ZMP
slc35f3
Ensembl ID:
ZFIN ID:
Description:
solute carrier family 35, member F3 [Source:RefSeq peptide;Acc:NP_001104675]
Human Orthologue:
SLC35F3
Human Description:
solute carrier family 35, member F3 [Source:HGNC Symbol;Acc:23616]
Mouse Orthologue:
Slc35f3
Mouse Description:
solute carrier family 35, member F3 Gene [Source:MGI Symbol;Acc:MGI:2444426]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42063 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11636 | Nonsense | Available for shipment | Available now |
| sa15772 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42063
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 |
|---|---|---|---|---|---|
| ENSDART00000109189 | Nonsense | 15 | 249 | 2 | 10 |
| ENSDART00000110773 | Nonsense | 15 | 249 | 2 | 9 |
| ENSDART00000127616 | Nonsense | 40 | 494 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 32390883)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 30611860 |
| GRCz11 | 12 | 30726762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGGACATGAGTCCGCGCCGCCTGTCAGATATCAGTCCTCAGATCAGA[C/T]AGCTGAAGTCCCTCGTCCTTGATGAAGATCTGAATGAAGAGTTAAAGTCG
Long Flanking Sequence:
TACTCGAAGCTTATATTAACTGGGATAATCAAGAGTTTTCGTCAGCGCAGGCGCATTGAGTTCACAGGTGGTCGTGTCTTCGTATCTCCATCCGCCCCAGCGTTCTGGATGCCCTTCTGACATTGTACAATTTATAAACGCTTGATTCTTAAGCTACTTTTTAAAATGGGCTCATCAGAATGTCGACTGAAGCAGCACATCTCTGTGTCAGAGTGAGTTGCTAGCAAAAAAACAACAACAACAACAAACTAGGCTACAGTCATCAAAAGGAGCGCGCGCACGAAAAGCTCGTTGAATTGAAATACCTCTTTTAAGTGCTTTTGCAGTTATCCATAATGCAGTAGTGCCGTGCCGCAGCTTTGTTTACATGCATTTTGGTACGTCCAACTGTATTTTTTTGCTAACATACTGTTTTGATGCGTCTTTTCAACTTCAGGGGAATGAGAAAGCCATCGGACATGAGTCCGCGCCGCCTGTCAGATATCAGTCCTCAGATCAGA[C/T]AGCTGAAGTCCCTCGTCCTTGATGAAGATCTGAATGAAGAGTTAAAGTCGTCGAGATCCGTCGAGTACATCCAAAATGCCTCCATAGAAGAGCGGATACTGAGGATCACTGGCTACTATGGCTATGAGCCTTGGAGCGCATCTGTTAGAGGTACTGCGCTTAAATGTAAGATGTTTTATAAGCGAAAAAAAATAAGGAAAATTACATGAACCCTAAAATAGTTCCAAACCCTTAAAGGGAAAGTCAATCAAATGTATTTATGTCATCATTTACTAATCCTAATGTCATTGAAAAAGAAGATTGTCATCCATGAAGATGTTAACCATACAGTTTTGTTTCCCATCGTTATTGTACGTACAAAGTAAATAAAAAAAATGCAGGTCAATGGGAAGTAGACTGCATGGTTATCAAAATATTTTTTTCTTTCTGCAAAAAAGAAAAAAAAAAGAAAAAACATCTACGATTTAATTTATTAATTTTAGCGGACTATACAAAAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11636
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109189 | None | None | 249 | 7 | 10 |
| ENSDART00000110773 | None | None | 249 | 6 | 9 |
| ENSDART00000127616 | Nonsense | 371 | 494 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 32398134)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 30619111 |
| GRCz11 | 12 | 30734013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTGCTCACWGGGGCAGAGGACTTCATTTCACCTAGAGATTTACCCTG[G/A]TCAAGCATATGTGGCATGTCTGCTTTACTACTRGGTAAGAGGATGGACAC
