ZMP
nelf
Ensembl ID:
ZFIN ID:
Description:
nasal embryonic LHRH factor [Source:RefSeq peptide;Acc:NP_001137373]
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 |
|---|---|---|---|
| sa33616 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38476 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40442 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33616
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 |
|---|---|---|---|---|---|
| ENSDART00000087763 | Nonsense | 116 | 568 | 3 | 14 |
| ENSDART00000129031 | Nonsense | 116 | 570 | 3 | 15 |
| ENSDART00000139253 | Nonsense | 116 | 297 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 30089067)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 27844365 |
| GRCz11 | 5 | 28444518 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTTCCAAGCGGCGGCTCTCCGTAGAACGCAGCCTTTCTTCTGAGGAT[C/T]AGCAGAATCAGAGGCGTACCGAGAGTTCTGTGAAGCCAGCACGTGTCTAC
Long Flanking Sequence:
ACCTTTCTCACACACACCCTGAGAACCGCAACAGATCAGGTTGGGTTCATTTCACCTCATGTTCTTCCACAATTTGTCCTCACATTTTTGTTTTTGCAGTTTGTTGTGACGTACTTGAGTGTCTCAGTCTTTGTAGTAGGTGAAGCATTATCCTTTAGGCTCAGTGTCAGTTCCACCTCAGACCATTCACCCAGTCAACATTTGATTGATCATTGCATTTTACAGGCACCTGTTGCTTTGACAGGACAAATCAAACTTTCTCCCTTTTTCTTCTGTCTCTCATTTCAGATCACTTGCTATCTGACACCTTCATTGGTCAGGAGACAGATTCCCCAGACATTAGCAGACTGAACAACAATAACAGCCTCCAGCCATACTCCCAACACACTCTAATAGTCAAGCCCAGTCAAGAAGAGCTTCAGCAAGGCAGTCAGTCTGCACCCCTTCCTACAAGTTCCAAGCGGCGGCTCTCCGTAGAACGCAGCCTTTCTTCTGAGGAT[C/T]AGCAGAATCAGAGGCGTACCGAGAGTTCTGTGAAGCCAGCACGTGTCTACACCATTACCAGGGAGCGAGATATGCTTGGGGGCCAGGGAAGCGAGGAGAGTTTGGAGTTAGAGGTTCTGAAGAGGACATCAGAGCCATCACAGATCAACCCTCCAACAGGTTTACGTGGAAGCCATCATCGAGGAAGCCAACATCGTGGGAACAACGGCCCCACCCACCAGCATCATTACGGTCATGCACCCATGGCACAACCTTTGCAGAGCTCAGGGAGCACCCATAACATTCGGGACTGGGGGTCGAGGCGGAGCAGGTCAAGGGAGGATTGCACACCCGATTGTGTGGCCTGCATTCGACCTCATTGCCAGAGTCAGCGCTCACTAGACCTTGATACATCTCCTCACGGTGGTGGCAAACAGCACAAGAAGCTAGAGAGGATGTACAGCGAGGACCGCGTGTCCTCTGAAGATCGAGGTAAGAACATCAGCAGGTTTTGTGGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38476
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087763 | Essential Splice Site | 315 | 568 | 5 | 14 |
| ENSDART00000129031 | Essential Splice Site | 317 | 570 | 6 | 15 |
| ENSDART00000139253 | None | None | 297 | None | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 30103936)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 27859134 |
| GRCz11 | 5 | 28459287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCGGAAACATCTGAGGATGGTGGGCAGCAGGAGGGTGAAGGCCCAGAG[T/A]GAGTTGTTTGTAGACATCTTTATGTGTGTTTGTGTTACAGAGTGAATGAG
Long Flanking Sequence:
AACACTCTAATTTTCCTAAAAGGTAAGCATTGGCTGTTTAGATTTCATGGTGACTTGAAGCTAACAACTCAGATGTGTGCTTTTAAAGTGCTAAATACAGAAATGAAATCTCATAAACTGTACAAATGGGTAAATGTGTTTAGAAGCCCAAAGCCTGCATGTCAAACTGTTTATTTTATTCAGTTTATTACAGAAGAACTGTGGGGACTGAGGATTTGTTTGGAGTGCACTGAGCTTGTTGTATAACTTCAAACACTCGTCTCTGTCCATTATCAGCCATGCTAAATGCTATACCATGTATAAAAGGATTGTTCGAAAATGTATTTAAAATTTTCATTTTTGTCTCCTCTTCCTCCATCTCCCATTCTTCTGATGTTTGTTCCACCTTTCCTGTTTTATACCTCTCATCCAACCCACTGTGCTTCTGCAAATTCTTTCTATCCTAGAAACTTCCGGAAACATCTGAGGATGGTGGGCAGCAGGAGGGTGAAGGCCCAGAG[T/A]GAGTTGTTTGTAGACATCTTTATGTGTGTTTGTGTTACAGAGTGAATGAGTGTGCTTATATATGGTTGTATGTCATCAGTACGTTTGTCTGATTTCATCTCTTTATTTATTTGTGCTATTTTATAAATGCACTATGAATATTTGAACATGCCATCGCTTGACAATAATTCATGGAGTCAGATGAATTATTTTCAGGGTTTACAAATGCTTCAGGCATCTGGTAAAAAGGATGAAAACAACCATTTGGTGCTCTTGTCTGACAACTAGCGGTGTGATTTGGATTCATAATAACTCACCTCTTTCTCATCAATATGGGTTACAGTATACGGGTTAAAATTGATTCTCATGTTTAAAGCTAAAATGGAAAAATCTTCAAACGTGCCACTTCCCAGCTTCAGGCAAGAGCCCAGAGTATGTATGTGTGTTGAAGAGCAGTGTGTGTGATGCTTTCCTCCTCCGCTTCGTTATTAGCATTTGTTGATCGCAAAGCGAAGAGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40442
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087763 | Nonsense | 436 | 568 | 10 | 14 |
| ENSDART00000129031 | Nonsense | 438 | 570 | 11 | 15 |
| ENSDART00000139253 | None | None | 297 | None | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 30110922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 27866120 |
| GRCz11 | 5 | 28466273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCATCTTTCCCCTCTTCAGAGGAGATTGAAAAGAAACTCACCGCCTA[C/A]AGAAAAGGCTGCAAAATCTGGAACATGCTCATCTTCTGTCAGGTTTGAGA
Long Flanking Sequence:
GATCATTGCTACCTAAAATGACCTCAATTTTGGTGCCTTCCTCAAAATTTGTGGAAAAATGTGTGGCATTTCATGCATTGTTTTGCTGTGGCTGAATGCCGAAGCACAGTGCTATGCTGTGTCTAGGACAACTCAAGGTATTGCACAGCAGATGAGCACTTTCTATATGCAAATATAATGTTATTAATTATTAAACAGTGAAAAATGTCCTGTGTGGACTGTGATCACAGAATCTTAAAATTCTGGAGGGACTGCTCAAAACATGAGCCTGGTTTACTGTTCATTATATAGGTCATGGAAATTCAGCTTCTTGGTCAGTGAAAATTAGGCAAAAATTTGGCATTTGACTTAGAGTGGTAATCCTGTGCTATTTGTTTTCTATGAAAAACTGGGCTGTAAATTCATACGACCCCCCCCCCCTCCCCTCTCTACCTCTCTGCTATCTGTCTTCTCTCATCTTTCCCCTCTTCAGAGGAGATTGAAAAGAAACTCACCGCCTA[C/A]AGAAAAGGCTGCAAAATCTGGAACATGCTCATCTTCTGTCAGGTTTGAGAAAAAAAATAAGAATATGTGTGTGATTAATTTGCATATCTTGCTTTTTCGTAAAAGTGCATGTGGAGTGTTTACGTTGGTGTTATTTTGTGCTGTGTAAATTGGTTTGTATGTTTTCTCCAGGGAGGCCCGGGTCATCTCTACCTTCTGAAGAACAAAGTGGCTACGTTTGCGAAAGTAGAGAAGGAGGAGGGCATGATGCAGTGAGTGTTCTCTTTCACAAAACAAATTCTAGCTCGTGGAATCTATCATTTTGTTCTACTTTTAAAAGTGCTGCATAATTAATAAAAAGAAATAAGATTATAGTGACGACTTTCAGAATCTATTTCAGGGATGCAAACATGATAGATTGAGCCAAACATCTTCAGTCAGAAGTAGGTCATCTCATGATTTCAATAAGCACAAGCAAAAATCTTGATTTTTTCCAAGCAAGGTTTGGCCAAAAATATGCA
Associated Phenotype:
Not determined