ZMP
wu:fb77g05
Ensembl ID:
ZFIN ID:
Human Orthologue:
EML5
Human Description:
echinoderm microtubule associated protein like 5 [Source:HGNC Symbol;Acc:18197]
Mouse Orthologue:
Eml5
Mouse Description:
echinoderm microtubule associated protein like 5 Gene [Source:MGI Symbol;Acc:MGI:2442513]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42987 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9672 | Essential Splice Site | Available for shipment | Available now |
sa12262 | Nonsense | Available for shipment | Available now |
sa10880 | Nonsense | Available for shipment | Available now |
sa23160 | Nonsense | Available for shipment | Available now |
sa36492 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11871 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42987
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112088 | Nonsense | 760 | 1908 | 18 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43191557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43156232 |
GRCz11 | 17 | 43146770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTAAAGGGGAAGTAAGGATAAGATATTTGTTATTAAAATCAACCCCTA[C/A]ATGCCAGACAAGCTGATCAGCGCTGGAGTGAAGCATATGAAGTTTTGGCA
Long Flanking Sequence:
ATTAGCCAAAGGAACATACATTTTTGAGCAAAATTTAGTGTCTGAGTGAGAAAAAAACTAACCTAATTTAAACAATGTAGTTGTTGAATGAATTTTGTCGTCACTAAAGTGTACCTTTTTAGACCTATAGTATTGGCCAAGAAAATTTTTTATTAGTGTTTCTTCATACAAATTAAATTATTTAATAACACAATAAATAATTATTACAAAGCATTTACGTTTTCAGTTTTCAAACATATGCATCCATTTTTGTCCTGAATTTTAATTTTGTGCAGTATAGTATGTGTCCGCCTATTGTATCAAAGTATATATGAATGCGTTCATGCACCCTCTGAGGAGAATAGCCTTCACAATGCCACTTCAGAAGTGCTTCTGTGCCACCTTTGCTGTGTAAATTTGACAGTTAGTCCCACTGATTGTAAAAACTAATAATAAAAGCTTCTCTTTTTGACTTAAAGGGGAAGTAAGGATAAGATATTTGTTATTAAAATCAACCCCTA[C/A]ATGCCAGACAAGCTGATCAGCGCTGGAGTGAAGCATATGAAGTTTTGGCACCGAGCAGGTAAGACTATAAAGTGAGTCACTCTTGTGAAGCTTGTGAATACCTAAACGCCATCATCTCACACTTTTTTTGTTCTCAGGTGGAGGATTGATCGGGAAGAAGGGCAGCATGGGAAAAACCGAGACCATGATGTGTGCGGTATACGGCTGGACTGAAGAAATGGTCTTTTCTGGAACCTGCACTGGAGACATCTGCATCTGGAGGGACATGTTCTTGGTGAAGACCGTCAAAGCTCACGACGGGCCTGTTTTCAGCATGCACGCGTTGGAGAAGGTGATAACACATGCAGCTGGAAACAAGAGGAAGTTGCTCCAGAAATGTGATTTTGAATATCTTGTTGTTAAGGGTTTCGTGACTGGTGGAAAGGATGGAATAGTGGCTTTGTGGGACGATACCTTTGAAAGATGCCTCAAAACATATGCCATAAAACGAGCGGTGCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9672
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112088 | Essential Splice Site | 780 | 1908 | 18 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43191497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43156172 |
GRCz11 | 17 | 43146710 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTGATCAGCGCWGGAGTGAAGCATATGAAGTTTTGGCACCGAGCAGG[T/C]AAGACTATAAAGTGAGTCACTCTTGTGAAGCTTGTGAATACCTAAACGCC
Long Flanking Sequence:
