ZMP
LAMA1
Ensembl ID:
Description:
laminin, alpha 1 [Source:HGNC Symbol;Acc:6481]
Human Orthologue:
LAMA1
Human Description:
laminin, alpha 1 [Source:HGNC Symbol;Acc:6481]
Mouse Orthologue:
Lama1
Mouse Description:
laminin, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:99892]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13584 | Essential Splice Site | Available for shipment | Available now |
sa17699 | Nonsense | Available for shipment | Available now |
sa10397 | Nonsense | Available for shipment | Available now |
sa44203 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24576 | Nonsense | Available for shipment | Available now |
sa44204 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37969 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13584
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 |
---|---|---|---|---|---|
ENSDART00000078414 | Essential Splice Site | 293 | 2660 | 6 | 67 |
ENSDART00000108598 | Essential Splice Site | 293 | 2680 | 6 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43476115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41815541 |
GRCz11 | 24 | 41715594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCTGCTATGGCCACGCCCAGAGCTGCCCCTGGGACCCTGTTACCAAG[G/A]TAACCGTYAACACATTGKAGCTGAAGCTGCCAATCAAACTATAGTGTGCC
Long Flanking Sequence:
AGCCGTCTGTCCATTAGCCATTAGAGTGTTTGAGCTGCTGAAGATGATGTCAGCATAGACTAAGAGCATTATAGATGTGGAGTTCTAGATATATTTTCATTTAATATTCTGCATTAATATTTAATACCTTTCTTTAAATAAATTGGAACTATACCTAAATTCAATTTCAATGATTAGTGATAAGAAAGCTGTTCAAACTTATCGAAGTTGTGCTGTGTGCTTAATATTTTTAATATTTCATGTGTGTTTCTTTGTTTTTTTCTAATCTCTTTCTTACTATACTCAATTTAATTTCTTACTATAGTTCAGTTTAGTTATTAATTTCTTAATTGTAAAATTATTTTAGGGGGTTACGATAGTGTATATTAATATCTTCTGAATGAATAACTGTATTATGGTCTGTTTTTCAGTATTATTACTCCATCAAGGACATCTCAGTGGGCGGGATGTGCATCTGCTATGGCCACGCCCAGAGCTGCCCCTGGGACCCTGTTACCAAG[G/A]TAACCGTCAACACATTGGAGCTGAAGCTGCCAATCAAACTATAGTGTGCCATTAGCCCCGCCTCTCTAAACAAACAAATACATTAATGAAGTATAAATACAAAATAATCTTTGGTAACAAGTTTAAAGGGTCGCGAAACACCCAAACACATTTTTGACATGTTGACAGTCATATATATATATCTGTGTCTCACGATGCTAAAAACAAAAAAGTGAAAATTGGTTGTTTTTGGGTTATTTCGAGCAAATTTATTCTTCTGGTTTGAAAATGAATGTTGAAGCTGTGTCAGAGTGATTAGATCCTTGTGTGTGTATTCCAGCGTGGAGACTGGATGTCAGTACAGGCAAGTACTACGTGACGTCTTTGAGACTTCATTATTAATTCATGACAAAGACTTGGTTTGAACCAATCAGCGTGCTCTATTGTGAATGAGGCAACCCAACCTCATTCTGGAAACGTAGCCCCGCGGACGTTTCTGGAGACCGCGATTTACGTGGGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17699
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 |
---|---|---|---|---|---|
ENSDART00000078414 | Nonsense | 436 | 2660 | 10 | 67 |
ENSDART00000108598 | Nonsense | 436 | 2680 | 10 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43481786)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41821212 |
GRCz11 | 24 | 41721265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGATGTTGTTTGTGTCGTGCAGGTCTGTCTCCAGGTCAGTGTGTGTG[T/A]AAGGAGGGTTTTGCGGGAGAGAAGTGTGACCGMTGTGCGTTCGGCTTCAG
Long Flanking Sequence:
CCAAAACTTACCCCTGTCAGATTTAGGTGGGGGAATAATAATAATCTTCATCATCATTAATAAAAAATATGAAATCTAAACACCAAACACCAATCGCACAACTTCTGTTCAACAGCTCCATTTATCACAAAGCCTCACACATATTACAAAACTCAGTAATTTTCAGAGGTTACATATCTGAGCTTTTCAGGATGTTCAAGATGGCTTTCAGCTCCAGAAGTGCTGGATTCAGCTGCTCATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGGTGTCTCCGTATGCAGAAGAGCCGTGTGTGGAGTGTCAGTGTGATATGAGGGGTTCAGTGAGTCCTGTGTGCATCAGAGATGATAATCACGCAAACCCAGACGCAGGTAGAGTATCGCCATCTGTTTCTGCAGATTCAGCATGAGTGTGTGTGTGCAGTGTGTGATGTTGTTTGTGTCGTGCAGGTCTGTCTCCAGGTCAGTGTGTGTG[T/A]AAGGAGGGTTTTGCGGGAGAGAAGTGTGACCGCTGTGCGTTCGGCTTCAGAGATTTCCCGGTGTGTTCTCGCTGCGAGTGTAGCCTGGATGGGAGCCACAACACCGATCCCTGTATGGAGTGTGTGTGCAAGGTACTAAAACACACACACACACGCACACACACACACACACGTCACTCACAGGGTTGGGTAATAAACTTTAAAAAAAAAAAACTTTTTAAAAGTTTTTTGTTTTGATTTTGTTTTGTTTTATTTTATTTTGTGTATTTTTGTTTTGTTTTTGTGTTTTTCTTTTGTTTTGTTTAGTTTTTTTTGTTTTGTTTTTGTTTAGTTTTTTGTTTTGTTTTTGTGTTTTTTTTTTTTTTTTTGCTTAGTTTCTGTTTAGTGTTTTTTGTTGTTTTTTGTTTTGTTATGGATTTTAAAAATTTAGATTTTGTGTTTTTTTGTTTAGTTTTTTGTTTAGTTTATTTTTTGGGTTTTATGTTTTCTCTTTTGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10397
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 |
---|---|---|---|---|---|
ENSDART00000078414 | Nonsense | 675 | 2660 | 14 | 67 |
ENSDART00000108598 | Nonsense | 675 | 2680 | 14 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43487513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41826795 |
GRCz11 | 24 | 41726848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGAGACGAGCTGATGACRGTGCTGGCGGACGTTGCTGCGCTCAGGGTT[C/T]GAGCCGAGCTGGARGACAGCGCTGAGGGAACGCTCAGGTCAGACACATGC
Long Flanking Sequence:
GGGCGGGGCTTTCCCCCTCTGATGACATGTACAAAGGGAGAATGTCAATCAAAGTGTTTCATTCATCAAGTCTGATTATATCAAACACAATTAATACATGTTGAGGCTGTTGGAGATATTCACACACTGCTCACACACACACAACTTGGGTTAAACATCACATAAATGTGACTTCTGCATTATAAAATAGTACTTAATTGTGTTTATATCACTATAATGTGGCTGTGTACACACAACAAACAGCTATCCAAATGTTGGTTTTGCATAATAGGAGCCCTATAATATCATGTGTGTGTGACTGAGTGTGAATGTGTGTGTTACAGGGTAACGGGCGCACGCTGAGGCAGGCGCAGTCGGCTCGTCTGCTGCTGAACGCTCACACACACCAGCGTGTGTTTGTGCAGATGCTTCCGCAGATCTTCATAGACTCACACAGCGGCAGGAGCGTGCAGAGAGACGAGCTGATGACGGTGCTGGCGGACGTTGCTGCGCTCAGGGTT[C/T]GAGCCGAGCTGGAGGACAGCGCTGAGGGAACGCTCAGGTCAGACACATGCAGAACATATCCTGATGAATGCTTGACTCTGATTGGCTGATGATAGACAATACAGTCTGTACACTATAAAAACAATGGAAACCTATGGAAGGTCCCGACAATTCACAAAAACAAACCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCGTCCACAGGTTGAGTCACGTGTCTTTAGGTGTTGGAGACTCAAACTCCGATGTGTCTAAAATCTCTCTAGATGTGGAGCACTGTGAGTGTCCGTGGGGGTATTCAGGCACTTCCTGTGAGGTAACAAACCACTTCCAGGTCACTTCATCAGTATTTTGCTGTATCCCAATTCGCATGCTGTCCATTTTAAATATTCAAGAGTTCACACTTAGCTGATGATTGATTATAAAGCTTGTTTGGCATGCTGTCCCGGGAGAGAGCCCTGAGCTCATGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44203
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078414 | Nonsense | 1017 | 2660 | 23 | 67 |
ENSDART00000108598 | Nonsense | 1017 | 2680 | 23 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43498099)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41837438 |
