Busch Lab

ZMP

mpll

Ensembl ID:
ENSDARG00000039222
ZFIN ID:
ZDB-GENE-060421-1
Description:
thrombopoietin receptor [Source:RefSeq peptide;Acc:NP_001003858]
Human Orthologue:
MPL
Human Description:
myeloproliferative leukemia virus oncogene [Source:HGNC Symbol;Acc:7217]
Mouse Orthologue:
Mpl
Mouse Description:
myeloproliferative leukemia virus oncogene Gene [Source:MGI Symbol;Acc:MGI:97076]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa20736 Nonsense Available for shipment Available now
sa881 Nonsense F2 line generated Not yet available
sa26776 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20736
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
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057297 Nonsense 304 655 8 13
ENSDART00000124917 Nonsense 277 614 7 12
Genomic Location (Zv9):
Chromosome 6 (position 33670542)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33988207
GRCz11 6 33972897
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGTTGTGTCCCAATTGCAATAACTCCATCCATCAGTGTGTCCTGTA[T/A]GGCCAGAAGTCCAATGTCTTTAAGTTTTACCTCAATACAGGGTTGCAACC
Long Flanking Sequence:
TACTGTACACTTTTAGAGAGACTACTGCATACTTTTAAAGAATACAAAATCTTTTATCATTTATAATTAGTTACATTATTTATAATACCAATTATTCATAATACCAATTAGTTTTACAATAGTAAATAATGACTAAACGTTCATTTTCTGAGAAAACTAAAAAATCTACATTGGTGAAAATATCAGTTAAATGCCCATTCACAATTCAGTATCTTTTGAATTTTCAGGTGACATAGAGTTCAGGTGCCACACTTCTGATCTGATTCAAATCATTTGCAAATGGAGGGGAGACTTATATAAGGACAATACATACAGCTTCTACTATAAACAATTAAACAGGTGTCATTTTTTTATATATCTTCTGTCTGAAACATTTAATAAAAACACTGAAAAGGTAGCTTACTAACTTTGATCCTTCTTGTCTGGTGTTTCAGAAGTTCATGGAGCAGTTGGAAGTTGTGTCCCAATTGCAATAACTCCATCCATCAGTGTGTCCTGTA[T/A]GGCCAGAAGTCCAATGTCTTTAAGTTTTACCTCAATACAGGGTTGCAACCATTCAGCCGAACATTTTATGCAGAGACTTTCTATATGAACAGTAAAGGTAAGTGTGAAGGAAGAATTGCAGAAAGTCATGTTAGATATGGTTTCTTACATTTAATTTTGATGGTCTCACAGACTGTCAAGTTACTCTCTTTAGTAAGCATTATCACACAGTAAGGTTAAGACTTGAGTGAGGTTATGTTAAGTATATTATGTTGACATATACTCAATGTTGGTTCGTAGACAATCAAAATAAAGTATTAGCTGATTTTAAAGGGATTTTCACCCAAATATAAAATGTCATTACAATTAACTCATACTCTAATGCATAGGTCTCGAACTCAATGCCTGGAGGGCCGCAGCTCTGCAATTTGCTCCAACCCTAATCAAACACAGCTGATCCAATTAATCAAGTGCTCAAGAATACTAGAGACTACTAAGCAGGTGTGAGTTGGAGGTGGTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa881
Status:
F2 line generated
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
ENSDART00000057297 Nonsense 346 655 9 13
ENSDART00000124917 Nonsense 321 614 8 12
Genomic Location (Zv9):
Chromosome 6 (position 33652540)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33970205
GRCz11 6 33954895
KASP Assay ID:
554-0788.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTTCTGTTTTTGACAGTTCAGACAAGGCCTCCAGAAGGTCTGAAGGTA[C/T]AGATTGGGGAAGAAAGGCTTTGTTTGACATGGGATTCACCATTTCTGATC
