Busch Lab

ZMP

EVPL (2 of 2)

Ensembl ID:
ENSDARG00000059002
Description:
envoplakin [Source:HGNC Symbol;Acc:3503]
Human Orthologues:
EVPL, EVPLL
Human Descriptions:
envoplakin [Source:HGNC Symbol;Acc:3503]
envoplakin-like [Source:HGNC Symbol;Acc:35236]
Mouse Orthologue:
Evpl
Mouse Description:
envoplakin Gene [Source:MGI Symbol;Acc:MGI:107507]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa15141 Nonsense Available for shipment Available now
sa19938 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15141
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082000 Nonsense 474 1706 10 15
Genomic Location (Zv9):
Chromosome 3 (position 6509445)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN149912.1 61878
GRCz11 KN149912.1 61878
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTCATCAACATGCCCAACAACAAGGTGCAGCCTGGTGAAAGTATGACR[C/T]AAGTCTATGCCAAGCAAAACTCGCAGATGGTCAGTATTAAATTKKATTGT
Long Flanking Sequence:
AAAAAATGCTGGGTTCCACACAATTCCTTCACGCAGACATTTGATGGTGGACTCCGGGTGCTCCGGTTTCCCCTACAGTACAAACACATGCGCTGTAGGCATAATTGTGTTGGCTAAATTAGCCGTAGTGTATGAGTGTGAATGCAATAATGGAAAGGTGTTTCCCAGTGTTGGGTTGTGGCTGAAAGGGCATCCGCTGGAGAAGTTGCTGGACAAGTTGAAGGTTTATTCCGCTGTGGCGACCCCTGATTAATAAAGGAACTGAGCTGAAAAGAATATGAATGAATGATACCGAATTAATTTTATTAATTGTTTACTTGAGGCTTTCTCGAGTAAAAATTCTTTTGACATTTGAACTGCATCTGTATTTTCTTAACAGGGCAACTCTGTTGAAAGAAGCTGTCAGTAAGTACCAGGAGTTTCAGAGCGTCAACCAATCGCTCACTGCTTTCCTCATCAACATGCCCAACAACAAGGTGCAGCCTGGTGAAAGTATGACG[C/T]AAGTCTATGCCAAGCAAAACTCGCAGATGGTCAGTATTAAATTGTATTGTTGGGTTTGCGTTTGAATTATTTGATAAATAATTTGATCATTCTGTGTAAAAACAACTTTAACTTTTGTTCTTTTTCGTTGTGCGGAAAATTTAATCGTTTGAATTTGTTTTCGGTTGCAGAGAGCAGTTGAAGACATCAAGAGGAAGCAGGACGATGTGAACAGGATCGTGAAACTTTCCGAGGAGCTGCAGGGCGTTCTCAATGTGCGTTGGCCATCTTGAACTTGAACTCATATTGCAATGTATTTCAGTAGAGATGTGGTCATAATCGTTAATGTATTGTTAAAAACACCCTTGAGCGCCATCTGCAGTTAAAAGCTGTCCTAAAGCACTATCTTCTGTAAAAAACTAAGTTCGGATTCAATTCAAGAGAGAAAAGCAATGGTCAGAATAGGTGCAAAATTGATTTCTCTAACAATCACAGCTCTTCATTCCAGATTCAATTTTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19938
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
ENSDART00000082000 Nonsense 1110 1706 14 15
Genomic Location (Zv9):
Chromosome 3 (position 6506944)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN149912.1 59377
GRCz11 KN149912.1 59377
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAGAACTGGAGGTGCAGCAGATGAGATCTGTAATCCTGGAACTGGAG[A/T]AAAAACTGGAGCTTGTGGATCGACAGAAGAAGGTAATGGTTGAGACAGAG
Long Flanking Sequence:
CTCGAGAGGTTGTGAAAGAAGAGAGGAGCCCTGAGATTATCAGAGAAATTAAGAGGCTGAATGAGCAGCTTACCATTTTGCGTACCAACTACGATTCTACTACGAGTCGTGTGTTTCGTCTGCGCAAGGACAGGGATGAGTGGAAGGCTGAAAGATCCAAGGTGGAAACGAAAGTGGTGACCAAAGAGTTGATAAGGTATGAAAATGACCCTCTTCTGGAGAAAGAAGCTGAACGTCTTAGGAAGGAAGTCAGAGAGGAAATTCAATGCCGCCGAACAGTGGAAGAGAATGTGTTTGATCTTCAAAACAAGTACATTGTGCTCGAGAGACAGAAACCAGAGGAAAGAGTTGTGGTCCAAGAAATAGTGCGTCTCCAGACAGATCCGAGTCAGATTCAGACTCATGAGAGATTAGTCAGGACTTTGGAAGAGACTATCAAGGTTCGACGACAGCTAGAACTGGAGGTGCAGCAGATGAGATCTGTAATCCTGGAACTGGAG[A/T]AAAAACTGGAGCTTGTGGATCGACAGAAGAAGGTAATGGTTGAGACAGAGTTGAGACAAATCAAGGCTAGAATCTATGAACTTGAGAACTGCCCAAAACCTGTTGAGGAAAAGATCGTCATTGAGGAGGTTTTGAAAGTTGAGAGAGACTCTAAAGTCGACAAACTTATCACTGGGCTTCGCACTGAGATTGACAATGAGGGTGCCAGCATTTCAAGACTGGAGAGAGAGATCCGAAACCTCAGAATTAGGATTGAGTCCCTGACCAAGGAGAAATCTGTTGAGAGGATCATCCACAAAGAGGTGATCAGGGTTGAGAAGGACCAAGCAGTGGAGGCAGAGAGAGAGAGCCTTCTGACCCAAGTCTCTCAAGTGAAGAGTACCAGGACCCTTAAAGATGAAGAACTGCTGAGATTGAAAAACAAAATCACCCGAATTCAGACCACCAGGACAAACTTCTCTCAAGAGGAGACCACCTTGATTGCCAACAGGGATAGGATC
Associated Phenotype:
Not determined