ZMP
dab1a
Ensembl ID:
ZFIN ID:
Description:
disabled homolog 1a (Drosophila) (dab1a), mRNA [Source:RefSeq DNA;Acc:NM_001040685]
Human Orthologue:
DAB1
Human Description:
disabled homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:2661]
Mouse Orthologue:
Dab1
Mouse Description:
disabled homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:108554]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14868 | Essential Splice Site | Available for shipment | Available now |
sa15478 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14868
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 |
---|---|---|---|---|---|
ENSDART00000083906 | None | None | 543 | None | 17 |
ENSDART00000083908 | Essential Splice Site | None | 541 | 1 | 24 |
ENSDART00000145841 | Essential Splice Site | None | 537 | 1 | 13 |
The following transcripts of ENSDARG00000059939 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 8596902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 8431171 |
GRCz11 | 20 | 8418910 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGATTTTTATCATGAGAAGTATGGAATCTGAACGCACTACTTTAAAGG[T/C]AAGRCGGTTTGTCTTGTGGATGACATATGGAAAGAAAAACRGCGCTGTTG
Long Flanking Sequence:
GGTGCTCGTGCATGTTGAGTCTCAGCAAATAAGATGCGCTTCATTTCTGATCTCTCATCCATCCCCCCCAAACGCATCCTTTTTGTCTTTATATTCTTTTGCACATCTTAGCTTTTTGGCATCGAAAACTCTCGCTCACCCCTCCCACTCCTTGCGTTTTCCCCTGAAAGCAAGAAACCAGGACAGCGCGGCGCGCGACGGGTTAACGCGCACTCACGCTCGTGATTGGCTGCGGGAGCGGCGCTTTTAGAGAGAGGTAACCAGGCAACTTCAGCTGGAGCAGCGGAGAGAAAGAACAGGGTAAAGGGGAAAAGAAGCGCAAAAATCCCATCAGTTTTGGTGTGCGATAGAAAGGATGTAGTCCAGGTCTGTGGCTGTCTGTCCCCGGCATGGGAAAGTGGATTACTGCTCTTCTACAGACGGTAGAGACTGGATACGGAGTGATTGCGCGTGGATTTTTATCATGAGAAGTATGGAATCTGAACGCACTACTTTAAAGG[T/C]AAGACGGTTTGTCTTGTGGATGACATATGGAAAGAAAAACGGCGCTGTTGCAGTGAAACTTGTCCATGTGGAACGCGAGGACGCCTCTCCGTGCTTCGGTGATGGAGTTGTGTCGGTTGATTGAATTCACGCATCTAAAGCGATTGGAAAGATATTAAACAGTTACCACATATTTGGCTTGCGAGGAAATGAGCGGAACCAACTGCCACCAGTTGACGGTGATCATGCGTCCACGCGCGTATGGAGAGGAGCGGCGTTTGCTGCATTGACATCCATGTTCTGCCCCGCACGAGAGCCATTGATCAACTGAGATTTACTACAACGCTTCATATGTATCACCCTATTCATTCACAGCCGTGCAGAGCTGGTATATACACTTAATTAGTGCTGTATGCGCATATAAACTGCAGTGGAAAGGTTCTCGGTATTCCTGCTCGGGTTAAAACGCACGAGTGTCAAAGAGCGTGAGATGTCAGTATGCCGAAGCGGATTACGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15478
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083906 | Essential Splice Site | 186 | 543 | None | 17 |
ENSDART00000083908 | Essential Splice Site | 186 | 541 | None | 24 |
ENSDART00000145841 | Essential Splice Site | 186 | 537 | None | 13 |
The following transcripts of ENSDARG00000059939 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 8371368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 8205637 |
GRCz11 | 20 | 8193376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGAAGAAAGCTCAGAAAGACAAACAGTGCGAACAWGCTGTTTATCAGG[T/A]AACACWCTCACCATAAACCTTYATGAACTCAAAGCCTTAAAGAGAATTCA
Long Flanking Sequence:
ACATACATACATACATACATACATACATACATACATACATACATACATACATACATACTTACTTACTTACTTACTTACTTACTTACTTACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATACATGATAGTTAGCTAGCTAGCTAGCTTCTGAAATGCTTTTATTCCGGTTATGCAGTTGCCAGCATGAACGGATCATTTTCATTTCTAACTGTGAGAAGTTGGTGTCAGTCTTTTTTCTCTGTGTTTGTGAATCTCTATGTCTTTGCTCATCTTTCCTCGTGTGTTCTCAGGCTGAGCCGGTGATCCTCGACCTCCGCGACCTTTTCCAGTTGATTTATGAGATTAAGCAGAGGGAGGAGATCGAGAAGAAAGCTCAGAAAGACAAACAGTGCGAACAAGCTGTTTATCAGG[T/A]AACACACTCACCATAAACCTTCATGAACTCAAAGCCTTAAAGAGAATTCAGTGTTTGTGAAGCTCTTACACGAATAGGCATCAGCGGGCAATTGAAGAGCAACAACAAACTCAAAAAGGGATGATGAAATATGCAATACAATAGGATGAAGACACGGAAAACAACACATTTCGAAAATAGGACATATATATTATTTATGTCAGAGAGTAGCATAATTAGATATAATATGAGGCAGAGTGCACGCTGAGATTAAAAAAAAATAAAAAATTTATACAACTGTTGCTTTTCACATTGTAAATTAATGAGATCTTGGGTAAAACCTAAAGTAGACTGCACAACAATACCTTACTTTTATGTGTATCTATAAATAATGAAATTTATTTCATGACATGATTTTCAAAAGTGGCTGATATTCAAAATAATTTTATGGGTTTAGCATTTTAATGTATATTTATTTCACCCATTTATTTTAATTATAATTTTTATAAACACTTAGATTG
Associated Phenotype:
Not determined