Long Flanking Sequence:
AGCTTTAAATGTTGAACCGGCCGACAGCGTAAATCTTACAATAGACAGACAGTAATATGCAATAAAGCTGACAGCAAACAAATACATTATAACAGATAAATTTACCTGATGATATAACAAATAACAATCTTCAAATGTTAAACAAAATAGCAATATACAAATGAAGCATACAAACAAGCAAAAATATTGTATCTATTGGTCTACCAATCTGACAACATAACAAATGGCATTCTATGATTAAAAACAGGCTACTAAAGAAGATAACAATACACAAACTAGAATTAAAATTATATCAAAAGTCATCTACATTATATTAAAAGTCATGTTATCTACAAAAAATATGCTTTAAGAAACATCTTTACATACCACTAATGTCAGCGATAGTCTATGCTGCATTGTAATGACACTTAGTGTAATGGCACTGGCAGTGAAAGCTCAGTTAGTCTGTCTCTTTTCTGTTTTTGACAGTTCAGACAAGGCCTCCAGAAGGTCTGAAGGTA[C/T]AGATTGGGGAAGAAAGGCTTTGTTTGACATGGGATTCACCATTTCTGATCATTTCTAAGCATCTAATGTACCAGATCCGTTATCAGCATCATGAAGAGAATCAGTGGAAGGTGAGTTTAAATAAATAATGAGAAATGAAAAATTCACTTATTATGGAAAGATAATATGAACTCATTTATTGCCATTATGTCTTTTTTTTTTGCTTTAAATCATTTATGCAAATAACTGCAAATGTTATGGTGAAATATAATTTTTGTGTCAGGGTTTTAAAGCTTCTGGATCCAAGACCAGCACTTGTCTAGATGTGCACAGAGGGGGTCGATACACCATCCAGGTTCGAGCACAACCCAATGGATCTGTGTACAGCGGAAACTGGAGTGACTGGTCAAAACCTGTTACAACCAACCTACCTTTAAGCAAAGGTTAACATTCTATTCATAATGTTAAATGTGCCTACTAGATACTTTCTGACAAAATAATGTGCTAAAGGAAATAGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26776
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057297 Essential Splice Site 436 655 10 13
ENSDART00000124917 Essential Splice Site 411 614 9 12
Genomic Location (Zv9):
Chromosome 6 (position 33652116)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33969781
GRCz11 6 33954471
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGTGACTGGTCAAAACCTGTTACAACCAACCTACCTTTAAGCAAAGG[T/G]TAACATTCTATTCATAATGTTAAATGTGCCTACTAGATACTTTCTGACAA
Long Flanking Sequence:
GCAGTGAAAGCTCAGTTAGTCTGTCTCTTTTCTGTTTTTGACAGTTCAGACAAGGCCTCCAGAAGGTCTGAAGGTACAGATTGGGGAAGAAAGGCTTTGTTTGACATGGGATTCACCATTTCTGATCATTTCTAAGCATCTAATGTACCAGATCCGTTATCAGCATCATGAAGAGAATCAGTGGAAGGTGAGTTTAAATAAATAATGAGAAATGAAAAATTCACTTATTATGGAAAGATAATATGAACTCATTTATTGCCATTATGTCTTTTTTTTTTGCTTTAAATCATTTATGCAAATAACTGCAAATGTTATGGTGAAATATAATTTTTGTGTCAGGGTTTTAAAGCTTCTGGATCCAAGACCAGCACTTGTCTAGATGTGCACAGAGGGGGTCGATACACCATCCAGGTTCGAGCACAACCCAATGGATCTGTGTACAGCGGAAACTGGAGTGACTGGTCAAAACCTGTTACAACCAACCTACCTTTAAGCAAAGG[T/G]TAACATTCTATTCATAATGTTAAATGTGCCTACTAGATACTTTCTGACAAAATAATGTGCTAAAGGAAATAGAATATCAGAATTTAAAAGCATTGCATGCAGTCTCAGCTTGCTTGGGCAACCGGTCTGCAGCCAAACCCTTCAGAATTTTTTTAAATATATACACAAAAAGTACTTAAATTCATATTCACCATATTCATATGCTTTTTAATGTTCAGATTAAAAGGTAGAATATTTAAAAAACAAATTGACTAGGGATCACTTTTTCAAAACAATACTGAAGACCAGGGGCGGATTTAACCAATAAGGAAGGTAAGCAGCCCAAATAAATACCTAGAAGTATAAACAATACCTATAAATTATTTATAACATTGTTTTCTATCATAATTTGTACAGTGAGGGTCTACATTTTTTAGTTCAAATTTAATTATTACATCTGCACAAATGTGTCCCACTTCTTAAAATCATTTAGCAGTTCAGCAGTCAAATTAGTAAAGATT
Associated Phenotype:
Not determined