Busch Lab

ZMP

si:ch211-45m15.2

Ensembl ID:
ENSDARG00000025983
ZFIN ID:
ZDB-GENE-040724-127
Description:
Novel protein similar to human and mouse l(3)mbt-like 3 (Drosophila) (L3MBTL3) [Source:UniProtKB/TrE
Human Orthologue:
L3MBTL3
Human Description:
l(3)mbt-like 3 (Drosophila) [Source:HGNC Symbol;Acc:23035]
Mouse Orthologue:
L3mbtl3
Mouse Description:
l(3)mbt-like 3 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2143628]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9692 Nonsense Available for shipment Available now
sa30715 Nonsense Mutation detected in F1 DNA Not yet available
sa39266 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa9692
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039249 Nonsense 62 490 2 14
ENSDART00000047308 Nonsense 61 739 2 20
Genomic Location (Zv9):
Chromosome 20 (position 2163970)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 2118255
GRCz11 20 2144961
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAAGCAGGATTCTCCTTGGGGTCAGCGCGGCCTGGTGYGTGTGCGCTG[T/A]AACAGGAAGGGCTCTGCGGTGGACTTCCTGCCTGATGGCCTTCACTGCAG
Long Flanking Sequence:
CGCGTTGCCCTGCATGCAGTCATTTTGACCAATATGGTAATTAAAGGTAGAAATGCTCAGTTCTTTACTGTTTTGTAATTTTAAAAATAACAATGTTAGAAAGAAATACATAGATATTTAGAAAACGTCAGGGTGGATAGATATGTTTATTTCAAAGAGTTATTAAGTTACAAAAAATAGTGCCAATAGTGTTCAGCTTTTTCTGACGGCTCCTCCCTCAAAATTTCATTGGCTGTGGTTTGGTAGCTTGACTGAGCTGTTGGGGAACGAGTTGTTGTCAGATCATGTAGTGTGTGATCATTTACGTCGTGTCGCATAGTGTGAACACCAGCGACACAAAATCAAGTCATGTAGTGTGACCGGCACATCGATCTGCCGATGTTTAAATGCATGTGGTGTGAACTAGGCTTAACTGTCTGTTTTCTCTCAGCTCTCTCTGAAGGGTCAGTCTTAAAGCAGGATTCTCCTTGGGGTCAGCGCGGCCTGGTGTGTGTGCGCTG[T/A]AACAGGAAGGGCTCTGCGGTGGACTTCCTGCCTGATGGCCTTCACTGCAGCGAGCGCTGTCTGCAGCAGGAGCAAGAGTGAGTCCTACACTCAACATCTGCTCTCCTCTTGTTTATTTAAGGATGAATCACAACAGTACATTAACCTGTTTCAATCATAGGCAAGATGTATGCTGTCAGAGTATAGCAGAATGCTAATATACACCTGCAGTCACCGAGAGTTCAGTCATTCATTCATTGTTTTTTTCGGCTTAGTCCCTTTATAAATCCAGGGTCGCCACAGTGGAATGAACCGCCAACTTATCCAGCATGTTTTACACAGCGGATGCGCTTCCAGCTGCAACTCATCTCTGGGAAACACCCATACACTCTCATTCACACTCATACACTACGGACAAATTAGCCTACCCAATTCACCTGTACCGCATGTGCTTAGACTGTGGAGGAAACCGGAGCACCCGGAGGAAACCCACATGAATGCAGGGAGAACATGCAAACTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30715
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039249 Nonsense 263 490 7 14
ENSDART00000047308 Nonsense 256 739 7 20
Genomic Location (Zv9):
Chromosome 20 (position 2176888)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 2131173
GRCz11 20 2157879
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACTCCAACTCTCCCGACATTCACCCTGTGGGCTGGTGTGAGAAAACC[G/T]GACACAAGTTACACCCACCGAAAGGTGTGCGGGTGAATATGTGATGTGTG
Long Flanking Sequence:
