ZMP
si:ch73-47d4.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate quaking homolog, KH domain RNA binding (Mouse) (QKI) [Source:Uni
Human Orthologue:
QKI
Human Description:
quaking homolog, KH domain RNA binding (mouse) [Source:HGNC Symbol;Acc:21100]
Mouse Orthologue:
Qk
Mouse Description:
quaking Gene [Source:MGI Symbol;Acc:MGI:97837]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22202 | Essential Splice Site | Available for shipment | Available now |
sa22203 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22202
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018737 | Essential Splice Site | 47 | 345 | 1 | 7 |
ENSDART00000131553 | Essential Splice Site | 47 | 95 | 1 | 2 |
ENSDART00000139958 | None | None | 159 | None | 4 |
The following transcripts of ENSDARG00000002026 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 3319227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 3534148 |
GRCz11 | 13 | 3667375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCAACTTCTGCGGGATCTTCAACCACCTCGAACGGCTTCTCGATGAAG[G/A]TAATGTTGATGGACTGACTTGTGTCCGTCAAATCCCACCGGGATGAAATG
Long Flanking Sequence:
GAGGGGCACGCGGGAGTCGCCGTTTCGAGTAACTTGTGGAATTTATCAGGAATTGTTTATTTATATTTTTAAAAGGAGACTTGGCTTCCCTCTTCACCCGTTTTGAATTTCTTTTGTCCGTTTAATTTCATCTCATCAGCTGCCCTAAAACAACTGTCATCCCCAGAATTGCAGTAGCCCATTGCAGCAGCAGCGGATTGTGCGTGAAGAGACAGCAGCCTTTCCCGCGGACGAGTCAGGCACTTGCCTTCTTCCCTTGCCTTTTTTTGTGCTCTATTTATTATTTATACTCCAGCCTTTATTTATCCTGGGACTTTTTCTGTCTATTTTGGGGCGTCGGTGGTGATTTCTGTGGAATATGGTGGGGGAAATGGAAACGAAAGAGAAGCCGAAGCCGACCCCAGATTATCTGATGCAGCTCATGAACGATAAGAAACTGATGAGCAGTTTGCCCAACTTCTGCGGGATCTTCAACCACCTCGAACGGCTTCTCGATGAAG[G/A]TAATGTTGATGGACTGACTTGTGTCCGTCAAATCCCACCGGGATGAAATGAAAGCTGTTGCAAACAGCGCGTTTTACGCGCGTAAGAAAGCCGGTTAAAAGCGTCAGCTGCTTGTTTTGGTGTCAGTCATTCATGCCTATTCATGTTTACTTTCATAGTCATACAAATAGACTCACATGGCCGTTTAGTTCAGCTTTAACTGCGGCTTAAGTTTACGCGCATTCAGCAGTCGACACTTGTCTGTTGTAAACCTGTGGATTTTACAGTGATTCAGTTGGATGCTAATGTGTTGTTAGAACATATGTTTTGGTTTTATTCACGTAAGAACGAATTCACAATTTCACCCTAACACTATATGCATTTTATAGCATAGTTCTTCATGAGACTTTCTCTGAGGTAAATAAAAAACTGTAGCCTAGTAGAATTCATCTCACTGCACATTGAGTTATTTACGCCAAGAGATACATCTCAAGAGTCTAGATTTTATCTTCTAGACCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22203
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018737 | Essential Splice Site | 95 | 345 | None | 7 |
ENSDART00000131553 | None | 95 | 95 | None | 2 |
ENSDART00000139958 | None | None | 159 | None | 4 |
The following transcripts of ENSDARG00000002026 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 3370626)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 3585547 |
GRCz11 | 13 | 3718774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTCAGCTCCAAGAGAAACTCTATGTGCCTGTTAAGGAATATCCTGATG[T/C]GAGTCTCAAAGCCTAAACACACCGACTGACACGCTTCCCTGCAGATGCGC
Long Flanking Sequence:
GCTATTTTAATTAGGCAATCGCTATATGCCGGAATAATTGGTGGTTCATTCCGCTGTGGTGAGCCCTGATTTTTAGGGGACTAAGCCGAAGTTGAATGAATGATTATATTATAAATCTAGTAACGTGCTATTCTGTTATGTGACTGTAGACCCTTCAACATATCGGATGGTTCATTAGGTTTAAGAGCGGTGTTTAGGAAGCATTTGCACTCCTTTACTGCCACATTAAAGCCACATATAATCCACGGGTAAAGCAAATGTAGCGTTTAGCCTGCCAGTGTATGGTCTAATCCTGTTTTTGCTCTGTCTGCATCCTGATTGATGTAGTTAACTCATGTGCTTCCTCTTTCTTTCAGAGATCAGCAGGGTACGAAAGGACATGTACAACGACACGTTAAACGGCAGCACGGAGAAGAGAAGCTCCGAGCTCCCGGACGCCGTCGGCCCCATCGTTCAGCTCCAAGAGAAACTCTATGTGCCTGTTAAGGAATATCCTGATG[T/C]GAGTCTCAAAGCCTAAACACACCGACTGACACGCTTCCCTGCAGATGCGCATGTATTTACGGTTTGTTTTTGATCACCAGCCACTGTGGCTAGTAGTTTTCCGACGCTACTAGCCACTCGCCAATTTCACTAGCCACAATTTTGTTGTTGGGAAAATATATTTTATGTGCATAAATTAACTTTGACATGCTAAAATTACTTGATTCAGACGTGTCATGTTCTCACGCCTCCTCTTTCATCTAACTTTTTCGTGTGTTGTGTTTGAAGACTCGTATTTGAAGGTCAGTCAAATATGATTTCAACAAATCTCTGAATACAGCACACACTCAAGCTCTTTACTGAACGTCAGTGAGTAAATGGAATAGTAAATAACCGTGCGCTGCTCCTCGGTATGGCTCTTATTTAATTACACAGACATACAAGTCAATGTAATCTAGTTTTCCTTGCATTAGGACATGGGCCCACATCCAGTGTATTGATTTCATTAAGACGTACTGAAG
Associated Phenotype:
Not determined