ZMP
zgc:172271
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100000381 [Source:RefSeq peptide;Acc:NP_001107938]
Human Orthologues:
LTF, TF
Human Descriptions:
lactotransferrin [Source:HGNC Symbol;Acc:6720]
transferrin [Source:HGNC Symbol;Acc:11740]
transferrin [Source:HGNC Symbol;Acc:11740]
Mouse Orthologues:
1300017J02Rik, Ltf, RP24-421P3.2, Trf
Mouse Descriptions:
RIKEN cDNA 1300017J02 gene Gene [Source:MGI Symbol;Acc:MGI:1919025]
lactotransferrin Gene [Source:MGI Symbol;Acc:MGI:96837]
signal recognition particle receptor subunit beta [Source:RefSeq peptide;Acc:NP_033301]
transferrin Gene [Source:MGI Symbol;Acc:MGI:98821]
lactotransferrin Gene [Source:MGI Symbol;Acc:MGI:96837]
signal recognition particle receptor subunit beta [Source:RefSeq peptide;Acc:NP_033301]
transferrin Gene [Source:MGI Symbol;Acc:MGI:98821]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14356 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14356
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021969 | Essential Splice Site | 596 | 733 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 6 (position 40818229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 40889829 |
GRCz11 | 6 | 40887365 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGAWGTGGCCTTTATGGAGCACCACAATCTAGAAAGCAACATTGAACG[T/C]AGGATATAATMTCTCTSTCTTTCTTTTTTTGGTAGGTTTAAATATGTTCA
Long Flanking Sequence:
GTTTTGGAAAGGCTGTTTGCCTGGGGGTCAGGGTAATCTGTGTAAGGTGTGTATGGGTGGAACTGAGGAAGCTGCCACGAAACGTTGTGCTGACAACCATAATGAGCGCTACTACGGCAACATGGGTGCATTAAGGTGAGGATTTGAACTCGATGAAGATCAAATAAAACATTGTACTACATATACTTGACTGTTTTTATTTCATTACGAAGGAACAGTGCACATCTAACAACCTTTCTCAAGAAAGTTAATGTACCCAAATTAGCCCAAAGCTAGTTTTCACTGAGACTCCCTTTGCCAGAAGTTATAGGCCTAAAAATGTTAATTGTAGCAATATATAGGATTATTTTTTATTGGTAGTGCCACATTGCTTAAACCAAACCGCTCTTCAGGGCTTATATTGTCTTTCACTCCAGGTGCCTGGTTGGAGACCCAACTGGGAAAAGTTTTGGAGATGTGGCCTTTATGGAGCACCACAATCTAGAAAGCAACATTGAACG[T/C]AGGATATAATCTCTCTCTCTTTCTTTTTTTGGTAGGTTTAAATATGTTCAGAGAAAACGTTTTAAATTTTAACTCCTTCAATTTTATTATTTAATTGGCAGTTTTCTTTAATTCTTTTAAAATCAAGAATTCATCTTGAGTTTTCATTATTCCAAACCTTTGATCTTCCGTGTTTTGACCCCCCCCCCCCCCCCCCCGCCCCCCGTATACATATTCTTCTCTTTTTTTCTATTTTTAAGTACTTTTTATTTAGATAATGTATTGATGGGGGATGCAGTGGCGCAGTAGGTAGTGCTGTTGCCTCACAGCAAGAAGGTCGCTGGTTTGAACCTCGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCATTCGAGTGGGTTTTTTCCGGGTGCTCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATAAGTGTGTGTGTGAATGTGTGTGTGGAT
Associated Phenotype:
Not determined