GAACAGATCCAGGAATTTTTCGCAGTATTTCCTCTAATATTTTTTCTCCTGGCGAAAGTCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTTAATTTTTAAACCATTTTAAGGTCAATATTATCAGCCCTTAAGTAATATTTGTTTTTGGTTGTCTACAGAACAATCCACTGTTATACAATGATTTGCCTAATTACCCTAACCTGCCTAGTTAATCAAGTTAAGCCTTTAAATGTCAGTTAAAGCTGAATACTAGTATCCTAAAAAATATAAAGGGCGGCTAATAATTCTCTCTTCGTTTCTCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGCGTGTGTGTGTGTTCAGGTGTCAGGGCATCGAATCAGACTCCACTTTGATCACTTTTCTGACTGCTATGACTTCTGGGTAAACTCCAACTCTCCCGACATTCACCCTGTGGGCTGGTGTGAGAAAACC[G/T]GACACAAGTTACACCCACCGAAAGGTGTGCGGGTGAATATGTGATGTGTGTTTATGTGTGTGTATGTAAATATCAATGTGTGTGTTTATGAATGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGAATTTGTGTGTACATGAATGTGTGTGCATGCATGAATTAATTATCTAAATGAATGTGTGTGTGTGTGTGTGTGTGTATGTGTGTCTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTATGAATTTGTGTATATAATAATATGTGGATATGAATATGTGTGTGTGTGTGTGTGTATCAATTTGTGTGTAAGAATGCATGTATATATATTAATTTGTCTGTATATGAATGTGTGTGTATATATATAATTTGTATGTACAATTGTGTGTATATTAATTTGTGTGCATATGAATGTGTGTATATATATCAATTTGTGTGTATATGAATGTGTGTCTATAAATGTATTTGTGCGTATATGAATGTGTGTGTGTATATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39266
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
ENSDART00000039249 Nonsense 453 490 13 14
ENSDART00000047308 Nonsense 446 739 13 20
Genomic Location (Zv9):
Chromosome 20 (position 2193755)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 2148040
GRCz11 20 2174746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGTAATTCTCTCTTTCAGATCCATTTTGATGGCTGGACAGATGAATA[T/A]GATTACTGGATCGATGCAGACAGTCCAGACGTTCATCCAGCTGGCTGGTG
Long Flanking Sequence:
TGCACTAAATCACACTTCAGCCGCGTTTATTTGAGGGCGCACAAGAAAATCTGCACATGAGCAGCGTATTTTTGAGGGCGCGCAAGAAGTTTTGTGCACGAACAGGAAATCGGCGCTCAAGCAGAGATTGACATGCTCGTAGGCTATTACATGAATGCGATCTCGACTTAATACTGTGCCCATGACATTTGTCAATGAAATAACGCCACATGTAGTGGTAAATATGTGTAAAATGGCCAATAGAGTCTGCCGCCACAGCTTTAAAAAATCCTAGAGGAAACACTGAACAGATTGAAATGTTCATGTGTTCTTTGTGGGCTTGATTTGCTGATTTTTAATGGGAAGAAGTAGTTGCTGTTTTTAACACTATTTATGTTGTTTAATGTTTGTCTTAAGTGTTTGGTTTGATTATGTGATATATGTGTTGTAAATCTATCATGCTGCTGAACAAACTGTAATTCTCTCTTTCAGATCCATTTTGATGGCTGGACAGATGAATA[T/A]GATTACTGGATCGATGCAGACAGTCCAGACGTTCATCCAGCTGGCTGGTGCGCCAAAACCGGACATCCTCTGCAGCCTCCAATCAGTGAGTATGGACATCTTTCACCCGGAAGAGAGGAGTTAAACACTCCCGATAGAAAGACTGCCGCAGATGAATAGCAGCAACATTATTTTGCCATCATATATGATCATTCCATCACAATGCATTCTTATGGAAACTCTGAGGGCCCTGATAAACACTTACTATTTTCACATTGCACTCATTTGTGCACCCATGGGTGTGCTGGTTTGAAAAGCAGATGTGTTAAGGTACATTGACATGTTACCATTTTGAGAAAATGGAAATAGACGGTGCCATTGACCATCTGAAACTGCTCTAAAGTCAATGGCACATTAGTGAAAAGTGGCTTCAAAATAACCCACGTTGCTTATTACACACACAGGGATGTGCAGCAGCACAGAAATGTATTTAAATATTAAAACTTAGATGTAAAATATAT
Associated Phenotype:
Not determined