ZMP
si:dkey-248f6.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
NELF
Human Description:
nasal embryonic LHRH factor [Source:HGNC Symbol;Acc:29843]
Mouse Orthologue:
Nelf
Mouse Description:
nasal embryonic LHRH factor Gene [Source:MGI Symbol;Acc:MGI:1861755]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23883 | Essential Splice Site | Available for shipment | Available now |
sa25152 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23882 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23883
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087766 | Essential Splice Site | 320 | 501 | 10 | 17 |
ENSDART00000139568 | Essential Splice Site | 62 | 123 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 11675852)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13377026 |
GRCz11 | 21 | 13473755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAGACTGGCCTGTGAGGGAGACGACTTTATCCCTCCCAAAATTATGG[T/A]GCAGTATTGATTTAAAATGTATTTTATTGTATGGTCTAGTGTTCATTCAT
Long Flanking Sequence:
TCCCATTAATCTTATAGCAGAAGTTGAGAAAAACACTAGCTTTTCATAAAGCCCATTGCAAACAATATAAAAACAACATGATGCTATAAAACAAACATGGTTGTGTTTGACATATCTAGAGCAAACTATCTTTCAACGGGACTTCCTCAAACATTCTCTTTACATTTTTCCACGTAAAAAATAGCAGCATGAAGGTCTGGAATAACGTTTTTAGGTGGACTCCTCCTTTTATCTGGATGTTTTTTAGTGAGCAGAAGCAAAACTAAAAATAAAAGCCGACAGTCCATGTAGACAGATCTGTGTCTGTGTGTCTTCTGATTGCATTGTCATGTCTCTATGGTGATGGTGTGTGTGTTGTGTTGCTGTGACAGGTGGAGAGCTGCAGGGCACCTGCTGCACCCCAGATGAGGCCAGATGTGAAGACATGGACTGGGAGGAGGAGAGAGAGATGGAGAGACTGGCCTGTGAGGGAGACGACTTTATCCCTCCCAAAATTATGG[T/A]GCAGTATTGATTTAAAATGTATTTTATTGTATGGTCTAGTGTTCATTCATTTGACTCTTGGTTCATTTGTTTTTATTTGACTTAAGCTCAATTGCATTTAATTTCAAACTTTTTATGTAAATAACTAGGGGAGAGGGTGTCGGTCTAGGTTTTTTATTTTTGAATGCTTATTTATTTTTAAAATAAATTCATAAAAATGTATCATTTATATTTTCTTATTCAGTTTTATAAACTGTTATACAGTATATTTACTTTTATTTATTATTTTATTTTATTTTATTTTTACTTATAACAACTTATAAAGTAAAACTTTTTTTTAAATTTATATTTACTTTAATTCAAATTTTCTTTTTTATTTAGTAGGGGAACAGCTGCATGCCATCTCCATATCCATTTCAGAACTTTTCTAAGCATAATAGTTTTAAAATCATATTTATAATAACTGATTTATTTTATCTTTGTCATGATGACAGTAAATAATATTTTACTAGATATTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25152
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087766 | Nonsense | 331 | 501 | 11 | 17 |
ENSDART00000139568 | Nonsense | 73 | 123 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 11673298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13374472 |
GRCz11 | 21 | 13471201 |
KASP Assay ID:
554-7453.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAATTTGTATTTTCAGCTGATCTCATCTAAAGTTCCCAAAGCCGAATA[T/A]CTTCCCAACATCATCAAAAGAGACGATCCTTCTATTATCCCCATTCTCTA
Long Flanking Sequence:
