ZMP
eml1
Ensembl ID:
ZFIN ID:
Description:
echinoderm microtubule-associated protein-like 1 [Source:RefSeq peptide;Acc:NP_001180527]
Human Orthologue:
EML1
Human Description:
echinoderm microtubule associated protein like 1 [Source:HGNC Symbol;Acc:3330]
Mouse Orthologue:
Eml1
Mouse Description:
echinoderm microtubule associated protein like 1 Gene [Source:MGI Symbol;Acc:MGI:1915769]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36453 | Nonsense | Available for shipment | Available now |
sa13937 | Nonsense | Available for shipment | Available now |
sa16731 | Nonsense | Available for shipment | Available now |
sa14062 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36453
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 |
---|---|---|---|---|---|
ENSDART00000104307 | Nonsense | 233 | 281 | 7 | 7 |
ENSDART00000126414 | None | None | 813 | None | 22 |
ENSDART00000134998 | None | None | 101 | None | 3 |
The following transcripts of ENSDARG00000042840 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 31059353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30983280 |
GRCz11 | 17 | 31000243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCTCGCAGTCCACCAACAACCCATCAGAGGTCAAGATTCTGTCTGAC[A/T]GAGCGGCCCGACTCGGATACCGAAAGATCCCTCCGTTTAGTCTTCCTCTG
Long Flanking Sequence:
TTGCAGTGTGCTTTTTGAGGCCTGTTCACACCAAGATCAATAACTATTTTGGAAATGAATGCTGTAGTTACATCAACAACACAATAACGTTCTGTCTTTTATAGAATTATGCTCCAAGATGAGCAGTCAAGTATTTTTTTTTTTTTTTTTTTTTTTTTTATCTCCAATGGACCACAGTTTATATTATTAAGTGAATACATCTTTGGAAGGCTCTCTTTGGTGTGAATATGTCTTTTAGTCTTGTGAAAGCCTTGTCGTCTTGTTATTATGATAAAAATCTAACAATTTTAGGCCATGCATGATCATGATTATACTTCATCCCACCTTTCCACCCTGTCCCGCCCCTGCCCTGTCCAATTTGACCACTTCACCCAGTAACTGTGCAGATCTACTTGCACCGGCCGTCCAAAAGGACCAGATCCGCCGAACCCCCCAAATCATCATCAGCCGTGCCCTCGCAGTCCACCAACAACCCATCAGAGGTCAAGATTCTGTCTGAC[A/T]GAGCGGCCCGACTCGGATACCGAAAGATCCCTCCGTTTAGTCTTCCTCTGAGGAAGTGCACATCTCAGCCTGTCCACTCACCCTTAGAAATGCCCACTTACAGGAGCCCAGTCAAATCTCCCAGCCAGTACTTTCAGATCTGTTACTAATCCCAACAGCTATAATAATAGACGTGACCTGGTGTTTATAAGGAGTTTTGTGTTCTGTTTCATTCTTTTTGTTTTGATTTTGTGTCACTTTGCTTTGATTTAGGTTATGTTTGTTGAGCTGCGTGTTCATCTTTTTTTTTGCTTCTAAATAGGTTCATTTTCTTTCAAGTGTGCGTTATCATCTGTATTTTTGTCTTTTCCATTGTGTTTGCATGCAGGCCTGTCTGTTATTTTTGTTTTGTGTTTATTACTAATTCATTAACTCATGGACCTGTTGCATTCACATGCTTTTGCATTTGATTTTGCACTGTTTGTCTTTACTTACATTGAACGCATCTCGAATACTGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13937
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 |
---|---|---|---|---|---|
