ZMP
im:7145112
Ensembl ID:
ZFIN IDs:
Description:
Im:7145112 protein [Source:UniProtKB/TrEMBL;Acc:Q6DG69]
Human Orthologue:
ELAC2
Human Description:
elaC homolog 2 (E. coli) [Source:HGNC Symbol;Acc:14198]
Mouse Orthologue:
Elac2
Mouse Description:
elaC homolog 2 (E. coli) Gene [Source:MGI Symbol;Acc:MGI:1890496]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13936 | Nonsense | Available for shipment | Available now |
sa40004 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26000 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9564 | Essential Splice Site | Available for shipment | Available now |
sa11507 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13936
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 |
---|---|---|---|---|---|
ENSDART00000048095 | Nonsense | 217 | 865 | 7 | 25 |
ENSDART00000122518 | Nonsense | 173 | 821 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 3 (position 11477135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 10609110 |
GRCz11 | 3 | 10575653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCMGSCCTTACACTGAGCCTCAGTATAAAGACGAAACCATGACCGTCAGC[C/T]AGATTCCTCTMTTCTGTGAGTCTCACCGTAGTTTTACAGCATTCTCAACA
Long Flanking Sequence:
CAGAAACTGCATTTGAAAAACACCAGCATTCATTTTAAGAAATATTATTAAAGTTCTTTGAATGTGACTTCTCACAACGGTCAAAGATTTTAATGTCAATATTAGGTGCAAGTGAAATGTGAAGTGCAGTAAGGACTTTCATAGTGTTACATATGCTGGGTATGAATGCTGCTTTAAAGTCCTTGAGTCTGCTGAAAGCATGGAAACCCTGCTCACACCAAAATGATAAAACTTAAACATAATGGGGGGGATCATAATGAATTCTTTTCTTCTGTTTCAGGACAGGTTTTTAAAAGCCATTAAAGTGTTTTCAGGACAGCTGGAAGACATTAAACTAGGTTACTAGTGCACTGTTATCTTTATTCTATCTGTGTGTATATTAGATTTCTGTATTCTCACAGCTGAGCAAGTGATGCTGATGTGTTTTTTTGTCTTTCATTTTTACAGCTGTCAGGCCTTACACTGAGCCTCAGTATAAAGACGAAACCATGACCGTCAGC[C/T]AGATTCCTCTCTTCTGTGAGTCTCACCGTAGTTTTACAGCATTCTCAACATTTTTAAGGTGACCTATTATGCCCCTTCTTACAAGATGTAAAAGAAGTCTCTGATGTCCCTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAATTTTTAGCTCAAAACATCACAGGTCATGTTTTAAACATCACAGATAACATTTGTGACCTAGTAACTCTGGCCACTCCCACCCGCAGTCTTCGTTCCTCATCTGCAATCTTGCTGTATCAGCCGCTTGTAAAGTGAAGACTGTAGGTGGTCGTGCTTTTCCGTACAGTGCGCCTAAGCTATGGAACGTCCTATCCACCAACATCAGGAATGCTGTTTCTCTGGATTTTTTAAAGAAAATTCATAAGACTCACCTTTTTACCGTTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40004
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048095 | Essential Splice Site | 222 | 865 | 7 | 25 |
ENSDART00000122518 | Essential Splice Site | 178 | 821 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 3 (position 11477118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 10609093 |
GRCz11 | 3 | 10575636 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAGTATAAAGACGAAACCATGACCGTCAGCCAGATTCCTCTCTTCTG[T/G]GAGTCTCACCGTAGTTTTACAGCATTCTCAACATTTTTAAGGTGACCTAT
Long Flanking Sequence:
AAACACCAGCATTCATTTTAAGAAATATTATTAAAGTTCTTTGAATGTGACTTCTCACAACGGTCAAAGATTTTAATGTCAATATTAGGTGCAAGTGAAATGTGAAGTGCAGTAAGGACTTTCATAGTGTTACATATGCTGGGTATGAATGCTGCTTTAAAGTCCTTGAGTCTGCTGAAAGCATGGAAACCCTGCTCACACCAAAATGATAAAACTTAAACATAATGGGGGGGATCATAATGAATTCTTTTCTTCTGTTTCAGGACAGGTTTTTAAAAGCCATTAAAGTGTTTTCAGGACAGCTGGAAGACATTAAACTAGGTTACTAGTGCACTGTTATCTTTATTCTATCTGTGTGTATATTAGATTTCTGTATTCTCACAGCTGAGCAAGTGATGCTGATGTGTTTTTTTGTCTTTCATTTTTACAGCTGTCAGGCCTTACACTGAGCCTCAGTATAAAGACGAAACCATGACCGTCAGCCAGATTCCTCTCTTCTG[T/G]GAGTCTCACCGTAGTTTTACAGCATTCTCAACATTTTTAAGGTGACCTATTATGCCCCTTCTTACAAGATGTAAAAGAAGTCTCTGATGTCCCTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAATTTTTAGCTCAAAACATCACAGGTCATGTTTTAAACATCACAGATAACATTTGTGACCTAGTAACTCTGGCCACTCCCACCCGCAGTCTTCGTTCCTCATCTGCAATCTTGCTGTATCAGCCGCTTGTAAAGTGAAGACTGTAGGTGGTCGTGCTTTTCCGTACAGTGCGCCTAAGCTATGGAACGTCCTATCCACCAACATCAGGAATGCTGTTTCTCTGGATTTTTTAAAGAAAATTCATAAGACTCACCTTTTTACCGTTGCATTAACTTAGATTGATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26000
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048095 | Nonsense | 365 | 865 | 12 | 25 |
ENSDART00000122518 | Nonsense | 321 | 821 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 3 (position 11470819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 10602794 |
GRCz11 | 3 | 10569337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGACTGTCCGTCAGAGGACTTCATAAAGCCGCTCTGCTCCAATCCCATCT[T/A]GAAAAGGTCAGCTGTGGTCCAATGTTGAGCAATTTCAGGATGAGCTTCAA
Long Flanking Sequence:
AAGGTGAAAAACTTAAATAATTACAAAAAAAACCAAGGTGCACTAATTGTTAATTGCATTGTTTTATTGTATATTAATTAACGTTTCTCAAGAATGTAAATGCACCCAAATTAGCCCAAAGGCTTGTTTCCATTGGTCGTCTTTTTTGCCAGATGTTATAAACCTGGGGTGTTGCTTCAACACACCTGCCAGGAGGTTTCTAGTATATCCGGCAAAAGCTTGATTTGCTGGTTCAGGTGTGTTTGATTAGGGCTAAACCCTCCAGGACTGAGTTTAGACACCCCTGTTATAAACCAATACAAATACCGAATTCAGATTATAAAGAAACCTCCAGTGTTGAACAGTGGGGAGGATCAGTGTTATTTTGTTGTTGAGTGTTCAGTGTGTGTTTCAGATCCGGCCAGAGGAGCTCTGCACACCTGCTGATCCCGGACCAGTCTTTATAGTCGTCGACTGTCCGTCAGAGGACTTCATAAAGCCGCTCTGCTCCAATCCCATCT[T/A]GAAAAGGTCAGCTGTGGTCCAATGTTGAGCAATTTCAGGATGAGCTTCAAAACAGTCAGGCTTGATCGTGTCAGATCAACAGCAGTGAATGGTTTGATATTTCTGCAGGTTTCAGAGTGGCGGATCTGAGGACTCTGCTGCTCTCGTGGTGCACATGACTCCTGAAGCGGTGCTTAACACACAGGAGTACAAGAGCTGGATGGAGAGGTGCGCATAGTATGCACTGTGTGTCTCTGTGTTTGGTGTTTCTCTGTGTGTGCATTTGTTTTGTTTGTGTGGTTGTTGTGTGTGCCTGTGTGTCTATGTTTGTGTGTACATGTGTGTTTGTGAATGCTTGCATGTTTGCGTCTCTGTGTCTGGTGTGTCTCTGTGCCTGTGTGTATTTTTGTGTATGATGAATGCTTGTATGTTTTGTGTCTGTGTATCTCTGTGTATGTGCGCATTTGTGCGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGCATGCTCGCGTGCAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9564
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 |
---|---|---|---|---|---|
ENSDART00000048095 | Essential Splice Site | 367 | 865 | 12 | 25 |
ENSDART00000122518 | Essential Splice Site | 323 | 821 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 3 (position 11470811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 10602786 |
