ZMP
sp5l
Ensembl ID:
ZFIN ID:
Description:
Sp5 transcription factor-like [Source:RefSeq peptide;Acc:NP_919352]
Human Orthologue:
SP5
Human Description:
Sp5 transcription factor [Source:HGNC Symbol;Acc:14529]
Mouse Orthologue:
Sp5
Mouse Description:
trans-acting transcription factor 5 Gene [Source:MGI Symbol;Acc:MGI:1927715]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11869 | Nonsense | Available for shipment | Available now |
sa43999 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3223 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa11869
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024283 | Nonsense | 53 | 357 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 28268984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28098037 |
GRCz11 | 23 | 28024578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGYCACCACATGCAGTCAGGCTTGGCAGGAAGGCTCGCAGCTCCCTTAC[G/T]AGGGTCCGGTGGGCTCCGCATCCAGCATGTTCCAGCTCTGGAGCAACGAC
Long Flanking Sequence:
TATTATACTCTAAATATACTGATTAACATAATACATAACATTTAAATTAGGTGAATTTCAAACTTGTTTTTAGTTTTTATCATTGTAAAACAATTCCAAAATAATAGTAAGATAATAAACTTAATTTACTAAATAAATTGATAAAATAGATGTAAGCTGCCTTGTTTTCAGTTTTGATTTTGTAATTATACCATTTTTTTTTACATTTCAAAAAATAATTTAACATAAAAAATAAAAATAAAATGGAAATTAAACTTAAGATTATTAACAATTAATATTAAATAAGAAAGAAATTAAATATATTTTACTTTTTGCATCTCCAACTCAAAATATTAAATGTGAAAAATATGAAGAAAAAAGCATGACTTATTTACAAATATTTGTTTTCTTCCCCCTAGGACCGCACTCCCAGCTCATCTCCAGAAAGTGGTCCAAACACCCTCTCCTTTCTGGCCACCACATGCAGTCAGGCTTGGCAGGAAGGCTCGCAGCTCCCTTAC[G/T]AGGGTCCGGTGGGCTCCGCATCCAGCATGTTCCAGCTCTGGAGCAACGACGTGGCCCCGAACTCCAGCTTAAGCGCTCACCAGATGACCTTCACCGTGCCCAAAATGCAGTTTCCCAGCCACATGCAACCCACTCTGGGCTCGCACTCCCATCACCACCATCACCACCATCATCACCACCACGAGCTTCCCCTCACTCCTCCAGCGGAGCCTCCGTCTGCATATTCATTCGAGCTTTCCCCGGTTAAAATGCAAGGGAATGCGCCATACTACACGCAGCACAACGCCGTCAGTCAAAACTTTCCAAGCTTCCTCCAAAACCCCTCAGGAAGAGCTCACCTGCCTGGAGGTCACGTTGAGGATGGCCAGCAGTGGTGGAGTCTCCCCCAGGGTAACAGCGCTCCCTCCGGGCACCCTTTCTCCTTGGGACGGCAGCTGGTTTTGGGCCATCAGCCTCAAATTGCAGCACTTCTGCAGGGAACCTCCAAAGGTCTGTTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43999
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 |
---|---|---|---|---|---|
ENSDART00000024283 | Nonsense | 87 | 357 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 28268882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28097935 |
GRCz11 | 23 | 28024476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCCCGAACTCCAGCTTAAGCGCTCACCAGATGACCTTCACCGTGCCC[A/T]AAATGCAGTTTCCCAGCCACATGCAACCCACTCTGGGCTCGCACTCCCAT
Long Flanking Sequence:
AATAGTAAGATAATAAACTTAATTTACTAAATAAATTGATAAAATAGATGTAAGCTGCCTTGTTTTCAGTTTTGATTTTGTAATTATACCATTTTTTTTTACATTTCAAAAAATAATTTAACATAAAAAATAAAAATAAAATGGAAATTAAACTTAAGATTATTAACAATTAATATTAAATAAGAAAGAAATTAAATATATTTTACTTTTTGCATCTCCAACTCAAAATATTAAATGTGAAAAATATGAAGAAAAAAGCATGACTTATTTACAAATATTTGTTTTCTTCCCCCTAGGACCGCACTCCCAGCTCATCTCCAGAAAGTGGTCCAAACACCCTCTCCTTTCTGGCCACCACATGCAGTCAGGCTTGGCAGGAAGGCTCGCAGCTCCCTTACGAGGGTCCGGTGGGCTCCGCATCCAGCATGTTCCAGCTCTGGAGCAACGACGTGGCCCCGAACTCCAGCTTAAGCGCTCACCAGATGACCTTCACCGTGCCC[A/T]AAATGCAGTTTCCCAGCCACATGCAACCCACTCTGGGCTCGCACTCCCATCACCACCATCACCACCATCATCACCACCACGAGCTTCCCCTCACTCCTCCAGCGGAGCCTCCGTCTGCATATTCATTCGAGCTTTCCCCGGTTAAAATGCAAGGGAATGCGCCATACTACACGCAGCACAACGCCGTCAGTCAAAACTTTCCAAGCTTCCTCCAAAACCCCTCAGGAAGAGCTCACCTGCCTGGAGGTCACGTTGAGGATGGCCAGCAGTGGTGGAGTCTCCCCCAGGGTAACAGCGCTCCCTCCGGGCACCCTTTCTCCTTGGGACGGCAGCTGGTTTTGGGCCATCAGCCTCAAATTGCAGCACTTCTGCAGGGAACCTCCAAAGGTCTGTTGAGCTCTACTCGTCGCTGTCGCCGATGCAAATGCCCAAACTGCCAGTCCACAGGAAACGGAGGTGCTGCATTGGAGTTTGGAAAGAAAAGACTACACATTTGTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3223
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000024283 | Nonsense | 211 | 357 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 28268510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28097563 |
GRCz11 | 23 | 28024104 |
KASP Assay ID:
554-2931.1 (used for ordering genotyping assays)
KASP Sequence:
TGGGACGGCAGCTGGTTTTGGGCCATCAGCCTCAAATTGCAGCRCTTCTG[C/T]AGGGAACCTCCAAAGGTCTGTTGAGCTCKACTCGTCGCTGTCGCCGATGC
Long Flanking Sequence:
GGCAGGAAGGCTCGCAGCTCCCTTACGAGGGTCCGGTGGGCTCCGCATCCAGCATGTTCCAGCTCTGGAGCAACGACGTGGCCCCGAACTCCAGCTTAAGCGCTCACCAGATGACCTTCACCGTGCCCAAAATGCAGTTTCCCAGCCACATGCAACCCACTCTGGGCTCGCACTCCCATCACCACCATCACCACCATCATCACCACCACGAGCTTCCCCTCACTCCTCCAGCGGAGCCTCCGTCTGCATATTCATTCGAGCTTTCCCCGGTTAAAATGCAAGGGAATGCGCCATACTACACGCAGCACAACGCCGTCAGTCAAAACTTTCCAAGCTTCCTCCAAAACCCCTCAGGAAGAGCTCACCTGCCTGGAGGTCACGTTGAGGATGGCCAGCAGTGGTGGAGTCTCCCCCAGGGTAACAGCGCTCCCTCCGGGCACCCTTTCTCCTTGGGACGGCAGCTGGTTTTGGGCCATCAGCCTCAAATTGCAGCACTTCTG[C/T]AGGGAACCTCCAAAGGTCTGTTGAGCTCTACTCGTCGCTGTCGCCGATGCAAATGCCCAAACTGCCAGTCCACAGGAAACGGAGGTGCTGCATTGGAGTTTGGAAAGAAAAGACTACACATTTGTCACATTCCAGATTGTGGGAAGGTTTATAAAAAAACCTCTCACCTCAAAGCGCACCTGCGCTGGCATGCTGGTGAACGGCCCTTCATTTGCAACTGGCTCTTCTGCGGGAAGAGCTTCACGCGTTCAGATGAGCTGCAGAGGCATCTCCGTACACACACCGGGGAGAAGCGTTTCGGCTGTCAGCAGTGTGGAAAGCGGTTTATGCGGAGCGATCATCTCTCCAAGCATGTGAAGACCCATCAGAGCCGGAAGAGCCGGTCCAGTCAGCCTCCTCACAGCGGGACTGATGCTCTGCTGAGCAACATCAAGAGAGAGTAAAAGATGCACAAGTACTAAAAACAATATGAACAAGAGCTAAGAGAGAGAACTTTTTTA
Associated Phenotype:
Not determined