ZMP
klf12a
Ensembl ID:
ZFIN ID:
Description:
Kruppel-like factor 12 [Source:RefSeq peptide;Acc:NP_996945]
Human Orthologue:
KLF12
Human Description:
Kruppel-like factor 12 [Source:HGNC Symbol;Acc:6346]
Mouse Orthologue:
Klf12
Mouse Description:
Kruppel-like factor 12 Gene [Source:MGI Symbol;Acc:MGI:1333796]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa868 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
| sa32708 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa868
Status:
Confirmed mutation in F2 line
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000012873 | Essential Splice Site | 211 | 373 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 34178817)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 33813568 |
| GRCz11 | 1 | 34546136 |
KASP Assay ID:
554-0770.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGTGCGCACATATTGTAAATCAACTCCCCCTACCTTTTGTTTTTATTC[A/G]GTGATGCACCGAATGGCAGATGGACTGTCACCGCGACGATCTCTGAGYGA
Long Flanking Sequence:
ATAGCATCATCGTGGAGTTTTTTTTTTATTGTTATTTCAGCAAATACGATCGTAAGAAAAAATATTTGTTGTATTCTCCTATTCACTGCGCTGTAAGTTTTCCCAATTATGACGACTTCCACTACTGAGAAACCCAGAAATGTAAAAAGTGTCTATTTATATAGCACATTTCATACACAATGGTAATTCAAAGTGCTTTGCATAAACAAGAAACATAAAAATTATTAAAATATAATAAATTAAAAATGATTAAAACAGATTTAAATGTGTTAAATCACATTTTAAAACTAAAGAGCCAGTACAACTGATTCATTTCCCAGTAAACAGCAGAACCTAAGATCACAACTCTCTTGACAAATATCATTCAATTAAATATGCAAACGATTCACAAACTGTGAATCAAATACAGAAAACTGACACTGGGATGTATTTTAACAATATGTTGGTCATACAGTGCGCACATATTGTAAATCAACTCCCCCTACCTTTTGTTTTTATTC[A/G]GTGATGCACCGAATGGCAGATGGACTGTCACCGCGACGATCTCTGAGTGACAGCGAGGATGACGACTTGCCCAACGTGACCTTGGAGAGTGTGAATGAAACAGGATCCACCGCCTTGACCATCGCCCGCGCTGTCCAAGAGTAAAGACACTTTCATCATTCATCTGCAATATTTATAATCCATCTACAACTAACCTATGTCTATCTATTAATGTGATCAATGATTTTTTATAGCCCTGCCTGCAATAACATGATCCTGTGGAATTTTAAAAGATGTAAGATTTAAGATACAATAATAACCTTTATTTTTATATAGCGCCTTTAAAAGTAGCATCGCAAGGCACTTTACAGACATTTACAATGTGCAGCAGTAAAAAACACATACAAGGATGTATGCAAAGAAAAAATATAATAATAAAAAATAATTAAAAACACATGAAATAAAAATAATAGCAATAGATCTAAAAATCAAACAAAAGTTACCCTAAATATGTAAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32708
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000012873 | Nonsense | 346 | 373 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 34188192)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 33822943 |
| GRCz11 | 1 | 34555511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACTGACGCGACATTACCGCAAACACACCGGCGTCAAACCGTTCAAATG[C/A]AGCGACTGTGACCGCAGTTTCTCCCGCTCGGACCACCTTGCCCTCCACCG
Long Flanking Sequence:
AAATACTTTGATTTCACAATGATAGGCCTACATTATAGAAAAAAGACACTAATTTAGACATAAGAAATCATGATTTTTGGCAATATAAGACACTTTTTTAACGAAAATATTGTTGTTATGGCATTTAACATCTTGCTATCTATATTAACAAGTGACAAATTTCTATAAATAATTAAACATGTAAACATTTTTTTAAGCTGAAAGAAAATTACGGCCTTTTGGACACCAAATGTACATGCAATTACAGAAACACCCTTGTACTTAATGGAAAATACTGTTAATAGCATGAAAATAGAAATTAAACGATGTATGGGCTTGCCATGAATGGTCTCTTCCTGTCGCGCAACACGTCTCTTTTATTGACATGTCACTGGTTTTCTCCATCTCGCAGGTGAAAAGCCATATAAGTGCACGTGGGATAACTGCACATGGAAGTTCGCTCGCTCTGACGAACTGACGCGACATTACCGCAAACACACCGGCGTCAAACCGTTCAAATG[C/A]AGCGACTGTGACCGCAGTTTCTCCCGCTCGGACCACCTTGCCCTCCACCGCCGCAGACACGCTCCACAAACATGCCTAGTGTGAAAAAACACACTCAACGGACAAAACAAGCAGAAAGAGCGGGTCTCTTTCTGCCAGTGCCGCATGCAGAAGCTCTGGAAATATTCCCCGCACAACAATAATGAGGAGAAAGGTATGGTCAGTTCATGGAATTGGATAGATATGTATCAGCATTTATTTGCCTTTCCCTCATACGGTTTATTGTTCTGCACTTTTAGGTGAGGTTTATTCGTGAAGGTGGGAGCCTTGAGTCTTTAATAATGAACTATTAAAAGCCATGTGCTGTTAAATGTGTTTTATATAGGCCTACAGGTTTCCTTCAGGTTTACTCATGGACGCCTAATGGAGTTGAAGGTTTTTCTTTTAACTCTCAAAACTATTTAGAAATCATGTTGTACTTATTTTTCTCGTTTAAAAAGCATCAAAGAGGAGCCTGAATA
Associated Phenotype:
Not determined