ZMP
abl2
Ensembl ID:
ZFIN ID:
Description:
tyrosine-protein kinase ABL2 [Source:RefSeq peptide;Acc:NP_001116177]
Human Orthologue:
ABL2
Human Description:
v-abl Abelson murine leukemia viral oncogene homolog 2 [Source:HGNC Symbol;Acc:77]
Mouse Orthologue:
Abl2
Mouse Description:
v-abl Abelson murine leukemia viral oncogene homolog 2 (arg, Abelson-related gene) Gene [Source:MGI
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21232 | Nonsense | Available for shipment | Available now |
sa13684 | Essential Splice Site | Available for shipment | Available now |
sa13149 | Nonsense | Available for shipment | Available now |
sa11098 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21232
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 |
---|---|---|---|---|---|
ENSDART00000041697 | Nonsense | 171 | 1135 | 3 | 11 |
ENSDART00000138548 | Nonsense | 171 | 587 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 15485188)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 14930532 |
GRCz11 | 8 | 14968237 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGGGAAAGCGAGAGCAGCCCCGGCCAGCTCTCCATCTCTCTTCGCTA[T/A]GAGGGACGGGTCTATCATTACCGCATCAACACGGCCTCTGATGGAAAGGT
Long Flanking Sequence:
GACAGAAACCTGCTCTTTGTTGATTGATAGAGCTGATACAGATGTTTTGGAAAAGTAACAATGGACCTGTTGTAGCTCGCATTTTCTAATCTCTTTTTAATTCCATTCCATTGAAGGGAGATGCATTGGTATGAATTACTGAAATTCTCAACTCAAAGTACATTCACAAATATGTCGAAAGGGCCGAGTAACAAGTCTTGTTATGTACAGTGTTGTGTGTATATCTCACTCTTTTTTTTTTTTGGGATTGCAGGAGAGAAGCTGCGAGTGTTGGGTTATAACCAGAATGGAGAATGGAGTGAAGTCCGCTCAAAGAACGGCCAGGGCTGGGTACCCAGTAACTACATCACCCCCGTAAACAGTCTGGAGAAGCACAGCTGGTACCATGGGCCCGTGTCCCGCAGCGCTGCCGAGTACCTGCTCAGTAGCTTGATCAACGGCAGCTTCCTGGTGCGGGAAAGCGAGAGCAGCCCCGGCCAGCTCTCCATCTCTCTTCGCTA[T/A]GAGGGACGGGTCTATCATTACCGCATCAACACGGCCTCTGATGGAAAGGTATAAGAGCTTTACTTTGCCATCGTGCTTCTTTTGCCTAAAAGGGAGGGATGGTTCACCCCAAAATTTTTTATTCTGTAATTTTTTTTTCTCCCTTCACTTGTGCCAAACCTGGTTACATTTCTTTTTATTTATTTTTTTACACTGGCACAAAAATTCTTACACTGGTGCAAAAAAACAGATGCACTGCATAGAAAAGGACTTGATCATCCCAGTCCCTCTCACTGAATAAAATCTTTCTAAATAGAGCTATTCAAATCATCTGGTGAAATTATGTTCATCTCGCTATATATAATGCAGCCAAAACATATTGCAATGTCAGATTTTTCCAATATTGTGCAGCACTAGTATACATTATTTTTTTACAACCGCTTTTAAAATCTTATACTGTATATGAGATAAAGGGGGGACAAAGGGATCAAAGGGAAAAATGGAGAAACAAACTAAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13684
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 |
---|---|---|---|---|---|
