ZMP
ablim3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate actin binding LIM protein family, member 3 (ABLIM3, zgc:158673)
Human Orthologue:
ABLIM3
Human Description:
actin binding LIM protein family, member 3 [Source:HGNC Symbol;Acc:29132]
Mouse Orthologue:
Ablim3
Mouse Description:
actin binding LIM protein family, member 3 Gene [Source:MGI Symbol;Acc:MGI:2442582]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa306 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa184 | Nonsense | Confirmed mutation in F2 line | Not yet available |
Mutation Details
Allele Name:
sa306
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125109 | None | None | 183 | None | 5 |
| ENSDART00000141157 | Nonsense | 177 | 681 | 4 | 22 |
| ENSDART00000147084 | None | None | 132 | None | 6 |
The following transcripts of ENSDARG00000088168 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 35826693)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 34355919 |
| GRCz11 | 14 | 34696233 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATCTCTGCTGGCGTTGGAGAAGCAGTGGCACGTCAGCTGCTTCAGGTG[T/A]CAGACCTGCGGCCTCGTCCTGACCGGAGAGTATATCAGCAAGTGAGTCCT
Long Flanking Sequence:
TCACCTTTCTTCCCTATTCTGATGCTCAGTTTGAAATGCTGCAGATCGTCTTGACCATGTCTACATGCCTAAATGCATTGAGTTGCTGCCATGTAATTGGCTGATTAGAAACTTGCATTAATGAGCAGTTGGACAGGTGGACCTAATAAAATAGCCGGTGAGTGTAATATTGCAGAACGACTTGTCACATGTTTTTGCTGTTTGCTAACAGTAATTTCTTAATTCTATTATTCGAATAATGCCACATCATTGCACCCATTTTTTTTTAACATTACACTGATTAAATGATAGTTACTCTCACATTGGAGCAGGAAAAAAGTTAATAAATATATCAAGGCTGACTGGATGCTGGAAAGACTTTTGAACCTTAAGTCCATTATATAAGCTTTCTTCCCTTCCCCATGGCTCTTTTTAGACTGTGCAGGTTGTAAGGAGGAGATCAAACAGGGTCAATCTCTGCTGGCGTTGGAGAAGCAGTGGCACGTCAGCTGCTTCAGGTG[T/A]CAGACCTGCGGCCTCGTCCTGACCGGAGAGTATATCAGCAAGTGAGTCCTTCTGTTCACCTGACCTGCTTCTTTCTTTCAGACACACGTCACACTCACACACATTGTTCAAAGCGGCCTGTTTCTCATGTTGGAGCTTGCATTAAATTACTTAATTGCTTCATTTTATGACTATTGAAAAAAATTGGTTTAATTCAGGGTAATTGGTATTTTATTTATTTTCAGTCATTGCACATTCAGTTCCAGAAATACAGTACTTGACCTGTATTTAATGGGTGGATGGTTAGATAAATTTGCATTGGAATATTACACTGTTTATATACAATCTTTCAAATATCAAGTGACATTAACCCTGGAGAATTGGCTGATAAAGTTTCTCTTTTACCCTCACAGGAAATAAATGACATTATAAAAAATTTATAAATCAGAAAATTTTCATGGTGTTTCACAGAGTTGCTGTTTTACTGCATTTTTAAAAAAAAAATACAGCCTCTGTAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa184
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000125109 | Nonsense | 31 | 183 | 1 | 5 |
| ENSDART00000141157 | Nonsense | 328 | 681 | 9 | 22 |
| ENSDART00000147084 | None | None | 132 | None | 6 |
The following transcripts of ENSDARG00000088168 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 35805829)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 34336507 |
| GRCz11 | 14 | 34676821 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTAAGGTTAAAGCCATTTATGAAGTGCAGAGGCCAGACTACTGGTCCTA[T/A]GAGTCGAGTCACAGATACTGCTCCGATGACAGGCTAGAGCGCCTCAGCTA
Long Flanking Sequence:
ATCCAGACCTCTAGTTTGGACTGAAACCTGGCAGGAGCGGGATTAAAAATGTAGTCTCGTGCAGATCTCTAGTCTGGCATAGTTCAGTTCACCCAAATATGAATATACACTGGATCATTTCATTACATGACTTTCTTTGCTCTGCTTAACACAAAACAAAATATTTTGAGGATCATTTAAACTGTATAATGCAAAATGAAACTCAATGGGGACCTGACATTTTACACCATTAATGTGCTTCACAGTTTCAATCACATTGTTCCAGCAAACGTGCCTCCAGCTCATCCTGTGTTGTTGACATTGTCATCGGCTGTCACCATTGCTGTTTTTTGCAGTCCTGCTCATGGCGTTTGATGTGTGTCTGAGTGAGTGTGTGTATCTGTCCTGTGTCCTTCTCCTCAGGCAAAAATGGACAACGAGATCCTTGATTACAAAGACTTGGCAGCGCTGCCTAAGGTTAAAGCCATTTATGAAGTGCAGAGGCCAGACTACTGGTCCTA[T/A]GAGTCGAGTCACAGATACTGCTCCGATGACAGGCTAGAGCGCCTCAGCTATGGGGAGGTACAGGACCACTAGAGCCCCATCGCGTCCACTCTTAGCATGTCTCCCCTCTGTTGCTGAATGACCTGGTCTTAGCTGAGCTTAGCATAGCTTTTTGTCTGTGTTTTTTCATCTATGTCGCATTTGTTGGCTGGCTGTGTGGCTATGTTTGTGCATTTCTCCAACTGCTAAAAGTCAGTTAGCTCATTTCCACTGCATGGTGTGGCTCAGTACAGTTCAGTGTGACTCGTTTTTTTATGGGGATTCTACTTTGTGCTCTATCTGGTGTGTGCATTGTAAAAATAATGTAATGACAACAAATATATTTAGGTTTCTTTCTATTTTAATAAGTTAACCAGGTTTCAAGCTAAATCTTTGAGTTATACAAACTTTAACTTAATATTTTTGAGTGGTGTAAGTTGAGATGACAGGGAGCAAGATATTTTTCAGTGTGGTTTCGAAGT
Associated Phenotype:
Not determined