ZMP
slc39a5
Ensembl ID:
ZFIN ID:
Human Orthologue:
SLC39A5
Human Description:
solute carrier family 39 (metal ion transporter), member 5 [Source:HGNC Symbol;Acc:20502]
Mouse Orthologue:
Slc39a5
Mouse Description:
solute carrier family 39 (metal ion transporter), member 5 Gene [Source:MGI Symbol;Acc:MGI:1919336]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29976 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12403 | Nonsense | Available for shipment | Available now |
sa44023 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37758 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29976
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 |
---|---|---|---|---|---|
ENSDART00000112788 | Nonsense | 158 | 610 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 32576210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32411100 |
GRCz11 | 23 | 32337631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGCTGCTTGGTAGTTTGGGTTTGGGAGAAGTCAGTGTCCTGGAGATT[C/T]GACATGGTGAAGCAAAACATCCTTCTCAATCGATATCCCATTCCCACTCA
Long Flanking Sequence:
GGAACTCTTTGAGGAAGCATTTGAAGAGCAGGTATGATTATTTCAGAAACCTAAACTTAAAGTAATCAATGTTTGTTTGTTTGAGAAACCACGGCAGCCATTTTCTTTTCACGTCTGGTAAAGTGGATTATCTACATTCCTTGAGGGATATTACAAAGAGATCAAGTGGTTTTTGGCTTGGGGTTGACGCTGAGCTCGAAAATCCTATCAACTATTCTGATTCAATCAATCAAATTGAGCTAAGTTAGAGCTGCAGTTTCAGTGTCTGTGTTGGGTGGGATTTATAGTTGCAGACTGTTTATGACACCAATTCAATATGATAAAACTGTCACATGGACATTAAATGTTAGGAAAATAGTAATTCTCATTTTTCTTCTCTCAAGGGCTACTACTTGCAACGTCTGTTCCTTCAGTATGGAGACAATGGGACTTTGACATATGAGGGTCTACAGAAGCTGCTTGGTAGTTTGGGTTTGGGAGAAGTCAGTGTCCTGGAGATT[C/T]GACATGGTGAAGCAAAACATCCTTCTCAATCGATATCCCATTCCCACTCACATGAAGACCATCACCCTTCTCAAGGGACTACAAACTCACCTCCACTCAGAGAAAGGTACATTAACTAAAGCAATATTTTAATGTAGGCTGGAGCCTATAAAGTTAACTTTTTGAATATCCCAAATAGCAACATTATATATGGTAATATATGCAAATTAGATAAATGACATGCAAGTTCATATTTGGATTTTACATGTATAAAACATATATACAACATATTTCTCAGTACTGGGTTGAGGCTGAAAGGGCATCCGCTGCGTAAAACATATGCCGGATAAGTTGCCAGTTCATTCCCCTGTGGCGACCACATATTAATAAAGGGACTAAGCCGAAAGAAAAATGAATGAATGAATGAATGAATGAATGAATGAATGAATATACAACATACAGTATTTCCCAGTACTGGGTTGTGGCCTGAAGGGCATCCGCTGTGTAAAACATCTGCGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12403
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112788 | Nonsense | 277 | 610 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 32579889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32414779 |
GRCz11 | 23 | 32341310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTCCTGCCCACTTCACCTTCCTGTGCCCWGCCCTCCTRTACCAGATC[G/T]AGAGCGGAGTGTGTCTGCGGCACACNNNAGATCATTCACAGRCCAGCAAA
Long Flanking Sequence:
TTTAAGCAGAGTGATATGCAGCATCCCTAAAACACTGATATCAGGAGAGGGGTCTGGCTGCAGACCTGGTGCAGTGCAATCTGGGCTGCATCCAATGCTTTTTAACGGGCTCACCTAACCCCACCCCTAACCCTATTCATCACAGTGACGTCACTAGCTCCATTTGAGTGCATTGTGTCTGACATTGCACCTCTGAGTGATGCAATCTCAGCTTGCATCATAAAGGCTGCATCCAGATACTATTGGATATCAGAAAAATAAACATTGGCAGCTATCCAAAAATATCTCCCAGCTAAATCCCACAATTTGTCCAATCAAAATCAAGTATTCCAGAATTTAAGCCTTGTAATATTGAATCTGAACTTAATCTTACATTTCTTATTGCGTCATGGCAGTGTCTGAATGTGACCCAGCTCCTCTGGAACTTCGGGCTTGGCCAGGCGTCCCACATCACTCCTGCCCACTTCACCTTCCTGTGCCCTGCCCTCCTGTACCAGATC[G/T]AGAGCGGAGTGTGTCTGCGGCACACAGAAGATCATTCACAGGCCAGCAAAACCAGCGAGGGCTTCCTCATAGGTGTGTGTGTGTGTGTGTGTGTATATAAACAGTTTTATCAGAATCAATTGATCATAGCACAGGTTAAAACAAGGTCACTATGTCTCAGCTCTAGGATGGGCATCATTGGCGCTCCTGGTCATCAGCCTGCCCTCTCTGGTTGCTCTGGGAATGGCACCGCTGCTTCAGCCTTCTGTACTTCAAGTGTTTCTCTGCCCGATGGCTGGCATGGCGGTGGGCACGCTCTGTGGAGATGCCCTTCTGCACCTCATGCCTCATGTAAGTCACAAAATACAAATGCATTCAGTTAGGTAGATCATTGAATTCTGCAAAGATGCTTTTAAAGAAACACTTCACTGTTTTGAAAATAGAGTTAACAGCTAGGTTTCATTATTTTTTTGTTTATTAACAAAGCATACAGGCCGAATTAACAATTTCATGACATACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44023
