Busch Lab

ZMP

LYL1

Ensembl ID:
ENSDARG00000091603
Description:
lymphoblastic leukemia derived sequence 1 [Source:HGNC Symbol;Acc:6734]
Human Orthologue:
LYL1
Human Description:
lymphoblastic leukemia derived sequence 1 [Source:HGNC Symbol;Acc:6734]
Mouse Orthologue:
Lyl1
Mouse Description:
lymphoblastomic leukemia 1 Gene [Source:MGI Symbol;Acc:MGI:96891]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa44628 Nonsense Mutation detected in F1 DNA Not yet available
sa10760 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa44628
Status:
Mutation detected in F1 DNA
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
ENSDART00000127734 Nonsense 203 331 4 4
Genomic Location (Zv9):
Chromosome 6 (position 104739)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 151798
GRCz11 6 169849
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATAGTGTGTTGATTTGTGCGTGTGGTTCTCCTTCAGGTCCTCCTCAG[A/T]AGCTGGCTCGGCGTGTCTTCACCAACAGCCGCGAGCGCTGGCGGCAGCAG
Long Flanking Sequence:
AATCATTATTCAACATTACATGAAATGCCTCTAAACCTCAAAGCATGGACAAAAGAAATCTCTTTCTCCAGAAGAACTCAGTTATTTGGTCAAACTTTGAGGCTTTTAGAGTTATTAAATGTTTTAATGCTTCATCATTTTAATAACAAACACAACATTCTATATTTCACAAATCAAATTCCCCTGAAAAAGAAAAGTTAAACATAATTTCAAATATTAAATATTTTGATTCATATCAAAATATTCAAATAAATCAAAGCACAACACTGTAAATCATCAGTGCAGCATGCTGACATACGCAGATGCAATTCAATTCAGTCAGATTATAAACTGAAGGTGGAGTTTATTATGCAAAATATTTACCTTATAATATACTGTATATATATATACACTCATCAGATAGTGTGAGTCGTGTGATTAGCCGTGTGCAGTCGTATCCATCTTTAGTTGAATATAGTGTGTTGATTTGTGCGTGTGGTTCTCCTTCAGGTCCTCCTCAG[A/T]AGCTGGCTCGGCGTGTCTTCACCAACAGCCGCGAGCGCTGGCGGCAGCAGAACGTGAACGGCGCTTTCTCTGAGCTGCGCAAACTGATCCCGACGCACCCGCCGGACCGAAAGCTGAGCAAGAACGAGATCCTGCGGCTCGCCATGAAGTACATCGACTTCCTGGAGCAGCTGCTGAACGACCAGAGCCAGCCGGAGGAGACGGGTCAGCGCGCACATGCACACACACCCTCCACACACTCGCTGCTGCTGCTGACCGCATCCTCTGGATCCAGCTGCTATGGGGACACTGACAGCGAGGAGAGCACGGGCCCTCGGGCCTGCAGCACGGACCCCAAACACAGCAGGGAGCCCATACTGGCACTCACAGTGAGCGGGGGCCAGCGGTGACACACACACACACAGACTGACCACGTGTGCGGGAGTTTACTGATGTCTGCGTTTACACTGCATGCTTCAGGTGACCCGTGCGGCACAGACAGCACACGGCCCACACACACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10760
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127734 Nonsense 230 331 4 4
Genomic Location (Zv9):
Chromosome 6 (position 104820)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 151879
GRCz11 6 169930
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GYGAGCGCTGGCGGCAGCAGAACGTGAACGGCGCKTTCTCTGAGCTGCGC[A/T]AACTGATCCCGACRCACCCGCCGGACCGMAAGCTGAGCAAGAACGAGATC
Long Flanking Sequence:
TTATTTGGTCAAACTTTGAGGCTTTTAGAGTTATTAAATGTTTTAATGCTTCATCATTTTAATAACAAACACAACATTCTATATTTCACAAATCAAATTCCCCTGAAAAAGAAAAGTTAAACATAATTTCAAATATTAAATATTTTGATTCATATCAAAATATTCAAATAAATCAAAGCACAACACTGTAAATCATCAGTGCAGCATGCTGACATACGCAGATGCAATTCAATTCAGTCAGATTATAAACTGAAGGTGGAGTTTATTATGCAAAATATTTACCTTATAATATACTGTATATATATATACACTCATCAGATAGTGTGAGTCGTGTGATTAGCCGTGTGCAGTCGTATCCATCTTTAGTTGAATATAGTGTGTTGATTTGTGCGTGTGGTTCTCCTTCAGGTCCTCCTCAGAAGCTGGCTCGGCGTGTCTTCACCAACAGCCGCGAGCGCTGGCGGCAGCAGAACGTGAACGGCGCTTTCTCTGAGCTGCGC[A/T]AACTGATCCCGACGCACCCGCCGGACCGAAAGCTGAGCAAGAACGAGATCCTGCGGCTCGCCATGAAGTACATCGACTTCCTGGAGCAGCTGCTGAACGACCAGAGCCAGCCGGAGGAGACGGGTCAGCGCGCACATGCACACACACCCTCCACACACTCGCTGCTGCTGCTGACCGCATCCTCTGGATCCAGCTGCTATGGGGACACTGACAGCGAGGAGAGCACGGGCCCTCGGGCCTGCAGCACGGACCCCAAACACAGCAGGGAGCCCATACTGGCACTCACAGTGAGCGGGGGCCAGCGGTGACACACACACACACAGACTGACCACGTGTGCGGGAGTTTACTGATGTCTGCGTTTACACTGCATGCTTCAGGTGACCCGTGCGGCACAGACAGCACACGGCCCACACACACACATGAATATTCACAAACTCAATGCGAGTAAACCAGGGGTGTCCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined