ZMP
tfa
Ensembl ID:
ZFIN ID:
Description:
transferrin-a [Source:RefSeq peptide;Acc:NP_001015057]
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 are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32879 | Essential Splice Site | Available for shipment | Available now |
sa19720 | Essential Splice Site | Available for shipment | Available now |
sa12059 | Nonsense | Available for shipment | Available now |
sa44526 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32878 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15651 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32879
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003845 | None | None | 675 | None | 17 |
ENSDART00000108611 | None | None | 673 | None | 17 |
ENSDART00000124119 | None | None | 286 | None | 6 |
ENSDART00000125647 | None | None | 674 | None | 18 |
ENSDART00000127207 | Essential Splice Site | 152 | 169 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 16590088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17114895 |
GRCz11 | 2 | 16783485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACTATATAATACATTTTGGATATGCTAAAATGTTTATTATGCTTTTTT[G/A]TGTTCTCCAGCTGTGTCAGAATTCTTCTCGAGCAGTTGTGTCCCTGGTGT
Long Flanking Sequence:
TATTGTTGCACTCTCAGAAATAAAAGTATAAGAGTTGTCACCAGGGCAGTCCCTTTTCAAATGATTATTTTTAGGTAATGTATAACTTTAAGATACCAATATGGAACATTCTGTTAAAAAAGAAGCACCTCAGTGGCAGTTCCCATACTTTTTTTTTTTTTTTTAAGAGAGTGGAAACTAAGGTAGTTGTAGTATTTTAAATATAGGGGTATAGGTTTGAGGTCTGCTTTGTAACTATTATTAAATAGGCAATTTGCTACCCATGCTAATGTACTATTGCTACACTGCTAAAAATATTCTTACTTTAATTACTTTAAAGTAATTTTTTACTTTAAGTTTTGTCTTGTGTCTAGTCCAAATTGAACTGTACTATATTTAGTAAATCTTGATTTTATTTATTACTCCCAAAATCTTTATGTTCATTTGTTGATTGATTGACGGATTGTTGAGCAACTATATAATACATTTTGGATATGCTAAAATGTTTATTATGCTTTTTT[G/A]TGTTCTCCAGCTGTGTCAGAATTCTTCTCGAGCAGTTGTGTCCCTGGTGTATCTAAACCCAAATACCCAAACCTGTGCAAAGCCTGTCAGGGTGACTGCAGCTGCTCACACAACGAGAAGTACTTCGGTGATGACGGAGCCTTCCAGTATGAGCCACACTAATACAATCCCTTATATAAGTATACACCAAGTTCAATTTCAAGTAAAAACAAAGAAAAAAACTGTTATAATTTAAAATAGTAAACACACTATAATCAATCTATGAGTACTATACTTGAATTCAGTATTGTGATTAGATTAGACCACTTTTTAATTGATTACACTCAAACTGTAAATGAGTTCACGACTAGTTAATCACTACATTTTTCATTTGGACTGCCACTTTACACTAAAAGTAAACTTATAGTTACTAGTTTAATACTTTTATATGACACTGAACCACAAAACAAGTCTAATGTTGCATGAGTATATTGTATGAGTCAAAATGATCCTTCTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19720
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 |
---|---|---|---|---|---|
ENSDART00000003845 | Essential Splice Site | 204 | 675 | 5 | 17 |
ENSDART00000108611 | Essential Splice Site | 204 | 673 | 5 | 17 |
ENSDART00000124119 | Essential Splice Site | 214 | 286 | 4 | 6 |
ENSDART00000125647 | Essential Splice Site | 205 | 674 | 6 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 16589940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17115043 |
