ZMP
klf2b
Ensembl ID:
ZFIN ID:
Description:
Kruppel-like factor 2b [Source:RefSeq peptide;Acc:NP_571932]
Human Orthologue:
KLF2
Human Description:
Kruppel-like factor 2 (lung) [Source:HGNC Symbol;Acc:6347]
Mouse Orthologue:
Klf2
Mouse Description:
Kruppel-like factor 2 (lung) Gene [Source:MGI Symbol;Acc:MGI:1342772]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43252 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45666 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43252
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 |
|---|---|---|---|---|---|
| ENSDART00000059188 | Nonsense | 11 | 363 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 17847772)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 17832802 |
| GRCz11 | 2 | 55665354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCGAGCACGCGTGGACATGGCTTTACCTTGCCTTTTGCCTTCGATTT[C/A]AACGTTTGCAAACCAGAAGGAGAAGCTCTGGGAGGATGTAAGTATTTGAC
Long Flanking Sequence:
GACTAAATTACGCACGGGTGAATGTAGGCTGTCGGGCGCTGGAATTACACTTGGATCAATTCGAGCTTTTCTTTGAAACGCCTTGGTAACAGTTTTGTGTGTGTTTCTACTACAGAGATGATAGTGACACGCCTCCTGTCAGCCGCGCCTCCGCGAGGGAGGTGTGCGCGCGCATCAGCGGCTCTGGTTTAAAAGCGGCGGAGCGTGCACTGTCCCGCACTGAGAAACGAGAAGCGCTGGAGAGAGCGCACTGTGCCTTATATATAGACTATCTTTGGGAACTCTGAACGCGGTTTCCACCGCGCACACAATTGGTCTAGGAGCCGTATTTATTAAGTAGGAGGCGCTCCTGCCGGGCAAACTTTGTTCATGACTGTGGAAGTTCACTCGAGGAAAAAGCGCGCAGAAGTTTGACATCTCTTCAGGAGCAAGTGCATTAATACTGAATACACACCGAGCACGCGTGGACATGGCTTTACCTTGCCTTTTGCCTTCGATTT[C/A]AACGTTTGCAAACCAGAAGGAGAAGCTCTGGGAGGATGTAAGTATTTGACACTTTTATGCACTTTTAAACGAGGGTGAAGTCAGGGCAATGCGGGAAACCTCACCTCAGATGTGGTTAAAATTGGGTTAACACTCGAAAAACACTTGCATTTCCTACTTGTTTTTGCGCAAAATACAATATATTGGAGATATAAGTCAAAAACACGCTTAAGAAATTTAGTTTTTATACGTATTTTATGCTTATAAGGTAAATATATCTTGTTTAAATGCATGTTTGATAAAAATGTTTAGTGCAAAACTTAATCGGAAAAGTGGGGGAAAGTAATGTTATAGTTTTTACTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTATTTATAAAAACACACTAAATTATAATACACTATAGTAGGTTACTAAAACACTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45666
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059188 | Essential Splice Site | None | 363 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 19 (position 17852448)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 17837478 |
| GRCz11 | 2 | 55670030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTGGTGTTAAAATCTAGCCTAGAGCACACTGTGGTGTTAAAAACTAG[C/A]CTAGAGCGCCTTCTGCTGCTCAAAACTAGCCTAGATTTCTGTTAAAAATT
Long Flanking Sequence:
TTTTGTTGCTTAAAACTAGCCTAGACCTCAGTTTAAAAATTAGCCTACAGTGCATCTGCTGATAAAAACTAGCCTAGAGCGCTCTCAGGTGTTAAAAACTAGCCTAGAGTGCTGTCTGCTTCTCAAAAACTAGTCTAGACTTGATTCCTTTGCTTAAAACTAGCCTAGACCTCTGTTAAAAAATTAGCCTATAGTGCGTCTGCTGTTACAAACTAGCCCAGAACATCCTCTGGTGTTAAATAACTAGCCTAGAGCACCATCTGTTGCTCAGAACTAACCTAGACCTCTGTTAAAAATTAGCCTTTATTGCGTCTCCGGTTAAAAACTAGCCTAGAGCGCCCTCTAGTGTTAAAAACTAGTCTAGAGCGCCCTCTGCTGCACAAAATTAGCCTAAACCTATGTTAAAATTAGACAAGAGTGCGTTTGCTGGTAAAAACTAGCAAAGAGCGCCCTCTGGTGTTAAAATCTAGCCTAGAGCACACTGTGGTGTTAAAAACTAG[C/A]CTAGAGCGCCTTCTGCTGCTCAAAACTAGCCTAGATTTCTGTTAAAAATTAGCCAAGAGCGCCGTTTGCAGTTCAAAACTAGCCTAGATTGCTGTTAAACATTAGTCTAGATCCCATATGCTGTTATAAACTCACCTAGAGCGCCATCTGCTGTCAAAAAACTCACCTAGAGCGCCATCTGCTGTTAAAAACGGATCTTAGAATTGATTCCAGAGAGAATCGGGACGCAGTTAAAAATCTAACAATCGATTCATGAATAACAATACAATGATTTATCAATTCCAGCCCTAATTTTTTACATATTTCTTTCCAAATGTTGGTAACGCTTTACAATAATGCTGCATTTAGTAAATGCATTGAGCAAAAAAAGTGTGTAATTTAGGTGCATTGGATCACACCAACAGATGCAACTTTTGTAAGTGTTAAAGGGACGGCTCACTCCAAAACTGAAGATGACCTCCATTGACTTTCATAGTAATTGTTTTTTATCCTATGGAAGT
Associated Phenotype:
Not determined