Busch Lab

ZMP

esrp2

Ensembl ID:
ENSDARG00000018814
ZFIN ID:
ZDB-GENE-030131-9824
Description:
Epithelial splicing regulatory protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVR8]
Human Orthologue:
ESRP2
Human Description:
epithelial splicing regulatory protein 2 [Source:HGNC Symbol;Acc:26152]
Mouse Orthologue:
Esrp2
Mouse Description:
epithelial splicing regulatory protein 2 Gene [Source:MGI Symbol;Acc:MGI:1924661]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa21001 Splice Site, Nonsense Available for shipment Available now
sa18119 Nonsense Available for shipment Available now
sa18517 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21001
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009698 Splice Site, Nonsense 489 736 12 16
ENSDART00000075089 Splice Site, Nonsense 489 711 12 17
Genomic Location (Zv9):
Chromosome 7 (position 36265980)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34539823
GRCz11 7 34811300
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACACCATTGACATCAAACCTCATGGAGTGCACATGGTCCTCAACCAG[C/T]AGGTGCCTCAGAAAGGCCTGATGTTTCTCGAAACTTGTCATGGGGTCTTT
Long Flanking Sequence:
AAATATTTTTTCCACCAATTCCTAGCAATGCATTTTTGCTGCTCTGTATTGCTATTGTGTATTTGTATATGCATGTCTATATATAAGTGTATGACATAAATATATAATTTAATCCCAAATATAGTGAAAATTAGGCTTTATTTAATTACCTTTTACAAATAGTAGTATATCTGATGATTAATCAGGACTGAAATCCCCCAAAAAACTGTTTATTTGAAAGACTAGAAGATCTTGTCAACTTGACTTTTTTTTGTCTTATAAACTAGGTGTTGAATCGCTATATGTCCACTCCACTGATCTCCACACTTCCACCTCCTCCTCCTCCAATGGTGTCTGTGCCAGTGTTGGCCACTCCACCCTTCATCACCACTGGCAACACACGCGACTGCATCAGGCTGAGAGGCCTGCCGTACACCGCCGCCATCGAGGACATCCTGGAGTTTATGGGGGAACACACCATTGACATCAAACCTCATGGAGTGCACATGGTCCTCAACCAG[C/T]AGGTGCCTCAGAAAGGCCTGATGTTTCTCGAAACTTGTCATGGGGTCTTTAACTTATGTTGAGTATTTTTGTTCTTCTTTTTAGGGTCGACCCTCTGGTGATGCCTTTATTCAGATGAAGTCAGCTGACCGTGCATTTATGGTGGCTCAGAAGTGCCACAAAAAGATGATGAAGGATCGTTATGTGGAGGTTTTCCAGTGCTCCACTGAGGAGATGAGCTTTGTGCTGATGGGGGGAACACTGAACCGCAGCGGTCTGTCACCACCTCCATGCAAACTGCCATGTAAGAGACTGCCTGAAAACCCCTATTCTCAGTGCATGCAATCAATATTCCAAAAATATTTATGCATAATACCAGTTCCAAACCACAGTTGACAATTAAGGGTTGGTTTAATTCTAGGTTTAACACCTACCTTTTCATCTTCATTCTTCCCTCAGTTGAGTGTGCTTTACTTCTAGTCGTTGGTAAAAATTATTCTACATCACTTTACATTAATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18119
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009698 Nonsense 579 736 14 16
ENSDART00000075089 Nonsense 579 711 14 17
ENSDART00000009698 Nonsense 579 736 14 16
ENSDART00000075089 Nonsense 579 711 14 17
Genomic Location (Zv9):
Chromosome 7 (position 36267940)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34541783
GRCz11 7 34813260
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGCGTTTCCTGCGGCTCCAGCTATGCTTCCCACTGAGGCAGCGCTGTA[T/A]CAGCCCCCCCTGCYGGCCACTCCAAGAACTCCACAGGCCYCAACACACAG