ENSDART00000041697 | Essential Splice Site | 563 | 1135 | None | 11 |
ENSDART00000138548 | None | 563 | 587 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 15492320)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 14937664 |
GRCz11 | 8 | 14975369 |
KASP Assay ID:
2260-0316.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGAGAACAAAGAGAATATGGRGGAGGCAGGACCCCAYGGCCCTGCAGG[T/A]ATACAGGCTCAACTCCGGCTCAGTCGGCTCAGAAAGAAGCTCAAGAGAAT
Long Flanking Sequence:
ATGAAATGAAATTAAATAATTAAATATTAATAAGTTATGTTATATACATTAAACAAAAAATATGAACATACAATCCACAGATACTTATACGACACACTCTGTAGAAGAGGTACTCGCATACTCTTAAATGGTTGCATGCCTCTGAAAGAAGATATTCTGATGTATGTTGTAAACTGGTGTCTTGATTTTCAAAATTGTTAAAAAAAATTCTTTTGTGTTCAACAGAAGAAAAAAACTTTTTTGAAATGTTTTGAAACAAGTGGAGGATTCAAGTGAACATTTAACGAAGATTTGACTAATACTATTTTGATATTAACATGCCCCTTCTCTCTGACAGAGGTAGCTGAAGAGCTGTGTAAAACTGCGTCTGGTGGGCAGAGTGGAGTTGCCCACACCTTCGGCCCTGATATGCCACTCTTGCCCTCAAAGTCTCGTGGGCAGAAGAAACACTCAGAGAACAAAGAGAATATGGAGGAGGCAGGACCCCACGGCCCTGCAGG[T/A]ATACAGGCTCAACTCCGGCTCAGTCGGCTCAGAAAGAAGCTCAAGAGAATGGGAGTGGTGTTCCTTATTGATTAACACAACTACCCAGTATATAACCTCTTTAAATATATTTAATGTGGATTGGGTTAAGAAAGTTATGTGTTGTATTTATATCATTGTCTTTATTCACGTGTATCAATATGAGAAGACTCGCATGTTTATAAACAGTCAACAGTTTTTACTCATGGTTTGTTTTTCTTGCTGTAAATGCATCTGATTTAATTCTGGTTTGACCCAATTTGCTGCATGTTACTAAACCCCAAGTATGCACAAGCACCTCACCCACTGCATGTTCATCTATATTATGACTCAAATCTGTTTAACCCAATGGCCTGTTTCCACTGATTGGTACAGTATGGTACAAGTCGGCAGGGGTCACCTTTATGAGGCTTGCGTTTCCATGGCCAAAAGGGTACCACTGGTACTTTTGGTGGGCATAGTGTACAACAAAGTTTCAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13149
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041697 | Nonsense | 988 | 1135 | 11 | 11 |
ENSDART00000138548 | None | None | 587 | None | 10 |
ENSDART00000041697 | Nonsense | 988 | 1135 | 11 | 11 |
ENSDART00000138548 | None | None | 587 | None | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 15497005)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 14942349 |
GRCz11 | 8 | 14980054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGWCCGTCAATACCACCACCACAAGTGCCTCCAGCCCCTGTAGTTCCCT[C/A]GAGTAACAACACMACCCAAACCAARTTGGCTAATGGTGCTTCAAGTGGCG
Long Flanking Sequence:
