Busch Lab

ZMP

si:ch211-223p9.1

Ensembl ID:
ENSDARG00000079248
ZFIN ID:
ZDB-GENE-080917-23
Description:
Novel protein similar to human meningioma (Disrupted in balanced translocation) 1 (MN1) [Source:UniP
Human Orthologue:
MN1
Human Description:
meningioma (disrupted in balanced translocation) 1 [Source:HGNC Symbol;Acc:7180]
Mouse Orthologue:
Mn1
Mouse Description:
meningioma 1 Gene [Source:MGI Symbol;Acc:MGI:1261813]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa33765 Nonsense Mutation detected in F1 DNA Not yet available
sa26622 Nonsense Mutation detected in F1 DNA Not yet available
sa33764 Nonsense Available for shipment Available now
sa33763 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33765
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109566 Nonsense 284 1204 1 3
ENSDART00000129197 Nonsense 284 1211 1 2
Genomic Location (Zv9):
Chromosome 5 (position 69697341)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66022524
GRCz11 5 66701629
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGACAGGGCGCCAGGTACCAGGGTCCAATTTTCCTGGAAACACAGGGT[T/A]GTCTCGCGCTCCTGGAATGCAGGGCATCGCTAAAGAGCACCCCCATGCCC
Long Flanking Sequence:
CTTTGGGGGAAACTTTGGACCTGAACCAGGATCCTCTTGTTTACACAGTGGAAGGGTGATGGGTTACAACAGCAGTATGGGACTCCAGCAAGGGTTCACAGAGGGTTTTGACTCGCTCTCTGAAGGACAGTCAGCAGATGGTGGCTTCTCTCAGCAGCAGCAAAGGACAAGCTCTATGTCGGATTTTCAGCACCATGGACCACCCAGTGGAAATCACCCTGTTCCAGCCCCGTGTCTCCCCTTGGACCAGTCACCTAATCGTGCCGCCTCCTTCCATGGCCTGTCTTCCTCATCCTCTTCATCAGAAAGTCACAATCTTGAGCCAAGGCGAATGCCGCCGCCAGCCGCTGTCGAAGGACTGGACTATAGCTTTCCTAACGAGCCCTCATCCAGACATTTTGACGTGCCTGTGTACTCCCCCTCTGAATCTGATTCTCAGCTTTCTCATTTTGGGACAGGGCGCCAGGTACCAGGGTCCAATTTTCCTGGAAACACAGGGT[T/A]GTCTCGCGCTCCTGGAATGCAGGGCATCGCTAAAGAGCACCCCCATGCCCCTCCTCAGCAGCAGCAGCCGTCAGCCCAGCACAGTGTGTTCTTTGAACGTTTTGGGGGTGGACGCAAAATACCAGTGGGGATAGAACCTGGTGCCAGGCATCCTCTCATGCAACAGCAGCAGCCAGGCTTGATTGGACGACAGAACACTTGCCCACCATCTCTCCCACAACCCCCACTATCAGAGACAGCTTCTGCTAATGTCGGCATGCAGGAGGGTGGCGTCATGATGCCTGGCCAACATAATCAGTTTGAATACCCTATTCACAGACCAGAGAACAGACGGATACATAGTTATGGTGACCCCATCTTCAACATGCAGCAGCAGCCTCCCCCTCCTCAGCAGCCTCCCAACCAGAGGTTGCAACACTTTGATTCTCCTTATTTAAATATGGGTAAGAGGCCCAGGTTTGATTTCCCCAATGCCACTCATGGCAGGGAGAGCTGCGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26622
