ZMP
znf668
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 668 [Source:RefSeq peptide;Acc:NP_001012507]
Human Orthologue:
ZNF668
Human Description:
zinc finger protein 668 [Source:HGNC Symbol;Acc:25821]
Mouse Orthologue:
Zfp668
Mouse Description:
zinc finger protein 668 Gene [Source:MGI Symbol;Acc:MGI:2442943]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16082 | Nonsense | Available for shipment | Available now |
| sa17530 | Nonsense | Available for shipment | Available now |
| sa22122 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16082
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 |
|---|---|---|---|---|---|
| ENSDART00000033878 | Nonsense | 325 | 643 | 2 | 2 |
| ENSDART00000123417 | Nonsense | 325 | 643 | 3 | 3 |
| ENSDART00000139347 | Nonsense | 325 | 643 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 30507652)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 28844589 |
| GRCz11 | 12 | 28959491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCCACAGTGTGGTAAGATGTTCTCGGATCCCTCTAGTTTCCGCCKAYAC[C/T]AACGGGCACATCAAGGATTCAAGCCATACCCTTGCGACAAGTGCACTAAG
Long Flanking Sequence:
CACAGCACAGTGGCGAAAGGCCTCACTCGTGTCCTCTCTGCTCCAAGAGTTATCCCACACTTTCCAAACTCAAAGTGCACCAACGATCCCACACCGGTGAAAAGCCTTACTTTTGTGTTGAGTGTGGGAAGAGTTTTGCAGACCCTTCAGTTTACCGCAAGCATCGGCGTAATCACCTAGGCCACCGGCCGTATTCCTGTGCGCAGTGTGGTAAAACTTACACAGAGCTGAAGGACTTGAAAAATCATGAGCGTTCACACACAGGTGAGAAGCCTTTCCTGTGCTCAGACTGCGGCAAAGCCTTCTCCCGATCCTCATCATTGGCGTGCCACTTGCGAATTCACTCCAAAAGCAAGCCATATCAGTGTGAGCAGTGTGGAAAAGGTTTTACCCAACTGTCCTCATACCAGTCTCACCTTCGCACACACTCTGGTGAAAAACCATTCTTATGCCCACAGTGTGGTAAGATGTTCTCGGATCCCTCTAGTTTCCGCCGACAC[C/T]AACGGGCACATCAAGGATTCAAGCCATACCCTTGCGACAAGTGCACTAAGAGGTTTCGGCAACCCGCAGATCTTGCTGTGCATCAACGTGTGCACTCTGGCCAGCGACCCTATAAATGCCAACGTTGTGATAAAGCTTTTGTAGCTTCTTGGGATCTTCGGCGCCACATGCTAGTGCATTCCGGACTGCGTCCTTTCGCTTGCACTGAGTGTGGCAAGTCTTTTACGGAGCGTTCCAGCCTGAACAAACACAGAAGGGTGCATTCAGGAGAGCGTCCATACAAATGCCAGCTTTGCTTCAAGTCGTTTGTTGTGTCTTCGAGTTTGCGCAAGCATGAGAGGACACACTTATCCGAGAGGCCGATACAGGTTCATGTCACTCCAGAATCAGCTTCAGTGTTTCCCAGCACCCTTCCCCAGTTCTCCTGCTCTCACTGTGATATGATATTTGGGACATGGGAGGAGGTGCAGGCCCACACCAGCCTTCACACCATCTCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17530
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033878 | Nonsense | 369 | 643 | 2 | 2 |
| ENSDART00000123417 | Nonsense | 369 | 643 | 3 | 3 |
| ENSDART00000139347 | Nonsense | 369 | 643 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 30507784)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 28844721 |
| GRCz11 | 12 | 28959623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWCAACGTGTGCACTCTGGCCAGCGACCCTATAAATGCCAAYGTTGTGAT[A/T]AAGCTTTTGTRGCTTCTTGGGATCTTCGGCGCCACATGCTAGTGCATTCC
