ZMP
itgb3a
Ensembl ID:
ZFIN ID:
Description:
integrin beta 3a [Source:RefSeq peptide;Acc:NP_001032312]
Human Orthologue:
ITGB3
Human Description:
integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [Source:HGNC Symbol;Acc:6156]
Mouse Orthologue:
Itgb3
Mouse Description:
integrin beta 3 Gene [Source:MGI Symbol;Acc:MGI:96612]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18375 | Essential Splice Site | Available for shipment | Available now |
| sa18576 | Nonsense | Available for shipment | Available now |
| sa40040 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40041 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33142 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40042 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18375
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025358 | Essential Splice Site | 377 | 820 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 19517869)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 19480904 |
| GRCz11 | 3 | 19630644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCAACCYCATCTTTGCTGTAACCAGCAATGTGGCTCCACTGTATCGTG[T/C]RAGTTTCTGCAMTTTGTCTAWCATCTGTCTATATAACANTTACACMCGTT
Long Flanking Sequence:
TCACTTTACAAGCACAAGTCCTTTGACAGACACCCATATGCTTCATACTAACTTCTTGATTGTTCTTCATTTGATTCAAAATGAAGAGCCTGATGTATGTGGTATATCTTTCAAAAACAGAAATAATGATTGCAAATTTGCCCTTTTTAGTCATCAAACTCAGAGCACAGCTAAGGCTGTTTAATTGTGTTGTCTTACAATAAATATACAGTAAATGTAAGTTAAAGTGTCACTGACATAATCTGTTCACTTTGGCAATGAGGTCTTAAAATGTATGAAAAGTGTCTTTAAAAGGTTTTTAAAAGGTATTAAATTTATCTTAATGATTCCTGTATATACCGTTGGATGGATGGTTGGATGGTTGGATGGATGTCTGATAGTGCACATATTTTTGTATTTGTAGGACTACCCTTCAGTTGGCATGATCACGGATAAGATATCTGAGAACAATATCAACCTCATCTTTGCTGTAACCAGCAATGTGGCTCCACTGTATCGTG[T/C]GAGTTTCTGCACTTTGTCTATCATCTGTCTATATAACATTTACACACGTTTATGGGAAATGTCCTGTTTCTCACAGAACTACAGTGAGCTGATTCCAGGCTCAACAGTGGGAACGCTCACTAAAGACTCATCAAATGTTGTGCAACTCATTCTGGAATTGTATGCGGTAAGTCACTGCGCCAGGAGTTATACCTCGGTGTGAGTTCTGAGAATTGGTTACTTTTTACAACATTTTAGCAAATTTTAAAGTTACTTTTATTAAGTTTTATTAAGGTTTTTTCTTTTCTTTTTTTCAGTTTATATGCTATGGTAATAACACCAGTAGTACTTAATAGTTAAGTAAATCCCATTATATCAATCAGCATTATAAGATATTGGGGAAATAAATCCCAGAAAAGGCTCACTTGAGGAAGAGAAACAAATAAAACAGCATAAAAAGGTGGGGGGTGCGTTGAAAGAGAAAAGAAGTGAATAAAGAGGAGAAAATATTAGGAAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18576
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 |
|---|---|---|---|---|---|
| ENSDART00000025358 | Nonsense | 406 | 820 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 19518032)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 19481067 |
| GRCz11 | 3 | 19630807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCTCACTAAAGACTCATCAAATGYTGTGCAACTCATTCTGGAATTGTA[T/A]GCGGTAAGTCACTGYGCCAGGAGTTWTACCTCKGTGTGAGTTCTGAGAAT