Long Flanking Sequence:
CCTTGTTATTATAAAGTTGTTGGTGTTTATCTGTATTCTCATCATAGAATCCATTGTTTATTTCGTCATTGTTTATTTTTATTGTTTCATCCATTGATTATCTGTATTCTATCTCAGATTGTGGCGGCCGTTTTAGCCATCGGTGGGATTGTTATGATGACATATGCCGACGGTTTCCACAGTTACTCTGTGATCGGCATCTCACTTGTCGTTGGGTCTGCATCTACAGCAGCTATTTACAAAGTAAGAGATGATTATTAAGCAAAACAAACACATTTTTCAGTGTCATACAGTACTGACCAGTGATGTTTATAATGAGCATTCAATTATGTGTTTCTTCAGGTTCTTTTCAAGCTTGTTTTGGGTAGTGCGAAGCTGGGTGAAGCGGCGGTGTATCTTACCATTCTCGGCGGAGCTAATTTGATCTTCATTAGCGCTGTACCTCTCATACTGCTGCTCACAGGGGCAGAGGACTTCATTTCACCTAGAGATTTACCCTG[G/A]TCAAGCATATGTGGCATGTCTGCTTTACTACTGGGTAAGAGGATGGACACAAATACACAAACTTGGTAAATCCTAAAAGCTTGTTATCTCCTCTTCTAATGTCATAATAACATTCTTCTTTGGTTGCACTCCTAGTGTTCAACTTCCTGTTGAATTGTGGTGTTTTGATAACACTTCCTACTCTGATTTCTCTGGGTGTTGTCCTCAGTGTGCCGGTCAATGCTGGTGAGTCATACTGGAATAAGTTGCTGATTTTAAAGGGAAAGTTACATGAAAGATGTATTTGATCATCATTTACTAAGCTTTAGGTTTTTACATATGAAAGCATATAAGTGTTGCTCTTTTCTATTGATTAGGAGAGGTGACTGGGAGCTATCAATCTGCAAAAATAGTAAACAAACTAAAGAATTAATAAACTAACCTTCCAGTTGTGTTCAGGTCAAATCTGACCGATTTACAACTTAAAACACAGCGTTTCACATCTGATTGCCTTAAGGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15772
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 |
|---|---|---|---|---|---|
| ENSDART00000109189 | None | None | 249 | 8 | 10 |
| ENSDART00000110773 | None | None | 249 | 7 | 9 |
| ENSDART00000127616 | Nonsense | 388 | 494 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 32398285)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 30619262 |
| GRCz11 | 12 | 30734164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCATAATAACATTCTTCTTTGGTTGCACTCCTAGTGTTCAACTTCCTGT[T/A]GAATTGTGGTGTTTTGATAACACTTCCTACTCTGATTTCTCTGGGTGTTG
Long Flanking Sequence:
TTATGATGACATATGCCGACGGTTTCCACAGTTACTCTGTGATCGGCATCTCACTTGTCGTTGGGTCTGCATCTACAGCAGCTATTTACAAAGTAAGAGATGATTATTAAGCAAAACAAACACATTTTTCAGTGTCATACAGTACTGACCAGTGATGTTTATAATGAGCATTCAATTATGTGTTTCTTCAGGTTCTTTTCAAGCTTGTTTTGGGTAGTGCGAAGCTGGGTGAAGCGGCGGTGTATCTTACCATTCTCGGCGGAGCTAATTTGATCTTCATTAGCGCTGTACCTCTCATACTGCTGCTCACAGGGGCAGAGGACTTCATTTCACCTAGAGATTTACCCTGGTCAAGCATATGTGGCATGTCTGCTTTACTACTGGGTAAGAGGATGGACACAAATACACAAACTTGGTAAATCCTAAAAGCTTGTTATCTCCTCTTCTAATGTCATAATAACATTCTTCTTTGGTTGCACTCCTAGTGTTCAACTTCCTGT[T/A]GAATTGTGGTGTTTTGATAACACTTCCTACTCTGATTTCTCTGGGTGTTGTCCTCAGTGTGCCGGTCAATGCTGGTGAGTCATACTGGAATAAGTTGCTGATTTTAAAGGGAAAGTTACATGAAAGATGTATTTGATCATCATTTACTAAGCTTTAGGTTTTTACATATGAAAGCATATAAGTGTTGCTCTTTTCTATTGATTAGGAGAGGTGACTGGGAGCTATCAATCTGCAAAAATAGTAAACAAACTAAAGAATTAATAAACTAACCTTCCAGTTGTGTTCAGGTCAAATCTGACCGATTTACAACTTAAAACACAGCGTTTCACATCTGATTGCCTTAAGGCAGGGGTGTCCAAAGTCGGTCCTGGAGGGCCAGTGTCCTGCTGACTTTAGCTCCAACTTGCTTCAACACACCTGCCTGGAAGTTTCTAGTATATCTAGTAGGAGCTTGATTAGCTGGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTCTC
Associated Phenotype:
Not determined