ZMP
itgb4
Ensembl ID:
ZFIN ID:
Description:
integrin, beta 4 [Source:RefSeq peptide;Acc:NP_001019557]
Human Orthologue:
ITGB4
Human Description:
integrin, beta 4 [Source:HGNC Symbol;Acc:6158]
Mouse Orthologue:
Itgb4
Mouse Description:
integrin beta 4 Gene [Source:MGI Symbol;Acc:MGI:96613]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14803 | Splice Site, Nonsense | Available for shipment | Available now |
sa21220 | Nonsense | Available for shipment | Available now |
sa21221 | Nonsense | Available for shipment | Available now |
sa18596 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14803
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029308 | Splice Site, Nonsense | 188 | 1893 | 7 | 41 |
The following transcripts of ENSDARG00000028507 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 13633526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13078870 |
GRCz11 | 8 | 13116575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACNTTTTTTATCACACACTCATAATGTAGTWTGTTTTCTSTTTTACAGAT[T/G]AGCTGAGCCGTGGTCCAATAGCGACCCTCCATTTTCCTTCCGTAAMGTCA
Long Flanking Sequence:
AACAGGATGTGTTCTAGCTATTTTTACATTGGCTGTCATGTCACGTCTTGTTGTTCAATTTCATCTTGATTCATCAGTGTTGCTGTAGTTATATGGTCGTTCAAGAAATTCAGCTTTTAAATCCATATACTGAGTCCCTATTGGAGTCTGTTCCTTTCCAAATAATGTTGTCTTCTCATTTTTAAATCCAAAAACATTTTATAATTTGACGTACACTCATGAAGCATACTGTAAATTTGTGTGACCCACTTACAAAATACACAGGCCATGTGTCTATTTTAATATTCATTCATTGCCTGGTTTCACATCATTGCAGCACGGCTTGTTGGCGATCTCTCTGACGATTACACCATCGGATTTGGCAAGTTTGTGGACAAAGTCACCGAGCCTCAGACAGACATGAGGCCAGCCAAGTAAGAATCATGCAGTGTTACTGCAGCACACAGTTTGACTTTTTTTATCACACACTCATAATGTAGTATGTTTTCTGTTTTACAGAT[T/G]AGCTGAGCCGTGGTCCAATAGCGACCCTCCATTTTCCTTCCGTAACGTCATCAAGCTCACCAGCAACATCACCTCCTTCAGACAGAAGCTACAGAAAGAGCGTATATCTGGCAACCTTGATGCTCCAGAAGGTGGTTTTGATGCCATCTTACAGACTGCTGTCTGCCAGGTACTGACAGTTTTTCTTCAGGGGCAATTGAAAAATAAAACTGAATGGCTTGGCTGACATTTACAATGCTGTAAACAACAACTTACTTCTTAGCGGTGGAGTTAAGGCTTAAAACCAATATTTTGTTTGGTTATATTTTATTTTTTATAGTTATTATATTTTTTATATTATATTTTTTGTCATTTAATATTAATATTAATATTATATCCTTTATTTCGCCAGTAAAAAAGCACATTAAGATTAAACATCTCTTTTACAAGAACGTCCTGACCAAGATTAAGCAGTAGACAGTTCACATAGGTTTAACAAAAATAACAGATAACATTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21220
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 |
---|---|---|---|---|---|
ENSDART00000029308 | Nonsense | 766 | 1893 | 20 | 41 |
The following transcripts of ENSDARG00000028507 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 13644119)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13089463 |
GRCz11 | 8 | 13127168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGACAGGTCGTATGGTGGGCTTTAAAGAAAACCAGTACCTGCTACGT[C/T]AGTCTTTTCTGCAAAATGATTATTTGGACACCCCAATGGTGCGCAGCGGC
Long Flanking Sequence:
AAAATAAACAGCGGGGCTAATAATTCTGACTTCAACTGTATGTATATATATATATATATATATATATATAGAAGCTTGTCCGGGACACACAAAGCTCACAAGCATTGTTGCATGAAATGTTTTGCTAGACAATGCACTTTTTTTTTTTGGTGTATTGCAATACTGTAAAAATACAGTAAAGGCAAATGTTAGATAAGTAATTGCAAAGTTTCTTGAGGTCACATAACTTGTATGAGAAAACGCAAATATTTTGTTTTTGAGAAACTATTTTTGTCAGGAGAACACAATATTTCACCATAGATCTATTTATAATTGATGTCTGTCTCCAACAGTCCTGTCTTGCTCTTCTCCCGTGCTGTGCAAGAGGTAGTTATATGCTTTCATACGTACTTTAAGTTACGTTATCTATATTTTGGTGGAAACACACATAATTAATTGTCCTTAATATGTAATGGACAGGTCGTATGGTGGGCTTTAAAGAAAACCAGTACCTGCTACGT[C/T]AGTCTTTTCTGCAAAATGATTATTTGGACACCCCAATGGTGCGCAGCGGCCCGCTCAAGAGCACAGACGTTGTGCGCTGGAAAGTGGCAGACAATGTTCATCGAGGAACGAATCACCCCCAGAACCAAATCAGACCCAACCCCAAAGAGACCAGTGAGTCTAAACATTGTTTTTTATATTGTTTTTATTATTATTATTAATATTATTATTAAACAAATACTGGTAACACTTTACAGTGTTTTTGCTCCATGTAGTTAGTATAGAAATACCTTTAAAAAGTTTGTATATTTGCATGAAAGCAACCGTTAACCTAACATCATGCTAACAATTACCATATACTTTGTCGTTTCAAAGCCAGAGTCAAATAAAAGTTCATAAATGATATACATATCCATTAATCCCTCTGTATTTTTCCTCCTAGTCCAGTATCCTGTTTCTCTTCGTCTGAACCGCCAGTTTTCAGAAGTTCTTTCTAACCCTGACGCTCGGGACACAGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21221
