ZMP
AXL (2 of 2)
Ensembl ID:
Description:
AXL receptor tyrosine kinase [Source:HGNC Symbol;Acc:905]
Human Orthologue:
AXL
Human Description:
AXL receptor tyrosine kinase [Source:HGNC Symbol;Acc:905]
Mouse Orthologue:
Axl
Mouse Description:
AXL receptor tyrosine kinase Gene [Source:MGI Symbol;Acc:MGI:1347244]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22558 | Essential Splice Site | Available for shipment | Available now |
| sa6360 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22558
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000093249 | Essential Splice Site | 60 | 304 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 33480)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 3402 |
| GRCz11 | 15 | 77973 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTGGCTTCTGCTAATGCTAATGCTAATGCTCTGCTTTACTGTGTTGC[A/C]GAAACAGGCCAGTCCAGAGGTGAGTGTTCACCATCTCCTGTTCACTCTTA
Long Flanking Sequence:
TAAAGAGACAATTGTGCTGCAGTAAGAGGAATACAGTCGTACAGTTAATAAAGCTGAAGCGGCCTCAGTCACAGTGAGTCTGACAGTCCTGCAGTACATCAGAGAATCAGTCGCTCAGTCAGTCCGTATTCAAGCATGTGTGTTTCTGTGTGTCTGACGCTCTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGCAGGCAGTGCTGGACGTGGGTTTAGACACAGAGCAGAGTGTGAATCTGTCAGAGCCGCTGTCCAACATTTCCTTCAGAGTGTGTGCGTACACTGGAGCGGGCCCGGGGCCCTGGACTGCCCAACACACACTCACACTCATCCCCACAGGTTAGACACATACACACACACACACACACACACACACACACACACACACACACACAATCACTCTCTCTCACACACACACTCACTCAGAAGCATACATTGGCTTCTGCTAATGCTAATGCTAATGCTCTGCTTTACTGTGTTGC[A/C]GAAACAGGCCAGTCCAGAGGTGAGTGTTCACCATCTCCTGTTCACTCTTATTGATTAGTAATGACTATTATTACATGACTCTCTTTATTTTTGCATGGTAATTGGCCGGTCATGGCAGTCCAAGGCAGGTTATTCGCCGATAAGAACTGATTAAACTAGTAACTCGGTGGTCCTCTTGAGCATTAGTGAACATACTCCTGCATTCGTGATCATCATCACTCTGCTGTTCTTGACGGGTTGACGTCGTCTTGTGATTGAATGCTGATGATAATACACCAGCATCACGCTTAATAAAGAGTTAGAATCCGCTCAGATCAGGGTTTTGTGTCTAATAGATTTGTTTTGTGTAATAATCAGCATAATGTACATCCAGCCGGTGGTTATTCACAATAAACCCGTCAGTCTTCTACAACAGCTTCATTCTGCCAGAACAGACGGCCGGATGTCCTTTATCTCTGACCAGAACAGCTCTGTTCATTTGTCATAACTGAGGTTTAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6360
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000093249 | Nonsense | 187 | 304 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 28740)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 8142 |
| GRCz11 | 15 | 82713 |
KASP Assay ID:
554-5344.1 (used for ordering genotyping assays)
KASP Sequence:
TNNNNNNNNNNNNNNNNNNTCAGGTGAGYTTGGCTCTGTGATGGAGGGTTCTCTCTCTCAGGAGGACT[C/A]GGTGCTGAAGGTGGCAGTAAAGACCATGAAAAGTGAGTGATGTTCATCTC
Long Flanking Sequence:
TCCAGGGTGGAGGGTTTACGTCATCTGGACGAGCTCCATCTGCATTCCTGCACTCACATCTGGGTTCATTTGTAGAGCAAAACACTCCTGCGTCAATTCTAACATCATGTGCTCCTCACTGGAGCTTTACTCTCAGTATATAGCTGTATTCTCACTCCAGCATACTAGTGTGTGTGTGTGTGTGTGTTATTGTGGTGTTGAAGGTGTGTGTTGTCTCCTCAGTGAACTCTCTGGGCATCAGTGATGAGCTGAAGCAGAAGCTGCAGGATGTGATGGTGGACAGACACAGACTGACCCTGGGAAAAACACTGGGAGAGGGTGAGCACTGACCCATGCGCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATTCAGATGCTTAATGTTCTGTGTGTGTGTGTGTTCAGGTGAGTTTGGCTCTGTGATGGAGGGTTCTCTCTCTCAGGAGGACT[C/A]GGTGCTGAAGGTGGCAGTAAAGACCATGAAAAGTGAGTGATGTTCATCTCTGATGGAGATATATATCTATATATGTGCATGTGTGCGTGCGTGCGTGTGACTAACCTGATCCTCCGCTCTACAGTCGCCATCTGCACCCGCACAGAGATGGAGGATTTCCTCAGAGAAGCGGCCTGTATGAAGGAGTTTGACCACCAGAACGTCATGAGGCTCCTGGGTGAGTGTGTGTCCACTGCTACAACACACACACACACACGCACACACACAAACACACACACACACGCACACACACACACACACACACACACACACACACACACACACACACACACAAACACACACACGCACAAACACACACACACACACAAACACACACGTGCGCATCTAAACGCAGATATTTCATGCACACACTTGAATAAACTCTTGTGATCTGCTGTTCCTGGCTGCTGTGTGTTTAATGTGGTGTAAGGATTATTATGGGTTATTGAGATATTGGCATG
Associated Phenotype:
Not determined