ACCTAATTTAAACAATGTAGTTGTTGAATGAATTTTGTCGTCACTAAAGTGTACCTTTTTAGACCTATAGTATTGGCCAAGAAAATTTTTTATTAGTGTTTCTTCATACAAATTAAATTATTTAATAACACAATAAATAATTATTACAAAGCATTTACGTTTTCAGTTTTCAAACATATGCATCCATTTTTGTCCTGAATTTTAATTTTGTGCAGTATAGTATGTGTCCGCCTATTGTATCAAAGTATATATGAATGCGTTCATGCACCCTCTGAGGAGAATAGCCTTCACAATGCCACTTCAGAAGTGCTTCTGTGCCACCTTTGCTGTGTAAATTTGACAGTTAGTCCCACTGATTGTAAAAACTAATAATAAAAGCTTCTCTTTTTGACTTAAAGGGGAAGTAAGGATAAGATATTTGTTATTAAAATCAACCCCTACATGCCAGACAAGCTGATCAGCGCTGGAGTGAAGCATATGAAGTTTTGGCACCGAGCAGG[T/C]AAGACTATAAAGTGAGTCACTCTTGTGAAGCTTGTGAATACCTAAACGCCATCATCTCACACTTTTTTTGTTCTCAGGTGGAGGATTGATCGGGAAGAAGGGCAGCATGGGAAAAACCGAGACCATGATGTGTGCGGTATACGGCTGGACTGAAGAAATGGTCTTTTCTGGAACCTGCACTGGAGACATCTGCATCTGGAGGGACATGTTCTTGGTGAAGACCGTCAAAGCTCACGACGGGCCTGTTTTCAGCATGCACGCGTTGGAGAAGGTGATAACACATGCAGCTGGAAACAAGAGGAAGTTGCTCCAGAAATGTGATTTTGAATATCTTGTTGTTAAGGGTTTCGTGACTGGTGGAAAGGATGGAATAGTGGCTTTGTGGGACGATACCTTTGAAAGATGCCTCAAAACATATGCCATAAAACGAGCGGTGCTGGCCCCAGGCTCCAAAGGTGCGTTTTTGTTGCTCTATCTCTCTCTCTCTCTCTCTCTCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12262
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 |
---|---|---|---|---|---|
ENSDART00000112088 | Nonsense | 1247 | 1908 | 28 | 44 |
ENSDART00000112088 | Nonsense | 1247 | 1908 | 28 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43127441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43092116 |
GRCz11 | 17 | 43082654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGAGAGAAYGAGATYGTCTATGTAATCAAAGCCTTATCTACAAACATG[C/T]GACCCATGACGGGGGYCAAGCCCCATTTAYAACAGAAGGAGCCAACTGTA
Long Flanking Sequence:
CAACATTATTCAGCTTAGTTTAGTTGAATCATTAATGTTGAGTCAGATCATTTGATTCAATTCATCTAATTGACATGTTTATTTGTTCATTATTTCAACAGGGAAAATATGCCAAGTTTAAACGGTACATGGCCCACAGTACCCATGTGACTAATGTGCGCTGGTCACACGATGACTCTTTGCTGGCATCGGTGGGCGGCTCTGACACCTGTCTAATGATCTGGAACCACGAGACCGAGAGCTGCAGAGAGGCCAGACAGTGTGACAGCGAAGAGTCAGACATCGAGAGCGAAGATGATGGAGGTGAAAAAGATCATGTATAAAAGAGCAGTTATTACTGTCCTCCACCCTCTGCTTGATTTTGAAAGGATAGCTATCTGTCATATGAAAAACCGTTCATTTAAACTCCATATGTGCTGCTGCTTTTTGTAGGCTATGACAGTGATGTAACGAGAGAGAACGAGATTGTCTATGTAATCAAAGCCTTATCTACAAACATG[C/T]GACCCATGACGGGGGTCAAGCCCCATTTACAACAGAAGGAGCCAACTGTAGACGAAAGGTAAGTTAGAACTGACATCAGTGTACAGTATAATGTACAGTTCTGTAAATGCACAAGGACAAGAAGGAAGGATCAGCTGGAAATCTTAAACTTCACACTTATATTTTAGGGATGCAGTAGGAACACTTGAAGGCAAAATTATTAGCCTAATTGTATTTTTATTCTTTTACACATATCAAGAGCTGTTTAACAGAGCTAGGATTTTTTTTAGTTTTTTTTTCTAATTGAGAAAGTCTTATTTCTTTTAGTTTGGCTGGCATTAATCTAGTTTACTTAAAAAAATATTTTTAAGTTATATAATATAATAATAAAATAAAACTATAACAAAAAAGTGTGTATTGTCATTATGGCAAAGATTAATGTTATAAGAATTCAGTTAATAAAACTGTTACAATTAAAATTGGGTTATAATGTAATGAAATGTACTACTAAAATAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10880
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 |
---|---|---|---|---|---|
ENSDART00000112088 | Nonsense | 1247 | 1908 | 28 | 44 |
ENSDART00000112088 | Nonsense | 1247 | 1908 | 28 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43127441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43092116 |
