ZMP
zgc:63514
Ensembl ID:
ZFIN ID:
Description:
four and a half LIM domains 3 [Source:RefSeq peptide;Acc:NP_001093448]
Human Orthologue:
FHL3
Human Description:
four and a half LIM domains 3 [Source:HGNC Symbol;Acc:3704]
Mouse Orthologue:
Fhl3
Mouse Description:
four and a half LIM domains 3 Gene [Source:MGI Symbol;Acc:MGI:1341092]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16053 | Essential Splice Site | Available for shipment | Available now |
| sa13682 | Nonsense | Available for shipment | Available now |
| sa29137 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16053
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082192 | Essential Splice Site | 110 | 290 | 2 | 5 |
| ENSDART00000132380 | Essential Splice Site | 110 | 290 | 4 | 7 |
| ENSDART00000139225 | Essential Splice Site | 110 | 225 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 4891886)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 4165447 |
| GRCz11 | 19 | 4096273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATGAGTTTTCTTCTAATTGTGTGGCCTGCGGGAAGACWGTGATGCCAG[G/A]TAACCTTMACACAMACACGYATATGCTAGWATTTTATTTWTATACACACA
Long Flanking Sequence:
GGAATGAAGGAAGATAACTGAATGCTTTTAAGAATACTTCGTTTACACATCCCTGCACAAATTGCATGTAAGCACATTCACTTTTCACTGTGTAATACTCACTCACTACTCTTGAGTACTTTTGAAAGGTCTACTTTTTACTCATACTTTGAGTAATATTTACAACTCTCTACTTGCACTACATTTTTGGGCAAGTAATGGTACTTGTACTTGAGTATGATTTTTCAGTACTCTTTCCACCACTGAGGGCTAATAATTTTGACCTCAACTGTACATCTTATAAGAGTGTGTTCATGTGTTTCTCCTGTGCTGTGTGTGTGTTCAGGAGCTGTATCATGAGGACAGGCATTATCATGAGCAGTGTTTCCGCTGCTCGCGCTGCAGTCGATCACTGGCTAAAGAGTCCTTCACCTGTCAGGAAGACGCTCTGGTGTGTAACAACTGTTACTGCAATGAGTTTTCTTCTAATTGTGTGGCCTGCGGGAAGACTGTGATGCCAG[G/A]TAACCTTCACACAAACACGTATATGCTAGTATTTTATTTTTATACACACACCTTTCGAAAGTTTGGGGTGAGTTTTTTCTTCAGGAAGGATGGCTTAAATTCAGAATACGATTCAGAATAACTGTGTAATCTCAAATAAATTCTTAAAGCACATAGAAAATATATAATATACATAGACAATAATGGGTAAAGCTATTCATTTATATACATATATTTATATACGGAAATATTTTATATTATAGTGCTCTTCAATGGAGAGATTTGAACAATTTTAAAAATACCAACTAATTTAATAACTAATTAACTTTGTCTTTGTGTCTTTTGTGCTATGATGACAGTATATAATATTTGTGTATTTTTGCAAGACACTATTCAGCTAAAAGTAATAATAAAAAAAAGAATGATTCGTTAAGGGGGCTAACAAGTCCGTTCATTCATTCGTTCGTTCATTCGTTCCAAGGTTATTCTAGTTATTATAAATAACTATAATAGATATAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13682
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 |
|---|---|---|---|---|---|
| ENSDART00000082192 | Nonsense | 120 | 290 | 3 | 5 |
| ENSDART00000132380 | Nonsense | 120 | 290 | 5 | 7 |
| ENSDART00000139225 | Nonsense | 120 | 225 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 4890092)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 4163653 |
| GRCz11 | 19 | 4094479 |
KASP Assay ID:
2261-2828.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTTATATATTGTCCTCTCAGGCTCTAAGMGGCTGGAGTATGAAGACTG[T/A]GTGTGGCATGAGGAGTGTTTTGTTTGCTGTGGTTGTGAGCAGCCCATCGG