GRCz11 | 3 | 10569329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTCAGAGGACTTCATAARGCCGCTCWGCTCCAATCMYATCTTGAAAAGG[T/G]CAGCTGTGGTCCAATGTTGAGCAATTTCAGGATGAGCTTCAAAACAGTCA
Long Flanking Sequence:
AAACTTAAATAATTACAAAAAAAACCAAGGTGCACTAATTGTTAATTGCATTGTTTTATTGTATATTAATTAACGTTTCTCAAGAATGTAAATGCACCCAAATTAGCCCAAAGGCTTGTTTCCATTGGTCGTCTTTTTTGCCAGATGTTATAAACCTGGGGTGTTGCTTCAACACACCTGCCAGGAGGTTTCTAGTATATCCGGCAAAAGCTTGATTTGCTGGTTCAGGTGTGTTTGATTAGGGCTAAACCCTCCAGGACTGAGTTTAGACACCCCTGTTATAAACCAATACAAATACCGAATTCAGATTATAAAGAAACCTCCAGTGTTGAACAGTGGGGAGGATCAGTGTTATTTTGTTGTTGAGTGTTCAGTGTGTGTTTCAGATCCGGCCAGAGGAGCTCTGCACACCTGCTGATCCCGGACCAGTCTTTATAGTCGTCGACTGTCCGTCAGAGGACTTCATAAAGCCGCTCTGCTCCAATCCCATCTTGAAAAGG[T/G]CAGCTGTGGTCCAATGTTGAGCAATTTCAGGATGAGCTTCAAAACAGTCAGGCTTGATCGTGTCAGATCAACAGCAGTGAATGGTTTGATATTTCTGCAGGTTTCAGAGTGGCGGATCTGAGGACTCTGCTGCTCTCGTGGTGCACATGACTCCTGAAGCGGTGCTTAACACACAGGAGTACAAGAGCTGGATGGAGAGGTGCGCATAGTATGCACTGTGTGTCTCTGTGTTTGGTGTTTCTCTGTGTGTGCATTTGTTTTGTTTGTGTGGTTGTTGTGTGTGCCTGTGTGTCTATGTTTGTGTGTACATGTGTGTTTGTGAATGCTTGCATGTTTGCGTCTCTGTGTCTGGTGTGTCTCTGTGCCTGTGTGTATTTTTGTGTATGATGAATGCTTGTATGTTTTGTGTCTGTGTATCTCTGTGTATGTGCGCATTTGTGCGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGCATGCTCGCGTGCAAAATTGTCTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11507
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048095 | Essential Splice Site | 718 | 865 | 23 | 25 |
ENSDART00000122518 | Essential Splice Site | 674 | 821 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 3 (position 11449773)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 10581748 |
GRCz11 | 3 | 10548291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGTGKGNNAGGCGAGGAGAGAGTTTGATTCATCTTTTGGTTTGTTCTC[A/T]GGCAAAAACGCAACTCTTTTGATTCATGAAGCCACGCTGGAGGACGGGAT
Long Flanking Sequence:
TTTTCTACACATATTCATATATACGTTTCGCTCAAAGTCTCCCTTCATTCAGAATCAGGTCATTAAACGACCATCAGTCCAGCGGTAGAGAGAGAGAGTGAGTCTGTAATTGCGTCTGAATCTCTGTAGTGACTCGCGGGTCGATACGGATGAAGCCTGCGTTTAAATGCTGCTTCCTGTCTTTATCAGTGGCGCAATCGATCACTTCTGAGTCTCCCAATCCTCTTTAATGGCTCCTGAGGGAGTCTCCCCCCTCCCGAACGCTGGAAATGGTTCGCTCCACTCGTCTCATTAGGAAAGGCCTTTGTCGTCTCGGCTCTTGCTGGAGTTTTCATGATTGATTTCTGGAGGGAGGGAAAAATGGAGTGTGTGTTGGTGTGTGAATGTTAGAGTGTGTTTTACAATGGGATGAAAGGGGGAAGAGCGTGTCAGATGTAATTTATCTGTGTGTGTGTGTGTGAGGCGAGGAGAGAGTTTGATTCATCTTTTGGTTTGTTCTC[A/T]GGCAAAAACGCAACTCTTTTGATTCATGAAGCCACGCTGGAGGACGGGATGGAGGACGAGGCCTTCGAGAAGAGACACAGGTGAGGAAACTGATTTAGTGGCAAATTCTGAGCTGTTAAAAGGGGGCCTGTTATAGAAAAATCACTTTAATAAGAGGTTTAAACATCATTTTGTGACAGAAATGGGTGTTTATAATCAGCTTCCAACGATAAAGATTAATTTTATTTGTTATAAACACACTTGATAAAAACTGTCTGCAGAAACACTTTGATTGAACAGTTTGTATATGTCTTCAGAGGGGGAAAGCCCCGCCCACTAGTGACCATTTCTCTCTCATAAGCATAGGACGTCAGTCTTGTTTTTGAATTTGCCACTATGCTGACACGCAGGCATTTGTAGCTTCCCACGCTCTTTTAAAAATTACACAATCTCATTTGAATTTAAAGTGACGATCACCAAAATGGCTCATAATAGGTCCCCTTTAAGAGCAATTCTGAATT
Associated Phenotype:
Not determined