ZMP
si:dkey-202m22.4
Ensembl ID:
ZFIN ID:
Description:
Asxl1 protein [Source:UniProtKB/TrEMBL;Acc:Q6P6X8]
Human Orthologue:
ASXL1
Human Description:
additional sex combs like 1 (Drosophila) [Source:HGNC Symbol;Acc:18318]
Mouse Orthologue:
Asxl1
Mouse Description:
additional sex combs like 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2684063]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45806 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32451 | Nonsense | Available for shipment | Available now |
sa45807 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44017 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45806
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042944 | Nonsense | 246 | 1632 | 7 | 11 |
ENSDART00000134141 | Nonsense | 233 | 1619 | 8 | 12 |
The following transcripts of ENSDARG00000036956 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 30985967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30820857 |
GRCz11 | 23 | 30747388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTCTCATCAACACACGGACCTTTGCTGCTTTTCCTTCTCACTCCCAG[C/T]AGCAACTACTCCAGCTTTTACCAGAGGTGGACAGACAGGTATATGTTATT
Long Flanking Sequence:
TTAATATAATGTGGGACCGATTTTTGTCCTAGAATATTTTGTAGCATAGTACTGTTAAAGCATGACACTTTCTGATAATTGCATAATTGGCTGAGGTAATATTCAGTTGTTTAATTTTAAAGCACAATGGATTAGACGGTTGTTTATCTAGAATTAAAATAAGACTTGTTTATTAGAGGTCTGATAGAGCACTCTACACATAAGCAGATATACCAGCAATTTATTCATATAGATTTACAAATGTGTGTGAATGCAGACCTGAATGTGCTTTAAGTTTCTATGTAATCATATCCCGTTCCATTCATTCACAAATCCTTAGGACTCATTAAACCAAGTTCTTATATATACTCAATCTAATACTGTATTTTGCAGGTCCCATGAAAAGGAGTCGAGGAGGAGTGGAGGTGGATTTTGAGACTCCAGGATCCATCCTGGTCAACACCAACATTCGTGCTCTCATCAACACACGGACCTTTGCTGCTTTTCCTTCTCACTCCCAG[C/T]AGCAACTACTCCAGCTTTTACCAGAGGTGGACAGACAGGTATATGTTATTTTTCTTGAGGACTTTTTAAAAGTATCCCTTTATTCATGTCTATGCAGTTTCTTATTGTTGCCTAATTTTCCTAACTTTAATATGTAGGTCGGCCCCGATGGCCTTGCTCGTCTAAGCAGTTCGGCCCTCAATAATGAATTCTTCACTCATGCCTCCCAGAGCTGGAAAGAACGTCTAGCTGAGGGTAAGCCTCTTAACATTTTCTTGTGACATCTAAAAAATGACCAAGACAAGTGGATCTAGGCAATTTTACTATAATAGATAAAGTTGGAATATTTTTACTTTTCTTGAAGGTGAGTTTACACATGAGATGCAGGTTCGCTTCAGGCAGGAGATGGAAAAGGAGAAGAAAGTAGAAGCATGGAAGGAGAAATTCTTCGAGGAGTACCATGGCCAAAGGTTCAGTGGCATTTTATTTTTATTTCTGAATTATTTATAGTGCTAGAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32451
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 |
---|---|---|---|---|---|
ENSDART00000042944 | Nonsense | 934 | 1632 | 11 | 11 |
