ZMP
slc30a2
Ensembl ID:
ZFIN ID:
Description:
zinc transporter 2 [Source:RefSeq peptide;Acc:NP_001038485]
Human Orthologue:
SLC30A3
Human Description:
solute carrier family 30 (zinc transporter), member 3 [Source:HGNC Symbol;Acc:11014]
Mouse Orthologue:
Slc30a3
Mouse Description:
solute carrier family 30 (zinc transporter), member 3 Gene [Source:MGI Symbol;Acc:MGI:1345280]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43504 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23776 | Nonsense | Available for shipment | Available now |
sa23775 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43504
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 |
---|---|---|---|---|---|
ENSDART00000050474 | Nonsense | 30 | 398 | 2 | 8 |
ENSDART00000110307 | None | None | 336 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 38635116)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38707528 |
GRCz11 | 20 | 38610407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTGAAATGGCGTCACTCTACCTCATGCTTTGTTCTTATAGTGAATTCT[C/A]AGGATCCAAAGAAAGTTGCCCAAACCTGCCTTTGGGAAATGGTGAAATGG
Long Flanking Sequence:
CATTGAAGGTGAGAACCACCCAAGTGGCTCTGCAGCAAGCACCTTCCCTTTATCGCAGCTAGTTGGCAAGAAAATATTTCTCACTTTCAATTTATTTCAAAATATTTTCAAAATACCCCCCACCCAAAAAAAATTAATAAAAAATAAAAAATGAATAAATAAATAAACAAATGACAAAAATATTTCATAAAATAGTTCAAACTAATAATCTATCAAGAAGATGCATGATACATACATAAACATAAGTATACTAATTACTCTTGTTCTGAAAAGTATATATTTATCCATCTATCTCTCTATTCTGCTAACTGCTTATCCTCTAACAGGTGATGTGCATATGACAAAAAACAATTTGCATCTTTTTATTATTTGCATAACTCCCTGATATCAGCAAGGAGCATTATTCAGTATAGTGCTGATGGACTGTACACATATATGGATTTAAACATTGACTGAAATGGCGTCACTCTACCTCATGCTTTGTTCTTATAGTGAATTCT[C/A]AGGATCCAAAGAAAGTTGCCCAAACCTGCCTTTGGGAAATGGTGAAATGGCTGGTGCTATTGAGCTCAAGAGGCCTGTTGGAACGCATTGCCATGGGAAAAAAGCAGCCTATGATGACAGCCGCGAGAAGCTCTTAGCCAAGAAGAAATTGTTCATCGCCTCCATAGTCTGTCTGGTTTTCATGATTGGAGAAGTTATAGGTGAGAACATTTTAGATTTGATGTGTCCTTAAATATTCATTTAACTACTTAGTCATTTTAATTATTACATGTACTAATGGTTAGTGGGTTAGATTTAGAGTTAGTTGCATGTAATTAGGTGTAATTAATTGTAATTACTAGGATGCACTAAAAGTATATGTATTATATATTACTGATTTCAATATATACAGTGTTACACTATATTGATCAGTTTGCAGGGTAATATACAGTACTACACTGTAAAACCCAAAAGGTTAAGGTAACTCAAACTATTTGAGCAAATCAATTGCAAAACTCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23776
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 |
---|---|---|---|---|---|
ENSDART00000050474 | Nonsense | 78 | 398 | 2 | 8 |
ENSDART00000110307 | Nonsense | 33 | 336 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 38634973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38707385 |
GRCz11 | 20 | 38610264 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGAAAAAAGCAGCCTATGATGACAGCCGCGAGAAGCTCTTAGCCAAG[A/T]AGAAATTGTTCATCGCCTCCATAGTCTGTCTGGTTTTCATGATTGGAGAA
