ZMP
si:ch211-263p13.7
Ensembl ID:
ZFIN ID:
Human Orthologues:
SLC35F3, SLC35F4
Human Descriptions:
solute carrier family 35, member F3 [Source:HGNC Symbol;Acc:23616]
solute carrier family 35, member F4 [Source:HGNC Symbol;Acc:19845]
solute carrier family 35, member F4 [Source:HGNC Symbol;Acc:19845]
Mouse Orthologues:
Slc35f3, Slc35f4
Mouse Descriptions:
solute carrier family 35, member F3 Gene [Source:MGI Symbol;Acc:MGI:2444426]
solute carrier family 35, member F4 Gene [Source:MGI Symbol;Acc:MGI:1922538]
solute carrier family 35, member F4 Gene [Source:MGI Symbol;Acc:MGI:1922538]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41674 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41674
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110501 | Nonsense | 298 | 417 | 5 | 7 |
ENSDART00000136122 | Nonsense | 207 | 293 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 27455461)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26858255 |
GRCz11 | 10 | 26819968 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCACACACGTGGAATACTGGCCTCCCTCTCAGCATATCCCCTGGGAC[A/T]AACTATGCGTCATGGCTTCTCTACTGCTGGGTATTTATTTTATGCTTTAC
Long Flanking Sequence:
TTTAGTCTTTAAAATCTATAATTTGTTGGCAAAATACAGGAGGTACTTATTTACTAATTCATTAACTAATTAATCAAGTGAACAAAAACGCGTTAAGTACTTATTAATTAAAATCACATGATAAACAGTTGTGCCAGCAACAAGTGACATTTTATATTACGAAGGAGCTACTTAATTATTAGGTAAGCGTAATCTTTGTGAGGGAAACTTACTAACCCCCTACAAATATCCAATTTGTATTTAAAGGCAGTTGTTTTAAAGCTTTGTATGTATAAATGTTTTATATGAACGTAACTTTCTAGAGGTTTTTAGTAAATGTGGATGGCTTTATGTTTCAGGTGCTTTTCAGAAAGTGCGTAGGGGAAGTGCAGCCAGGTCCTGCCAGCGTGCTGTTGTCCTGCGTGGGTCTGTGCAGCTTTGTCCTGCACTCGTGGGTGTGTGTGTTGCTTTATTTCACACACGTGGAATACTGGCCTCCCTCTCAGCATATCCCCTGGGAC[A/T]AACTATGCGTCATGGCTTCTCTACTGCTGGGTATTTATTTTATGCTTTACACTATGCTTTAAATTACATTGAAATAAATGTATTTAAATTGTATTCATTACAGCCGGATCAATACTGGTAATTATCAGATTATATTTTCTATATACTAAACAATGATATTTAGCCCTTATTGAATTAAAACTTGAGAAATTAAAAAAAATTATGCAACATATACATACAGTTGAAGACAGAATTATTAGCCCTCCTGAATTATTAAACTTTTTTTAACACATTTCTCAACATAATAGTTTTAAAAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTACTAGATATTTTTCAAGATACTAGATTTCAGCTTAAAGTGACATAAAGTGAAGTTTGTTTCTCACCGCTGCCACTGACTTGCTTGGTTGGGACTCATAGAGCTGTGCATCGATGGATTTGCTCTTCAGTCTTTGGACTTTCAGCAT
Associated Phenotype:
Not determined