CATTCATACACACCCATTCACACACATACACCATGGACAACTTAGCTCACCTATTTAAACTATTGTATAGCACATGACTTTAGACTGTGAAAAAGCCGGAGCACCCGGAGGAAACCCATGCAAACACGAGGAGAACATTTAAACTCCACACAGAAATGCCAAGTGACTCAGCTGAGGCTCAAACCAGCGACCTTCTTGCTGTGAGGTTACTGTGCTACCCACTGCACCACCGCGCCACCCTAATTTACCTGTATATTTATTTAAATATTTAATTTAATTTACATTACAAATGAATTCCTAGATCCTTTTTCATCTTTTTATATAAAGAAAGGTACAACCTCCATCTCTCCATCTCTTTTCAGTGTAAGACCTCTCCATCTGTCACTCTCATATTTTCAATGTTTATTTGTATGTTTTACAATATTTCCCTATGCTCATTATTTTCATCTCTACAATTTGTATTTTCAGCTGATCTCATCTAAAGTTCCCAAAGCCGAATA[T/A]CTTCCCAACATCATCAAAAGAGACGATCCTTCTATTATCCCCATTCTCTACGTAAGCCAAGCCTGTTTTTACTCTACATCGTTTATTGTCATGACTGATCATCCAGATAAATATACACGATACAGTTTCCTTGTCAAGTTGTAAAGCTTGTAAAGTGTTTGTTTTGTCCTGTGCAACAGTATACAGTTGAAGTCAGAATTATTAGCCCTCCTAAGTTGTTACCCCCCTTGTATGTTTTTGCCCTAATTTCTGTTTAGATTTTTTTTTCAACACATTTCTAAACACAATAGTTTTAATAACTCATTTTTAATAACTCATTTCTTTTATTTACTGTCATGATGACAGTAAATAATATTTCGCTAGATATTTTCAAGACACTACTATTCAGCTTAAGGTGACATTCAAAGGCTTAATTAAGTTAATTAGGCAAGTTAGTGTAATTAGGCAAATCATTGTATAACGATGGTTTGTTCTGTAGACAATCAAGGAAAAAAGTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23882
Status:
Available for shipment
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:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087766 | Nonsense | 471 | 501 | 17 | 17 |
ENSDART00000139568 | None | None | 123 | None | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 11657500)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 13358674 |
GRCz11 | 21 | 13455403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGAATCATATCTTCTTCTCTATTCTACCTCTCTTTTTCTTTTAGGC[A/T]AAGAAATGATTGAGATGTACTTCGACTTCCGCCTGTTTCGACTTTGGAAA
Long Flanking Sequence:
TGCGTCTACTGTGTATATTATTATGTGTATGTAAATGCACACATATATACTTAAAAATAATTAGACATTAATATTTCTATATAATTTATGGTATATGTAATTATTTTATAAATAAATAAAAAACTTTTTATCCATATATATAATATTTAAATATACACAGTACAAACAAGATTATTGTGTAAATGTGAACTTTTAATTAATCATTTTAAATCGAATTAATCGATTAAACAGCACTAATCTATTTAACAATATTTTCATTTTTTTTATCTTAATTTTCCCTACCTGTCCTGATCTGACATACCCTCTATTCTCTGACTCTCAATTTTCTTTATCATTTCTTTCTCATCTACATTGTCTCTCACATCATGCTGTTTTCCAATTACCAGCAGAGCGAATCTGCGTGGAAGTGTCTGTTCATCACAGAAAGAGACGTGCTCTCATTGAAATGTAGTTCAGAATCATATCTTCTTCTCTATTCTACCTCTCTTTTTCTTTTAGGC[A/T]AAGAAATGATTGAGATGTACTTCGACTTCCGCCTGTTTCGACTTTGGAAAACCCGACAGCACTCAAAACTCCTCGACTACGAAGATCTCTTGTGACCCCGCGCAGGTCTGCGTGTAGCATTCCGGGCAGGACGTCCCACTATAAAACTCCATTCCACCAGCTTTCATTTCAGAAAACGGGAGGAAGAGGAAAACAAGTGGAAACGGACGCAGCCACTTTGCGTCTCAAGTCTTATTTCAGCTCGCCGTTGTGGATTTCAGCCACCTCTGGACGGTAACACACAAAAACAACTGACAAACGCTCCAAAATCCAAGACAAACCGGGATAGAGCAAAGGGAAGGTGTTCTTCTGAACTAGCTGTCAGTCTGTTGACTGTTTTTAAACTAACATATCGCCTACAGCTATTGATCACTAGCCGAGACAGTTGTGCTTTTGAACGAGTCCTGCGTGCAATATCGAGTCAAGCGTACCTACCAGTACCCACGGAAACCGTCATATAC
Associated Phenotype:
Not determined