GRCz11 | 24 | 41737491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCACACACTCATGGGAACTGCAACGATCAGACGGGCGAGTGTATCTG[T/A]CCTCCACACACACACGGGCTGAAGTGTGAACAGTGTGATGAAGGTCACTG
Long Flanking Sequence:
GGTCGGAAAAACCTGCGACCGCTGCCAGGTATGACAACTCGTGTGCTGCACATAAAACATTACAGTGTGTCATAATTCTCCTATTGTAGTTCTGCTTTAGAAAGAGCCTTACAGTTGCGTGTGTGTGTGTGTGTGTGTGTGTTTCAGGAGGGTTATCACGGTATTAACAGTGGTGAAGGCTGCAGACCGTGTGAATGTAACCAATCAGGCGCTCTGTCTGCGTCATGTGATGAGGAGGGGCGGTGCCAGTGCATAACTGGGGTAACGGGTGACAAATGTGATCGATGTCACCATGGATACTACAACTTCAAAGAGAACGGATGCACAGGTAACACATGCGCTATAGGGGAACTGATCAACTAAATTGGCCTTAGGATAGTCTAAATAAGAATGACTCTGTACTGTCCAATGAGTGCTCAAAGCTGATTTATTGATCCTCCAGCATGCGACTGCGCACACACTCATGGGAACTGCAACGATCAGACGGGCGAGTGTATCTG[T/A]CCTCCACACACACACGGGCTGAAGTGTGAACAGTGTGATGAAGGTCACTGGGGTCACGACGGAGTGTCCGGCTGTAAGGTACGACTCTACAAAGCCATGTGTGTGTTTGATCATGTGTGTGTGTGATCATATATGTGTGTGTGCCATCATGTGTGTGTGCGTGTGTGGGTGTGTTTGTGTGTGTGTGTGTGATAATGTGTGTTTGATCGTGTGTGTGTGTTTGTGTGTGTGTGATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCTCTAAGATGCAGTGTGTAATTGATGATTAATGCTGATGTTGTGCTCAGGATAATGTGGGCGGCAGAGGCTGTGACGAGTGTAAGAGCGGCTCCTTCGGGCTCTCGGCCCTCAATCCGGCCGGCTGCAGCCCCTGCTTCTGCTTTGGCCTTTCAGACGTGTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24576
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078414 | Nonsense | 1203 | 2660 | 27 | 67 |
ENSDART00000108598 | Nonsense | 1203 | 2680 | 27 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43500489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41840825 |
GRCz11 | 24 | 41740878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTCTCTCTCCTCACCGGACCGTATTACTGGAGACTCCCACAGAAATA[C/A]AACGGCAACAAGGTACAAATACACAACACACCCACAGAAACACCAGGGTA
Long Flanking Sequence:
TACATATGTCAAAATAGTAACATCCTAAATTAAATGCAAACAATTCACATTTATTTATAGCATGCATAAAAACAGTTATATAAATACACATCTCAAAATAGTAACATTTTAAATGCAAACCATATACATTTATTAATAATATGCAAAAAAAGTTTATTCTTAAATGCACATCTCAAAAGAGTAAAATGAAAAATAGATGCAAACAATATGCATATACATGCATGCATATTGTAATAATTATAAAAACTACTATAAAAATGATGTTGCTGAATGAATCGTGTGTGTATTTGACTAGTAATAATCATCTATTAATCGTGTGTGTGTGTTCAGATTGTTCTGGGTTCATCTCCGGCTCTGCTGCGTGTAGTGTCTCAGAGTGACCTGCAGGGGACGCTGGAGGGCGTTTATTACAGCGATGACGAGATGCTGCTGGACGTGGATCAGCTCAACAAACTCTCTCTCCTCACCGGACCGTATTACTGGAGACTCCCACAGAAATA[C/A]AACGGCAACAAGGTACAAATACACAACACACCCACAGAAACACCAGGGTACAACACCATAGATATACCATGGTAGTACAGTTTGCAGAAACAGAGACAGAGAGGGCCAATAGTATCTGGGTGCAGACTTGGGTTTGTGAGCTGAGACTGTGTATCTCAGATTTGCTATTAGAGCTTAGAGATCCCAAAAATTAAACCTAACCCTATCCGAGCCCGTGCACCCCATGCCCAAGCCCGACCCAGTCTCAGACATTAACTGTAATTAAGAATTAAAAATTAAAACAGATGTTCTCAGCTACAATTCTGAGTCATTTGAACTGCAAACATGAATTTAAGGGTGACAAATAAGGACATTGAAGGCTGACTATCATCCTGTCTGCATACCTGTCAACCCTCCCATGTTTGCAGGGATTCTATCCTGTTATCATCCTGTTTTCAAGAGTTCACACTTAGCTAATCAATAATCAGATAATTGATAATCAGCTAGATAATCAATAGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44204
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078414 | Essential Splice Site | 2300 | 2660 | 57 | 67 |
