ZMP
zgc:110788
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC503601 [Source:RefSeq peptide;Acc:NP_001013306]
Human Orthologue:
SFT2D2
Human Description:
SFT2 domain containing 2 [Source:HGNC Symbol;Acc:25140]
Mouse Orthologue:
Sft2d2
Mouse Description:
SFT2 domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1917362]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13673 | Essential Splice Site | Available for shipment | Available now |
sa40735 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13673
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104160 | Essential Splice Site | 81 | 166 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 6 (position 36789928)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36863518 |
GRCz11 | 6 | 36841412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTTTTGTTGTGTTTTATACATTGGGAAACGTTTGCTCCTTAGCAAGG[T/A]GAGTCATCWGGTTTATARCAACTAAAATTCTGTGACTATTTGCATTGTAT
Long Flanking Sequence:
AATTTAAACATTATTTTCAGTTTTGCCTTTTTTTTGTAGCTCAGCAATTAAACAAAATGTTATGTAAAATTGAAAAGGATGAATTCGGTTTGAGGGATTTACCCCAACCTTCCCCATTTTTGGTCCATTTCTTCTCACGGGCCCTAGTTTGGGCAACTTTCTTGGAAACACTGTTTTGATTCTTGCATGTGCAAAAAACACTTTATAACACCTCACTGCATCATCACAAGCTACGGGTATTAATTTTATTTACTCTGCATATTATTTTGACTGTGATAGTGCCAGTAGAAAATGTTGAATCTGCAAGGACTGTGGTTTCACTTCAAAATATTCTGATGAAAAAATAAATGCTTCTTCTAGAAATATCCTTTTAACTGTCATATTAATAATATACATTTTTTTATCTACCTCAGGGAGTAGGTTGCCTGTTTATTCCCAAAATTGGGATACTTCTTTTTGTTGTGTTTTATACATTGGGAAACGTTTGCTCCTTAGCAAGG[T/A]GAGTCATCTGGTTTATAGCAACTAAAATTCTGTGACTATTTGCATTGTATTTTAATTAATTTCATTTGAACTCCTCAACAGCACCATGTTTTTAATGGGACCAGTGAAACAGCTGAAACGCATGTGTGACAAGACCAGAGCCTTTGCTACTGTTGTGATGATAGTGAGTTAATCTTTTCCACACCACACTCTGCTTGACTTTACATGTAAAGCCATCAATGAGGATGTGACTTGTTGTAAAAATAATGCAGACATGTTAGTTGTCTTGCAGTTTCTGGCTTTTCAAGTTTTAAAGCAAATGACGCTTGAAAGAAGTTTATTAATTACTAGGGCCAGACAGAATCTGTGGACATTTTTGCTATTTCTGCAGAGAATTTTGTAAAAAAAATTGCAGTTTTATGCGGAATCAGTTTGGGAGTATCATAACTGCAAATTTAATAAATGAAATAAAATATAATAGGTTTTTAACCTTTATTTAATGTTTACAATGCAAATCCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40735
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 |
---|---|---|---|---|---|
ENSDART00000104160 | Essential Splice Site | 150 | 166 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 6 (position 36792076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36865666 |
GRCz11 | 6 | 36843560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAACCAAGTACAGTATTTTTAATTCTCTATGCTGTCTTTGTCTTAACC[A/G]GGGATGCTGTACTGAAGTTTTTCTCCATGTTGTGCAACATGTGTATGAAA
Long Flanking Sequence:
TTAATTTAAATTCATCAATTTGTTTTAAAAGCTTATTAATTAACTAAAAAGTAACTCGCATGACATTTTTGAAAAACTTACTCAAATATTACTTATTTGTTTAATGCAATACTTTACTTGTTACTTAGAAAAGTAAAATTATTACGTAACTCTTGTTACTTGTAATGCGTTACCACCAACACTGCTTTTTCCTGTACTGAAATACATTTGATCAATTTATTAATTTTTCTTTATAGGTATGGCCTCTCATACATCCCTTTTGCAAGGTTAGTCATTATTTGTGATTTTAACATATTATTTTGTCTTAAAATATTGAATTAGATAAAACATATTAAGCATTTGATGGATGTGTGAATATTTGTTAGGTGGTTCATTCTGCTGTGGCGACCCCTAAAATAGAGACTAAACTGAAGAAAGTAAATGAATGCTAGAAAATAAATATGACACAATTGAAACCAAGTACAGTATTTTTAATTCTCTATGCTGTCTTTGTCTTAACC[A/G]GGGATGCTGTACTGAAGTTTTTCTCCATGTTGTGCAACATGTGTATGAAATGAAGAGCTGATGTTTATCCTTTCATCACTCTGGGAACTGGGAACACTCTGCTCAAGTATTCTGCAATTCTGGGGTCCACAAATAATCACTGAGACTATGGGATGGTGCTAGTTGTAATCGCTAACGTTAGCTGGACGACATGCTAAATCTGACTGTACAAAAGATTACATTTTACTGAATGTGTTTTAAATGTGTTGTAAAACAGATTTGTAAATGTTATGAAATGTCTTAAAATTGATATTTATTAAAGTAGATATTGCAGTTATATACTAAAAAGCTGACCTTCTATTTTTTTCTGTATCTTTGTCTGATACTATTTGTAAATGAAGTCTAGCTCAATTTTTTTTTCTGTGTCAGAATGTTGAATATAATTCAAAGGATAATCCGAGATTTGAGAATTTAAGATCTTTACACACGTATTCTTTATAAAATATACATATTTTAAATAT
Associated Phenotype:
Not determined