GRCz11 | 17 | 43082654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGAGAGAAYGAGATYGTCTATGTAATCAAAGCCTTATCTACAAACATG[C/T]GACCCATGACGGGGGYCAAGCCCCATTTAYAACAGAAGGAGCCAACTGTA
Long Flanking Sequence:
CAACATTATTCAGCTTAGTTTAGTTGAATCATTAATGTTGAGTCAGATCATTTGATTCAATTCATCTAATTGACATGTTTATTTGTTCATTATTTCAACAGGGAAAATATGCCAAGTTTAAACGGTACATGGCCCACAGTACCCATGTGACTAATGTGCGCTGGTCACACGATGACTCTTTGCTGGCATCGGTGGGCGGCTCTGACACCTGTCTAATGATCTGGAACCACGAGACCGAGAGCTGCAGAGAGGCCAGACAGTGTGACAGCGAAGAGTCAGACATCGAGAGCGAAGATGATGGAGGTGAAAAAGATCATGTATAAAAGAGCAGTTATTACTGTCCTCCACCCTCTGCTTGATTTTGAAAGGATAGCTATCTGTCATATGAAAAACCGTTCATTTAAACTCCATATGTGCTGCTGCTTTTTGTAGGCTATGACAGTGATGTAACGAGAGAGAACGAGATTGTCTATGTAATCAAAGCCTTATCTACAAACATG[C/T]GACCCATGACGGGGGTCAAGCCCCATTTACAACAGAAGGAGCCAACTGTAGACGAAAGGTAAGTTAGAACTGACATCAGTGTACAGTATAATGTACAGTTCTGTAAATGCACAAGGACAAGAAGGAAGGATCAGCTGGAAATCTTAAACTTCACACTTATATTTTAGGGATGCAGTAGGAACACTTGAAGGCAAAATTATTAGCCTAATTGTATTTTTATTCTTTTACACATATCAAGAGCTGTTTAACAGAGCTAGGATTTTTTTTAGTTTTTTTTTCTAATTGAGAAAGTCTTATTTCTTTTAGTTTGGCTGGCATTAATCTAGTTTACTTAAAAAAATATTTTTAAGTTATATAATATAATAATAAAATAAAACTATAACAAAAAAGTGTGTATTGTCATTATGGCAAAGATTAATGTTATAAGAATTCAGTTAATAAAACTGTTACAATTAAAATTGGGTTATAATGTAATGAAATGTACTACTAAAATAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23160
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112088 | Nonsense | 1274 | 1908 | 30 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43122125)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43086800 |
GRCz11 | 17 | 43077338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGATTACTGATGTAAGTCTGATTAAGTTGCTGTGTTTTGTTTGGGTGC[A/T]GACCCCCAGTGAGCAGGGCTCCACCAATGCCAGAAAAACTACAAACCAAC
Long Flanking Sequence:
TATGGGCCATTTTGTGTTGAAGTAAACATGATATTTTGTTGTCACTGACAACTTCAATGCATTTTGTTGTATTTTGTTTGCGTTCTCAATGTCCCTGTGCTGTGCTTTGTTTTCCGGAGCACTTGACAGAACTGCTCAGCTGTCACACTTCTAATGTTTTCTCTTTTTTTTTGTTGATGCTGCATGTAAAGGGGCTCAAGGTAAGACTAGACCGATCTTTTATTCCTAAATTCACCTGATACCTTAGATTGTTTTATACAAATTTATACAAATTTATACAGATTATTTCAGCTTTCTGAATGTTTCACATAAGCATTATTTGTACATTACAAACTGTCCCATATAGTTCTGACCTTTTAGTCAATTCTAGTTAGATGCCACTGTGAAATCTTAAAGTGAAACTGAAGCATGCCAGATGTCTGGTGTCCCTTTCACCTGGTCTCTGTCTGACCTGATTACTGATGTAAGTCTGATTAAGTTGCTGTGTTTTGTTTGGGTGC[A/T]GACCCCCAGTGAGCAGGGCTCCACCAATGCCAGAAAAACTACAAACCAACAATGTGGGCAAGAAAAAGAGACCAATTGAGGTAAGTAATTTCCAGATAAGAACAATATAAATGTGTGTTTTGTGAAATAGATCAAGATGTAATCAAACCGTTCATTCCCTTTAAATTTTACTTTTCCATCCCATCCAATCCTATCCTATCCTATCCTATCCTATCCTATCCTATCCTATCCTATCCTATCCTATCCTATCCTATTCTGTCCTTTTTTCTATCATGTCCTATCCCATCCTGTCCTATCTGGTTTTCCCTGTCCAATCTATTCCAATCTTAGTCTATACTAATTTGTTTCGTATCCTTTTCTGTCCTGTCCTATCCTATCCTATCTGTTCCTCCCTTTCCAATCCATTCTAATCTTATCCTATCCTATTTTTTTCATATCCTATTCTGTCCTATCCTGTCTTTTCCCCCGTACAATCTAATACAATACTATCCTATCCCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36492
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112088 | Nonsense | 1670 | 1908 | 39 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43113443)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43078118 |