ENSDART00000108598 | Essential Splice Site | 2302 | 2680 | 55 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43534657)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41881892 |
GRCz11 | 24 | 41781945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTGTGTGTGTTTTCCTGCAGTGAAAGAGGGCTATAATGTGGGCTCA[G/T]ACGTGACGGTGAGTCTGGAGTTCCGCTCCACGGCGCCGGATGGTGTTTTA
Long Flanking Sequence:
GTGCTGTTTTTTAGCTATATTTATACTAATATGTANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAATTAAGCAGATCAATCTTATATTACTGATAAATAACATATGCATATTAATCAGGGCGGTAAAATACATATTTATTAAACAATCCAGTTTACACAATAGACACTTCTTGATTCTGTAATCGTATTACTTTTCACAAATAGATCATCATAGAAAATCAGCAGCTGACCTATCTAAATTAACAGGGGTAAAATTACATACCTCTGTTCATTGAATGGAGACAGTACACTTTATAGACAGTAAACTAATGAAAGAAGAGAATTAGACATGCCGTGCTTTCATTCAAAATAAGAGTGCTTTCAGATCTTGAATGTGTGTGTGTGTGTGTGTGTTTTCCTGCAGTGAAAGAGGGCTATAATGTGGGCTCA[G/T]ACGTGACGGTGAGTCTGGAGTTCCGCTCCACGGCGCCGGATGGTGTTTTATTAGGAATCAGCAGCACTAAAGTGGACGCCATCGGCCTGGAGCTGCTCAACGGACAGGTCAGTGTTCGCTCTACAGTGTCCAATAAACAGCGTTCCCACCACGGGTCATTCATTTCTGGAGGTTTAAAAGGTTTTTCCACACATTGAAAGTCAGGAAATTTGTGTTTTTATTTTTATTATTAATTGTCATTTTACATTTTTGTTTGTCGCATTAAATTTTAGTTTCCATTTATCAAAATGCGATTTTTTTCTAAAAACGTAAAGTAGATCCAGCAGGTTTTTATCTCAGAATTAAGTTTATCAGCCCGATTATCAGTATTAATAAAAATTAATGGGCATGATCAATAAACACACATTGATGGTGTTGAATAACGTGTTTCTCCTCATCTCAGGTGGTGTTTAATGTGAATAACGGTGCGGGCCGCATCTCGGTGAGCAGCAGGAGCAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37969
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:
C > A
Consequence:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078414 | Nonsense | 2647 | 2660 | 66 | 67 |
ENSDART00000108598 | Missense | 2650 | 2680 | 63 | 63 |
Genomic Location (Zv9):
Chromosome 24 (position 43542645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41873695 |
GRCz11 | 24 | 41773748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATATGGACAGCTGTTTGCTGGAGCCGCGGCCCAGACGAGTACTGCTG[C/A]CTGATGACCCGGAGCCGACCTCTGACCCCGACACACGACCTCTGACCCCT
Long Flanking Sequence:
TCTACATCGGCGGCGTTCCTCCAACAGAGGGAGACACACACACACTCACACCTGCCTTCTACGGCTGCATCAGGAACACTGCGGTCGACGGCATGTGAGTCTCACACACACACATACACACACACACAGAGACACACTTACAGTCATGCACACTTACATTCTAAGACACACACACACACATACACACATATAGAGACACACATTATCACATACACATACATAGAGACACACACACACACATTTAGAGACTAAACCATGTATGCAGGTGTGCGTGTGTGTGTGTATGGTATCATTACATCTGAGCAGCTGATGTGTCTACTATTGTAAAAGAGTTGTGGGTCTGTGATGTTCTGCTGGTCTCCAACTTTTATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGGTTGTTGGATCTGTCCGCTGCGCTGCGCTACGAGCAGGTGGATATGGACAGCTGTTTGCTGGAGCCGCGGCCCAGACGAGTACTGCTG[C/A]CTGATGACCCGGAGCCGACCTCTGACCCCGACACACGACCTCTGACCCCTGCAGCAGCGGAGCTGAGTGCGCTCACACCAAACAGCGGCAGCGTGAGTCTCACACACAACACAAATGATCTATCAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATTTATCCATCATCCATCCATCCATCCATCCATCCTTCCATCCATCCATCCATCATCCATCCATCCTTCCATCCATTTATCCATCCATTTATCCATCCATCCATCCATCCATTTATCCATCATCCATCCATCCATCCATCCATCCTTCCATCCATCCATCCATCATCCATCCATCCTTCCATCCATTTATCCATCCATTTATCCATCCATCCATCCATCCATTTATTCATCCATCCATTCAACCATTTATCCTTCCATCCATCCATCTATTTATCCATCCATCCATA
Associated Phenotype:
Not determined