ZMP
lamb4
Ensembl ID:
ZFIN IDs:
Description:
Laminin subunit beta-4 [Source:UniProtKB/Swiss-Prot;Acc:Q8JHV6]
Human Orthologue:
LAMB4
Human Description:
laminin, beta 4 [Source:HGNC Symbol;Acc:6491]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6002 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30287 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9508 | Nonsense | Available for shipment | Available now |
sa24711 | Nonsense | Available for shipment | Available now |
sa6808 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18559 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6002
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058400 | Nonsense | 458 | 1827 | 11 | 35 |
ENSDART00000123330 | Nonsense | 458 | 1827 | 11 | 34 |
Genomic Location (Zv9):
Chromosome 25 (position 32653180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31264349 |
GRCz11 | 25 | 31675310 |
KASP Assay ID:
554-3915.1 (used for ordering genotyping assays)
KASP Sequence:
AACTTATTTATACATATCAAGTGTGCAGGTGTAATTTCCTGGGAACCAYA[C/T]AAGTGGGCAACCCTTGCGATCCGACAACAGGAAGGTGTATCTGTGAGCAC
Long Flanking Sequence:
GCAAGGTTGGGTTTTACGGATTCAGCCGGGACGATCCTAGCGGCTGCCAGTGTAAGTGTTGATTCACCCACCGAAGGGTTTTTCACAGCTGAAATAGGTAACCCTGGAGAGTTAATAACTCAAACGTGGTGCTAATGGGACTCCAGAACAGGGTTTCATAAATGCAATTAAAAGGCATAGTTTAGAACAGGGGTCACTAATCTCGGTCCTGGAGGGCCGGTGTCCCTCCAGGGTTTACCTCCAACTTGCCTCAACACACCTGGCTGGATGTTTCAAGTATACCTAATAAGACCTTGATTAGCTTGTTCAGGTGTGTTTGATTAGGGTTGGAGTTAAAATCTGCAGGACACCGGCCCTCCAGGAACAAGTTTGGTGACCCCTGGTTTAGAATAACAAGTGGATTCTGAAAATCCTAAATTCATTTATACATTTACTAATTTATCAATCCTTAACTTATTTATACATATCAAGTGTGCAGGTGTAATTTCCTGGGAACCATA[C/T]AAGTGGGCAACCCTTGCGATCCGACAACAGGAAGGTGTATCTGTGAGCACTTCGCTTACGGCTCACAGTGTGACCAGTGTCTGGTGAGTGTCTCAATCAGACCCAAGCACATAACCATAACTGAGTTACACTTTAAAGAGCCCATATTATACATGAAATAGGGTCATATCTTGGTTGTAAGGGTCTCCAACAACCGTCTAATATGCATGCAAGGTCAAAAAACACTTTCATGGTCTTATAATCTGCATTTATTTTTACCTAATTATTCCAGCGACTCCCGTATGAATCGTCCAGTGATTCATTTGTTCCCAAACCCCTCCTTAGCGCGAAGCTAATCTGCGCTGATTGGACCGATGACAGTCTGTTGCGATTGGTCGACTGCCTTCAGTCAGAGAGTGAAATGCACACAAACACACATATTGCCCTCGTCCTTGCGCGCGCGCGCGCACACACACACACACACACACACACACACACACACAAACCCACACACACCTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30287
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058400 | Nonsense | 546 | 1827 | 13 | 35 |
ENSDART00000123330 | Nonsense | 546 | 1827 | 13 | 34 |
Genomic Location (Zv9):
Chromosome 25 (position 32651202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31262378 |
