ZMP
si:ch211-241e1.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8DZG5]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19647 | Essential Splice Site | Available for shipment | Available now |
sa13307 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19647
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 |
---|---|---|---|---|---|
ENSDART00000058281 | Essential Splice Site | 644 | 1368 | 15 | 31 |
ENSDART00000140540 | Essential Splice Site | 623 | 1347 | 15 | 31 |
The following transcripts of ENSDARG00000022615 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 1149327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1095148 |
GRCz11 | 2 | 965556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTAAGTGCTTACACATTTGTATTTCTTTTTTTGTTCTGTTGTTTCA[G/A]GATGTCAGTCAAGGGGATTTAATCAACAGAGCACAAGATCTGAAAACCAA
Long Flanking Sequence:
TAAATACAGTGCATCCCGAAAGTATTGATAGGGGAATACGGGAAAATACCTTTACAGGATGATAGCGGGATAGAACAGTAAAATACGGGAGAATCCCGGGAAAAACAAGAGGGTTTGCAATGATTTCAAAAACTCTTTTTTCCTCATTGTCATTATGGGAGATTGTGTGTAGAATGTTGTGGAAATAAATTAATGTAATCCATTTTGGAATAAGGCTGTAACAAAAACAAACGTGGAAAAAGTCAAGCACTATCAATAATTTTCGGATGCACTGTATGTTTTTGGGAGTAGGTGATCGGGTAAGGTGACAAAGTGAGACGTGGTTCCGCTGCTGAACCCGTGTTGACATGTTAACTCCATGTATAAGCATTGCATTGATGCAAAGCACACGTTGAATGTACCTGCCGTGTTTGTAAGTGCTTTGAGTATTAAATAATCCTCTTGCACCAGTGTGTTAAGTGCTTACACATTTGTATTTCTTTTTTTGTTCTGTTGTTTCA[G/A]GATGTCAGTCAAGGGGATTTAATCAACAGAGCACAAGATCTGAAAACCAATGGCAGTAACCTGCTTAAAACTGCCAAAAACACAGCCAAAGATCTTAAAGGTGATGTCAACAACATGTACACTGCAAAAAATGCTTGCTTACTTAGAGATTTTGCCTTGTTTGTAGTCTAAATATCTACACATGATGAAATCAAGCAGCATTATCTAGACCAGAGTAAAATATTGTCTTGTTTTCAGAAAGAATGCATCAAAATTAAGTAGTTTTTGTTCTTAAAACAAGCGAAATAAGCTTGTTTTCACTTTGAAATAGAATTATTTTGCTTGCATTATGTCTTAAAGCAAGACTATATTTAGTGCTTGTCCAGAAAATGCTTCTTGATTTATGAATATTCAGATATTTGGACTGGAAACAAGACAAAAGTTCAGATGCAAAACCTGAGCTGTATTTTATCGTCAGTCATTTATAGTTTCTCACTGTGGTTTCACCTTCACCAGGAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13307
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058281 | Nonsense | 1156 | 1368 | 25 | 31 |
ENSDART00000140540 | Nonsense | 1135 | 1347 | 25 | 31 |
The following transcripts of ENSDARG00000022615 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 1136536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 1082357 |
GRCz11 | 2 | 952765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGACCACCGAAGTCAAAAGGGACGTCAATATTCCAAGGAAATTCCTTTA[T/G]TACTACATCGGTGGAATTCCCAGCATTTTGCGTGAGAGRTTTGTATCTTG
Long Flanking Sequence:
TGGCTACGCTAAAGTCCTGCTGGAAAGATTCCCCTCCAATCTGCAGCTCGTGCAGAGAGTGGAAACCCGAGCCAAAGATGCTCTACTGCTGTATTTAGGAGACAAGGATGATGTAAAAATCTGTTTACACCTATTAATTATTATTCTCTTGTGTCCTTTACACACATCACATCACTGTACTCCTTCAACAGGACTTCTACTACAGTGCGTCTCTTGAAGGCGGTTATCTAGTTCTACGAGGACAAGAGAAGGATACCATTTTGGAGCCCATCAGAAGTAACGAACAACCAGTTCTTTCTCCGGTAAGGAAGAAAATGATGCTGACTTTTACTTAAGGATTCTGCACACAGTCATGGAGGTGGAAAATTAATCGACTTTTTTCTCTTCTGCATTAAGGGAATAGACGTGAGACTCATTCTTGTTAATCGAAAAAATCTAAGGGTAATAATAGGGACCACCGAAGTCAAAAGGGACGTCAATATTCCAAGGAAATTCCTTTA[T/G]TACTACATCGGTGGAATTCCCAGCATTTTGCGTGAGAGGTTTGTATCTTGGTGGCTTCCCTTTAGGATGTATATATTTTCTAAACACTCGCATTATGGTTTATTACAACCCTTGCTCATGGGAAATAAGTTCTTCAGCACAACATGTTTTGTAAACCTAAGATACATTGCTCCGGGTACATTGTGTTGTACGTGTCAGATAACAAATCCACTAGAGGGCAGTGTCGCATTTTTGTGAATCTGAAACATGCAGTTAGGTTATGTTTTGTTGTACATTTCAGATGACAAATCCACTAGAGGGCGCTGTCTACATTATCGTGAAACTAAAATACATGACTTTCAGGCCGCTTCATTGCACGTTTTAGATGACAAGTCCACTAGAGGGCGCTGTCTACATTCTTTCGAATATGAAATTGTCATGAAATTGTTCTTTCGAACACTTAAATGATGGTTTATTACAATTCAGGCTGATTGGAAATATATGCCTTAGCCTACATTCAT
Associated Phenotype:
Not determined