ZMP
si:dkey-83f4.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate DAB2 interacting protein (DAB2IP) [Source:UniProtKB/TrEMBL;Acc:B
Human Orthologue:
DAB2IP
Human Description:
DAB2 interacting protein [Source:HGNC Symbol;Acc:17294]
Mouse Orthologue:
Dab2ip
Mouse Description:
disabled homolog 2 (Drosophila) interacting protein Gene [Source:MGI Symbol;Acc:MGI:1916851]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41139 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9948 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41139
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 |
---|---|---|---|---|---|
ENSDART00000091612 | Nonsense | 250 | 1162 | 6 | 16 |
ENSDART00000135812 | Nonsense | 237 | 1147 | 5 | 15 |
The following transcripts of ENSDARG00000069484 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12700598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12145361 |
GRCz11 | 8 | 12183066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCCCTCGGTCAAGAGCATCACCGTTCATCTTTACAAGGAAACGGAC[A/T]AAAAGAAAAAGAAGGACAAAAATAATTATGTGGGCCTGGTCAATATTCCC
Long Flanking Sequence:
TATCTAGTGTAATTGGGGTTGGAGTTAAACTCTGCTGGACACCAGCCCTTCAGGACTGAGTTTGGGCACCCCTGCTTTAAAGGCAAATTAAAAGATGCGCATTAAAGGTATAGAATTCCCAAAAATGAAACATTGCTGCAGATTTCAGGCCTTCGAAGATGTAGGTGACTTTTTTCTTCAGTAGAAAATTTGAAAAGATTTCATTACATGCAAGTCAAGTCAACACTTACTTTGAGAGAAAAAAAAAACATGAACTGTGTTTATATTTTCTGCAGGATAACACCCGTCGGGTGGAAAATATGCTGAAATGTTGGATTATCGAAGCCAAGGACTTGCCAGCAAAGAAAAAATACTTCTGTGAACTCTGTCTGGACGACACATTATACGCACGGACTACCTGCAAACTCAAAACGGACAACGTTTTCTGGGGCGAACACTTTGAGTTCAACAACCTGCCCTCGGTCAAGAGCATCACCGTTCATCTTTACAAGGAAACGGAC[A/T]AAAAGAAAAAGAAGGACAAAAATAATTATGTGGGCCTGGTCAATATTCCCATTGCGACAGTCACCGGGCGGCAATTTGTGGAAAAATGGTATTCGGTTAGTACGCCGAATCCTAACAAAGGGAAGAGTCCGGGACCCATGGTCCGCATGAAGTCCCGCTATCAGAGCATGAGCATCCTCCCCATGGAGCTTTACAAGGAGTTTGCAGAGTATATTACTAATAACTATATGCTAATGTGCTCAGTGCTGGAGCCGGCGCTCAGTGTGAAGAACAAGGAGGAGATGGCGTGTGCACTTGTGCATATCTTACAAAGCACAGGCAAGGCCAAGGTAAGACCACTGCTTTTATAACTCATCGCGTATTATGCATGATTTATCAGCACAAATCATTGAAAAATAAAGAATATACAGTTAATGTAAGAATTATTAGCTCCCCTTAGATTTTTTAAAAAATTTTTCCAAATGATGATTAACAGAGCAAGGAAATTTTTACAGTATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9948
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 |
---|---|---|---|---|---|
ENSDART00000091612 | Essential Splice Site | 359 | 1162 | 6 | 16 |
ENSDART00000135812 | Essential Splice Site | 346 | 1147 | 5 | 15 |
The following transcripts of ENSDARG00000069484 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12700267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12145030 |
GRCz11 | 8 | 12182735 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGGCGTGTGCACTTGTRCATATCTTACAAAGCACAGGCAAGGCCAAGG[T/C]AAGACCACTGCTTTTATAACTCATCGCGTATTATGCATGATTTATCAGCA
Long Flanking Sequence:
CTTGCCAGCAAAGAAAAAATACTTCTGTGAACTCTGTCTGGACGACACATTATACGCACGGACTACCTGCAAACTCAAAACGGACAACGTTTTCTGGGGCGAACACTTTGAGTTCAACAACCTGCCCTCGGTCAAGAGCATCACCGTTCATCTTTACAAGGAAACGGACAAAAAGAAAAAGAAGGACAAAAATAATTATGTGGGCCTGGTCAATATTCCCATTGCGACAGTCACCGGGCGGCAATTTGTGGAAAAATGGTATTCGGTTAGTACGCCGAATCCTAACAAAGGGAAGAGTCCGGGACCCATGGTCCGCATGAAGTCCCGCTATCAGAGCATGAGCATCCTCCCCATGGAGCTTTACAAGGAGTTTGCAGAGTATATTACTAATAACTATATGCTAATGTGCTCAGTGCTGGAGCCGGCGCTCAGTGTGAAGAACAAGGAGGAGATGGCGTGTGCACTTGTGCATATCTTACAAAGCACAGGCAAGGCCAAGG[T/C]AAGACCACTGCTTTTATAACTCATCGCGTATTATGCATGATTTATCAGCACAAATCATTGAAAAATAAAGAATATACAGTTAATGTAAGAATTATTAGCTCCCCTTAGATTTTTTAAAAAATTTTTCCAAATGATGATTAACAGAGCAAGGAAATTTTTACAGTATGTCTGATAATATTTTTTCTTCTGGAAAAAGTTTTTTTTATTTTTATTTTGGCTAGAGTAAAAGCAGTTTTTAATTTTTTAAACACCATTTTAAGGTCATAATTATTAGCTCTTTAAGCTATATATTTTTTCGATTGTCTACAGAACAAACCATCATTATACAATCACTTGCCCAATTACCCCAACCTGCCTAGTCAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATGTAGTCAAATATTATATTACTGTCATCAAGGCAAGGATAAAACAAATCAGTTATTTGAAATGAGGTATTAAA
Associated Phenotype:
Not determined