Busch Lab

ZMP

ENSDARG00000088125

Ensembl ID:
ENSDARG00000088125
Human Orthologues:
C16orf5, LITAF
Human Descriptions:
chromosome 16 open reading frame 5 [Source:HGNC Symbol;Acc:13234]
lipopolysaccharide-induced TNF factor [Source:HGNC Symbol;Acc:16841]
Mouse Orthologues:
5730403B10Rik, Litaf
Mouse Descriptions:
LPS-induced TN factor Gene [Source:MGI Symbol;Acc:MGI:1929512]
RIKEN cDNA 5730403B10 gene Gene [Source:MGI Symbol;Acc:MGI:1913876]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa44574 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa20122 Essential Splice Site Available for shipment Available now
sa20121 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa44574
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123317 Splice Site, Nonsense 49 190 1 5
Genomic Location (Zv9):
Chromosome 3 (position 46413071)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48422624
GRCz11 3 46374958
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGGCCATGCTCATTCAGTTCAAGAAAAACAACGGGCAAAACGAGCAA[C/T]GTCAGTATGATCAGATCGAACCAAATAATTGTTTGCTTTTTAATGATTTA
Long Flanking Sequence:
TAGTAAAATACAGGTAAACCACATACTTTAAATATTACCAACATGTTCCTCGCTACAGTATACAACCAAGCACATATTTCCTTATTACTGGAATGTGGAAAGCTACTGATGGGACGCTACAGTATGCATCGGTAAGTTTTTAATCCAATTTTAACCACTTCTGCTTTTACTGTTCATTCATATTATAATCACACACTAAAAGTGGTATTTGTAATACAAAAGCCTTGATTCTCCTGCATTCCTGCCCTAAAGCGAAGTTCTGTTGCGTAACTGTGTTGTATTTCTTTCAGAGAAGACTCTTTATGATGGTTTGAGAATTGTGGATGTTTAGGTGAGCGGTCATCTCAACCCTCAACATGCCTGAGCAATCTGAAGATCAGCTGTCGAACATCTTTGAAGACCTCAACCTTCTGTCTCTTAAAAGACAGCAATTCACCGATAGACGCAATGTGTTGGCCATGCTCATTCAGTTCAAGAAAAACAACGGGCAAAACGAGCAA[C/T]GTCAGTATGATCAGATCGAACCAAATAATTGTTTGCTTTTTAATGATTTACAACAGAAGCCAGATATAATGTGAAAGACATCTAGGAATGATTTTTAAGAGGAAAATTCTGGTTATAATTGACACTGGACTACATTTGTATTGAGATTTTCACATAATGGATAAATAAGCTTTTCATTGATGTGTGGTTTGTTCGGATAGGACAATATTTGGCTGAGATACATCTGTTTAAAAGTCTGAGCGTAAAAAAAAAACTTTTTATATACACTAGAAAAATGTACAAATATCTCCATGGAACACAGTTTTTACTTATCCTAATAATTTCTGGCATAAAAGAAAATAATAATAATAAAATAATAATAATTTTGACATATACAATGTATTTGTAGCTATTGCCAAATATATACCCCTATGACATAAGTTTTGTCATCCTGGGTCACATATGGTTGCATGTATGTGTGTGTTTTTACAGTAAATTTCCTATTTTAGTGAACTGATGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20122
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123317 Essential Splice Site 48 190 1 5
Genomic Location (Zv9):
Chromosome 3 (position 46413070)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48422623
GRCz11 3 46374957
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGGCCATGCTCATTCAGTTCAAGAAAAACAACGGGCAAAACGAGCAAC[G/A]TCAGTATGATCAGATCGAACCAAATAATTGTTTGCTTTTTAATGATTTAC