Long Flanking Sequence:
GACTGTCTGAATGTACTAAGAGGATAAAATTACAACTGAAAGTGGCAGCGCTCTCTCTCCTCCCTCTTTCATTCAAAACACACTTTAAGATCAGGTGAGCCGTTTCCTACCAAACCTGTATGCTGCAACTCGTGCATTTTTCAGATTCCACGTGCGTTTCTGTGGATACACACTTCCAGCCCACAGATTTCACACAGCTGAAATGGAACTCAAAACACGAGCGGCTTTTGTAGATATAGAGTCATTCAGCAGGAATATGACATCACATCATGTGTAGTTGGTCATGATAATGCAAAGGTTTAACTGTGTGGTATTTGCTTATCGAATGTGCTCAGTCACCTGAAACAGTAAAAGTGCTTGAGAAAGAACCTGTCGTGGATAATTAGGCCTGTTTTTCTGAGTAAATCATCCATTAATCATGCAATGATTTAATGACCTAAAAGTTATATGAAGTTATATATTGTCCTCTCAGGCTCTAAGCGGCTGGAGTATGAAGACTG[T/A]GTGTGGCATGAGGAGTGTTTTGTTTGCTGTGGTTGTGAGCAGCCCATCGGCGCCCAGTCCTTTATTCCCGATAAGGACGAGTACTACTGCGTGCCCTGTTATGAGGGACGATTCGCTCCGCGCTGCGCTCACTGCAAACAGGTGACACAAAAACTACTCATTTTATTATAATTCATCCATTAAAGATGAACTATTATGCCTCTTTTTTTATAAGATGTAAAATAAATCTTTGTTGTTCCTAGAGTGTGTATGTGACGTTTCAACTCAAAATACACAACAAATAATGTTTTTTAAGTCTTTGAAACTGCCGTTTTGATGCTAATTATGAAATTTTGGTGACTTGTCACTTTAAATTCAAATGAGATTGTGCTCTTTTTTTAAAGAAGGGGGAGCTACAAAAGCATGTGTCAGTAAAGTGGCAGATTCAAAAACAAGACTTTTGCTCTATGCTAATGAGAGAGATTGTCACTAATGGGCGGGGCTTTCCCCCTCTAATGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29137
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082192 | Nonsense | 122 | 290 | 3 | 5 |
| ENSDART00000132380 | Nonsense | 122 | 290 | 5 | 7 |
| ENSDART00000139225 | Nonsense | 122 | 225 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 4890086)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 4163647 |
| GRCz11 | 19 | 4094473 |
KASP Assay ID:
2261-2827.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATTGTCCTCTCAGGCTCTAAGCGGCTGGAGTATGAAGACTGTGTGTG[G/A]CATGAGGAGTGTTTTGTTTGCTGTGGTTGTGAGCAGCCCATCGGCGCCCA
Long Flanking Sequence:
CTGAATGTACTAAGAGGATAAAATTACAACTGAAAGTGGCAGCGCTCTCTCTCCTCCCTCTTTCATTCAAAACACACTTTAAGATCAGGTGAGCCGTTTCCTACCAAACCTGTATGCTGCAACTCGTGCATTTTTCAGATTCCACGTGCGTTTCTGTGGATACACACTTCCAGCCCACAGATTTCACACAGCTGAAATGGAACTCAAAACACGAGCGGCTTTTGTAGATATAGAGTCATTCAGCAGGAATATGACATCACATCATGTGTAGTTGGTCATGATAATGCAAAGGTTTAACTGTGTGGTATTTGCTTATCGAATGTGCTCAGTCACCTGAAACAGTAAAAGTGCTTGAGAAAGAACCTGTCGTGGATAATTAGGCCTGTTTTTCTGAGTAAATCATCCATTAATCATGCAATGATTTAATGACCTAAAAGTTATATGAAGTTATATATTGTCCTCTCAGGCTCTAAGCGGCTGGAGTATGAAGACTGTGTGTG[G/A]CATGAGGAGTGTTTTGTTTGCTGTGGTTGTGAGCAGCCCATCGGCGCCCAGTCCTTTATTCCCGATAAGGACGAGTACTACTGCGTGCCCTGTTATGAGGGACGATTCGCTCCGCGCTGCGCTCACTGCAAACAGGTGACACAAAAACTACTCATTTTATTATAATTCATCCATTAAAGATGAACTATTATGCCTCTTTTTTTATAAGATGTAAAATAAATCTTTGTTGTTCCTAGAGTGTGTATGTGACGTTTCAACTCAAAATACACAACAAATAATGTTTTTTAAGTCTTTGAAACTGCCGTTTTGATGCTAATTATGAAATTTTGGTGACTTGTCACTTTAAATTCAAATGAGATTGTGCTCTTTTTTTAAAGAAGGGGGAGCTACAAAAGCATGTGTCAGTAAAGTGGCAGATTCAAAAACAAGACTTTTGCTCTATGCTAATGAGAGAGATTGTCACTAATGGGCGGGGCTTTCCCCCTCTAATGACGCATACA
Associated Phenotype:
Not determined