ZMP
si:dkey-121a11.10
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate laminin, alpha 3 (LAMA3) [Source:UniProtKB/TrEMBL;Acc:Q1LXE7]
Human Orthologue:
LAMA3
Human Description:
laminin, alpha 3 [Source:HGNC Symbol;Acc:6483]
Mouse Orthologue:
Lama3
Mouse Description:
laminin, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:99909]
Alleles
There are 15 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24130 | Essential Splice Site | Available for shipment | Available now |
sa11864 | Nonsense | Available for shipment | Available now |
sa15223 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24130
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062705 | Essential Splice Site | 160 | 1657 | 6 | 41 |
ENSDART00000126827 | Essential Splice Site | 165 | 1681 | 6 | 41 |
ENSDART00000130840 | Essential Splice Site | 179 | 1028 | 7 | 27 |
ENSDART00000135987 | None | None | 1263 | None | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 16619989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16371747 |
GRCz11 | 22 | 16398017 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATAGATTGTTATGAGGCTGATGACCCAGACACCGACAACTGCTTTGG[T/C]TTGTCATAACAGAAAAAAAACATGAATGTATGTATGGATGAACATTACTA
Long Flanking Sequence:
AAAGGTGTGATGCCAGCTTTTTTCTAAAGCAGAACTATATAGTTTAGTTTCAGGATGACTTTGTTGTTTATTTACTGAATATTTGTTTATTCATTTGTGCAGTTTTGCTGTTGGATGTCTCGGAGTTGGAGATGAGTTTGAATGTTTGTGTAAACCTGGCTACTCTGGAGTTCGATGTGAACGGTCTGTCTGCCTTTTGAAACATGGTCACATTTGGTTTCGATTGAATTAATGATTTAGGCAATTTAATTTAATTGAGTGTTTTCTCATTTACTCCACATTATAGGTGCGCGCTTGGATACTATGGCAGTCCTTTGGCAGAAAGAGGAAGTTGTCAACCATGTGACTGTGAACACGGTTACGTGTGTGACCCGTTAACAGGCGGTAAGCAAATTCTCATGATTTACATAATAATAGTAGTAATGATATTAATGAATCCATTTGTTTGTCTTTATAGATTGTTATGAGGCTGATGACCCAGACACCGACAACTGCTTTGG[T/C]TTGTCATAACAGAAAAAAAACATGAATGTATGTATGGATGAACATTACTATGATTGACTAACTCCAGTCTCTCTCCCATTAGACTGTGATATCTGTGTGGTTAAGTTAATGGATGATCTTGCAGCGATGGATGAGGAGTTTGCCAGACTGATTGATCAACTTGGGTCTTTTAGTCCGAATGCTACTTCATATACGGGACTTGAAAAACTTGAAGATGCCATTGCTGATACAAAGGTCCCTACAACAATTTTCCTAAACAATTATTTGGAATGGCTCTAATACACTGTTTATGTTTGTGCACAACTAAAAAAGAAATTCCACTTTCTTAGGTGTTGGTGCAGAAGTATACTGAATCTGTCTTCAAATTGAAACCAAAGATTTCAGAGCTTGAATCTCATCTCCAAAATGTCAAAGATGACCTAACTGCTCTCAATGACAAGGTACGATTACTATTCAGAAGGGTTTATCTTTATGTTGGCTGTAAAATAGATTTCAACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11864
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062705 | Nonsense | 836 | 1657 | 20 | 41 |
ENSDART00000126827 | Nonsense | 844 | 1681 | 21 | 41 |
ENSDART00000130840 | Nonsense | 859 | 1028 | 22 | 27 |
ENSDART00000135987 | Nonsense | 806 | 1263 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 16612848)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16364606 |
GRCz11 | 22 | 16390876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACCAAGTCCAGCAATGATAAAGCCTTTATGGATAGGGTGGMTTTCCGC[A/T]GGTAAACAACGTYTTAGTCATTGTAGATCCCCTGTTCTGTCGATTTGTCC
