ZMP
znf451
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate zinc finger protein 451 (ZNF451) [Source:UniProtKB/TrEMBL;Acc:B8
Human Orthologue:
ZNF451
Human Description:
zinc finger protein 451 [Source:HGNC Symbol;Acc:21091]
Mouse Orthologue:
Zfp451
Mouse Description:
zinc finger protein 451 Gene [Source:MGI Symbol;Acc:MGI:2137896]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31900 | Nonsense | Available for shipment | Available now |
sa22195 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31900
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110828 | Nonsense | 556 | 871 | 9 | 14 |
ENSDART00000145867 | Nonsense | 556 | 916 | 10 | 13 |
The following transcripts of ENSDARG00000076939 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 1287916)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1285268 |
GRCz11 | 13 | 1415559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTCGTGGCTTTGTCGAATGTGCGAGGATTTGTTTGATTCGGAGAAGT[T/A]GGTACGAAAGCATTGCGGAGATTTGAGCAGCCATAGTTTCCAGAGGTTTG
Long Flanking Sequence:
CGAAGACCATTCAGCCAAACGAAAGAGAGCTGAAGACTCGGATTCGCAAGTCAAACGAGAAAGAAAGCATTCGAATGTGGCTTGGTTTTGCGAGTGCGGCCTTCGCTTCGTTGAAGAAAACCACGCAAAGAGACACCAGCAAGCCGCCAATCAGATCTTTCACAAATGTGCAGTGTGCGGGAAACTAACCGGCGAATCCTCCATCGCGCGCTTGCATATGAGTCGTTTCCATGGTGGCGCGCATCTATCCAACTTCCTGTTTTACTGTAGGAAGTGCAAAGTGGAAATGCCCAGGATGGAGGATATAATGGCGCACGTTAGCGCTAGCCATCAAGGACACAACTACTATGAAGAACGAGAAGATAGCGGCAGCGTAATTGATCAAATATCGGCAAAACCATCAACCAGCAAAGAATGTGAACCAATCAGAAGCGTCTCCCCAAAAAAGACAGAGTCGTGGCTTTGTCGAATGTGCGAGGATTTGTTTGATTCGGAGAAGT[T/A]GGTACGAAAGCATTGCGGAGATTTGAGCAGCCATAGTTTCCAGAGGTTTGCATGCGGTCACTGTCCGCAGAAGTTCTTCAAGGACTCGACTCTACGACGACATTGCGCTAACGAGCATAACGGTGATGTAGCGTTGCGCTACTTTTGTGGGCTTTGCGATAGCATGCTGTTCGATACCGAAAACGAGTTCCAGGTGCACTACGACAATCTGCACAGCCAAGATTACTACCGTTTGGAAACATCGACAAATCATTCGCAAAATGCACCGGAAGTCATTGTTAATAATAGTAACACGAGCGATTCCCAAACATGTCTTTGCATGGGATCAAAGAAATCCAGAGAGGAACGGAAGCCTGTTTATACAAACTGCATGAAGCAGTTGGCTGCTGAAAACAAATGCAGATACCGATGTCGCAATTGCGCTAAAAGCGCTCAGAGCTACGCTGAGATGAAGACGCACATCTTGTTGAAACACAAAGGAAATGGGAAGAGTTTTGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22195
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 |
---|---|---|---|---|---|
ENSDART00000110828 | Nonsense | 589 | 871 | 9 | 14 |
ENSDART00000145867 | Nonsense | 589 | 916 | 10 | 13 |
The following transcripts of ENSDARG00000076939 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 1287818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 1285170 |
GRCz11 | 13 | 1415461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCATGCGGTCACTGTCCGCAGAAGTTCTTCAAGGACTCGACTCTACGA[C/T]GACATTGCGCTAACGAGCATAACGGTGATGTAGCGTTGCGCTACTTTTGT
Long Flanking Sequence:
GCCTTCGCTTCGTTGAAGAAAACCACGCAAAGAGACACCAGCAAGCCGCCAATCAGATCTTTCACAAATGTGCAGTGTGCGGGAAACTAACCGGCGAATCCTCCATCGCGCGCTTGCATATGAGTCGTTTCCATGGTGGCGCGCATCTATCCAACTTCCTGTTTTACTGTAGGAAGTGCAAAGTGGAAATGCCCAGGATGGAGGATATAATGGCGCACGTTAGCGCTAGCCATCAAGGACACAACTACTATGAAGAACGAGAAGATAGCGGCAGCGTAATTGATCAAATATCGGCAAAACCATCAACCAGCAAAGAATGTGAACCAATCAGAAGCGTCTCCCCAAAAAAGACAGAGTCGTGGCTTTGTCGAATGTGCGAGGATTTGTTTGATTCGGAGAAGTTGGTACGAAAGCATTGCGGAGATTTGAGCAGCCATAGTTTCCAGAGGTTTGCATGCGGTCACTGTCCGCAGAAGTTCTTCAAGGACTCGACTCTACGA[C/T]GACATTGCGCTAACGAGCATAACGGTGATGTAGCGTTGCGCTACTTTTGTGGGCTTTGCGATAGCATGCTGTTCGATACCGAAAACGAGTTCCAGGTGCACTACGACAATCTGCACAGCCAAGATTACTACCGTTTGGAAACATCGACAAATCATTCGCAAAATGCACCGGAAGTCATTGTTAATAATAGTAACACGAGCGATTCCCAAACATGTCTTTGCATGGGATCAAAGAAATCCAGAGAGGAACGGAAGCCTGTTTATACAAACTGCATGAAGCAGTTGGCTGCTGAAAACAAATGCAGATACCGATGTCGCAATTGCGCTAAAAGCGCTCAGAGCTACGCTGAGATGAAGACGCACATCTTGTTGAAACACAAAGGAAATGGGAAGAGTTTTGATGTCGTGTGCATGATCTGCTCTCAGAGTCACAAAGATGTTCCCAGTTTTCATGCACACCATCATATACATCACTGCCAGGCAGAACCGTGCACTTATTCC
Associated Phenotype:
Not determined