ZMP
lama4
Ensembl ID:
ZFIN ID:
Description:
laminin subunit alpha-4 [Source:RefSeq peptide;Acc:NP_001034154]
Human Orthologue:
LAMA4
Human Description:
laminin, alpha 4 [Source:HGNC Symbol;Acc:6484]
Mouse Orthologue:
Lama4
Mouse Description:
laminin, alpha 4 Gene [Source:MGI Symbol;Acc:MGI:109321]
Alleles
There are 12 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23614 | Nonsense | Available for shipment | Available now |
| sa32265 | Essential Splice Site | Available for shipment | Available now |
| sa15496 | Nonsense | Available for shipment | Available now |
| sa10261 | Nonsense | Available for shipment | Available now |
| sa15046 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23614
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 |
|---|---|---|---|---|---|
| ENSDART00000002661 | Nonsense | 438 | 1871 | 11 | 40 |
| ENSDART00000133785 | Nonsense | 303 | 374 | 7 | 8 |
| ENSDART00000138931 | None | None | 955 | None | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 251716)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 242311 |
| GRCz11 | 20 | 230946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGAATTTGGGAAACCAAGTGGATCAAGAGACACTGAACAGCTCCACA[C/T]GAGCAAAGACCCTCACTGCTAACCTGTCATCGCTCAATGTCCTCATTGAA
Long Flanking Sequence:
TCTGGTGTTTCGTAACATCTAATTTTTTTTGAGGTGGGTCATTAGCCCAACGCTCAACCCCCAACCTGGAGGACCAGGACTAACACAGATACACTGCAGACAATTAGGCCTACCCAATTCCCCTATCGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCTGAGGGCGACAGCGTGACCCACTGCACCACCGTGCCGCCATTCACAAATGTGTAATGAAAAAAAGAAAGCATAATCATGTCAGTGTGTTCACGTCACGACTCTTCAACTGCACCAGTGCTACAACAGCACGTTCTCATTCTGTGTTCACATGGAGTCTGCATTAACATGAACAGCTTCCCTTGTGTTCATTAGAGATGACACTGAAATGATGGTTATTTTGTTTTGTCAGGAGAATGAAGTGCAGAATTTGGGAAACCAAGTGGATCAAGAGACACTGAACAGCTCCACA[C/T]GAGCAAAGACCCTCACTGCTAACCTGTCATCGCTCAATGTCCTCATTGAAGGTATCGAGACCTTCTGACTCTGTATTTGTGTGTGATGCTGTGCTGGATTAAGTGAAGCATGTCTGTGGTACCTGGAGAAAGGGCTGCCTGGTAACTGATATGTATTTGATGTACCTGCTCAGATTTACCTCAGGATGTTTCTGCCAAACCTTCAACCGTTTGTAAAGCTTTATAGTCTATCTGTAATGCCCTCTTAAACAGAAACCAACGCTTGTGTGTGCATTTCAGATATGATCAGGGACTGGGAATTATACGGTGTCTATCAGGAGTTGGATCCTCAGGTGAAGTTGCAGAAACTGGCTGAAGCTGAACGGATCTTGGGCTGGATGAGAAAACTGAACCTGTCACCCAAAGAACCGCTTGCTACAGATGAGTCCTCCGAGGCGCATGAGTGTACGATTGTTTGATTTCGCTCATGTCTAACTGCATTATCTGTGTGCTTTCCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32265
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 |
|---|---|---|---|---|---|
| ENSDART00000002661 | Essential Splice Site | 741 | 1871 | 17 | 40 |
| ENSDART00000133785 | None | None | 374 | None | 8 |
| ENSDART00000138931 | None | None | 955 | None | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 255318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 245913 |
| GRCz11 | 20 | 234548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGCAAAAGTGTTGAATGAAGCATCGTCCCTACACTTTCAGCAGCAAG[G/A]TACAGCAGAGAGAGCTCTTTCCATGCTTTTCTACTGTTTGTTTTTCAGCA
Long Flanking Sequence:
GCCCTATGCACTCTGTCACACTTGCTGTGCCCGTGCCCTAAGATGCTTGAGCTCCTCCACCTTGGGTAAAGACTCTCCTACAACCTGGAGATGGCAAATCACCTTTTCCCACTCAGCAATGTGATCTCAGACATGGAGTTGCTGGATTTCATTCCTGCCACATCATAGACCACCCCAGTCTACATTATACCACAGCGCTAAATGACTAGCAGATTCATTTGAGTGTGGTACTCCAGAGTACTCCCAGAATATAGTGACATTTCACACGTCTGAGGTCACCTCAGTTAAGATAGAAACTGATTACTCTTTTTTTAATGTCCTGACTGCGTGAAATGATTTTTAAGAGTTTTTATAGAGCATTGTACTGTATCTCTGTTAATGTGCTCTCTTCCCATGTTTCTCTCAGGCGGTCGATAAGCTAAGCTCTCAGCTGAACCTCATGCGCTCTCAGAGTGCAAAAGTGTTGAATGAAGCATCGTCCCTACACTTTCAGCAGCAAG[G/A]TACAGCAGAGAGAGCTCTTTCCATGCTTTTCTACTGTTTGTTTTTCAGCATTTCCATATTAAATACATTAACATTACTTTTACTGTAAAAACTGCAACCCAAGCTCATTCTGAAAACGTAGCCCCGCGGACGTTTCTGGAGACCGCGATTTACGTGGCCGGAGGTAGGTATGGCCGCATTTGTTATGGGGCGGTGTGACGCCGCTCCTCTTCTTCGTACTCTCCGGCTGTGTCGGCTCACCTCCGTGTGGAGGGCTTTCCCGCCGCAACCAGTTTGTCCGCTTAGCTCGTAGTGTTATGTCGGCGGAGCGGAGGCCTGGAGGAGGAGGAGCCGGCCGCGGCATCAAACAGGTTCGACTCCGGGAAAGAGCGGTTCCCGAAATCAGGTAAGATGAAAAACAGAATCCAAAAAATAAAAGTGATGGAGTTCATGACGGGGCGAGAATGCGGCAAAATCTGAAAAACGTGGTCAAAATCGGACGAGGGCTTTTGCTTTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15496
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002661 | Nonsense | 795 | 1871 | 19 | 40 |
| ENSDART00000133785 | None | None | 374 | None | 8 |
| ENSDART00000138931 | None | None | 955 | None | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 258076)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 248671 |
| GRCz11 | 20 | 237306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTRAAGATCGTACCCCGAAGCGTCTGCAGTTCACTCAGGAAGTRGCT[G/T]AGGGCACTCTGAACCGCTCCGCTGAGGTGTTGGAGAAAGTGACTCCCATT
Long Flanking Sequence:
TCTTCTGGAGAAAGTCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTAAATTTTTTTAAACACCATTTTAGGCTCAATATTATTAGCTTCTTCAAGCTATACTTATATTTGATAGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTACATGTCACTGTAAGCTGAACACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGGCATCATGACAAAGAGAAAATAAATCAGTTATTAGAGATGAGTTATTAACACTATTATGATTAGAGATGTGTTGGAGAAATCTGCTCTCCGTTAAACAGAAACTGGGGGTAAAATAAACAGGGGGGTGAATAATTCTGACTTGAACTGAATACATGTATATGCACATTTTGTAGTGATTTTGCATGTCTCTGTTGAAGATCGTACCCCGAAGCGTCTGCAGTTCACTCAGGAAGTGGCT[G/T]AGGGCACTCTGAACCGCTCCGCTGAGGTGTTGGAGAAAGTGACTCCCATTCTGAAGAGAGTGGAGCAGTGGGACGGCAACATGAAGAGTGAAGCCTATTCTGCTGCAGCGTTCGACCGCACTGTTCTGTCTGCTGGCGAGGCGGGTACGGCGGATCGTCTAATTCCACACAGCTGAAAATAACACGTGCACTGGCTTCTGCTCATGCTGTTAGCTAGTTTCATAAAATGATTCAGAAACACCCAGCAACTGCTGCCTTCTTGCTTTGACTACAGCAGTTCTAGTTTTTAGACATTTTTAATTGTTGAATATTTATTAGATATTATAACACAAATAAGAAAAAAACAGGTAACACTTTAGTTTAGATCATAATTGAGCATTAACTAACACTGCTAGCTTAATAAACTACTAATTAGCTGCTTATTAATAGCAATACTACTACTAATACTACTATATATTGTTTTTTTAAAGTCGTTTGGCTTCAAAATAGATCATAAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10261
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 |
|---|---|---|---|---|---|
| ENSDART00000002661 | Nonsense | 1105 | 1871 | 25 | 40 |
| ENSDART00000133785 | None | None | 374 | None | 8 |
| ENSDART00000138931 | Nonsense | 216 | 955 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 264363)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 254958 |