ENSDART00000134141 | Nonsense | 921 | 1619 | 12 | 12 |
The following transcripts of ENSDARG00000036956 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 30988450)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30823340 |
GRCz11 | 23 | 30749871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGAGCTTCACCCAGGGACAACTGGAGTTATCCAGCATGGCTCAGACT[T/A]GAAATTACCCAAAGAGACTCTTGTTACAGCCAGAAATGGATGGGTAGAAA
Long Flanking Sequence:
GCCTCAAACTTCCACCCCACTCACTGAACCATCTCCCTCTTCTGTGTCCTCAAACCCATCTCTACCATCATCAGAATCTCCAAAAATACTTGCGCTATCACCACCTGCAACCGACAGCCCTGCTTCCCAGGATCAGGTGGAGGAGATTTGTGGAGTGGAAGAGGTGACTGCCTGCCCAAGTGATAAAACCTCAGAGCAGACCTTAGACACCCCAGTGCCTACCCCAAGTGAATCAGAGTCTTTTTGCAGTCACCAAGATGGGAGAGGCGAGGAAGCAGAGTCGAGTGATAGTAGAACAAATACGCCTGTTTGCACCTCATCATCAAATGATGCTATTTCTTTAGTGCCCACCTCTATACCTGACTCGCTACCAAGATTTGGTGCCCAGGGTGTGGATGTCATCAGGACATTGGCAGCTTCCTCTCAGCCTTGGGAAGGTGAAAAGAAAGCGGTTGAGCTTCACCCAGGGACAACTGGAGTTATCCAGCATGGCTCAGACT[T/A]GAAATTACCCAAAGAGACTCTTGTTACAGCCAGAAATGGATGGGTAGAAAATAGAGAAGAGCATTCCATGAGAGAGGGTATGCTAGAAGAACATAGGAATGGAGGGAGTGATGCTAATGGTAAATATGAATCAGGCTCTTTACCTTGCCTACCACGATGTGCTGGTGAGGAAGACACTGGAGCACACAGTGATTCAACGGAGACAGCATCTGACTTTGAAAATGAATCACAAGAGGATGAAATGGTGGATTGGCATGGGACCCAGATGGATGGTAGTGGCATGCAAACTCAAAATACAAAATCACTGAATCGACCTGTTATTCAGACCTCAAGTCGACTCACTTCATCGATTGTTAATCCTCCTCAACACCAGCAACCGGTTATACAGGCCCATATATCTAATCAAAACCATACCCAAACTGTTATTCAGGCTTGCTTTCCTAATGGTGTGCCAAACCAACCAGTCATTCATCCTCACAAGCAGCATGCAATTAATACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45807
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042944 | Nonsense | 1268 | 1632 | 11 | 11 |
ENSDART00000134141 | Nonsense | 1255 | 1619 | 12 | 12 |
The following transcripts of ENSDARG00000036956 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 30989451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30824341 |
GRCz11 | 23 | 30750872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCTACGGACACTGTTAGTTCTGACTTCCAACACAAAACCCCACCTGCT[C/T]GAGTATCTCCTGGACCTGGTCGGAACTTTGGTTCTTCCCCGCCAGGTTCT
Long Flanking Sequence:
ATGCTATAAACCACTCTCAGGACCAGATTGCCTCTGCACCTTCACAAGCCCAAGTGCAAGCTTATCTGACCCAGACTGAGATGGACCAAAGCAGAAATCTACGACTGAATGATAATGGCAATGGTGTGAAGCTGTATTTGTCAGAGGATGACACCAAACCTCTTGGCAGGGAAGATTTAGTTTTAAAGAATTCTGCTGGTCCTCCAGTTGGCAGAAGAGTCCAAGTTTCATCTCGACCAGTTTCCACTGTAGAGGCCAACAATCCTCTTGTCACACAGCTCCTCCAAGGCAGTCTACCTTTAGAGAAGGTCTTACCCCAACCCCACTCAGCCAGCAAGTTAGAAATTAATCGACTTCCAGGTGCCAATTCAAGCAACTCGCTCAACCCAGCCAATCATCAAACACAGAGAAATCTGGCACCACGTTTTAGAGGCCCACCTGAGTCGGGAGGGCCTACGGACACTGTTAGTTCTGACTTCCAACACAAAACCCCACCTGCT[C/T]GAGTATCTCCTGGACCTGGTCGGAACTTTGGTTCTTCCCCGCCAGGTTCTGCTCCATCAAGAATGGCATGCCTGTTTGAGGAAGCCAGCCCCAGGTCTGCAAACTCTCAGTTCAGTTCTCAGCAACCAGGAGGCGTTGTGCCTCCAGGAGCAGTACCTGTCATAACATCCCTTCCCTTAAACTCCACCACTAGAACCTCAATGGATATGAACTCTCAGAATGCTCCAGTTTATGAATCAGCTGTTATTAAAGAGCACCCTGGACCTCTTTCTCAACGGAGTGAAACTCCTGAGAGGCCAAGTAGCTTTCAGCAGCATCCTAATAATGTCTCCCAGTCCGTGTGCAGAAACACACCAGATGCTCCTTCACCTCCACATGGAGACCTTTGTCCATCAGAGGTTGTACCAACTGTTAAGATTAACTGGCGCCCAAACAAACCTCAGCAACCGATCTCCCCTGTAGCTACAGTAAAAAACGAAGTCTCCTTGCGCCCTTCGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44017
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 |
---|---|---|---|---|---|
ENSDART00000042944 | Nonsense | 1625 | 1632 | 11 | 11 |
ENSDART00000134141 | Nonsense | 1612 | 1619 | 12 | 12 |
The following transcripts of ENSDARG00000036956 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 30990524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 30825414 |
GRCz11 | 23 | 30751945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGTGGCGCTTTCTGCCATGATGATTGCATCGGCCCTTCGAAACTGTG[T/A]GTGTCATGTCTGGTTGTCAGATAGTTTGTTGCAGCTCCTTTAAAACTGAG
Long Flanking Sequence:
CCTCTGGATGGTTTTCATGGAGGTGGTGGAGCTATGGAAGGACTGCTAAATATGGAAATGTCTCTTGTCAGAATGGCCAAGAAGGAACAAGTCAAAAATCCATATACCCGCCAAGCAGACACCTCCGCTTCTCCTGTTTCTTCCTCTCCTTCCTCATCAGCCTCCAGTCTCCCTTTCCAGCTATATGGTAAGCTACCAAAACTTCAGCAGAGTGGGGGCAACGGAGGGTCCTCATCCAGCTTCAGTTACACAGCTAATGTGTCTGTGGTGGATGGTAGTGGCTTCACTCGCACCTTAGCCGATAGTGTGCTCCAACTAAGGCCACGTGTGAGCGTCGGCAGCGGTGGAGGTCAGAGTGCCACGCTTGGCATCCAGGCATTTACAGACAGTGCTGCCGAAGAAGTGGCTCTCAAGTGTTCCTGCCGACTCAAGGCTATGATCATGTGCCAGGGCTGTGGCGCTTTCTGCCATGATGATTGCATCGGCCCTTCGAAACTGTG[T/A]GTGTCATGTCTGGTTGTCAGATAGTTTGTTGCAGCTCCTTTAAAACTGAGCCGACTAATCAGAGCAAATACTTTGACCTCTCCAGACAATTCTAGCCCTTTGCCAGTGGTGGGACACTACCTGAAGTCTTGGACTCTTCTTGAGCAAGACAGTGACAGTACACTGCAGTGTTAAAACTGGACTGATTTTTCTTTTTGTTGCTGATGGGTCAGGCAATACAGTAGGGCTGGAAGATTACTTGTAAGATAAAAAATCAGTCTGTATTTTTGTTGCATATTTTTTCTATTTCTGTTATGATGGTGTTATTATTATTATTATTATTAATATTATTATGATTACAATAATAATGATATTGTTGTTATTATTATTGGTATTATTATGTGAATTTACATGGCACAGTTGATTGAAAATTGTGCCTTTTCTTTCCCCCAACAAAACATTTACCTCATCTACTTGACACCAGTCATCAGTTCAGTGTGATAATGGTGGCGTTCCTGTTT
Associated Phenotype:
Not determined