ZMP
lztfl1
Ensembl ID:
ZFIN ID:
Description:
leucine zipper transcription factor-like protein 1 [Source:RefSeq peptide;Acc:NP_955881]
Human Orthologue:
LZTFL1
Human Description:
leucine zipper transcription factor-like 1 [Source:HGNC Symbol;Acc:6741]
Mouse Orthologue:
Lztfl1
Mouse Description:
leucine zipper transcription factor-like 1 Gene [Source:MGI Symbol;Acc:MGI:1934860]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu2127 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa9216 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu2127
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000061544 | Nonsense | 68 | 298 | 3 | 10 |
ENSDART00000136357 | Nonsense | 68 | 247 | 2 | 7 |
ENSDART00000137245 | Nonsense | 68 | 298 | 2 | 9 |
The following transcripts of ENSDARG00000041997 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 11949094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 12017555 |
GRCz11 | 24 | 12157699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACGAGGTGACTGATATTCTAAATGGGCTTCAGGTTTTGGTGCGTGGA[G/T]AAGTGGAGATGGAACTCATAAACACAGCTCACACTAACGTGCTGCTGCTG
Long Flanking Sequence:
TATACTAATGTTAATACATATATTGGTTTAAAAAATATAATTTATGCTTGAGATAAAATCAGTTATATCTTTAAGCGACATATGCAAGTTGGTTTTTAAAGTTTTTTAACCTCTTCAATTACAATAAATTTGTTTGTATAGTAGGTTGGTGTGAAAATGCCATTCTGCTAGAAGATTAAATGTAATATTCTGTGCCTTCCCTATAGGCTGATTTTGGTTTTAATGAACACCATCAGCATGAGGTGATAAACTACATGCGATTTGCCCGCTCTAAACGGGCCCTTAGACTGAAGACTGTCGACTCCTGTTTTCAAGACCTAAAGGAAAGTAGGTGAGGAATACAAGCCAATGTATTTGAAATAAACTGCTGGTTTTTGTCTTTAGCAGAAGTTAATTTTTTACTTTTCTCTCTGTGTCCACATTAAAGGCTCATAGAAGAGACATACACAGTGGACGAGGTGACTGATATTCTAAATGGGCTTCAGGTTTTGGTGCGTGGA[G/T]AAGTGGAGATGGAACTCATAAACACAGCTCACACTAACGTGCTGCTGCTGCGACAACTTTTTTCTCAGGCTGAGAAATTCTACCTAAGGCTGCAGACAGACATTTCAGAGCTGGAGAACAGGTAAGGAAAGAAGAAAGGTTTGCCAGTACTAGGGGTGGGAAAAAAAAGTATGCATCATGATTCTTTTGTTTAGCGATTCTGAATTGATTCTCAAATGTTTAGTATCGATTCTGTATTCAAAGTAGACCTCTGCAAAGTATGGAAGCATACGAGTAGCATAATTCAATTCAAAATGTAATATGCAAAATGGCAATGCAATATGTTAAATGGCAATGTATTTCTGTATTTGAATTTGCATTTTCCAAGACATATGAGCAATGTTTGGTGCAGAATGAAAATGTAAATTAAATTACATTGTTTGCATTTCTCATTTCAAACACTGTTTTAATTTGTAAATTGTATCCACATTTTAAAGCTTTATAAGTAGCAAAATTAAATT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa9216
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000061544 | Nonsense | 113 | 298 | 4 | 10 |
ENSDART00000136357 | Nonsense | 113 | 247 | 3 | 7 |
ENSDART00000137245 | Nonsense | 113 | 298 | 3 | 9 |
The following transcripts of ENSDARG00000041997 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 11910909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 12055740 |
GRCz11 | 24 | 12195884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAATAAAATCTCTCTCCCTCTCACTCTTTTATTAGAGAGTTGCTGGAG[C/T]AAGTAGCTGAGTTTGAGAAGACTGATTTCAAACCCAACATCAAGGTGAGC
Long Flanking Sequence:
GTTTGCGGCCATCCGGGAGTCTCTATGCATTTGCAGGAAACTTCCGGAACACTTGGGATGTATGGGAGTACATTAACATTACTAGCCATTTTGCGAGCTAGTGTAGCGCATGCCTGACTTGAGTGGTGTTTGAGATTGGCTGTTTTGTGTCGGGGTCCAGGGTTGCGGGGGCAACAGGGGCGGAGCCAGCATGAACAGCATATATATATATATATATATATTAAGGGTGTAACGATACAGTGTCATATTTTGCACTGATTAAAAAAATGCTAGTAATGACGGCGTGGTCTGTCGACCTCAGAAGGTTCAATTACAGTGGTGTTATAATGATATTATCTGCGCTGTAATTGAGGATTTATTATTTATTTTTTACCTTGTTGTTATTATTATGTTATTAAAATTGTTTGTATGTGACAGTTTTTTGTGATATTGTTGATTAAAGTTTAATTCAAAAATAAAATCTCTCTCCCTCTCACTCTTTTATTAGAGAGTTGCTGGAG[C/T]AAGTAGCTGAGTTTGAGAAGACTGATTTCAAACCCAACATCAAGGTGAGCTCATTGCAGGTCTTGACAGAATTCTGATAGATGTAGTCTGCTAAAAACTTAATTAACTGACAAATTATAGCTGAAGCTTGCATAAAGTTCACGTTTGTGACATACATTTTTCTATTTTGCCATGACATGCATGTGATATTCTTAGTTTGATAATTATAGCGATTAAAATAAATTAAATTAGACTAGTGAAGTACTTTATGAGTTAATTTATTTACCAGTTTATTTAGTTTATTAAACAATGATTGCTTTGTTTTATTTAGCAAATAGAAGTACTTTAGATGGGCATATAGGTTGCTAATCAACCACACATTAAGTTAATATACCACAGCACACCAATTTTGAGAGAAAAAAAAAAATCTGTCCATAAAGAGTTGCCTTCAATATATATTTTTTTGTGCTTTTAGGCAAACCAGGAGACCACTAAGCCAAAATTAGCACCGCTGAATGAAG
Associated Phenotype:
Not determined