Busch Lab

ZMP

mlxip

Ensembl ID:
ENSDARG00000059474
ZFIN ID:
ZDB-GENE-060526-8
Description:
Novel protein similar to human and mouse MLX interactin protein (MLXIP) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
MLXIP
Human Description:
MLX interacting protein [Source:HGNC Symbol;Acc:17055]
Mouse Orthologue:
Mlxip
Mouse Description:
MLX interacting protein Gene [Source:MGI Symbol;Acc:MGI:2141183]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa40598 Nonsense Mutation detected in F1 DNA Not yet available
sa8759 Nonsense Mutation detected in F1 DNA Not yet available
sa11142 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa40598
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
ENSDART00000082702 Nonsense 385 860 9 18
ENSDART00000134673 Nonsense 380 525 9 10
ENSDART00000144092 None None 241 None 6
Genomic Location (Zv9):
Chromosome 5 (position 70325391)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66650535
GRCz11 5 67328904
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGGTGGCCAACCAGGACAATGGTAACTCCGTCGGTCCGTCCTACCAA[C/T]AGCCCTACATGCCTCTTTTCACAGAGCAAGTGAGCTCCTCCGTCCCGTCT
Long Flanking Sequence:
AGCTGATAAGAACTTTCAACCACTATTCAGGACGCGCGCGGCGACAACACCCGCTTTAGAGTTTTACAGCTCTTTTTGATCCCCGCTTCTAGCAGCACACTCCATTTCCGCATTACTGGATCTGTAGCGACAACAGACCGCAAGGGATTATGGCCAAGCCTGGGCTTATGGGAATTGTAGTTTTCCGGTACCTTCCGTTCGCTTCATTCGCCTGAGCAAATTTTCTCAGAAGACCTATAGTTTTACCGAGTCATGCGACTACGGTAATATCGAAAAAAATTAATATTGCGGTATGACGGTATTTACAATACCGTTACATCCCTATTCAATATCTATATCCGCTTTTTGTTGTTTAGGCTTCCCTGCTTTCATCCCTGCCGCTCTCCACGGAGCTTCCTTCTCTGCCTCTGGACTACCGCCTCATGCCCTCTGCTCCTCTGCCTGGCCATCTCTCGGTGGCCAACCAGGACAATGGTAACTCCGTCGGTCCGTCCTACCAA[C/T]AGCCCTACATGCCTCTTTTCACAGAGCAAGTGAGCTCCTCCGTCCCGTCTATCCTGCCTCCCCCAGCTCCACCTCTCCCCTCAGCCCCACAGCCTCTCAGCACAGTCACTACAGTCCCCCAGCCCAGCCAGAGCGTCCCGCCTTCATCAGTAATAACGCACACCGCCTCCTCCACAGTGACTCCCACTGACGCAGCCACTACCGTCAGCCACAGGTCCAGTTTTGAGCTGCCCCCTGCGCCATCTCCACAGCCTGTAGTCTCCAGCTCTGCCTCGCTCGGCTCACAGCCAGTCAACTTCGCCTTGCCCAAATCCATCCAGCCTCCCATCTCTAGCAAAAAGTCCAGACACTCACAGAGACCGATTGTCCCGGCGAATCCACTGCCGTCTCCTCAGCTCATACTGACAGGTTTGTGTCTCTCCTGAAATCGATTTTGTAACATGCTCGATATGCGATGGGATAGTTTACATAATTGTCGGTTCTGTTGTCTAGGATGTGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8759
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
ENSDART00000082702 Nonsense 480 860 9 18
ENSDART00000134673 Nonsense 475 525 9 10
ENSDART00000144092 None None 241 None 6
Genomic Location (Zv9):
Chromosome 5 (position 70325106)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66650250
GRCz11 5 67328619
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCGCCRTCTCCACAGCCTGTRGTCTCCAGCTCTGCCTCGCTCGGCTCA[C/T]AGCCAGTCAACTTCGCCTTRCCCAAATCCATCCAGCCYCCMATCTCTAGC