Long Flanking Sequence:
CTAGTCTGCACTCTTCTGCTGCCATTGGCACGGCTGTTTGAGCTTCAGTTTCAGATTATCTGCTAGAAAGCAGTGTGATCACCTCTGTCACAGATCTAAAGGTGCAACATTTTGGCATTTAGAAAGAGCAAGCCTGTTGCAGCACTAAAGGAGGGGCTGTTTGCTTAGTTATTTGATCTGGTTGTTTGACCTTGGCTTGAGAATTAGCCGTATGTGCTCACGCCACATCAGAGGAGACACTGGTTGTCCCTGTGCCAGTTCAGCTAAATATACATGACATTCACACACTCCAGCAAGGTTGGCTCCTCTCATTTTCACCAAACCACACAAAGTGGAAATGCTAAAAAGTTAATTTACTTAGTGATGATGCATTAGTTAACAAATTTACTAGGGCATCATAATAGAACTTTTTTTATCCTGTGTCTTTCAGGTCTCTCTCCACCAACATATGCTGCGTTTCCTGCGGCTCCAGCTATGCTTCCCACTGAGGCAGCGCTGTA[T/A]CAGCCCCCCCTGCTGGCCACTCCAAGAACTCCACAGGCCCCAACACACAGCCCTGCACCTGCTTTCGCCTACTATTCTCCACAGCTCTACATGAACATGAATATGAGCTACACCACCTACTACCCCAGGTACCACACTTACACAAGCTGGCTTGATTGGATAAATAAGACCTTTTAGCTTTTGTCTAAATTCACTTGATGCCATTTAAAGATACCTTTTAAGGCTGTAATTTTACCTGGTTAAGTTTTGTTGTTAGGAGTAACATATCTGAGATTGTCATTTAAGCATCTTTTAAATGAGCAATATCATACGAGTAGCAGTGTGATATGGCTGTAGGCACTGGTGGGAGGCATGCGTGCCTTAGTGTCCCACCAGTGATGATATACAGCCATTTCGCACTGCTACGCGTGTAATATTGTGTTCATCCAACAGTTTAACATCATCGTTTGTATAATCAAACACAGAGTCTCGAATTATTTTGTACAATGAACTACTTTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18517
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009698 Nonsense 579 736 14 16
ENSDART00000075089 Nonsense 579 711 14 17
ENSDART00000009698 Nonsense 579 736 14 16
ENSDART00000075089 Nonsense 579 711 14 17
Genomic Location (Zv9):
Chromosome 7 (position 36267940)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34541783
GRCz11 7 34813260
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGCGTTTCCTGCGGCTCCAGCTATGCTTCCCACTGAGGCAGCGCTGTA[T/A]CAGCCCCCCCTGCYGGCCACTCCAAGAACTCCACAGGCCYCAACACACAG
Long Flanking Sequence:
CTAGTCTGCACTCTTCTGCTGCCATTGGCACGGCTGTTTGAGCTTCAGTTTCAGATTATCTGCTAGAAAGCAGTGTGATCACCTCTGTCACAGATCTAAAGGTGCAACATTTTGGCATTTAGAAAGAGCAAGCCTGTTGCAGCACTAAAGGAGGGGCTGTTTGCTTAGTTATTTGATCTGGTTGTTTGACCTTGGCTTGAGAATTAGCCGTATGTGCTCACGCCACATCAGAGGAGACACTGGTTGTCCCTGTGCCAGTTCAGCTAAATATACATGACATTCACACACTCCAGCAAGGTTGGCTCCTCTCATTTTCACCAAACCACACAAAGTGGAAATGCTAAAAAGTTAATTTACTTAGTGATGATGCATTAGTTAACAAATTTACTAGGGCATCATAATAGAACTTTTTTTATCCTGTGTCTTTCAGGTCTCTCTCCACCAACATATGCTGCGTTTCCTGCGGCTCCAGCTATGCTTCCCACTGAGGCAGCGCTGTA[T/A]CAGCCCCCCCTGCTGGCCACTCCAAGAACTCCACAGGCCCCAACACACAGCCCTGCACCTGCTTTCGCCTACTATTCTCCACAGCTCTACATGAACATGAATATGAGCTACACCACCTACTACCCCAGGTACCACACTTACACAAGCTGGCTTGATTGGATAAATAAGACCTTTTAGCTTTTGTCTAAATTCACTTGATGCCATTTAAAGATACCTTTTAAGGCTGTAATTTTACCTGGTTAAGTTTTGTTGTTAGGAGTAACATATCTGAGATTGTCATTTAAGCATCTTTTAAATGAGCAATATCATACGAGTAGCAGTGTGATATGGCTGTAGGCACTGGTGGGAGGCATGCGTGCCTTAGTGTCCCACCAGTGATGATATACAGCCATTTCGCACTGCTACGCGTGTAATATTGTGTTCATCCAACAGTTTAACATCATCGTTTGTATAATCAAACACAGAGTCTCGAATTATTTTGTACAATGAACTACTTTCTT
Associated Phenotype:
Not determined