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112788 | Splice Site, Nonsense | 397 | 610 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 32585835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32420725 |
GRCz11 | 23 | 32347256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACCTTCTCTTCATCTTTGAGAGTCTTCTGGGACTTAAGCAGCATTTC[A/T]AGGTGAGCTTCAGCCAGTGCAAAACATGATGTTTTTGCTCAATTATTAAG
Long Flanking Sequence:
TTTGTGGGAAAATCTGATTTTTTTTTTTTTTTTTTTGTCGTATTGCCTGAGGAAAAATAGTTTTGGTTGTTCAAATAGAGTATGGGGCCTTGATCTCTGCTCTTATGTGGTAAATATAACTGTACAGTTTAAGACTATGACTTTTATTGACATTTTTTTTTATTTGAAACAATATATTGTATAAGAAAAATAAATAAATGTATTGAATAAAGAGGTAATATTAAATGAAATAAATAATATATAATTTTATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTTTTAATTGAGGTGCTATAGATGTGAGTTGTTTGTGATTTCAGGCCATCTTCAGTCAACACACTGATCACCAGAATGCTGTTTTCAAAGGTCTCAGTGTTCTGGGAGGACTTTACCTTCTCTTCATCTTTGAGAGTCTTCTGGGACTTAAGCAGCATTTC[A/T]AGGTGAGCTTCAGCCAGTGCAAAACATGATGTTTTTGCTCAATTATTAAGACCTGACGACTTAAATGAAACCTTCAGTTTGACAAAAGAGCTGAAGAGAAATATTTATGTTTGTGCATATATTTTTTCCCTTTTTAAACCAGAATTTAAAGAGAAGAAAGCATGACGCAGAGTGTGGAAGAGAGCTTGACGCACTACAGGGTTTGTTAATTTTCAGACATAAAATAAGCAAACATGCACACATAGATATGAATTAAAATGCAAATTGTAAAGTCACCTGGACTCTATCATAGGAACCTCATCAGCCAATCAGAATGAGAGTTCAGGGCACGGTCATTCCCATGGACAGGCTGAACCAGGGCAAACTGGTATCAGAAGCATGGCATGGATGGTGGTGATGGGTGATGGCATACATAACCTGACAGATGGACTTGCCATTGGTATACAAACATCTGTGAAAATTATTCAAATTAAATATCATCATTTAAGATAAGAAACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37758
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112788 | Essential Splice Site | 556 | 610 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 23 (position 32586784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 32421674 |
GRCz11 | 23 | 32348205 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTCACACTCACCGCCGGTGTCTTCCTCTATGTAGCTCTTGCTGACATG[G/T]TAATCATCTTAACTGTTCAAAACAAAGTTAAATGTAGTTGATAGTTGAAA
Long Flanking Sequence:
CATCTGTGAAAATTATTCAAATTAAATATCATCATTTAAGATAAGAAACTAATGGCAAAGACTATAGAATGTCTTACTTTGTTTACATTAATAGAAAGTTTATATAGGAGCAAAGGTATATTGAAAATACATTACTGTTGTTGTCCTCTAGGTGTCGCGTTTTCCCAGAGTTTGACTGGCGGCTTCAGCACCGCGATCGCCGTGTTCTGCCACGAGCTTCCTCATGAACTAGGTTTGAGTCGTTTACACATTAGTTTGAATGATCATTATGAATCATCAGTGGTTTAAATATACGTGTTTATTTTGCAGGTGATTTGGCGGTGTTGTTGTCTGCGGGCTGGCCTGTGCGCAGGCTGCTGGTGTTCAGCGGGCTCTCTGCTCTGCTGGGTTTTGTGGGTGTTTTGGCCGGATCTGCGCTGGGGAACCACTGGGCTTCACACTCACCCTGGATCCTCACACTCACCGCCGGTGTCTTCCTCTATGTAGCTCTTGCTGACATG[G/T]TAATCATCTTAACTGTTCAAAACAAAGTTAAATGTAGTTGATAGTTGAAAAAGTCTACTTCCAAATTTCATTTTAAGTTTGTTTAGTTTTATCTTTGTCTATATATATTAGCAACATTAGCAGTTGGAGTAAAACTGATTCATAGAAATAGGTCAGCCAAAAAACCAAACAAGCTCACACAGACACACAAAAATTCTGTCATCACTTACTTGCCCTATACTTTCAAACCTTTATGATTTGTTTGTATTCTGTTGAACAAAAGAAGGTATTTTGAAGAAATGTTGGACTGGTGTAGGGGAGAGCGGGGCACAAAATAACACTTTTTGGTTTTGGCCAAATAATGAACAGAGTAATGGGATTGGACAAACCATATTTTTTTTACCAACATCACACAAGCCTCTCCTACAAATGAGCACTGGTTGTATGATCGCCAGAAATATAGTTTCTGTGCAGTATTGCCAAAAGTGCCAGGAATAAAAATTTTACTATTTACCCCACCT
Associated Phenotype:
Not determined