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109566 Nonsense 524 1204 1 3
ENSDART00000129197 Nonsense 524 1211 1 2
Genomic Location (Zv9):
Chromosome 5 (position 69696622)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66021805
GRCz11 5 66700910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGATGGCGTCTCGGAGCCAGCAGCAGAGGATGAGACAACCCAGTCTA[C/T]AGCAGCTGGGTCACCACAATGATGTTTCTCAAGGGCCCCTGGGACCAGGG
Long Flanking Sequence:
AACCCCCACTATCAGAGACAGCTTCTGCTAATGTCGGCATGCAGGAGGGTGGCGTCATGATGCCTGGCCAACATAATCAGTTTGAATACCCTATTCACAGACCAGAGAACAGACGGATACATAGTTATGGTGACCCCATCTTCAACATGCAGCAGCAGCCTCCCCCTCCTCAGCAGCCTCCCAACCAGAGGTTGCAACACTTTGATTCTCCTTATTTAAATATGGGTAAGAGGCCCAGGTTTGATTTCCCCAATGCCACTCATGGCAGGGAGAGCTGCGGCAGTTGGAACAGCGCTATGGAGAATAATCTCTCTCCAGCAGCCTACCCTGGCCTGCCTGGAGAGTTCACCCCTCCTGTGACGGATGGCTTCTCGACAGGCCCATCGCTGCAGCTAACAGGCTCTGAGCAACAATCGATGCAGCAGCAGCAAAATGCAGCAATGATGATCAAGCAGATGGCGTCTCGGAGCCAGCAGCAGAGGATGAGACAACCCAGTCTA[C/T]AGCAGCTGGGTCACCACAATGATGTTTCTCAAGGGCCCCTGGGACCAGGGGGCCCAGTGGGAGGCATGCCTCAGTCAAGTTTTGAGAGAGAAAATGGTGGGAGGATGGTGAACTTTGATGGACGGAGTCCACACATGACTATGGAGAGCGGGTGGTTTCCTGGGCCACATCCACCGGGGGAAATGCTAGGTCATCGCATGGGTTCAAGTGGTGAGATGGGGGATCGAGACATCCAGCAAAATGGTCCTGGAATGATGTTCAGAGCTGGTGTGAGTGGAATGGGCATGCAGGAGTCTATGAGAGTCCCAGGAGAGGGCCACGTGCAGCCTTTACTGTCGCCTAACATACACTCACAATTCAACAGTGGCATGGGAAGCCTCTCGCAGATGCAGTCTCCCAGTGCAGGTGTTGGATTGCCCAACACGCCATCAGAAAGACGCTCAAATGACTTTCCAGGACCACCCATGGGTGGTCCGTCCCAGTTTCAATACGGAGGCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33764
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109566 Nonsense 607 1204 1 3
ENSDART00000129197 Nonsense 607 1211 1 2
Genomic Location (Zv9):
Chromosome 5 (position 69696373)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66021556
GRCz11 5 66700661
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTTCAAGTGGTGAGATGGGGGATCGAGACATCCAGCAAAATGGTCCT[G/T]GAATGATGTTCAGAGCTGGTGTGAGTGGAATGGGCATGCAGGAGTCTATG
Long Flanking Sequence:
CCAATGCCACTCATGGCAGGGAGAGCTGCGGCAGTTGGAACAGCGCTATGGAGAATAATCTCTCTCCAGCAGCCTACCCTGGCCTGCCTGGAGAGTTCACCCCTCCTGTGACGGATGGCTTCTCGACAGGCCCATCGCTGCAGCTAACAGGCTCTGAGCAACAATCGATGCAGCAGCAGCAAAATGCAGCAATGATGATCAAGCAGATGGCGTCTCGGAGCCAGCAGCAGAGGATGAGACAACCCAGTCTACAGCAGCTGGGTCACCACAATGATGTTTCTCAAGGGCCCCTGGGACCAGGGGGCCCAGTGGGAGGCATGCCTCAGTCAAGTTTTGAGAGAGAAAATGGTGGGAGGATGGTGAACTTTGATGGACGGAGTCCACACATGACTATGGAGAGCGGGTGGTTTCCTGGGCCACATCCACCGGGGGAAATGCTAGGTCATCGCATGGGTTCAAGTGGTGAGATGGGGGATCGAGACATCCAGCAAAATGGTCCT[G/T]GAATGATGTTCAGAGCTGGTGTGAGTGGAATGGGCATGCAGGAGTCTATGAGAGTCCCAGGAGAGGGCCACGTGCAGCCTTTACTGTCGCCTAACATACACTCACAATTCAACAGTGGCATGGGAAGCCTCTCGCAGATGCAGTCTCCCAGTGCAGGTGTTGGATTGCCCAACACGCCATCAGAAAGACGCTCAAATGACTTTCCAGGACCACCCATGGGTGGTCCGTCCCAGTTTCAATACGGAGGCTCTAATCGACAGGGAGCCTCTCATGGTAACTCTCAAGGGGTGAACACCTCACCGGGGAGCTTTACATGCCAATCAGACTTTCCCACTAGCCAGCGTTCCTCAGTCAGCAAACTTGGGGGACTGTCTTTAGGGAATTTTAGCAAAACGAATGGCAAGGACAATGTTTTTGGACAGAGCTGCCTGGCAGCCCTCTCTACTGCCTGTCAGAACATGATTGCCAGCCTGGGGGCCCCTAACCTCAATGTGACATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33763
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109566 Essential Splice Site 1152 1204 2 3
ENSDART00000129197 None None 1211 None 2
Genomic Location (Zv9):
Chromosome 5 (position 69691185)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66016368
GRCz11 5 66695473
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCATGTTCAAGAAACCAGTCGGCACATTCTGACCCTAGCATCCTGATG[T/C]CGGCAGCCCAGGCTCATTCTGAAAACGTAGTCCAGCGGATGTTTCTGGAG
Long Flanking Sequence:
GAGAAGGGTTACAAAGTGTTTGCGGCTCGTGAAATTGCATGGGATTCATTGCACGCCGACACACAAGGGGACTGTTAGACTCTATAAGACGTTCGTTCACATCGTCATTTTTTTACAGGCCTTTATAACACTTCAATCTCAAAGTGCAGGAATGCGTCTAGTCATTTTAATTAGGTGACTAAGTACGTTGATAATATGGATTTATGGGATGCTGTAATTCATTTTACAAGTCTCCTGATCATTTAAGTGGCCATGAAATGAACTCCTAAAATTGTGTTGTGAACCAATCTAGCAGATACGACCAACGTTTTTCTTGATTTAACATAAGGTATAATCATAGTCATGTATTGCACATCCATGATGTAAATCTCCCGTTACACCAAATCCCAAAGGTGCTCTATTGGATTGAGATCTGGTGATGTGGAGGCCATTTGAGTACAGTGAACTCACTGTCATGTTCAAGAAACCAGTCGGCACATTCTGACCCTAGCATCCTGATG[T/C]CGGCAGCCCAGGCTCATTCTGAAAACGTAGTCCAGCGGATGTTTCTGGAGACCGCGAAAAACGTCCCGGCAGGTACGTATTTGTGCAGTTTTTGTTTTCGCGAATCCGCAAGAGGCCGTTGTGTGCGCTTTTTCGTATCTCGAACGTCTCTCGCGAGTGCCGTTCACGCCCGCGCTGTTCTCGCGTCAACCCACCAGAGGCCGCTGTCTGACTGACCGAATGATTGACTGCGCAAGCGGCCAATCAGCTGACCCACCCTCCTCCTTCCGTGAACCCAACCAGTTTTACCAATTGACCCGCCCGCCCGCTTACTTCCCTAAACCCGAGCAACAAGTTAGAAAAGCCGTCTAGAAAAAAAAAAGCCCTCGTCTGTTTTTTTTTTTTTTTTTTTTTTAACCACTTTTTCGGATTTCACCACATTCTCACCCTGTTATGAACTCGTTCGCTTTATTTTTTGGATTCTGTTTTTGTCTTACCTGATTTCTGGAACCGCTCTTCCC
Associated Phenotype:
Not determined