Long Flanking Sequence:
TTGCGGTATGACGGTATTTACAATACCGTTACATCCCTATTCAATATCTATATCCGCTTTTTGTTGTTTAGGCTTCCCTGCTTTCATCCCTGCCGCTCTCCACGGAGCTTCCTTCTCTGCCTCTGGACTACCGCCTCATGCCCTCTGCTCCTCTGCCTGGCCATCTCTCGGTGGCCAACCAGGACAATGGTAACTCCGTCGGTCCGTCCTACCAACAGCCCTACATGCCTCTTTTCACAGAGCAAGTGAGCTCCTCCGTCCCGTCTATCCTGCCTCCCCCAGCTCCACCTCTCCCCTCAGCCCCACAGCCTCTCAGCACAGTCACTACAGTCCCCCAGCCCAGCCAGAGCGTCCCGCCTTCATCAGTAATAACGCACACCGCCTCCTCCACAGTGACTCCCACTGACGCAGCCACTACCGTCAGCCACAGGTCCAGTTTTGAGCTGCCCCCTGCGCCATCTCCACAGCCTGTAGTCTCCAGCTCTGCCTCGCTCGGCTCA[C/T]AGCCAGTCAACTTCGCCTTGCCCAAATCCATCCAGCCTCCCATCTCTAGCAAAAAGTCCAGACACTCACAGAGACCGATTGTCCCGGCGAATCCACTGCCGTCTCCTCAGCTCATACTGACAGGTTTGTGTCTCTCCTGAAATCGATTTTGTAACATGCTCGATATGCGATGGGATAGTTTACATAATTGTCGGTTCTGTTGTCTAGGATGTGGGTTTGATTTGGTTTAAAAAATGCATCAATAGCATTTAAATAAATCAGACATTAGTATACAATACACTACCTGACAAAAGTCTTGTTGCCTATCCAAGTTTTTGGAACAGCAAATAATATCACTACTGAGAGTTCAAACACTGAAGAGCGAATCCATCGATGTGCAGCTCTAAAGATCCCGAACCATGTAATATTTGGTATCAGAATATTTGGTATCAGAAGTGGCTTATATGAAAGGCAAAGGCCTCTAGATTACGCTTCTTTTACCTAAATAAAATATTATTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11142
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082702 Essential Splice Site 821 860 None 18
ENSDART00000134673 None None 525 None 10
ENSDART00000144092 Essential Splice Site 202 241 None 6
Genomic Location (Zv9):
Chromosome 5 (position 70316147)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 66641291
GRCz11 5 67319660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGTGTGTGTGTGTGTNNNNASAYTAACAATATGTTTCTCTGTCCTMC[A/T]GTGGTGCTCAGGACRTTACGGCAGCTCTGCACCAGCACCTCCATCCTGAC
Long Flanking Sequence:
TGTCTTCCTCAGCTTATTCAAATGTCAGCAACTAGAAAAACACTGAAAACTAATATTAACTGGACATTAATCACTCAGACTAATCTTCAGCCTTACATTAGGAAAGTGGCTGGTACGAGTCCCAGCTGGGCCAGTTCTGTGCGGCATTTGCATGTTCTTCCCTCTGGGTGCTTCGGTTTCCCCCATAGCCCAAAGACATGTGGTATAGGTGAATTGGATTAACTAAATTGGCCGTAGTGTGTGTGTGTGTGTGTGTGTGTGAATACAAGATTGTATAGGTGTTTCCCAGTACTAGGTTGCGGCTGGAAGTGCATCCGCTGCATAAAACATACGCTGGAATAGTTGGCGGTTCATTCCGCCCCTGATAAATAGGGGTCTAAGCTGAAAAAATGTGAATTAGTGAATGATTTTGTCTCCAGTTTGACTTGTTTGGCATCTGTTTGCTTGTTTCTTTGTGTGTGTGTGTGTGTGTACATTAACAATATGTTTCTCTGTCCTAC[A/T]GTGGTGCTCAGGACGTTACGGCAGCTCTGCACCAGCACCTCCATCCTGACCGACCCCTCACTTTTACCTGAGGAAGCCAAAAAGGCCGCTCTCAACCCCAAAAAACATTCCTCAGGGTCTTAGTTTTAACACAGTGACTTCTGAAATGTGCTTTTCAGGCATAACAGTCATGATCAGGAGCCTCCAAAACAACACCTTGCGCATGTGGATCTAAGGATCTGTGCTTTGCTGTTACTCACTGAACTCCTTCAGAGTGGTGAAAACTGCTCGATTGTGTACTTTACGCGTGTTTACAGAACAGTTTTGAGCTCTCTGTGTGTGTACCTGCTCAAATCTCTTCTGTTTGCCTCACTTATGCACTAAGGACACTACCCACAAAGCAGTCACGTTGAATTTATCTAAATGGGCCAGTCTAGGAACAAAAGCCTTTTTTACTAGAGCTGTGTCGAGAATTTGTTTCAAGTAATTGATTCTGTATTGATTCTAAATGTATCGCTCTT
Associated Phenotype:
Not determined