ZMP
zgc:92375
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC445475 [Source:RefSeq peptide;Acc:NP_001004112]
Human Orthologue:
FHL5
Human Description:
four and a half LIM domains 5 [Source:HGNC Symbol;Acc:17371]
Mouse Orthologue:
Fhl5
Mouse Description:
four and a half LIM domains 5 Gene [Source:MGI Symbol;Acc:MGI:1913192]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32141 | Essential Splice Site | Available for shipment | Available now |
sa45598 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa165 | Nonsense | F2 line generated | Not yet available |
sa337 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa23027 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32141
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010496 | Essential Splice Site | 53 | 280 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15452550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15603378 |
GRCz11 | 17 | 15611311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAACTGCTGCGAGGTGTGTTCGCTGCCCATTGGATGCAACTGTAAGG[T/A]AGGCATCCGAAAACCACTGGCGCCATCATAATTATTAAAAGCTTGAAATG
Long Flanking Sequence:
ATGCGCTCTGATTAGACTCCCATAAAAGGTGCAGAGATAAGCAACTGGCTCATTCTCCCCAGGGATTTCAGCTAATAAGAGCAATCGTATTTATAGAGGGTGTTTTAATGCATCCCCTCAATCACTGACCATCTCACCCTGAAGCCCTTCAGAAGCCCATTCAACCACCGAAGGTGAGTTTTACTAACTAATATAGATGATACGTACCCTCAAGCACCATGTAAGCGACCAAATGTGCAGAAACCATCAGTTTTGCATGTTGTGCTCGACGACACTTCTCTGATTGCTTTAGCCTGATACGTTGTAACATTGCTTTATGGTTCTGTTTACTGCTTTTAAGATGTCTACTGAAAGATTCGACTGCCATTACTGCAAGGACACTTTACTTGGAAAGAAATACATCCTAAAAGAGGACACACAGTATTGCACAAAATGCTACGAGAATCTGTTTGCCAACTGCTGCGAGGTGTGTTCGCTGCCCATTGGATGCAACTGTAAGG[T/A]AGGCATCCGAAAACCACTGGCGCCATCATAATTATTAAAAGCTTGAAATGAGTGATGGAAAGTCAGAAGAGATTTTCAAGCTCTTAACTATAATTTCTCTCCCTGCATAATGAAGGACCTCTCCTACAAGGACCGGCACTGGCATGAAAATTGCTTCAAGTGTGCTAAGTGCAGCAGATCATTGGTGGACAAACCGTTTGCTGCTAAAGATGAGCTTATGCTTTGCACCGAGTGTTACTCTCATGAGTATTCCTCTAAGTGTAGCACTTGCAAGAAGACCGTCATGCCAGGTACAGTTGAAGTCAGAATTATTAGTCCCTCCTGTATATTTTTTCCCCTAATTTCTGTTTATTGCAATAATTTATTTCAACACATTTTTAAACATAATAGTTTTAATAACTCATTTCTAATACCTAGAAATGCTCAGATCAGGATTTTTGCAGCCGATACAGAGTACTAATTCCTTGTTATGGTGGTCAGCCAATACCAAGAAATTCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45598
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010496 | Nonsense | 79 | 280 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15452359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15603187 |
GRCz11 | 17 | 15611120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATGAAAATTGCTTCAAGTGTGCTAAGTGCAGCAGATCATTGGTGGAC[A/T]AACCGTTTGCTGCTAAAGATGAGCTTATGCTTTGCACCGAGTGTTACTCT
Long Flanking Sequence:
