATTGTGGATGTGAACGACAATGCTCCAGTTTTTCCAAACAGCACATATATTCTTAGCGTTACAGAAAATGCGATTGAGGGGGACAGATTTCCTCTTCCAGTTGCAAAAGATTTAGATGTCGGCAGTAATGCTCTAAAAGACTACAAACTCAGTTCAAATGAACATTTTTCCTTAGATGTTCATAGCGGGCAAAGGAGTATATATGCTGAGTTAATACTACAGAAAGCTTTAGACAGAGAAAAGCAAGCTGTTATTCATTTAATACTAACGGCTATTGACGGAGGGAAACCTCCAAAATCTGGAACTTTGAGTATTGTTGTTAATGTTAAAGATATAAACGATAATAAACCTGTTTTCAGCAAATCTTTATACAAAGTTAAAGTGAAGGAAAACACGCCAGTTGGAACTAAAATAATCTCTGTAT[C/A]AGCCAGAGATTTGGATGAGGGCATTAACAGCGAAATTCAATATTCATTTCTTGGACACGGAAATAACGACGAACTGAACCGTTTTACAATTAATACCAATTCTGGAGAAATTACTGTTCAAGGTCAAATTGATCACGAGGAAGACTCTGCAATTGAACTGCGTGTTCAGGCAAGTGATAAAGGCAGTCCTTCAAAAAGTACACACTGTAAAGTTTTAATAGAAGTTGTGGATGAGAATGATAATGCCCCAGAGATAGTTACAACTCCACTGATGGAAAGTGTAAAAGAGGACGCAAAATCAGGAACCGCTGTTGCTTTAGTCACAGTTTCTGATAAAGATATGGGTAAAAACGGCATTTTACATTGTGCTTTAAAGGGTTCGTTCCCTTTTAAACTGGAGACATCATACAATAATCATTATTCTCTAGTGGTAGATGGACCACTGGACAGAGAGAGTGTTTCTCAGTATAACATCACTATTACAGCTGCAGATGAAGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21718
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100600 Essential Splice Site 789 789 1 4
Genomic Location (Zv9):
Chromosome 10 (position 21647659)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21609073
GRCz11 10 21566454
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTGAAGATACTTTTACGCGCACTCAAACTCTTCCTACCAACGAGAAG[G/A]TAAGACGGTAAATTGTTTTGTAATTCATAGCACTGCACTTGACTCAAAAG
Long Flanking Sequence:
CTAAGAGACGAATGAGTGACAATGACTTAAAAACTCACCCACAGATTATTACAGTGTCTGAAAATGGAGAGCCATCGCTCTCAGCGACTACGTCCATGGATGTTGTGGTTCTCGAGAGTCTGGATGACATAAAGACATCATTCAGAGAAGTTCCTGTTAAAGAGGAGAGTTTTTCAGATCTGAATCTGTATCTGCTCATCGCTATTGTCTCAGTATCAGTCATCTTTTTACTGAGTCTCGTGGGTTTGATAGCAGCTAAATGCTACAGGACAGACAGCAGTTTCAGCAGGTACGGCGCTCCAGTGATCAACACACATCCAGACGGCAGCTGGTCCTTCTCTAAATCTACTCAACAGTACGACGTGTGTTTTAGTTCAGACACAATAAAGAGTGATGTAGTGGTTTTCCCTTCGCCGTTTCCACCAGCAGACGCGGAGCTGATCAGCATTAACAGTGAAGATACTTTTACGCGCACTCAAACTCTTCCTACCAACGAGAAG[G/A]TAAGACGGTAAATTGTTTTGTAATTCATAGCACTGCACTTGACTCAAAAGTTATAGAAACCTTTCATATTTCCGGGAATGATCATTTTTTTTAAAATCTTTTTTTAAAATGAATATACACACATGTACTTTTTCTGTTTCTGAAAATGCTTAAAAGAAATACACTTAAATGCACTGTCAAATCAAAATAAGTAAAGCACTGGGTGCTTTTGAATAAGTGAAACGTTTTCATTTCCCACTTGTTATTCAGAGTATATGTTTCAAATACCTCTGGTTCATGTGCCTTATTTGTGGTTTTATTCGTAACAATGACCAGCATTGAAGTGAAATTTTGATTTGCATGGACTTGGCACATGGCACTAAGGGACGATATTGTTTTAATTATTTTTATTTGTTGTTATTAATATTATTGTCACAAAATTTACATTTAGCTCTTGATATCCTGCTCTTTGCTTGTTAGTTTGCGCTATAACCGAAACGTTACCTATTTTTAAATCAAGG
Associated Phenotype:
Not determined