GRCz11 | 2 | 16783633 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCTGCTCACACAACGAGAAGTACTTCGGTGATGACGGAGCCTTCCAG[T/C]ATGAGCCACACTAATACAATCCCTTATATAAGTATACACCAAGTTCAATT
Long Flanking Sequence:
TTTTTTTTTTTTTTTTAAGAGAGTGGAAACTAAGGTAGTTGTAGTATTTTAAATATAGGGGTATAGGTTTGAGGTCTGCTTTGTAACTATTATTAAATAGGCAATTTGCTACCCATGCTAATGTACTATTGCTACACTGCTAAAAATATTCTTACTTTAATTACTTTAAAGTAATTTTTTACTTTAAGTTTTGTCTTGTGTCTAGTCCAAATTGAACTGTACTATATTTAGTAAATCTTGATTTTATTTATTACTCCCAAAATCTTTATGTTCATTTGTTGATTGATTGACGGATTGTTGAGCAACTATATAATACATTTTGGATATGCTAAAATGTTTATTATGCTTTTTTGTGTTCTCCAGCTGTGTCAGAATTCTTCTCGAGCAGTTGTGTCCCTGGTGTATCTAAACCCAAATACCCAAACCTGTGCAAAGCCTGTCAGGGTGACTGCAGCTGCTCACACAACGAGAAGTACTTCGGTGATGACGGAGCCTTCCAG[T/C]ATGAGCCACACTAATACAATCCCTTATATAAGTATACACCAAGTTCAATTTCAAGTAAAAACAAAGAAAAAAACTGTTATAATTTAAAATAGTAAACACACTATAATCAATCTATGAGTACTATACTTGAATTCAGTATTGTGATTAGATTAGACCACTTTTTAATTGATTACACTCAAACTGTAAATGAGTTCACGACTAGTTAATCACTACATTTTTCATTTGGACTGCCACTTTACACTAAAAGTAAACTTATAGTTACTAGTTTAATACTTTTATATGACACTGAACCACAAAACAAGTCTAATGTTGCATGAGTATATTGTATGAGTCAAAATGATCCTTCTTTTATGCCGAAGCAAATCATTAGAATATGAAGTAATTATCATGTTCTATGTCACAGATGTCAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGACCTTCAGGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12059
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003845 | Nonsense | 267 | 675 | 7 | 17 |
ENSDART00000108611 | Nonsense | 267 | 673 | 7 | 17 |
ENSDART00000124119 | Nonsense | 277 | 286 | 6 | 6 |
ENSDART00000125647 | Nonsense | 268 | 674 | 8 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 16587983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17117000 |
GRCz11 | 2 | 16785590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGAGCCTGCCCGCACTGTCATTGCTCGCACCGATACTGATTTACAATA[T/A]GTTTATGATGTCCTGAAGCAGATTCCGGTATGCCCTTACAGTGTCACATA
Long Flanking Sequence:
TATAGGTCAAGCCAACTTTTGTCAGTGTCTGTCAGCATAAATCAAGGACACTTTATAGTGTGATTTATTAAGAACTACATGTAAAATATGCTGAAACTATAGTTAAAAAAAAAACTACAATGACATTAACTTATTTTCCCCATGTCTTCTATATGGACATTAATATGTCTTACAAATATGAAATATTTTTTCAGGTGCCTGAAAAATGATAATGGACAGGTTGCATTTGTTTGCCACCATGCAATCCCAGGTCGGTCAATATCTTTACCCAAAATCTTAAATGTTTTCTCTGTCTATGTCACAAAGCTGCTGGTTATAATACCAAGGTTTCTGGTTACAAGCTTCTTGTCTGTTGTGAATTTTTAAGAGAGTGAGAGGCAGAACTACGAGCTGTTGTGCATGGACGGCAGCAGGAAAAGTGTGGAGGATTATAAGACATGCAACTTCGCCAGAGAGCCTGCCCGCACTGTCATTGCTCGCACCGATACTGATTTACAATA[T/A]GTTTATGATGTCCTGAAGCAGATTCCGGTATGCCCTTACAGTGTCACATAAGTAACCTAACTACATTTCTGTTTAAGAACGCCTGTCCCCTTTAGAGATAAACAATGTCAATGTTAGAAACAAAAGGGAGTAAGATTGTTCTAGATCAGTGAAATCCAACTGAATGTTTAAACGTTTTGCTCAACAGGCCTCAGATCTTTTCTCTTCTCAAGCTTTTGGTGGTAAAGACCTGATTTTCTCAGACTCTGCGACTGAGCTGATGCTGCTTCCTAAAAGAACAGACTCCCTCCTCTACCTGAAGGAAGAATATTATGAGGCCATGCAAGCCTTTAAAGGTGACTAGAATTTTATTTATTTTTGTGCCAAATATTCAGATGAACATTGACACCATTGCATTCAAGAGTAACATTTCTTGTAGTTTTCTTATACATTTCTTATACATTTCATTTTAGACTTCTTTGACAAAAAGAAAGTTGACTGATTATTCTGCTTAGCCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44526