Long Flanking Sequence:
ATTACTGTTAATATCAGCCAATCATCAGTTGGGTCAGTTTCAGCTATCAGTATTGCTAGCAGCTAGAATTGTAATATGTGTGCATATATTACACATATTCAAGCTGTATATTGTAGGACAGGGGTGTCCAAACTCGGTCCAGGAGGGCCAGTGTCTTGGAGAGTTTAGCTTCAACTCTAATCAAACACACCCGAACCAGCTAATCACGCTCTTTCTAGATATACTAAAAACGTCCTAGCATGTGTGTGGAAGCAAGTTGAAGCAAAACTCTGCAGGGCACCAGCCCTCCAGGACCGATTTTGGACACCCCTGTTGTAGGGCATCATTTTATTTGTAGTTCTTTTGACCAACAGGAAGTCAAGGATTTCATTGGCCTGGTTGTAAGGAATGGTGTTCTTTTTTGCCTCTACAAACTGGGTGGCCAACTTCATGAAATAGAGACGAGTGAAATCACCAAGTCCAGCAATGATAAAGCCTTTATGGATAGGGTGGATTTCCGC[A/T]GGTAAACAACGTCTTAGTCATTGTAGATCCCCTGTTCTGTCGATTTGTCCTACCTTGTCAGATTGTCCTACCACCTTCCATTCAAAAAGTATTCAGTAAATTTTGATGCTACAAATCAGATTTGGCTACCAGTGTAAATTTTAATGTGGAGTAGTGTGATATGAAGCTGTAATAACACCCTAACCTACCCAATCCCTAACCCCAATCTCAAAACCATTTAAATACAGTGTTGGTAGCATATTCTGAGGGGTGGGATAAAATGTCAGGACACCCCCAAAGAGTTCATTTGGTTTTCTGAAAAATATTTTTTTTTCTCCTAAATTAGAGTTTATCAAGATGCACAAGTCATATACACACATACTTTCACTTCAACTGAACCCAACGAGCTGCCAGCAAGGATAAATCAGCCTAAAACCATGAATGGATTGCTCGATCTGGACCCCAATGATGTCGTTCTTTATGTTGGAGGATACCCAAGGGATTTTACGGTAAACAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15223
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062705 | Nonsense | 1434 | 1657 | 35 | 41 |
ENSDART00000126827 | Nonsense | 1457 | 1681 | 36 | 41 |
ENSDART00000130840 | None | None | 1028 | None | 27 |
ENSDART00000135987 | None | None | 1263 | None | 29 |
Genomic Location (Zv9):
Chromosome 22 (position 16607293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 16359050 |
GRCz11 | 22 | 16385320 |
KASP Assay ID:
2261-6652.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCGTTGAAAGGATTCACGCAGGAWTTGCAGTCTCCTGTCTATRTGGGA[C/T]AACTTCAGACTCGTCACCAAACATATGTATGAATGYTTAACGCCCTTTTT
Long Flanking Sequence:
AGCAAAATGCAGTTTGAATTAGATCCAGAGGAGCTCAATAACAGGTAAATTATGTTCATGACGTTTATTCTTAATTTTGCAGCACCTTTATGAGACCTTCTGCATCCTATAGGCCCCATTTCTCTCTAGACGTCCAGACCACATCATCTGAAGGACTTTTACTCCATCTCTCAGGGAAACATGGTGTTCCTCTTGTGGTCTTGTATTTATATGAAGGAAAAGTCAAACTTTCTGTTGGGGAAGATGAAATAGTTTCCTCTCGGAGGATCAATGATGGTCAATGGCACAGTGTATGTAGCAAACTCATATATATCTTAACCCAAACATATATATCTGCATAATCCCAAGTTTTGGTTCATGTTTTTGAAATATTGTGTTAACAGATCCAGTTCACGGTGAAGAAAAGATCGTCTCATCTTGCTGTGGATGACCTTCGAACACTCAATGGACAGCCGTTGAAAGGATTCACGCAGGATTTGCAGTCTCCTGTCTATGTGGGA[C/T]AACTTCAGACTCGTCACCAAACATATGTATGAATGCTTAACGCCCTTTTTTCAGGACACAGGTAAACCTCAAGTTTTGTAAACCTCTAAAAAGGCTTTTTTCCTCAGAAAAATGTCCCTCAGAAGAGTATAATCGGATGCATTCGTGAGCTCAGAGTTTCCAAGCTTCTCCTCATGAATCCAGCTGTCAATCAGGGAGCCACGCCCTGTTTTAAAGGCCGGACTGAGAAAGGGGCGTATTTTGCTGGAAATGGTGCACATTTAGTCTTAGGTATGGCTCTTCATTTTGGTACATTAGAGAATAGAGACAGAAAAATATGCTGAAGGAATTAAGAAATCTTTTTTTTTAACAGAAAAGTACTTTATCTCTGGTTCTACGTATGATTTAACTTTTGAACTTCGGCCAAGAAACCTCACCGGCCTCATCTTCCACAAAAGAGACAACCTTGGACAGACTGTCACACTATTTCTCAAGAAAGGAAAGGTGAGTGAAAATATGGT
Associated Phenotype:
Not determined