| GRCz11 | 20 | 243593 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTTTTCMGGCACAAGCTGGCTTTCTCTCAGAGTCGTGTCACCAGTTA[T/A]TTGTTTGACGGCACCGGCTACGCTTTAGTCAACAACATTGAGAGGCGAGG
Long Flanking Sequence:
GGCCCTATCATAAACATATGGGCCCTATCATAAACATATGGGCCATATCAAACCCCCGGCGCAATAAGGGGCAAGACGTGTTTAGTGTGTTTTTGTTTTAGAGCAGCGCAATAGTTATTTTGACATTTCCGGCACGTTGTTTACGTCCTTAACAGCGCTCAAATGTTATTAGGAAATGTACGTTTGTGAAATTTCAGTATTGATTAGTACCAAATTCCAGTGTTGTGACAATCCTACTACTGACTAAAGTGTCCTCAAACTACCAAAATGTGTGTCTAACAACTGTTTCAATGTGATCGTGAAGTGTGAATGCTTGGTTATGATCAACTCTTTTTCATGGTTTGTCTGTGCTTGTAAAGATCTGTATTTATATGATCAGTCCTGCTTTATTATGTGTTGTGTGGCTTTTTATTTCCACATGCTGTGTGTGTTTAAGAATGACAATCTCTCTGTGTTTTCAGGCACAAGCTGGCTTTCTCTCAGAGTCGTGTCACCAGTTA[T/A]TTGTTTGACGGCACCGGCTACGCTTTAGTCAACAACATTGAGAGGCGAGGAAAGATTGGCGTCGTCACTCGATTTGATATTGAAGTTCGAACTGTTGCTAACAACGGCATCCTCTTCCTCATGGTGAATGAGGTAAATGTAGATTCATTCCAAAGGTTTTCCTTTGTTTATATTCTTGCATTCTAGCACAAAACAAACATGTAATTCTGAAGATAATTCTTAAAACATTAGTAAAAAACTTAAAACATCATACATTTGAATCTCAAAGTAAAGTGTGTCAGTGTCTCAGTGGTCAGCATTGTGGCCTCACAGCAGGAAGGTCACTGGTTCATGAAACTGTAAATGAAAGACTGCAACTTAGAACAACACATACACAGAAACCCCTGGATATCATTTAAGATTGCTTAAAAAGGGCTTTATACTTTTGTCATGTGCATACTGTAAATATATGAGCAATATCACATGAGTAGCAGTGCGATATGGCATGTATATTGACACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15046
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 |
|---|---|---|---|---|---|
| ENSDART00000002661 | Essential Splice Site | 1193 | 1871 | 26 | 40 |
| ENSDART00000133785 | None | None | 374 | None | 8 |
| ENSDART00000138931 | Essential Splice Site | 304 | 955 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 266259)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 256854 |
| GRCz11 | 20 | 245489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGAGACTAACTTAGCCAAACTGCAGATCAATGACGCTCGCTATCACGAG[G/A]TAATGTTTTCCAGCAGTACATCACGTTATATCTTTAAACACAGCGTGGAC
Long Flanking Sequence:
GCTCAGTTGGGGTTTTTGTGTGGAGTTTGCATGTTCTCCCTGCATTCGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCAGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTATGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCCTAAAACCTTGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAATGAATATATATATATATATATACGCATTTTCCTAAATGAATGTGCAAAATAAATAAATGTATGCATTTGTGTTGGACTTTTGCAGACCAATTTCTTTGTGCTGGAGCTGAAAAATGGCTTTCTCCGTCTGATGTACGACTTTGGTTTCGCTAACGGTCCTGTCATCATAGAGACTAACTTAGCCAAACTGCAGATCAATGACGCTCGCTATCACGAG[G/A]TAATGTTTTCCAGCAGTACATCACGTTATATCTTTAAACACAGCGTGGACACTCTTTGTAACACCCTGTCATTTTCCCCTCAGGTGTCTGTGATCTATCATCATTCAAAGAAGATCATTTTGTTGGTGGACAGAAGCCATGTCAAGTCCTTTGAAAGTGAAAAGAAACCCCTACCCTTTTCTGATATCTATATAGGAGGAGCTCCTTCGAGAATTCTGCAGTCTAGGTAAGATCATATGCTCCAAATAAAGCGCAGAGAAATCAACTACCATTACTGATTTCTTACTTTTAACCAAGATAATTGGATGTCCAACAGGCCAGAGCTGACATCCTTGATTGGATTGAAGGGTTGTGTAAAAGGCTTCCAGTTCCAGAAAAAGGATTTCAACCTCTTGGAGGAGCAAGGAACCATTGGTATCAGCAGCGGCTGTCCTGAGGAATCGTTTGTAAGTTGCACACCTTCATGATGGCAGTGCTGATTATTTGATTACCCAGCAATT
Associated Phenotype:
Not determined