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003845 | Essential Splice Site | 408 | 675 | 11 | 17 |
ENSDART00000108611 | Essential Splice Site | 408 | 673 | 11 | 17 |
ENSDART00000124119 | None | None | 286 | None | 6 |
ENSDART00000125647 | Essential Splice Site | 409 | 674 | 12 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
ENSDART00000003845 | Essential Splice Site | 408 | 675 | 11 | 17 |
ENSDART00000108611 | Essential Splice Site | 408 | 673 | 11 | 17 |
ENSDART00000124119 | None | None | 286 | None | 6 |
ENSDART00000125647 | Essential Splice Site | 409 | 674 | 12 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 16585907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz11 | 2 | 16787666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATTGACATTTTTGATGAAACCTAACATTTTATTCACTACTCTTTTGC[A/C]GAAAGCTGCTCTAGTGGTTCAGGAGGTAAATATTACTATAATTATTTGGT
Long Flanking Sequence:
CGTAAGATTGAACATGACCTCATCAGTTCATAAGACATTTATTGCAATATGTTACATGGGTAGAAAATACATTATACAAGTCAAAATTATTTTTGTTTATGCCCAATATCATCAGAATATCAAGTAAATATCATCTTTTATTAAGAATGTTTGTACATTTCCTTCTGTAAATCTGTCAAAACTTAATTATTGATTAGCAATGAGTATTGTTAATTATTTAATTAGGAAAACTGTGATGTCAGTTTTCTCAATTCTTAGATTTTTTTTAACCTTTATATTTCAGATATACAAATAGTTTTATCTCGATCAAATATGATCCCAATCTCAACACACCGAATATCAATGAGAATCTTATTCATTCAGCTTTCATGTGTATAGATATAAATCAGGTGTATGAATCTCAATTTTCAAAAGCTGACTCTTATGGTTTTGTGGTTTACTGTCACCTTTAGAATTGACATTTTTGATGAAACCTAACATTTTATTCACTACTCTTTTGC[A/C]GAAAGCTGCTCTAGTGGTTCAGGAGGTAAATATTACTATAATTATTTGGTACTGATCTGCATTCATTCATCCTGTCAGCCATTTTCTGTGATCTAATTTGGTCTTAAGTGTTGTTTACACCGATGACAATGAGAAGAATTCTATAGTTTACAAAAAAAAAAAAAAAAAACAGTTTTAAACATAAAGGAATAGCAGTGTCTACCTTACAGCCATAATAATGATGACTTTTTAGGCTGATGAATGAATTAACATTTTTTGTATTTTGTGATTCATGTTTTTTCCTCCCTGTATATTTCTGCTTTTAAATTGCATAATGGCACATGGATCTTTCTTCCAACAACTTTTAACCTTCAAAAATTGGAAAAAGTTTTTTTTTTTAAATTTAGGTCTCATTAAGTGCTTTGAAATATGATTTTTTTTTTTATTTGATGTTTGAAATAATCTCAACTAAAAAACGAAAACAGGGTGGGACATTGAGTAGCTCCCATTTTAAAAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32878
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003845 | Essential Splice Site | 408 | 675 | 11 | 17 |
ENSDART00000108611 | Essential Splice Site | 408 | 673 | 11 | 17 |
ENSDART00000124119 | None | None | 286 | None | 6 |
ENSDART00000125647 | Essential Splice Site | 409 | 674 | 12 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
ENSDART00000003845 | Essential Splice Site | 408 | 675 | 11 | 17 |
ENSDART00000108611 | Essential Splice Site | 408 | 673 | 11 | 17 |
ENSDART00000124119 | None | None | 286 | None | 6 |
ENSDART00000125647 | Essential Splice Site | 409 | 674 | 12 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 16585907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17119076 |
GRCz11 | 2 | 16787666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATTGACATTTTTGATGAAACCTAACATTTTATTCACTACTCTTTTGC[A/C]GAAAGCTGCTCTAGTGGTTCAGGAGGTAAATATTACTATAATTATTTGGT