GRCz11 | 25 | 31673339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGTAATGATCCGGCTCCTGGATATTTCCTGGCTCCTCTTGATTTCTA[C/A]ATCTATGAGGCTGAGAACGCAGCACCTCTGGTAAGAATGAATGGTCACAT
Long Flanking Sequence:
AGTCGACTCTTTTATAGATGAATCAACAGTTTTAAACACTGTATTCTTACAGATTTAAGCCTTAGCTGGATACATCACTTCACTTAGAGCTGTGTTACACACTACATGGAGGGGAATTTTTAAAAACCCATAATACGGGCTCTTTAATATTTGATTCCCACTTTTCCAGCCAGGTTACTGGGGTCTGGGAAACACAGTCTATGGCTGCATACCCTGCGACTGTGACATTGGAGGGGCACTGAAAACAGAGTAAGCTACTATAGTTTCCTATCTACAGTACATTACTTCTTCTTCTTCTTTGGCCTTAGTCCCGTATGATTGCGGGGTCGGCTCCTACAGTACATTACTAATATTTGATAAATTGTTTACAAGATGGTATGTGTATATCCTCCACACAGATGTTCCTCGGTGGATGGCCAGTGTAAATGCAGGCCTAACATGGTCGGCCAAAAATGTAATGATCCGGCTCCTGGATATTTCCTGGCTCCTCTTGATTTCTA[C/A]ATCTATGAGGCTGAGAACGCAGCACCTCTGGTAAGAATGAATGGTCACATGTGATTTTTCGGTGACACTTTATTTTGATGGTCCATTTGAGTATTAGTAGACTTTCTGCTTAATATCTGTTGATAATGCTTCTTCAGCAGACATTTAACTGACTGTAAGAAACTTTGCAAGTACATGTCAACTTACACTAACCCAAACCTAACAGTCTACTTATAATTTAATGATAATTAGTTGCAATGTAACATAAATTCAACAAACCCACCACCAAAATAAACCGTGACCAATTTTTCAGCAAACACTCCAATATGACATTGCACAAAGTGAATGCCAATTCACAAAGTACGATACATGCTGATCAACGGCTAATCCATATCCATTTCCTTCCTCTAAACCCAATAACAGTTTAATAGCAATCATGTAGAAGTGCATAAATCCGTAAGCCTAAACTGTAAATGTATCCCTTAATTCTGATTGGCTGATTGAAATTTTGTTCCAGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9508
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 |
---|---|---|---|---|---|
ENSDART00000058400 | Nonsense | 670 | 1827 | 15 | 35 |
ENSDART00000123330 | Nonsense | 670 | 1827 | 15 | 34 |
Genomic Location (Zv9):
Chromosome 25 (position 32644195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31255371 |
GRCz11 | 25 | 31666332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGGACAATCCCCTTTGAACCAGGCTCACCTCTTCAGATCCTCCTGCGC[C/T]AACGTGCCAATGATCAGTCCATCACGTGGACTGGATTGGGTTTTGTGCGA
Long Flanking Sequence:
ACCTTGTTGACTCTATGCCACAAAGGATTAAGGCAGTTCTAAATATAAAAGGAGGTCCAGCCCGGTGCTAGTAAGGTGTACCTAAGAAAGTGGCCGGTGAGTGTATGTGTATAATGTATTTATATCTTGGCTCAAATCAGTTGCTCCTTGTTGTTCCATATTCTTGCTTAAATGTAAAGGAGATAGAGCTTTCTCTGTTGCAGCTCCAAGGCTCTGGAACGACCTTCATCTGTCTGTAAAATCTTCTTCAACACTAGCTTTATTCTGATTGTACTAAAACCTTTTTCTGTTGCTTTTAAAAAGGTCTTGTTGGATTTGTTTCTGTTTCTCAATATTGTTTCTTTTTTCTTTGGTTCCACATGTGCTGTTAAAAGTGCTTTAGAAATAAATTGAGTTCAGTATAATGGTGTGTGATCAAATGTGATTATCTTACCTTGGCTGTTCCCATGCAGAGGACAATCCCCTTTGAACCAGGCTCACCTCTTCAGATCCTCCTGCGC[C/T]AACGTGCCAATGATCAGTCCATCACGTGGACTGGATTGGGTTTTGTGCGAGTTCAGGATGGAGCTGGACTTAGATTTACCGTCAGCAACATCCCAGCAACACTTGACTATTATGTAGTTGTCCGCTATGAACCAGAGGTCAGCCAGTGTTTTTGTTCAATATTTGAATGTGGATGTTTGTTTGAGATGTTCTGGTCCATTTCACGTTTATGTTTTCTCAACATTATCTTTGCAGTCCACCGATGATTGGACAGCTATTGTGAGCATTTTATCTTTTGGATCAGAGGATGAACGGTGTCCGAATGACCAATCAAACAAAATGTTTACTCTTCCTGCCTCTGGAAGGTGAGAAGGTTATACAGTATTTTTGCATGTATTTAATGGCTATTTTGATATCTTTTGTTGTGTGCCAGTTTAGTAATGGTAAAAACCTGAATTTATTGTCTATCCATTGTTTAGTTGTACGTATGTCATTCTAGACTACAATGTTTTAAAGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24711