Long Flanking Sequence:
ATAAAAAATGAATAAATAAATAAACAAATGACAAAAATATTTCATAAAATAGTTCAAACTAATAATCTATCAAGAAGATGCATGATACATACATAAACATAAGTATACTAATTACTCTTGTTCTGAAAAGTATATATTTATCCATCTATCTCTCTATTCTGCTAACTGCTTATCCTCTAACAGGTGATGTGCATATGACAAAAAACAATTTGCATCTTTTTATTATTTGCATAACTCCCTGATATCAGCAAGGAGCATTATTCAGTATAGTGCTGATGGACTGTACACATATATGGATTTAAACATTGACTGAAATGGCGTCACTCTACCTCATGCTTTGTTCTTATAGTGAATTCTCAGGATCCAAAGAAAGTTGCCCAAACCTGCCTTTGGGAAATGGTGAAATGGCTGGTGCTATTGAGCTCAAGAGGCCTGTTGGAACGCATTGCCATGGGAAAAAAGCAGCCTATGATGACAGCCGCGAGAAGCTCTTAGCCAAG[A/T]AGAAATTGTTCATCGCCTCCATAGTCTGTCTGGTTTTCATGATTGGAGAAGTTATAGGTGAGAACATTTTAGATTTGATGTGTCCTTAAATATTCATTTAACTACTTAGTCATTTTAATTATTACATGTACTAATGGTTAGTGGGTTAGATTTAGAGTTAGTTGCATGTAATTAGGTGTAATTAATTGTAATTACTAGGATGCACTAAAAGTATATGTATTATATATTACTGATTTCAATATATACAGTGTTACACTATATTGATCAGTTTGCAGGGTAATATACAGTACTACACTGTAAAACCCAAAAGGTTAAGGTAACTCAAACTATTTGAGCAAATCAATTGCAAAACTCTATTTAAGTAAAAAAAAAAACTAATCCTAAAGAGTACTGTGAACCTAATCCATTTGAGTACACGAAGCAATTTGAGCACAGTAAAACCCAATGAATGAGGAGAACTTAAACCAACTACTGTAAAAACAAGTAAGGCAACTCAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23775
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050474 | Essential Splice Site | 197 | 398 | 5 | 8 |
ENSDART00000110307 | None | None | 336 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 38626178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38698590 |
GRCz11 | 20 | 38601469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGATTGATTTGATCCGCATCTGTGCATTATTATTGTTTTAATTTTGC[A/C]GAATGGCCTACATTCTGCACCACTCCACAACCTTCCACAGTCACGGGTCA
Long Flanking Sequence:
AGCAGCTAATATTATTTTACAATGATGAAAGGCAGAGGGTTGCTGAAAAACTACCGAGAGATTTTAGCTGCTGTCTGGGCCTTCACTGCCTTTCTACACCTCCCTATCTTCATGTGTTCAATACTTTTTCTCTGCGTCATTTTATTATGCATTTTATTACGCATAACATAATTTGTGTACTATTTAGATTAGCTTTCTCTTGATATATGGATTGCTTTTGGTTGTTATCAACATTCGAGGGCAATTTCAAGTCAACGGCACCTTTAGAAATATGTTTTCTGGGCAAATAGGTGATGTGTTCCTTACTTATAATCCTCGCTGTATATTCCGTTACCATTAACCCTCTTATTTTTAAAACCAACCCTGTTTATACAAACTGGAGAAATAAAATGTAAAAATCAAATCAAATGCACAGTCCCACAAGATTTTTAAACAATATACCACGACAAACATCGATTGATTTGATCCGCATCTGTGCATTATTATTGTTTTAATTTTGC[A/C]GAATGGCCTACATTCTGCACCACTCCACAACCTTCCACAGTCACGGGTCAGGCTACCACAAGATTGATGAGAGCGGGATGAGTCCTGTGGGCCACGGTCACTCGCACAGCCTCCTGGGGAATCATGGCAACACCAGCGTCAGAGCGGCTTTTATTCATGTGTTGGGGGATCTTCTGCAGAGCTTTGGAGTGATGGTGGCTGCTATTATAATCTACTTCAGGGTAAATCAACACGCATAGAGAATCACTATATAAATTCTTATATACTTCATAAAAACTTCTATATTTTGTTGTTGTATATGGTTTACTTTAGAGGCTCTCTCCATATAATAATATATAATAAAGAATTGTCCTTTAAAGAATGCGTTTTATTTTAGTTTTTTTTCAAAATAACAAACATTTTAATTGCTGTAACTCATAGGTCTCAACTCAATTCCAAGAGGGCCGCAGCTCTGCTTTGCTCCAACTCTATCAAACACAGCTGATTTATATGATCGGGGT
Associated Phenotype:
Not determined