Long Flanking Sequence:
CGTAAGATTGAACATGACCTCATCAGTTCATAAGACATTTATTGCAATATGTTACATGGGTAGAAAATACATTATACAAGTCAAAATTATTTTTGTTTATGCCCAATATCATCAGAATATCAAGTAAATATCATCTTTTATTAAGAATGTTTGTACATTTCCTTCTGTAAATCTGTCAAAACTTAATTATTGATTAGCAATGAGTATTGTTAATTATTTAATTAGGAAAACTGTGATGTCAGTTTTCTCAATTCTTAGATTTTTTTTAACCTTTATATTTCAGATATACAAATAGTTTTATCTCGATCAAATATGATCCCAATCTCAACACACCGAATATCAATGAGAATCTTATTCATTCAGCTTTCATGTGTATAGATATAAATCAGGTGTATGAATCTCAATTTTCAAAAGCTGACTCTTATGGTTTTGTGGTTTACTGTCACCTTTAGAATTGACATTTTTGATGAAACCTAACATTTTATTCACTACTCTTTTGC[A/G]GAAAGCTGCTCTAGTGGTTCAGGAGGTAAATATTACTATAATTATTTGGTACTGATCTGCATTCATTCATCCTGTCAGCCATTTTCTGTGATCTAATTTGGTCTTAAGTGTTGTTTACACCGATGACAATGAGAAGAATTCTATAGTTTACAAAAAAAAAAAAAAAAAACAGTTTTAAACATAAAGGAATAGCAGTGTCTACCTTACAGCCATAATAATGATGACTTTTTAGGCTGATGAATGAATTAACATTTTTTGTATTTTGTGATTCATGTTTTTTCCTCCCTGTATATTTCTGCTTTTAAATTGCATAATGGCACATGGATCTTTCTTCCAACAACTTTTAACCTTCAAAAATTGGAAAAAGTTTTTTTTTTTAAATTTAGGTCTCATTAAGTGCTTTGAAATATGATTTTTTTTTTTATTTGATGTTTGAAATAATCTCAACTAAAAAACGAAAACAGGGTGGGACATTGAGTAGCTCCCATTTTAAAAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15651
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003845 | Essential Splice Site | 608 | 675 | 16 | 17 |
ENSDART00000108611 | Essential Splice Site | 606 | 673 | 16 | 17 |
ENSDART00000124119 | None | None | 286 | None | 6 |
ENSDART00000125647 | Essential Splice Site | 607 | 674 | 17 | 18 |
ENSDART00000127207 | None | None | 169 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 16581925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17123058 |
GRCz11 | 2 | 16791648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATATGTCTTACAAATAAAGTTTTAAATCCCATCTCTTATCATATGTTTC[A/T]GAGCAAAAATAATGACCTTTTCACCTCCAAAGATGGGAAAAATCTCCTTT
Long Flanking Sequence:
TTGCTTTTATTAAGCACACTGTGGTCGGGGACTACACAGATGGTTAGTGTGTTTTACTTCAATTAATATTTGACACTTTTTTAAACTGTAAGGTGTTTCAATGGTCTTATCTTTTTCTTTAAAATTCTGTCTGCTTAGGTAAAGGAAAGGACTGGGCAAAGGATTTAAAGTCAGAGGATTTTGAACTTATTTGTCCAAACACACCAGACACAACAATGAAATACACTGACTTTGAAAAGTGTAACCTTGCCCAAGTGCCAGTTCATGCTGTGATTACCCGGGAAGATGCGCGCAGTGCTGTGGTGTCCTTTTTGTCTGACATTCAAGTGAGTTTTTACAGTTCTAAGTATGTTCCTGCTGTTTCAATATTTTGTCAATATTTTGTCAGTATTTGTTTTTAAAGTTGGGTCTTATTTTACCAGTCGTCTGTTTCTACATATTTTTCCCTGTTATATGTCTTACAAATAAAGTTTTAAATCCCATCTCTTATCATATGTTTC[A/T]GAGCAAAAATAATGACCTTTTCACCTCCAAAGATGGGAAAAATCTCCTTTTCACTGATGGCACTAAATGCCTTCAAGAGATAAAAGGATCTGTGGATGATTTCCTGACGAAAAAGTACATCGATATGATTGAGAGGACCTACAAGACTAGCCAGAATGTACCAGGTATAAAATGTACCTATAATATCCTACAATGTCTGGTTCAAAATTCTAGGTCAAAACAAGTTTTAGCCATATCTTGTTGTTTTTGACTTACAAAACTGCATCCACTTACAATGCTTTATTGTAATGATTCATTCTTTTAATGTTTTTTTTTTACAGATCTGGTGAAGGCATGCACTTTTGGCAACTGTATTAGCTCCTAGTACCTATCTTACGGTCAACAAACACATCAAACAGTCAGATGTGATCAGGTTTCTGTTTTATCACAAAAGGGGATGAAATGAAATTAAAAAAATATTTCTCAAAATGATGTTTCTGAGATTGTTTTTTAAATGCAAA
Associated Phenotype:
Not determined