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 |
---|---|---|---|---|---|
ENSDART00000058400 | Nonsense | 894 | 1827 | 19 | 35 |
ENSDART00000123330 | Nonsense | 894 | 1827 | 19 | 34 |
Genomic Location (Zv9):
Chromosome 25 (position 32640260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31251436 |
GRCz11 | 25 | 31662397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTATCGGCCGCTGCTGTGATTCTTGTGCTCCCCTGACATATGGGCTT[G/T]GACCCAATGGCTGCTCACGTAAGACATTTTCTCATATTTCTCATATTGTG
Long Flanking Sequence:
GATTGACTCTGTAAGCAAGCCAGATTTTGTTTTAGCAAGATCATTGGAAATGATGCAATTGAAAGTTCACCGACTTCTGCTTACCCTATGTTTTATTTTTAATCACAGCTAGGACTCATTCCCAAAGTGGAGTCCGTCCCAAACTTCTGCTCACAGTCATATCTATCTCAGTTTCAACAATACCGGTGTATTGAGCTGGCTGTACAGGCAGGAGGTCAGACACTTCCTGAAGTTTGTGAGATGCTTATTGGATCCATGTCAGCTTTTATTCACAATGGAGCAGTGTGTGAGTATCATCCATATTTACACCTCAGACATACACATACGCATTTAAACTATTACCACGAGTACATGTATATCTGTGCAAATCAACAGCTTGCAACTGTCATCACGTCGGAGCATATGGCTCATCTTGCAGTAAATTTGGTGGACAATGTCAGTGCAAACCCAATGTTATCGGCCGCTGCTGTGATTCTTGTGCTCCCCTGACATATGGGCTT[G/T]GACCCAATGGCTGCTCACGTAAGACATTTTCTCATATTTCTCATATTGTGGTCATGTATAAGGGCTTTTTGCATCGAAGGAACTTTTTTTTACAGTTCCTAGAACTACCACAGCAGAAGCTGGAAATGATTTTAGCTCTAGGAACCATTTCAACAGTTCACACTTAGATATTGTTTGACAAATGCTAGCAGGTTTGGCATGCTGTCCCTGGAGTGAACCCTGAGCTCGGAGATAATTGAGCCCCAGGCTCCCACCTGGTTGATAGAGCATGAAAGGGGGGGGGTTTAATGGCTCGTTTCCACTGACTGGTACAGTACGGTACGGTTTGGGTCGGTACGGGTCACCTTTATCAGGCTTGCGTTTCCACTACCAAGGGTACCCTTTTGGTGGGTGAGGTGTATGACAAAGTTTCAGTCGACATAATTTTCGCTCTAGAAAATGTCTACAATAAAGCTGCACAGGTCGCTCACATATCATATGAAAAGCACTTCTCACAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6808
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058400 | Nonsense | 973 | 1827 | 20 | 35 |
ENSDART00000123330 | Nonsense | 973 | 1827 | 20 | 34 |
Genomic Location (Zv9):
Chromosome 25 (position 32633531)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31244716 |
GRCz11 | 25 | 31655677 |
KASP Assay ID:
554-5365.1 (used for ordering genotyping assays)
KASP Sequence:
GTGACCCCATCACTGGAGACTGTCTGGACTGCAGGGAACACTCCGCGGGA[C/T]GAAACTGCGAAAGGCAAGGGACGAGTCTGAGATCACATTTCAAGATTATG
Long Flanking Sequence:
ACATGATACATTCTAGACATTATACACATTATATATATATATATATATATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATATATATATATATATATGTATAGTACAATTGTCCTGATAACAAAAACAAAGACATTTACCTTGATATATGGGATGTTTTAATGTTTTTAATTTGTTATTGACCCTTCTAGCATGTGACTGTGATCGTTCTGGCTCTACCACGGAGCTGTGTGACCAGACAACTGGTCAGTGCTCGTGTCGAGATGGAATAACTGGCCTTCAGTGCAATAGATGTTACCCTGGCTACTATGGGTTTCCCCTGTGCAGACGTTGCCAGTGCAACAGGTTGGCTGACATTTGTGACCCCATCACTGGAGACTGTCTGGACTGCAGGGAACACTCCGCGGGA[C/T]GAAACTGCGAAAGGCAAGGGACGAGTCTGAGATCACATTTCAAGATTATGGCAAAAATATATAAAGTATTTACTAGAATTTTGGTGTGTATAGGTGTGAAGAGGGATATGTTGGTGACCCTGTCTCTGGACAGCCATGTGAGCCATGCTTATGTCCAGATCTGAATGGAAGTGGACGCTTCTTTGCCTTTTCCTGCAATAAGGATCCCCGCTCTGGAGCACCTTACTGTGAATGTCTGCCTGGACATACAGGTCATCATACTTTATGATACACAACATTTCCATCAAGACCATCCAATTAACTGTTTAATGTAACTTACAGTAAGAAATTAAAGATACAGTCAGCACCAGTGGTGTAGTGGTTAGTGCGTCGACCTGGGTTCGACTCCGCCTCGCGGTCCTGTGCCAATCCTTCCCCTCTCTCTGCTCCCCTTGCTTTCCTGTCAATTCTCTCTACTGTCCTATCAAAAATAAAGGTGAAAAACCCCAAAAATAATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18559
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 |
---|---|---|---|---|---|
ENSDART00000058400 | Nonsense | 1226 | 1827 | 25 | 35 |
ENSDART00000123330 | Nonsense | 1226 | 1827 | 25 | 34 |
Genomic Location (Zv9):
Chromosome 25 (position 32625748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 31236933 |
GRCz11 | 25 | 31647894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGTGACTGTAACYTGGAGGGCACCGTTCATCCAGCTTGTGACGCTTA[C/A]ACGGGTGAGTGTTTGTGTAAGCCAGGRGTGACRGGCCCTTTCTGTGATGA
Long Flanking Sequence:
AAATGGAAACTCCCATTTTTATTCAAATCCTTCCCTCTTTTCCCTCCCCCAACACTCCCACCTAAACAGAACTAGACACACCCACTTTCCAGACTTTTTTTAAACTAGAGGTGTGAAAACACCCTGCTGAATCAGGGGGTTTCATGGCCCTTTAAAAATGTTTAGATCTTTAATCTAGAAACAAGACAAAAACTTTTAGTAAGATTTTTTGCAGCATACAAAGTCTATTATCAGATGCCTTTTGTGCTTCATGCATTCCCTGTACGACCTTCCAGATCACAGGCCAGTGTTTATGCCAGCCAGAATATGGAGGCAGAATATGTGACGAGTGTGGTCCGAATCACTTTGGAAACCCTGATTTACAGTGCATGTGTAAGCTATTATACAGAAAGTTTAGCTCTCTTCCAAGTCATGTTGGTCTGATTGACAAAACTTTTTATTCCTCCTTCAGTTTGTGACTGTAACCTGGAGGGCACCGTTCATCCAGCTTGTGACGCTTA[C/A]ACGGGTGAGTGTTTGTGTAAGCCAGGAGTGACAGGCCCTTTCTGTGATGAGTGTGCCCCGGGTCACAACAACAACTTTCCTGCCTGCGAACCCTGCCATGCTTGCAACTACCTCTGGGAGAAAATCATCTCAGATCTTAGTTTAGATGCGGAGAGGATAGAAACCATGATGCCTTGCCCTGAAGATTTTCGGTCTAGACCTGAATTACAACACCTACAGAATTTGCTGGAGAAACTGCAGAATGTTCTTAACATGGGCGCTCAGGACGAGCTTAAAAAACTGGAGGAGCTCTTGGCGCGGATTAGGTATGATAATTTTATGTCAGTTTAATTTTGAGTTGGCTGATTAGATATTTGCATTAACAAGCAGCTGAACAGGTGTAAAGTGGCAGGTGAGCGTCTAAAGCTTTTGCCACCAGATCCAAATCCACAGGTGGAACCAACAAAGAAAACATAAAATGGAGAAATGGCTATATGTTTGTGTTTATGAGTGAAGAATCT
Associated Phenotype:
Not determined