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 |
---|---|---|---|---|---|
ENSDART00000029308 | Nonsense | 1088 | 1893 | 27 | 41 |
The following transcripts of ENSDARG00000028507 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 13649436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13094780 |
GRCz11 | 8 | 13132485 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGGAGGACAAGCAGGTCAAACAGTTTGTCATGGATTTGACCAACCCA[C/T]GACAAAGTGCTAAACTAGGCCGTTACCCACGCACTGTTATCACCATCGCT
Long Flanking Sequence:
GCATAAAAATTTTTCATACATATATTTTTAGATTTTAATTTTCCAAAAAAAATAAATAAATAAAATAAATAAATAAATAAATATATAAATTAAATAAATATATTTATTTAATATATATATATATATTATATATTCTAATATATTTTATAGAAGTTCACTGATGTTGATGTAACTTCATAGTTATGTGCTCCATACATATTGAAAATGCAATGTTGTACCATTGTTTATAAATAATTATGGCTCTTAAAATATGTTTTAATTATTTTATTAGTAATGGGTAATGGGAACATTCAGTTGTCATTGTTTGATTGCAGTATTTTTTTATACTACTTTTTGCATTCTCTCCTGTACAGGACTATATTTCGGTAGATGGAGACTTGAGCTATGGAGCAGGTGAAACAGAGAAGATTGTCCCAGTGAAACTTCTGGAACTTGGAGAGCAAGATGGCCTGCTGGAGGACAAGCAGGTCAAACAGTTTGTCATGGATTTGACCAACCCA[C/T]GACAAAGTGCTAAACTAGGCCGTTACCCACGCACTGTTATCACCATCGCTGACAAACCAGGTACATATGAGCAATTCCATGCAAATGTCACCCTTGCCATGAAAAAATGAAGGTTTCACCAAAATAGCGAAATTCTTTCTACATTTTTTGTGTAAGCAAGTATTTTATAGTACTTCAAAAATACTGAAAAATGTCTGACAATGATTTCTAACAATTATATTTGATTTACCAAAGTCACACCAGTGGCAATTTCACATCTATCACATCCGTAACGGAGAGGTGTCACATCTATAAGGAAGCTTTTTCCTCATAAATGCAAAGATGTCACCTAAAATAAAATCAATCAATTTTGCTCTATAGAGAGCCGACTCTTACCCTTTTAAATAGCATTATTTCTTTTGGGTTGTGCGATTTAACTCACAGAATTTCTACAAAGTATGTTGTATACTTTAAACTCGCTAACTTTTTTGCTCACATCAATAAAGCATGACTATTTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18596
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 |
---|---|---|---|---|---|
ENSDART00000029308 | Nonsense | 1227 | 1893 | 29 | 41 |
The following transcripts of ENSDARG00000028507 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 13652322)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 13097666 |
GRCz11 | 8 | 13135371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAACATTTCAGGGGATGGTAAAAATCAGGATTTCCAGAAGATGGAMTA[T/G]GTTACTCAAACAGCCACATCCYCCGGAGGACGCCTCTATTCTCCAGCCAA
Long Flanking Sequence:
ATATTGAAAAATGAGAACGAGCAATGCATCTGGCTTTATGCTTCATTTTTATCCATCTTAAAATTATTTATGCTTGGTTATTTTATCAAGACATTAGCATTACATGCATATCTAAGGCCGAAACTCTTTTGAGTTCACTGTTTTATTCCTACAAATTGTCCTCTTTATATTCCATACAGTAAAGTAATAGTCCAAATTGCCATGCGAAGATTCGTGAGTTTTTTGGGGTTGTGTGTGGTCTGCTAAAAGTCATTTTGTTTATTCTAATAAATTATTTTTTAAAATTTTCAAATTGATAAACTTTGAGGAAAGTTATAACAAACTTGTCGTCACCCTTTTTTTAAAACATTGCAGATTGTTTACAGTTTAATATAAGTTACTTAAACATTTTGGCAGTAGGAAAAAGGTAGATAATCAGCAGATACTAGAAATGATAATTATTATTTGCATTTGAACATTTCAGGGGATGGTAAAAATCAGGATTTCCAGAAGATGGAATA[T/G]GTTACTCAAACAGCCACATCCCCCGGAGGACGCCTCTATTCTCCAGCCAACATTAAAGCCGTTGCTACCGGCCCTAAAAACATCCGCCTGAACTGGAAACCCAGCCAAAATGCCAATGGTTACAAGGTAGATCTTGTCAAATAATATCTACTGCATATATAGATCCTTTTTTGACTTATTTATTTATTTATTTATTTATTGTGTACATCTGTAGAATTTATTTATCAAAAAATAAACAACGGTATCCGTAAATGAACAAACTGTAAATGAAGAGTGTGAAATGTGTGAAGCCTTTAAGCAGTTCCTAAGTGTTTACTTTATGACCAATATAACCAGTATCATTACTGTGTCTTTTCTAAATAATAGGACATTTTTTGTTCTGTATAACATCACTGACCACAAACTTTTGAATAACAGTGTATGTGACATGAAATGACAGGTTAGCTTGATATTGGGCTGTTTTTTTTAGCCATTTTTCTTTTTAGAAACACCACAGGAGC
Associated Phenotype:
Not determined