Long Flanking Sequence:
AGTAAAATACAGGTAAACCACATACTTTAAATATTACCAACATGTTCCTCGCTACAGTATACAACCAAGCACATATTTCCTTATTACTGGAATGTGGAAAGCTACTGATGGGACGCTACAGTATGCATCGGTAAGTTTTTAATCCAATTTTAACCACTTCTGCTTTTACTGTTCATTCATATTATAATCACACACTAAAAGTGGTATTTGTAATACAAAAGCCTTGATTCTCCTGCATTCCTGCCCTAAAGCGAAGTTCTGTTGCGTAACTGTGTTGTATTTCTTTCAGAGAAGACTCTTTATGATGGTTTGAGAATTGTGGATGTTTAGGTGAGCGGTCATCTCAACCCTCAACATGCCTGAGCAATCTGAAGATCAGCTGTCGAACATCTTTGAAGACCTCAACCTTCTGTCTCTTAAAAGACAGCAATTCACCGATAGACGCAATGTGTTGGCCATGCTCATTCAGTTCAAGAAAAACAACGGGCAAAACGAGCAAC[G/A]TCAGTATGATCAGATCGAACCAAATAATTGTTTGCTTTTTAATGATTTACAACAGAAGCCAGATATAATGTGAAAGACATCTAGGAATGATTTTTAAGAGGAAAATTCTGGTTATAATTGACACTGGACTACATTTGTATTGAGATTTTCACATAATGGATAAATAAGCTTTTCATTGATGTGTGGTTTGTTCGGATAGGACAATATTTGGCTGAGATACATCTGTTTAAAAGTCTGAGCGTAAAAAAAAAACTTTTTATATACACTAGAAAAATGTACAAATATCTCCATGGAACACAGTTTTTACTTATCCTAATAATTTCTGGCATAAAAGAAAATAATAATAATAAAATAATAATAATTTTGACATATACAATGTATTTGTAGCTATTGCCAAATATATACCCCTATGACATAAGTTTTGTCATCCTGGGTCACATATGGTTGCATGTATGTGTGTGTTTTTACAGTAAATTTCCTATTTTAGTGAACTGATGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20121
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
ENSDART00000123317 Nonsense 125 190 4 5
Genomic Location (Zv9):
Chromosome 3 (position 46409039)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 48418592
GRCz11 3 46370926
KASP Assay ID:
2259-4014.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTATTTTGGATGTTCGGCAACTTCCTCCACAACCATCTCTAACACAGTG[T/A]CCATTCTGTCAGCAGTTTATAACTACAGATGTCTCAACCCAAGTTGGCAG
Long Flanking Sequence:
GCACAAACTCACACAAGCACACACACATACTATACCACATAGAATTCCACATAAAAGCCAGAAACTAAGAATTTTTTTTTATCTGATGATCAACAGTAAAAATGACAAAATCTTCAATAGGGAAAACCACCAGCTTTTTACCAACAATAAAGAATGTAAAATGATATGGTGTCATTGTAATGGTAGTCAAAAGCAAAAACAGCCATGAACACCAAAATGTGTCAATATAAGATTTGTCACCAAAACTCATTCCATTTGCTGAAATACAGAGAAAGTTTTGGTCAAATTAAGACTCAACATCACCAGTGGTTACAGTGGTTGAAAACGTCCCCAGCAGCACACAAGGGTTAAAATTGTGGTGAGGTTTGATGTTTTTTGAGATAAGAAATGGCTGCATAAATACAAAGCAGCTTCCTCACAGAAAGCTTGTTTGTTTTCTCAGCTCCGCAGGTTATTTTGGATGTTCGGCAACTTCCTCCACAACCATCTCTAACACAGTG[T/A]CCATTCTGTCAGCAGTTTATAACTACAGATGTCTCAACCCAAGTTGGCAGTGTGGCCTATCTTATGTGTTTCATCTCCATTATATTTGGGTGAGCTGCCCTTTATGTGCTTTATTGTCAACTATGCTGAATAGGATTGTTGAGATTCTCTAAAATTTCCATCCCTAACAGTCCTTTCAGTTTTCCATCTGATATGGTTTGAGGTCTGAAATCATTAAATATTTATTTTAGTGTTTCCTCAGTAGCACATGACTGACTGTTCATTTCATGCAAATAGCTTTGATAAACGACTATAAATAATTTGTAATTAATAGCTGTGTCAAATATTATATGGTAATAATATGAATTAATTAATCTCTAAGTTTTGTTAATGTTAAAAGTCCCACTGAAGTGCATTATCCAGTATGACATGAGGGGCTACATCTCCATTTAAAAATAAGGCCAATCAGGCCAATAAGCCCCCCCACCCCACCCCCCCCCCCCCCCCCCTAATTTCTGTTT
Associated Phenotype:
Not determined