ZMP
si:ch211-210c8.8
Ensembl ID:
ZFIN ID:
Human Orthologue:
TFCP2
Human Description:
transcription factor CP2 [Source:HGNC Symbol;Acc:11748]
Mouse Orthologue:
Tcfcp2
Mouse Description:
transcription factor CP2 Gene [Source:MGI Symbol;Acc:MGI:98509]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18190 | Nonsense | Available for shipment | Available now |
sa17044 | Essential Splice Site | Available for shipment | Available now |
sa9853 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18190
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084848 | Nonsense | 31 | 512 | 1 | 16 |
ENSDART00000138416 | Nonsense | 31 | 512 | 2 | 17 |
The following transcripts of ENSDARG00000060306 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 33893067)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 33752865 |
GRCz11 | 23 | 33679396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGAGTCTGGWCTGGTCCARGACTTTGATGCCAGTCTGTCAGGGATCGGG[C/T]AAGAGCTTGGAGCTGGTGCTTACAGCATGAGGTGAGATTCATCACTTAAC
Long Flanking Sequence:
TCTGATTGAATTACGTAATACAATACATGTGTTGGTCATGTGTAGAGCTGTACGTACTTCTGAATATATGAACTCATTTTGGGGGTTTGCTCTGTCCTTAGCGTCAAGTTTGGTCCAGTAAGAATTGTATTAATTAAGAATAATAGTTTAGAAAATGTTCAGGTGATATAATTTTTTTTATTTTTCCTGTTATAATAACAAACCTTTATGTATGTTTAATCTAAATCTTTTGTGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTTTTTTTTTTTCAGAGATGAGTCTGTGATCGTCCCTAAATCCAAAGGGAGGCTGCCAGAACTGTGATTCTTTTTTTGATTTTGTTGGTAAATTGTAAGTCTAAAATCATGGCTTGGGCTCTGAAATTACCTCTGGCCGATGAGGTGATCGAGTCTGGTCTGGTCCAAGACTTTGATGCCAGTCTGTCAGGGATCGGG[C/T]AAGAGCTTGGAGCTGGTGCTTACAGCATGAGGTGAGATTCATCACTTAACTTACACTTTTTTATTGTTTGCTTGATTAGGAATGTTTAAACAGTGTCTGCGTATTTTATTAATGTTTCCTGAGGCCTGTGGGTTTTGATGTAAGTTATTTTTTATTAATTAATAGCTACTGGTGCCTTATTGAAAAGCATTTAGTCTAGTTTACTTGCCTAGACACATTTCTCCTGCTGTTCACATGTCACTCCGGGGTGTTTAAATGTCATGATGAATGTGTTTCAGCACCGTCTGACCTTCCAGACTGGCACACACTGTATCTTGTAAGCTCTTACAGGACTGTTATGCAGAAAATTAACCATTTTGAAAAGTACTGGTCTATTTGTGCCAAGGTTATTGTGTGGGTTTTGGTGAGGTGTTTAGGAAAGGATCATTTGTAATGTACAGAGGCGTATTGACAAACTAAAGTTCTCTGTGATGATTTTAAAATGCATCTAAATGTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17044
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 |
---|---|---|---|---|---|
ENSDART00000084848 | Essential Splice Site | 324 | 512 | 9 | 16 |
ENSDART00000138416 | Essential Splice Site | 324 | 512 | 10 | 17 |
The following transcripts of ENSDARG00000060306 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 33883780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 33743578 |
GRCz11 | 23 | 33670109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCACCCAGTCACCAGCCAGAGCCTGTCGCACAGTTAGCGGATGTGAGTG[T/A]ATGTGTATTTTTTTTCTTCCTCTCTCATATCYGATATCCACTGCTCWCAG
Long Flanking Sequence:
ACGCAGAAGTATAAATCAGGCTTAATGCTTAACAAATAATGAATTCACTAGATGCTAATGCTTAGTATATGATTCATAGTGTGCAGTTATTATAAAGTGTTACCCAATATTTCACTTGGTCCAAGATTTTTTTTTATATTTGAACTAGAAACTAGACAAAACAAAGTAAGAAAAGCAATTTTTGCTTCGTGGTTATTCGATTTCTGTAACCGAAAACTCTTAGACTCCCTAGAAAACCATCAGATAGAGCTATTGTGTGAAGCTGCATTAATAACGTATTTATCGCAGAAAAATAAAATACCGTAATATCCGATCTTTCCAGTATCATGCAGCCCTGGTTATAGATCGTTTTATAGACTATGAAAACATTTATCTTTTTTGGAGCAACATGCAATAATTAAATGTTTATGTATGGCCATAATGACTCATAGTTTTGTCTTGCAGAAATGGTTCACCCAGTCACCAGCCAGAGCCTGTCGCACAGTTAGCGGATGTGAGTG[T/A]ATGTGTATTTTTTTTCTTCCTCTCTCATATCTGATATCCACTGCTCACAGTGGCATAAAATAACAATCATTTAACAAATGTATGTACATTGAGAAATGAAAGGCAAACTGCCTAGGACTTTAACCAAAATATAGATGCATCCCAGTGTTCCCTTATGTTTCTTTTCCTACATTTCTGCATTCTACATGCTATCCTTTAATTTAAATATTATGTTTGTGCTTCTTATCTGTGTTCCATTTGCATTTGTGTTTGATTTAGTTCATATTTAATAATACTGGCTTCACTCGTTAAGTAGTTGAGCTGTTTTGGGAATGAAATGGTAATTAGGTGTAGTGCTGTGTGTGTATTTGTGTATAAGGTATGCTCCATGCTTCCATCTACATTAATAATATCAGGACAACTACAGTAGTTCATCAAAAACCCTTTGTTCCATTCATAATATGGCAGCTGCTATGATTAATTCTGTAGAATGCTTTTTTGGTTGCTTTGCATGCTCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9853
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084848 | Nonsense | 437 | 512 | 14 | 16 |
ENSDART00000138416 | Nonsense | 437 | 512 | 15 | 17 |
ENSDART00000084848 | Nonsense | 437 | 512 | 14 | 16 |
ENSDART00000138416 | Nonsense | 437 | 512 | 15 | 17 |
The following transcripts of ENSDARG00000060306 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 33876971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 33736769 |
GRCz11 | 23 | 33663300 |
KASP Assay ID:
554-6199.1 (used for ordering genotyping assays)
KASP Sequence:
TGATTTGTTTTCATGTGGAATMTCATGTTTCTTTACCCAATGTTAGTGTA[T/G]CACGCCATCTATCTGGAGGATTTAACCGCWGTGGAACTGACGGAAAAGTT
Long Flanking Sequence:
CTGAGCTCAACCACTCTCACTGGCAGAGCTGTTATAAAACAAAATTCTATTGGCTGTTTTTTTTAAATGGGGAGGAGTTAGTTTATGTCCCGCCCTCTCTTCGTTTTACAGTTGAGATTACATCAAACCTCTTATTAAAAATGAACATTTCAAACCACTTGACATGAACTTTAATGTATTAAGTCTCTGTAAACTGAGAGCCAACTCTGCTCTGATTGGTCAGAAGCTCGAGTTTGTTGTGATTGGTGTACCACTTGCAGCGCGTTTTGGAAACCAAACCCTTATTACCATGTCTGAATTTCTGAGTTTGTGTTCTTTGATACTCTGCAAACCTTTTACATTCACAAATGATTACATTACACACAGTTAAATGTATTATTAAAAGCTATAATTGGGGCACTTCCAGATCCTTGCTAGCTTGTGGTTCGTTTTATTTTGATGTGTATCCTGTGATTTGTTTTCATGTGGAATCTCATGTTTCTTTACCCAATGTTAGTGTA[T/G]CACGCCATCTATCTGGAGGATTTAACCGCTGTGGAACTGACGGAAAAGTTGGCTCAACTCTTCAGCATCTCTCCACGCCAGATCAGTCAGATCTTCAAGCAGGGACCGACTGGCATCCATGTGTTAGTCAGTGATGAGGTAACTGCTTCTGCAGGATTTCTCTTTTGTTCATTAGGTTAAAGCACTGAAATTTCCTCACACTTAAAGGGTAGCTCATCCATGAATGAAAATTCTCCCATCATTTACTTACCCTTTACTTGTTTAACTTGCTATTTCCAGTTAAACACCAAAGATATTTCAAAGAAAGGTGGAAACCTGCAACCATTAACCCCTTTCACACAGTGATACCGGTAAATATCTGGAAAATTTCCGGAACGACTTTACCGGTAAATTCAAAAAAGCGCTGTTCACACAGGCGAGGACGTTACGGAATTTTTCCGGAAAAGAGCATTCACACATCCATCGCAAAATGCCGGTAAATTCTGTCATCATTAACCAGA
Associated Phenotype:
Not determined