ENSDART00000104307 | None | None | 281 | None | 7 |
ENSDART00000126414 | Nonsense | 212 | 813 | 6 | 22 |
ENSDART00000134998 | None | None | 101 | None | 3 |
The following transcripts of ENSDARG00000042840 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 31056904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30980831 |
GRCz11 | 17 | 30997794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KCACCATGTACATGCCCAAAGACCTGGTGGAYACTTATTGCCTGGAAACT[A/T]AAGCTGACTWGCCTCCTAAAAAACTGAAGCTAGACTGGGTGTATCCTTTA
Long Flanking Sequence:
AAAAAACAGTGTATAAAAGTATAATTTTATTCTGTGACTCAAAACTGATTCTTTAGCATTATACCTCCAGTCTGCAGTGTCACACCATCCTTGAAAACCTGAAATACAGTACCTATTAACATTGTTGAAAACACTGCTGCTTAATATTATAATAAAAACTGTCATTCATTTTCCTGATAAATAAGAAGTTAGTGTTTATTTGAAAATGAAATCTTTTTAATATGTCTTTACTGTCATGTTTGATCAATTTTTTTGCATTCTTTCTGAACAAAAGTATTACATTCTTTCAAGTTGCTGAGCCTTCATCTGGCTCAGTCGAAATCTGGTAATAAAAGCCACAACAGATGTGACAGGGATCCTTCAGTGACCCATGCATTTTCTTCTTCTGAAAATCTATGTTGCTTTTTCTAGATGAAGGGTATGTCAAAATGTATTTGAAGGGACGACCCATCACCATGTACATGCCCAAAGACCTGGTGGATACTTATTGCCTGGAAACT[A/T]AAGCTGACTTGCCTCCTAAAAAACTGAAGCTAGACTGGGTGTATCCTTTAATGCTGCTGCATGCGAAGAAAAAAAGAAGAAATATAGATTGATTCTGAACGCTCATAGCTGTAAAATTAAATTACCCATTGATTTATTATAGCCTAGAAAATGAGCTGGTTAAAATGCCAGAGCTAAATGATGGATATGGTTTCTAGGTCACTTTTATGTTGCGAGATTATTGTGGATAATGTATGTTCGCTGTGTTGTACTTCTGTATTCACATTCTAGGTTACTATAGGATGTTTAATCATGTACTCTGGTTTTCTCTCTGGATCTGCTGAGCACTGCAGTCTGCCAAAGTGGAATATTTTCTTCAGCTCTTACCCACAATGCATTTGGAATGTTCCCTGAAAAGGACTTTGTGCGGCAAAATTAAGACATTTATTATACCCAAAGCCTAGCAAATGTAAAATATTAAGTGGTCAGCTGGCACTTCTCCACAAATGTTCCAAAGATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16731
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104307 | None | None | 281 | None | 7 |
ENSDART00000126414 | Nonsense | 215 | 813 | 6 | 22 |
ENSDART00000134998 | None | None | 101 | None | 3 |
The following transcripts of ENSDARG00000042840 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 31056894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30980821 |
GRCz11 | 17 | 30997784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGCCCAAAGACCTGGTGGAYACTTATTGCCTGGAAACTWAAGCTGACT[T/A]GCCTCCTAAAAAACTGAAGCTAGACTGGGTGTATCCTTTAATGCTGCTGC
Long Flanking Sequence:
GTATAAAAGTATAATTTTATTCTGTGACTCAAAACTGATTCTTTAGCATTATACCTCCAGTCTGCAGTGTCACACCATCCTTGAAAACCTGAAATACAGTACCTATTAACATTGTTGAAAACACTGCTGCTTAATATTATAATAAAAACTGTCATTCATTTTCCTGATAAATAAGAAGTTAGTGTTTATTTGAAAATGAAATCTTTTTAATATGTCTTTACTGTCATGTTTGATCAATTTTTTTGCATTCTTTCTGAACAAAAGTATTACATTCTTTCAAGTTGCTGAGCCTTCATCTGGCTCAGTCGAAATCTGGTAATAAAAGCCACAACAGATGTGACAGGGATCCTTCAGTGACCCATGCATTTTCTTCTTCTGAAAATCTATGTTGCTTTTTCTAGATGAAGGGTATGTCAAAATGTATTTGAAGGGACGACCCATCACCATGTACATGCCCAAAGACCTGGTGGATACTTATTGCCTGGAAACTAAAGCTGACT[T/A]GCCTCCTAAAAAACTGAAGCTAGACTGGGTGTATCCTTTAATGCTGCTGCATGCGAAGAAAAAAAGAAGAAATATAGATTGATTCTGAACGCTCATAGCTGTAAAATTAAATTACCCATTGATTTATTATAGCCTAGAAAATGAGCTGGTTAAAATGCCAGAGCTAAATGATGGATATGGTTTCTAGGTCACTTTTATGTTGCGAGATTATTGTGGATAATGTATGTTCGCTGTGTTGTACTTCTGTATTCACATTCTAGGTTACTATAGGATGTTTAATCATGTACTCTGGTTTTCTCTCTGGATCTGCTGAGCACTGCAGTCTGCCAAAGTGGAATATTTTCTTCAGCTCTTACCCACAATGCATTTGGAATGTTCCCTGAAAAGGACTTTGTGCGGCAAAATTAAGACATTTATTATACCCAAAGCCTAGCAAATGTAAAATATTAAGTGGTCAGCTGGCACTTCTCCACAAATGTTCCAAAGATCTTTATCTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14062
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 |
---|---|---|---|---|---|
ENSDART00000104307 | None | None | 281 | None | 7 |
ENSDART00000126414 | Nonsense | 362 | 813 | 10 | 22 |
ENSDART00000134998 | None | None | 101 | None | 3 |
The following transcripts of ENSDARG00000042840 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 31048288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 30972215 |
GRCz11 | 17 | 30989178 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACYCCAATGACCACATGCTCTCTGTGTGGGACTGGCAGAGGGAAGAC[A/T]GAYTCGCTGAAGTCAAGGTGAGYGCTTCAGTATTCAGCATAGATTTATTA
Long Flanking Sequence:
GAAAGTCTTATTTGTTTTATTACAGCTAGAATTAAAGCAGTTTTACATTTTTAAAACCCTTTTTAGGTCAATATTATTAGCCCCTTTAAGCTAAATTTTGATCGATACAGAACAAACCATCTTTATACAATTACCCTAACCTGCCTAGTTACCCTATTTAACTTAGTTAAGCCTTTTAATGTCACATTAAGCTGTATAGAAGTGGCTTGAAAATTATATAGTAAAATATCATTTACTGTCATCATGGCAAAGATAAAATAAAGCAGTAATTAGAAATGAGTTATTAAACCATTATGTTTAGAAATGTTTTGAAAAAATCAGAAATGAGAGAAAAAACATACAGGGTTACTAATAATTCTGACCTCAACTTTATCTGTCAAAATGAGCTTCAGTGTTATTAAAAAAACTTTCATTACATTCAGAACGGTGGAAGCTGGTTGTGTGTTGTGGATGACTCCAATGACCACATGCTCTCTGTGTGGGACTGGCAGAGGGAAGAC[A/T]GACTCGCTGAAGTCAAGGTGAGTGCTTCAGTATTCAGCATAGATTTATTAGCATTGTCTACTTTGGGTCAGCATTGGGAGTGCAGAAATAACCTGATTTGCGCATCTATGTCTTTTTTTCTCTCCCCTTTTAGTGCTCCAATGAGTCAGTGTTTGCTGCTGATTTCCACCCGACAGATGCTAATATAATTGTAACATGTGGGAAATCACATCTGTGCTTCTGGTCATTAGAAAAGGGGTCTCTTGTGAAAAAGCAGGGTCTTTTTGAGGTAATCTCCCCTAAGCCACAAGACTATTTTTATGAAATCAGATTAATTTTTTTTTATTTTATTCGGAAAAACATGTGCATGTGCATCATAAGTGCCATGCAGTAAAATGTAGAGACATCTGCTCATCCTTTAATGCAACTGTTTTATGCTTCTATGATCAAAAACACACACATGGAAGTATTACATTATTAGTGCATTTTCATTTTTGAGTGAAATGTCTCTTTAAGGTCTG
Associated Phenotype:
Not determined