Long Flanking Sequence:
AGCACAGCTAAGGCTGTTTAATTGTGTTGTCTTACAATAAATATACAGTAAATGTAAGTTAAAGTGTCACTGACATAATCTGTTCACTTTGGCAATGAGGTCTTAAAATGTATGAAAAGTGTCTTTAAAAGGTTTTTAAAAGGTATTAAATTTATCTTAATGATTCCTGTATATACCGTTGGATGGATGGTTGGATGGTTGGATGGATGTCTGATAGTGCACATATTTTTGTATTTGTAGGACTACCCTTCAGTTGGCATGATCACGGATAAGATATCTGAGAACAATATCAACCTCATCTTTGCTGTAACCAGCAATGTGGCTCCACTGTATCGTGTGAGTTTCTGCACTTTGTCTATCATCTGTCTATATAACATTTACACACGTTTATGGGAAATGTCCTGTTTCTCACAGAACTACAGTGAGCTGATTCCAGGCTCAACAGTGGGAACGCTCACTAAAGACTCATCAAATGTTGTGCAACTCATTCTGGAATTGTA[T/A]GCGGTAAGTCACTGCGCCAGGAGTTATACCTCGGTGTGAGTTCTGAGAATTGGTTACTTTTTACAACATTTTAGCAAATTTTAAAGTTACTTTTATTAAGTTTTATTAAGGTTTTTTCTTTTCTTTTTTTCAGTTTATATGCTATGGTAATAACACCAGTAGTACTTAATAGTTAAGTAAATCCCATTATATCAATCAGCATTATAAGATATTGGGGAAATAAATCCCAGAAAAGGCTCACTTGAGGAAGAGAAACAAATAAAACAGCATAAAAAGGTGGGGGGTGCGTTGAAAGAGAAAAGAAGTGAATAAAGAGGAGAAAATATTAGGAAACATTTCATTTTGTGGTGAAAGCAATAGGGAATCATTGAATCATTGACAGAAAAACATAAAGTCTGATACCCATACATACCCGAAGTGCCTAGTGACAATCTCCAGCCACAGTATCCCTCTTTGAGCCAACTAAATAACTCAGGCCACTGAGGTAAGACAAGCTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40040
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 |
|---|---|---|---|---|---|
| ENSDART00000025358 | Nonsense | 418 | 820 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 19520444)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 19483479 |
| GRCz11 | 3 | 19633219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCATTTGTCTTTGCAGAAAATCAGGTCTAAGGTTGAGCTGGAGCTGT[T/A]GAATGTGCCGGATGAGTTATCGCTGTCCGTCACTGCAACATGTCTGGATG
Long Flanking Sequence:
CACTGTGTCGATCATGTGACTCGATACTTGATTTAAAACTCAAAAGATGCAGCAACTGGAGCAAGAGCAGTGTCAATTGCAGCTTTCACCTGTTCTGCGATGGTAGAGGTTAGCTCGGTGATCAGAGTGGCACAGAGATTTTCTAGATCCAGCGGCAGCCTGCCGCCATGACTCTTTGTCGCAGCCGCCAACACTTTTTCTGCCTTTCAGACGCCATAAATCCTTCCAAACTGTATCTGTTTGATGCCCGATACAAATAGGAAACCACCAAGTGTGTTTAAAGATTCAAGCAGTCAGCTAAATATATTGAAAGACGAAATTGTTCGGGAGCTCACTTCAAGCGTGATTACCGACTCACAATCTTAACCGGATGTCGTTTCAGCTCATTTTAAATAAGTAGTTTGAACAAACAACAAACGTCATTTTTTTAAACGTATATTTGTATTGTTTGTGCCATTTGTCTTTGCAGAAAATCAGGTCTAAGGTTGAGCTGGAGCTGT[T/A]GAATGTGCCGGATGAGTTATCGCTGTCCGTCACTGCAACATGTCTGGATGATGAGGTCATTCCAGGAGTACGGTCCTGTGACGGACTCAAAATTGGAGATATGGTCAGCAACTGACGCATAAACACTGGAGAAAACCATGCTTGTTCCATTTACCAAAGTGCAGTGAGCCAAAGCAACACTTCATCAATATGTTTTATCTCTTATTTTTATTGAGTTGTGGTTAATAGTAAAAGTTAGTTTGTAAACAGACAAAAGTTTACAGTCATAACCTATAATGACAGACAAACCTGAAAGCTGCAACTGACCAATCAGGGTCAAGTATTTTAGAAAGCTGTGTATATGGGGTCGCACAACAGTTGAAATTATCGCACACCTGATGCACACATTTACATGTTATTTAAAATGAAACTATTCATATGGCACTCTGTGGTGTGGCAGGAATATGAACAGTGTTCTGAACCATTAATCCTAATCCTAAACCAAACCGTCATCCTAACGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40041