CAAAGCCAAACTCTTGCCACGAGGGGTCGCAGGTGGAGTTAGGGCACCAGGTGTAGGGGGAGAGGCAGAATCGGACTCAAACACAAGGGGGAAAGATGGGCAAGATGACAGGCAAGGCTGGTCATCTCCATCCAAAACCTCTACCCTTGGTTCTGTCAATCTGCATAACCACAAAGTTCCAGTGCTGATCTCCCCGACTTTAAAGCACAGCTCGGGTGATGCACACCTAGTCGGCGTGGACTCTCAGGGCAACCGCTTCAAACTACTGTCCGATAGTGGGGATCGTGACCGACCACGTCTGGTGAAGCCAAAATGTGCACCTCCCCCACCGCCCATGCTACGCTCCCTCCAACACGCCTACAGTGCCGATGCAGCTGACGAAGTGGTCAGTGGGAACATGGAGGTCAATGGAGATACCATCAAAAGGTCGGGAAGAGAAGTCAGGGGAGCACGTCCGTCAATACCACCACCACAAGTGCCTCCAGCCCCTGTAGTTCCCT[C/A]GAGTAACAACACCACCCAAACCAAGTTGGCTAATGGTGCTTCAAGTGGCGGACCAGGCCCTACTTCAGCTAAACCCACTCTTAGACGGACTCGGCAGCAGACAGAAAGGATCCCTCTTGAGAAGATCAGTAAGGAAGCTCTTCTGGAATGTGCTGAATGTTTGAGTAGTGCTCTTCAAGGTAACTCCGAGCTTTCGTCCAGCAGCCAGGTCCTGGATGTGGGACACCAACTTTTGGACTACTGCTCGGGGTATGTTGATTGCATCCCACAGACACGTAATAAGTTTGCCTTTCGAGAGGCTGTAGGGAAACTGGAGTTGAGTCTACAGGAGCTGCGCGCTTGCTCTACGGGTGGGGGAGTGGGACTTAGTGGACCTGGGACCAGCCCAGCTCTTGACAACTTGCACATGTGCATTAAAGAGATCAGTGATGTTGTTCAAAGGTAGCCACTGTGTTTACCTGTAGCTACACCTTCCAAAACTCCTCCTCCTCCTGTACCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11098
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041697 | Nonsense | 988 | 1135 | 11 | 11 |
ENSDART00000138548 | None | None | 587 | None | 10 |
ENSDART00000041697 | Nonsense | 988 | 1135 | 11 | 11 |
ENSDART00000138548 | None | None | 587 | None | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 15497005)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 14942349 |
GRCz11 | 8 | 14980054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGWCCGTCAATACCACCACCACAAGTGCCTCCAGCCCCTGTAGTTCCCT[C/A]GAGTAACAACACMACCCAAACCAARTTGGCTAATGGTGCTTCAAGTGGCG
Long Flanking Sequence:
CAAAGCCAAACTCTTGCCACGAGGGGTCGCAGGTGGAGTTAGGGCACCAGGTGTAGGGGGAGAGGCAGAATCGGACTCAAACACAAGGGGGAAAGATGGGCAAGATGACAGGCAAGGCTGGTCATCTCCATCCAAAACCTCTACCCTTGGTTCTGTCAATCTGCATAACCACAAAGTTCCAGTGCTGATCTCCCCGACTTTAAAGCACAGCTCGGGTGATGCACACCTAGTCGGCGTGGACTCTCAGGGCAACCGCTTCAAACTACTGTCCGATAGTGGGGATCGTGACCGACCACGTCTGGTGAAGCCAAAATGTGCACCTCCCCCACCGCCCATGCTACGCTCCCTCCAACACGCCTACAGTGCCGATGCAGCTGACGAAGTGGTCAGTGGGAACATGGAGGTCAATGGAGATACCATCAAAAGGTCGGGAAGAGAAGTCAGGGGAGCACGTCCGTCAATACCACCACCACAAGTGCCTCCAGCCCCTGTAGTTCCCT[C/A]GAGTAACAACACCACCCAAACCAAGTTGGCTAATGGTGCTTCAAGTGGCGGACCAGGCCCTACTTCAGCTAAACCCACTCTTAGACGGACTCGGCAGCAGACAGAAAGGATCCCTCTTGAGAAGATCAGTAAGGAAGCTCTTCTGGAATGTGCTGAATGTTTGAGTAGTGCTCTTCAAGGTAACTCCGAGCTTTCGTCCAGCAGCCAGGTCCTGGATGTGGGACACCAACTTTTGGACTACTGCTCGGGGTATGTTGATTGCATCCCACAGACACGTAATAAGTTTGCCTTTCGAGAGGCTGTAGGGAAACTGGAGTTGAGTCTACAGGAGCTGCGCGCTTGCTCTACGGGTGGGGGAGTGGGACTTAGTGGACCTGGGACCAGCCCAGCTCTTGACAACTTGCACATGTGCATTAAAGAGATCAGTGATGTTGTTCAAAGGTAGCCACTGTGTTTACCTGTAGCTACACCTTCCAAAACTCCTCCTCCTCCTGTACCCC
Associated Phenotype:
Not determined