GRCz11 | 17 | 43068656 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCTGATTGAGATGTGCTCTTGTGTGGAACAACAGAAGATGCTGAAT[A/T]AAGTGAACCTCGGTCATCCGGCACGAACCGTCAGCTACAGTCCAGAGGGC
Long Flanking Sequence:
TTAAACATTGAAAGTTTCAAATTTGAAATACAATTTTTAAAATTCAATTTTAAGACAACTTTGATCAAATTATATTATATAAAGTGGACCTAACTAGCTACCTCCATGAGAAACTTCATGCTGGTTAATCATCACATGATTAATACAAAATATTGTTCATCAAGTGAGCAGCAGTTAAACTAGCTCTGTCCTCTCTGTCCTTCTGCTGGGTTCTCAAGGGGAAGATTCTGGTTGGAACTCGTAACGCTGAGATCATTGAGGTCGGTGAGAAGAACGCAGCATGTAACATTCTGGTGAACGGTCACATGGATGGTCCTGTCTGGGGTCTTGGAGCCCACCCGACCCGGGACGTCTTCCTGTCTGCTGCAGAGGACGGCACTGTGCGCCTCTGGGACATTTCACAGAGGGTAATTTATATCCTAATCATAAATAAATAAAAGAGTCTGAGAAAGGAGCTGATTGAGATGTGCTCTTGTGTGGAACAACAGAAGATGCTGAAT[A/T]AAGTGAACCTCGGTCATCCGGCACGAACCGTCAGCTACAGTCCAGAGGGCGACATGGTGGCCATCGGCATGAAGAATGGAGAGTTCATCATCCTACTTGTCACCTCGCTCAAGATTTGGGGAAAGAAGAGAGATCGCCGCTCTGCCATACAGGATATCAGGTCAGACTGAGGAAAGTTGTTTATTATTATTATGAGTCAAAAACAAAAAGGGGCTTTCAAAACATCAGTTAACAATTAAAGTGTTATACGTTTTTTTCTTACATTACAAGAATTTTTGTGCAAATTAGAAAGTGTTTAGGCAAGTAAACAACAATCATACATTTTGCCATGATTTACAGAAGACACCCACCAAATTCTCACAACAATTTTCTTTACGTATATAGTATAAAATATTAGTATTAAATTAAACCCAAAATACTAATTAATTGTAACTTTATATCTACTTTTCCACTGTCCTTAAAACCAATAGGTTTTACCCATTTCATTTTTAAAATGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11871
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112088 | Essential Splice Site | 1723 | 1908 | 39 | 44 |
Genomic Location (Zv9):
Chromosome 17 (position 43113282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 43077957 |
GRCz11 | 17 | 43068495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGATTTGGGGAAAGAAGAGAGATCGCCGCTCTGCCATACARGATATCAG[G/A]TCAGACTGAGGAAAGTTGTTTATTATTATTATGAGWCAAAAANAAAAAGG
Long Flanking Sequence:
AAGTGAGCAGCAGTTAAACTAGCTCTGTCCTCTCTGTCCTTCTGCTGGGTTCTCAAGGGGAAGATTCTGGTTGGAACTCGTAACGCTGAGATCATTGAGGTCGGTGAGAAGAACGCAGCATGTAACATTCTGGTGAACGGTCACATGGATGGTCCTGTCTGGGGTCTTGGAGCCCACCCGACCCGGGACGTCTTCCTGTCTGCTGCAGAGGACGGCACTGTGCGCCTCTGGGACATTTCACAGAGGGTAATTTATATCCTAATCATAAATAAATAAAAGAGTCTGAGAAAGGAGCTGATTGAGATGTGCTCTTGTGTGGAACAACAGAAGATGCTGAATAAAGTGAACCTCGGTCATCCGGCACGAACCGTCAGCTACAGTCCAGAGGGCGACATGGTGGCCATCGGCATGAAGAATGGAGAGTTCATCATCCTACTTGTCACCTCGCTCAAGATTTGGGGAAAGAAGAGAGATCGCCGCTCTGCCATACAGGATATCAG[G/A]TCAGACTGAGGAAAGTTGTTTATTATTATTATGAGTCAAAAACAAAAAGGGGCTTTCAAAACATCAGTTAACAATTAAAGTGTTATACGTTTTTTTCTTACATTACAAGAATTTTTGTGCAAATTAGAAAGTGTTTAGGCAAGTAAACAACAATCATACATTTTGCCATGATTTACAGAAGACACCCACCAAATTCTCACAACAATTTTCTTTACGTATATAGTATAAAATATTAGTATTAAATTAAACCCAAAATACTAATTAATTGTAACTTTATATCTACTTTTCCACTGTCCTTAAAACCAATAGGTTTTACCCATTTCATTTTTAAAATGTAAAATTGCTAAATTTTAGGACATTTGGAATCTTCACTGTCTTTTTATACATTTTAATAAGTACACGCCAGAATGTTTTGTTTCATTTTTACATAAATATATCTGTCATGACAACTCTCTGAGAGATTTAATATGGTAATAAATATGTACATGGCAATGTTGATG
Associated Phenotype:
Not determined