TATAGATGATACGTACCCTCAAGCACCATGTAAGCGACCAAATGTGCAGAAACCATCAGTTTTGCATGTTGTGCTCGACGACACTTCTCTGATTGCTTTAGCCTGATACGTTGTAACATTGCTTTATGGTTCTGTTTACTGCTTTTAAGATGTCTACTGAAAGATTCGACTGCCATTACTGCAAGGACACTTTACTTGGAAAGAAATACATCCTAAAAGAGGACACACAGTATTGCACAAAATGCTACGAGAATCTGTTTGCCAACTGCTGCGAGGTGTGTTCGCTGCCCATTGGATGCAACTGTAAGGTAGGCATCCGAAAACCACTGGCGCCATCATAATTATTAAAAGCTTGAAATGAGTGATGGAAAGTCAGAAGAGATTTTCAAGCTCTTAACTATAATTTCTCTCCCTGCATAATGAAGGACCTCTCCTACAAGGACCGGCACTGGCATGAAAATTGCTTCAAGTGTGCTAAGTGCAGCAGATCATTGGTGGAC[A/T]AACCGTTTGCTGCTAAAGATGAGCTTATGCTTTGCACCGAGTGTTACTCTCATGAGTATTCCTCTAAGTGTAGCACTTGCAAGAAGACCGTCATGCCAGGTACAGTTGAAGTCAGAATTATTAGTCCCTCCTGTATATTTTTTCCCCTAATTTCTGTTTATTGCAATAATTTATTTCAACACATTTTTAAACATAATAGTTTTAATAACTCATTTCTAATACCTAGAAATGCTCAGATCAGGATTTTTGCAGCCGATACAGAGTACTAATTCCTTGTTATGGTGGTCAGCCAATACCAAGAAATTCTGGTGCTTAAAGCATTATAATGCATAAAGCACATTTTAACTCTAAGTATGATACTTAAGAGAAGATCTTGTCTTACCTAAGAGATTAAATGAAAGATGTTGCATATAATTTTTTTAACATGTCTTATATAACCATTTAGTGTGGACATGTAATGAGCAGAAGCAGTTTATAGAAAATAATACATAAAACTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa165
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000010496 | Nonsense | 123 | 280 | 4 | 6 |
ENSDART00000010496 | Nonsense | 123 | 280 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15450962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15601790 |
GRCz11 | 17 | 15609723 |
KASP Assay ID:
554-0061.1 (used for ordering genotyping assays)
KASP Sequence:
ATWTTTTCCTCATTAGGATCACGGAAAATGGAGTACAAAGGGAACAGCTG[G/A]CATGAGACATGCTTTCTGTGTCAAMGCTGTCAGCAGCCAATAGGAACCAA
Long Flanking Sequence:
TATTGGCCTGTGTAATAACTGTTTCCTTTTATCTTTGATATTATAATACTAGATATTTTTCAAGATGTTAGTATTCAACTTAAAGTGCAATGTAAAAGCTTAACTAGGTTAATTAGGCTAGTTAGGGAAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTTGACAATTGAAAACAAAGAAGATGAATAATAATATTTAAATAGCTTTAAAATATTTTTTAAAAACTGATTTCAATTCAGCCAAAATAAATCAAATAAGACATTTTCTCCAGAAGAAAAAATAGTGTAGGAAATACTGTGAAAAGTTCCTTACTCTGTTAAACTTCATTTGGGAAATATTTGACAGAATCATTTTGGCTTCTACTGCATGCACAAGAATCAAAACAAGAATCTTGTTTTAAAACTAAAGTTTTTACAAAATTCAAGACTACAGTGTATAAAGGTGATTTTTTCCTCATTAGGATCACGGAAAATGGAGTACAAAGGGAACAGCTG[G/A]CATGAGACATGCTTTCTGTGTCAACGCTGTCAGCAGCCAATAGGAACCAAGTCTTTCATCCCAAAAGATAACAATTACTTCTGTGTTCCTTGTTTCGAGAAGCAGTTTGCCTACCAGTGCTGTGCTTGTAAAAAGGTAAGTGTCGAAAGAAGTCAAACATTTGGAAAACAATATTGCTGTTAATTAAAGTTGTGGGGCGCAGTGGGTAGCACGATCGCCTCATAGCAAGAAGGTTGCTGGTTCGAGCCTCTGCTGGGTCAGTTTGCATTTCTGTGTGGAGTTTGCATGTTTTCCCCGTGTTCATGTGGGTTTCCGCCAGGTGCTCCGGTTTCCCCCACAAGTCCAAAGACATGAATGAGAGTGTGTGGGTGTTTCCCAGTGAGTTGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAAACATATGCTGGATAAGTTGGCGGTTCATTTTGCTGTGGCGACCCCTGATTAATAAAGGGACTAAGCTGAAAAGAAAATGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa337
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010496 | Nonsense | 123 | 280 | 4 | 6 |
ENSDART00000010496 | Nonsense | 123 | 280 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15450962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15601790 |
