ZMP
cyth4b
Ensembl ID:
ZFIN ID:
Description:
cytohesin 4 [Source:RefSeq peptide;Acc:NP_001108375]
Human Orthologue:
CYTH4
Human Description:
cytohesin 4 [Source:HGNC Symbol;Acc:9505]
Mouse Orthologue:
Cyth4
Mouse Description:
cytohesin 4 Gene [Source:MGI Symbol;Acc:MGI:2441702]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38532 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
This allele has been removed from public view.
Allele Name:
sa3604
Status:
Allele not cryopreserved
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:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028022 | Essential Splice Site | 53 | 394 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 6 (position 605235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 373641 |
GRCz11 | 6 | 396348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAGAATGTGATGGCTGATATTCAGGACTTCAAGTCGGCAGAAGACAAG[T/C]GAGTCCAGCATCTCCTGGGGTGTTGTTGGTGTTGTTAGTGTTGTTTGTAA
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTAAGTGTGTGTATGTGTGTTTTTGGGTCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTTGTTAAACGTGTGTTTTTGGGTCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTTGTTTGTTAAACGTGTGTTTTTTGGTCAGTGTCTGTGTGTGTGTGTGTTTGTTTGTTTGTTAAGTGTGTGTATGTGTGTTTTTGGGTCAGTGTGTGTGTATGTGTGTGTGTCTGTGTGTGTGTGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGTCATCTGATGTGTCCTGCTGTTTTCCAGAAACTGAAGAGTCAGATTGAGAATGTGATGGCTGATATTCAGGACTTCAAGTCGGCAGAAGACAAG[T/C]GAGTCCAGCATCTCCTGGGGTGTTGTTGGTGTTGTTAGTGTTGTTTGTAATATTATCTGTGTTGTGTCTCTCTGTAACTCCGGCTCAGGTGTAAAGGGTTGTTGTTGTTGTTGTTGTTGCAGTAAGACACTGGAGAGAGAAAAACGCTTCAGCAGTGGAAAGAAGAAATTCAACATGGACCCTAAAAAGGTGAGAGGGTGAAGAGGATGATGATGAGGATGATCAAGATGATGATGATGATGAAGAAGATGTTTTCCACTGTGGGGTGACGATTGGAGCGTCTGTCTCTCTGTCTCTCCTTTATTGATCTGAGACCCCCATGTTAAACAGAGGTCGGAGCCAGCTGGAGGTCTTATTTATTGAAAGTCTTGTGCTTGACACAGAGTCCAGTGTTGTGCTTTATGAACGTCTACACCCACCTCAACCCTAAACCCAACCTCACACTCACCTGATGTGTCTTATTAACATCTGCTCCACCCACTCCACCTAAACCCAGCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38532
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 |
---|---|---|---|---|---|
ENSDART00000028022 | Essential Splice Site | 293 | 394 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 6 (position 593115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 385761 |
GRCz11 | 6 | 408468 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAATGTAGGTGTGTTTGTGGATCAGGGTTGATGACGGTGTGTGTGTTC[A/G]GGATAAAGAGCCACGCGGGATCATTCCTCTGGAGAATCTGTGTGTCAGAG
Long Flanking Sequence:
CTTAAAAGCTACTTAACACATGACTTTTTACAGCAAAATTGCAATGTTACTTTTAAAAGACTACTATTGAGTTTTTAGCACTGTTTTATTTTTGTTAGTTTGTTTTGTATTTAATATAAAATTAAAATTAATTTCAGAAACTGTTGTTTTATATTGTTGAAAGCAAGCAAGCACACAAATGAACACAAACTTAATTAATTATTTTATTTTATAAATAATTAGAGCAACATTTTAAAGCATTACTTTTAAAAGACCACTACTACTGTTAAGTTTCTTTTGTTTTTTTTATGTAATGTATAAAATGTAAGCTATCAGCATTAATCCTGTATTGTTGTCACCTGCAGGCGGTCGTGTGAAGACGTGGAAGCGCCGCTGGTTCATCCTGACTGATAACTGCCTGTATTATTTTGAATACACCACGGTAAGAGTGATGTTTATTAATATTAATGATTAAATGTAGGTGTGTTTGTGGATCAGGGTTGATGACGGTGTGTGTGTTC[A/G]GGATAAAGAGCCACGCGGGATCATTCCTCTGGAGAATCTGTGTGTCAGAGAAGTCATCTTTCAACGCAAACCGGTGAGAACACATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTATCTATCATCTGTCTGTCTTTACATTTTTCCATCCATCCATAGACTAGACTGTGGGTTTGGTTAACATTAGTAATAGTTGACCTTTGACCTCTGACCTTTGACCTATGCAGTACTGTCTGGAGCTCTACAACCCCAACAGTCGAGGGCAGAAGATCAAAGCCTGTAAGACGGAGACAGACGGACGCGTGGTGGAGGGAAAACACCAGTCATACACCATCAGCGCATCTACAGCGGAGGAGAGAGACCAGTGGATAGA
Associated Phenotype:
Not determined