ZMP
ern2
Ensembl ID:
ZFIN ID:
Human Orthologue:
ERN2
Human Description:
endoplasmic reticulum to nucleus signaling 2 [Source:HGNC Symbol;Acc:16942]
Mouse Orthologue:
Ern2
Mouse Description:
endoplasmic reticulum (ER) to nucleus signalling 2 Gene [Source:MGI Symbol;Acc:MGI:1349436]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17230 | Essential Splice Site | Available for shipment | Available now |
sa12750 | Nonsense | Available for shipment | Available now |
sa18038 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17230
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081355 | Essential Splice Site | 91 | 950 | 3 | 24 |
ENSDART00000143587 | Essential Splice Site | 95 | 927 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 8264186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 8503991 |
GRCz11 | 1 | 9188102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACGGMAGTCTGTATGTTCTCGGAGGAAAGAGGAAAGAAGGTCTGATGG[T/G]GAGTRTTGTGAGCGTGGCWGYGGATGTGTTTATCAGAGAGTGACAGCTCT
Long Flanking Sequence:
ACATTATTTCTGTTAATTAACAAGACGTTTGTCTAAGCAAACTCAGACCTTACTGTCCTATTTGAATAGCTAAAAATTAAGGCATGATCATATTTTTTAGGAAACAAGTCAAATAAGCGTAATCGAGAGGCCTTTGCCTTGTGATGATCAACTAAAAGTCAAGTTATTATTTGTTGGTACTAAAACTTGGATAGGCAACTAGACTTTTGTCAGGTGGTGTAGAAAGGGCAAATGTATACTGTGAAAAATGGCATTTCGTTTCATTTTTCATAAATATTTCCACAGACCACCCAACACTTAAAAATCTCTGATTTAGGCCAAATACAAAAAAAGTTTAGTCCTGCATTCAGGTGTGCTTTCAGTCTTGTTTGTAATGCAAACTTTTTCTTGATCAGACTTTAAAGTCGTGTCCGCTTCCTCTTGTAGGCCAGGCTTTTTACCAGACCCCAATGACGGAAGTCTGTATGTTCTCGGAGGAAAGAGGAAAGAAGGTCTGATGG[T/G]GAGTATTGTGAGCGTGGCTGTGGATGTGTTTATCAGAGAGTGACAGCTCTTGACATTTATATGAATGTTTTCCTCAGAAACTGCCATTCACTATTCAAGAGCTGGTGCAGTCGTCTCCCTGCAGGAGCTCAGATGGAGTACTCTACACCGGTATCAGCAAACCTCTTTATGATGTTTTATGGTCAAATTCGTGTTTGATAACTGTGTTTTGTGGCAGTGAAGGATTGCTGTGGTCATGTTAGATTTTATTTGAAGAAAGAAAGTTAGGGAAATGAGCTAATATAACCTGAACTAATACATTCATTCATTCATTTTACTTCGGCTTAGTCCCTTATTTATTAGGGGTCGCCACAGTGTTTTTGCCTGTTGTGTCCTGCCTTGAAATTCAATTCTGTTTTCACAGAATACTACAACACATAATCAACTCAATTTGGATTTTAGTCTGTGTTTGATGCAGCACAGGCTCATTGTGAAAACATACGCCTGTATACATTTCTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12750
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081355 | Nonsense | 191 | 950 | 6 | 24 |
ENSDART00000143587 | Nonsense | 195 | 927 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 8262594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 8502399 |
GRCz11 | 1 | 9186510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATACAACGATTACTCAGCTCCTCTATATGACGACAAAAAATATGAATA[T/G]AGYAGGYTCCTCACAATGCAYGATTGTAGATATTTACATACAGTTGAGGT
Long Flanking Sequence:
CTCTGGTGGATTTGCGGAAACAAAAACTGCAAAAAACTTACCTCCTGGAACATATTGTGCGCTGTCTAGCAATGTATGCAGGGGTTGGTTTGATAGCATTAGTCAATGGGTGTGGGAAGCCTGATAGTATGGTTATAAAATGATAAAAAGCTGTACATCCTTGTATGCTCTCCTTTATTGAACTCTGTGTATTCCCAGGTAAAAAACAGGACACCTGGTTTGTGGTCGATCCTCAGACAGGTGAAAAACAGACAAGTTTGAGCACCTCGTCTTCAGACTCCATCTGTCCCTCTGCACCTCTGTTGTACATCGGTCGCACAGGTTTGAACACACACACAGCACACTCTTTTCTATGCATATGTATTGATATGCATTTCATACATGTTTCTCTCTGCAGAATATATGATCACCATGTATGACACGAAGACTCAGGAGCTCCGCTGGAATGCCACATACAACGATTACTCAGCTCCTCTATATGACGACAAAAAATATGAATA[T/G]AGTAGGTTCCTCACAATGCATGATTGTAGATATTTACATACAGTTGAGGTCAACATGCTTAGCCCTCCAGTGATTTTGTTTTATTTTTTCAACTATTTGCCAAATAATGTTTAACAGAGTAAGGAATTTTTCCTATAATATTTTTTCTTCTGGTGAAAGTCTCATTTGTTTTATTTTAGCTAGAATAAAAGCAGTTTTCAATTTTTTAAAAACCATTTTAAGGCATATCTGTCAACCCCGTTTTTCCCAGGATTCTCCTGTATTTTACAGTTCTATCCCGCTATCATCCCACAAAGGTATTTTCCATTATTTCTCCCATATTTTCAGTCTTTCTCTGAAGGGTGGCAACAAGCATTAAAGAGCCGAGCCTCTATCCTCTGCGCAACCATACCGCCGAACCACCAGGTGACGCCCTAACGCTCTTAAATGTGAGTCCGTTCTGTGCTTTCGGTTTATTAATATATGAAAACAGTTTGAAATAAATATATAAACGATGGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18038
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081355 | Nonsense | 691 | 950 | 17 | 24 |
ENSDART00000143587 | Nonsense | 668 | 927 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 1 (position 8253576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 8493381 |
GRCz11 | 1 | 9177492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGATTTAAAGCCCAGGAATATTTTGCTRTCTCTKCCCGGGGMACTGGGT[C/T]GAGTGCGGGCGCTSATCTCAGATTTYGGCTTGTGTAAGAAGCTTCCAGAT
Long Flanking Sequence:
AATATTAAAGGTTTAATTAAAATGTTTAACACAAAAAGTATAAACAATCAATTTTAAGTTCATCAGATTTTAATTTATCTAGCCTGTAAGATCTAAAAAAAGAAAAAACCCTGGTGTAATAAGCAGTATAACCACATGCATCTTACTCTGTTTTTCTGTTGTTGCTGGATGCAGTATGTAGAAGACCCGAGCTGTCCTCACTCAGAGCTGAACCCGGTGTCCCTGCTGGAGCAGACCATGTGTGGCCTCAGTCACCTGCACTCCCTCAACATCGGTCAGCACCAAAATATGAGTCCAACCTCAACATCCCTTTCTGAAACTATATCATAATGCATCACAGTTGCACATGGCGGTGTTGCATTGCACTGATGTTTATTAATTGCTATTGAGTAACTGCATGCAAGCACACTGCCATTAGTAATCACATGACCCTCTCATTCTCAGTCCACAGGGATTTAAAGCCCAGGAATATTTTGCTGTCTCTGCCCGGGGCACTGGGT[C/T]GAGTGCGGGCGCTCATCTCAGATTTCGGCTTGTGTAAGAAGCTTCCAGATGGTCGGCACAGTTTCAGCCTACGCTCCGGGATACCTGGAACCGAAGGCTGGATCGCCCCTGAATTACTCATAAACGCTCCGAAAGGGAACCCTGTATGTCTGCTAGTGAATATGCATACAAACACGCACACACACAGCACATGTTAACTGTAAAAAACAGATACTGTACAGCTTTACTGAATGTGCATGTGATTTCCCTTCACTCAACAACAAATCTTTTCAATTTAATGGTATTCAGAAGAGAAAAAGGGATGTAAAAATATAATTATCTAGCAGGACGTATTTATAGAGGCATTCAAATGTCACAGTCTAGCACTTATTTTAGGAGAACTGAAACTAGTTCATTCACTCATTCATTTTCCTTCGGCATAGTCCCTTTATTTATCAGGGGTTGCCACAGCGGAATGAACCGCCTACTATTCTGGCATATGTTTAACACAGCGGATGCCC
Associated Phenotype:
Not determined