GRCz11 | 17 | 15609723 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTTTCCTCATTAGGATCACGGAAAATGGAGTACAAAGGGAACAGCTG[G/A]CATGAGACATGCTTTCTGTGTCAACGCTGTCAGCAGCCAATAGGAACCAA
Long Flanking Sequence:
TATTGGCCTGTGTAATAACTGTTTCCTTTTATCTTTGATATTATAATACTAGATATTTTTCAAGATGTTAGTATTCAACTTAAAGTGCAATGTAAAAGCTTAACTAGGTTAATTAGGCTAGTTAGGGAAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTTGACAATTGAAAACAAAGAAGATGAATAATAATATTTAAATAGCTTTAAAATATTTTTTAAAAACTGATTTCAATTCAGCCAAAATAAATCAAATAAGACATTTTCTCCAGAAGAAAAAATAGTGTAGGAAATACTGTGAAAAGTTCCTTACTCTGTTAAACTTCATTTGGGAAATATTTGACAGAATCATTTTGGCTTCTACTGCATGCACAAGAATCAAAACAAGAATCTTGTTTTAAAACTAAAGTTTTTACAAAATTCAAGACTACAGTGTATAAAGGTGATTTTTTCCTCATTAGGATCACGGAAAATGGAGTACAAAGGGAACAGCTG[G/A]CATGAGACATGCTTTCTGTGTCAACGCTGTCAGCAGCCAATAGGAACCAAGTCTTTCATCCCAAAAGATAACAATTACTTCTGTGTTCCTTGTTTCGAGAAGCAGTTTGCCTACCAGTGCTGTGCTTGTAAAAAGGTAAGTGTCGAAAGAAGTCAAACATTTGGAAAACAATATTGCTGTTAATTAAAGTTGTGGGGCGCAGTGGGTAGCACGATCGCCTCATAGCAAGAAGGTTGCTGGTTCGAGCCTCTGCTGGGTCAGTTTGCATTTCTGTGTGGAGTTTGCATGTTTTCCCCGTGTTCATGTGGGTTTCCGCCAGGTGCTCCGGTTTCCCCCACAAGTCCAAAGACATGAATGAGAGTGTGTGGGTGTTTCCCAGTGAGTTGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAAACATATGCTGGATAAGTTGGCGGTTCATTTTGCTGTGGCGACCCCTGATTAATAAAGGGACTAAGCTGAAAAGAAAATGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23027
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010496 | Essential Splice Site | 169 | 280 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 15447575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 15598403 |
GRCz11 | 17 | 15606336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTTTAAGTCTATATTTACGGTACTGAGATCCACACTTTCACCTCTCC[A/T]GGCCATAACAACTGGCGGTGTCACATATCACGATAAGCCCTGGCACCGAG
Long Flanking Sequence:
GCCACCGTGCCGCCCCCTGATAATTATCCAAATGTTGAATATTACATATTGGAAAGTTGATGAGTCAATTATGCACTTTCGCAGAATCTGCTCACTACTTTTTTTTAGAAAATGTTCTGTGCAAATCAAATTGTATTTATGTATGAGATCATTACCTTATCATAATTAAAATTATTGTTTCTTATAAAATTGGGTTGGAATTTTCCTTTTTGTGTGAACTATTTCTTTAAAGGGATTGTTCACTCAAAAATAAAATAGTGACCATTTACTCCCCCTTAAGTGGTTATAAACCTTTATGAGTTTCTTTTTTCTGCTGAACACTATGGAAGTTACAGGTTTCCAACATTCTTCAAAATATCTTCTTTTGTGTTCAACAGAAGAAATCAAATCAAACAAGTTTGGAAAAACTGAAGGATGAGTAAATGGTGACAGAATTTTCATTTTGAACTATCCCTTTAAGTCTATATTTACGGTACTGAGATCCACACTTTCACCTCTCC[A/T]GGCCATAACAACTGGCGGTGTCACATATCACGATAAGCCCTGGCACCGAGAGTGTTTCACTTGCATTGGATGCAAGAGACAACTAGCAGGCCAGCGCTTTACCTCCAGAGAAAACTACCCATACTGCCTGGACTGTTTCAGCAATCTCTACGCCAAGAAATGCGTGGGCTGCACCAAGGCGATTACTAGTATGTTCTAATTTCTGACATCTGGTGGCTATTTTTACATGCCTCTAGATTAAAATTGAAAAATCTACCAGAATTCTACATGACTGTAAAACAACTATGTGTGTATGTTTGTGTCCAGGCTTGGCAGGTGCTAAATACATCTCGTTTGAGGAGCGCCAGTGGCACAGCGAGTGTTTCACGTGTATGCAGTGCTCAGTGTCTCTGGTGGGTCGTGGCTTCCTTACACAGCGGGACGACATACTGTGCACCGACTGTGGCAGAGAGAAATGAGCTCAGACGACCACAAGAGCCTCTACCAATATTGCAGGAGAG
Associated Phenotype:
Not determined