Long Flanking Sequence:
GTTTTGCAGACCCTTCAGTTTACCGCAAGCATCGGCGTAATCACCTAGGCCACCGGCCGTATTCCTGTGCGCAGTGTGGTAAAACTTACACAGAGCTGAAGGACTTGAAAAATCATGAGCGTTCACACACAGGTGAGAAGCCTTTCCTGTGCTCAGACTGCGGCAAAGCCTTCTCCCGATCCTCATCATTGGCGTGCCACTTGCGAATTCACTCCAAAAGCAAGCCATATCAGTGTGAGCAGTGTGGAAAAGGTTTTACCCAACTGTCCTCATACCAGTCTCACCTTCGCACACACTCTGGTGAAAAACCATTCTTATGCCCACAGTGTGGTAAGATGTTCTCGGATCCCTCTAGTTTCCGCCGACACCAACGGGCACATCAAGGATTCAAGCCATACCCTTGCGACAAGTGCACTAAGAGGTTTCGGCAACCCGCAGATCTTGCTGTGCATCAACGTGTGCACTCTGGCCAGCGACCCTATAAATGCCAACGTTGTGAT[A/T]AAGCTTTTGTAGCTTCTTGGGATCTTCGGCGCCACATGCTAGTGCATTCCGGACTGCGTCCTTTCGCTTGCACTGAGTGTGGCAAGTCTTTTACGGAGCGTTCCAGCCTGAACAAACACAGAAGGGTGCATTCAGGAGAGCGTCCATACAAATGCCAGCTTTGCTTCAAGTCGTTTGTTGTGTCTTCGAGTTTGCGCAAGCATGAGAGGACACACTTATCCGAGAGGCCGATACAGGTTCATGTCACTCCAGAATCAGCTTCAGTGTTTCCCAGCACCCTTCCCCAGTTCTCCTGCTCTCACTGTGATATGATATTTGGGACATGGGAGGAGGTGCAGGCCCACACCAGCCTTCACACCATCTCTCCCCCATCTGATCCTTCAGTTTTGGCTGTACCTGTCAGCCCACATGTATGTGTGACTTGCCAGGAAGAGTTTGTTAATCTGGCTGATCTTCAGGCACACGAGAAACTGCATCCCAAGCCTCGACCCCACATTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22122
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033878 | Nonsense | 556 | 643 | 2 | 2 |
| ENSDART00000123417 | Nonsense | 556 | 643 | 3 | 3 |
| ENSDART00000139347 | Nonsense | 556 | 643 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 30508346)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 28845283 |
| GRCz11 | 12 | 28960185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGGTTTTCTGAATAAAGCTGGTCTTCGTAAACACCAGCGTATCCACT[C/A]AAGTAATCGGCCACATAGTTGCAATGTTTGCGGGAAGGCTTTTCTTTTTG
Long Flanking Sequence:
TTTCGCTTGCACTGAGTGTGGCAAGTCTTTTACGGAGCGTTCCAGCCTGAACAAACACAGAAGGGTGCATTCAGGAGAGCGTCCATACAAATGCCAGCTTTGCTTCAAGTCGTTTGTTGTGTCTTCGAGTTTGCGCAAGCATGAGAGGACACACTTATCCGAGAGGCCGATACAGGTTCATGTCACTCCAGAATCAGCTTCAGTGTTTCCCAGCACCCTTCCCCAGTTCTCCTGCTCTCACTGTGATATGATATTTGGGACATGGGAGGAGGTGCAGGCCCACACCAGCCTTCACACCATCTCTCCCCCATCTGATCCTTCAGTTTTGGCTGTACCTGTCAGCCCACATGTATGTGTGACTTGCCAGGAAGAGTTTGTTAATCTGGCTGATCTTCAGGCACACGAGAAACTGCATCCCAAGCCTCGACCCCACATTTGTGACCAGTGTGGAAAAGGTTTTCTGAATAAAGCTGGTCTTCGTAAACACCAGCGTATCCACT[C/A]AAGTAATCGGCCACATAGTTGCAATGTTTGCGGGAAGGCTTTTCTTTTTGCTGCTTATCTACGCAAGCACTTACGCACCCACCGTGACACAGAGTCCTTACCGTCTCTGCCTCAGACAGACATGGCACACACCCAGCCCTTGCCATCCCCACCAAGTGCTGCGTCACCTTCGGGATCAGAACCCACCGCTATTTCCCTTACTGTTCCTGTAACCTTTCAGACAATACCAGCCCATGTGTATATGGACAAAGAAGACGGACTCTGAACTTATTGATGACTTTGTCGGATGCTTTGAACATTTGTTTAGACAATGTTCACATTTTTGTTACTGCTATTCTATACTAACAGGACAGTGAAAGCGTTGAAAACAGAAAAGCCAATGCATTGTTTTTTTTGTTTTTTTTTAAAGATGGATTAAATGCATCAGTACACAAAATTTCTCATAAAATATTGTCTTTGAATTTCTTTGATAATGTAAGAGAACATTTATATTTAGGTAT
Associated Phenotype:
Not determined