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025358 | Nonsense | 450 | 820 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 19520539)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 19483574 |
| GRCz11 | 3 | 19633314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATGATGAGGTCATTCCAGGAGTACGGTCCTGTGACGGACTCAAAATT[G/T]GAGATATGGTCAGCAACTGACGCATAAACACTGGAGAAAACCATGCTTGT
Long Flanking Sequence:
TGCGATGGTAGAGGTTAGCTCGGTGATCAGAGTGGCACAGAGATTTTCTAGATCCAGCGGCAGCCTGCCGCCATGACTCTTTGTCGCAGCCGCCAACACTTTTTCTGCCTTTCAGACGCCATAAATCCTTCCAAACTGTATCTGTTTGATGCCCGATACAAATAGGAAACCACCAAGTGTGTTTAAAGATTCAAGCAGTCAGCTAAATATATTGAAAGACGAAATTGTTCGGGAGCTCACTTCAAGCGTGATTACCGACTCACAATCTTAACCGGATGTCGTTTCAGCTCATTTTAAATAAGTAGTTTGAACAAACAACAAACGTCATTTTTTTAAACGTATATTTGTATTGTTTGTGCCATTTGTCTTTGCAGAAAATCAGGTCTAAGGTTGAGCTGGAGCTGTTGAATGTGCCGGATGAGTTATCGCTGTCCGTCACTGCAACATGTCTGGATGATGAGGTCATTCCAGGAGTACGGTCCTGTGACGGACTCAAAATT[G/T]GAGATATGGTCAGCAACTGACGCATAAACACTGGAGAAAACCATGCTTGTTCCATTTACCAAAGTGCAGTGAGCCAAAGCAACACTTCATCAATATGTTTTATCTCTTATTTTTATTGAGTTGTGGTTAATAGTAAAAGTTAGTTTGTAAACAGACAAAAGTTTACAGTCATAACCTATAATGACAGACAAACCTGAAAGCTGCAACTGACCAATCAGGGTCAAGTATTTTAGAAAGCTGTGTATATGGGGTCGCACAACAGTTGAAATTATCGCACACCTGATGCACACATTTACATGTTATTTAAAATGAAACTATTCATATGGCACTCTGTGGTGTGGCAGGAATATGAACAGTGTTCTGAACCATTAATCCTAATCCTAAACCAAACCGTCATCCTAACGCTGATCTTATAGTAAGTAAATGTAGTTAATTACTTTTCATTTGGTACTTTATGTATGGTTAAACTGTAACAAGAACAAGGCGTGATGGCGCAGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33142
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025358 | Essential Splice Site | 453 | 820 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 19521800)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 19484835 |
| GRCz11 | 3 | 19634575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTACCATGTGAATTGACCTTTAACTTCTTTTTCTCACTCTCCATGAAA[G/A]GTTTCGTTCAGCATTGAGGCCAAACTTCACGGCTGCCCCAAACAGAAGAG
Long Flanking Sequence:
GTTAATCACACGACTAACACGTCTTGCGCCATATAACGCTAGGTGTATGATCGGGCCCTTTACTTTGGTCCACTTGAGTATTAGTAGACTGTCTGCTTAATACCTGTTGATATTCTCCTTTAACAGACATTTAACTGACTATAAGAAACTTTGCAAGTACATCTCAACATACACTAACCTCAACAGTCTACTTAAATCTAATGAGAATTAGCTGTAGATGCAATGTAACTTAAATTTGACAAACGAACCATCAAAATAAAGTGTGACCGAGACTGAATATTTATACATATAATGAACTATGTGGTCACATTTAGAGATTATTGATTTGAATCATTGTTCAATCATCAATTTTATTATTCATATTAAATGCTCTTATCCAAAGCACTTTGCATTTAAGCAGTACATTTTGTCAACCTCATAACTTCATCATTTTTTCTCCATCCTCTACTGTTTTACCATGTGAATTGACCTTTAACTTCTTTTTCTCACTCTCCATGAAA[G/A]GTTTCGTTCAGCATTGAGGCCAAACTTCACGGCTGCCCCAAACAGAAGAGTCAGACTTTTACAGTGAAGCCAATTGGTTTTAAAGACGCTCTTCAGGTCACTGTGGACTTTGCTTGCGATTGTACCTGTCAGCAGAACTCGGTGCCTGCCAGCCCATACTGTCATGAAGGCAATGGGACGCTGGAGTGCGGCACGTGCCTGTGCGACCCGGGCCGACTGGGCTCCCGATGCGAGTGCAGTGAGAGCGAATATAAACCCACTCAACAGGACAGCTGTAGCCCCAGTCCAGAGGCACGGACCTGTAGTGGACGTGGAGACTGTGTGTGCGGCCAGTGTGCCTGCCGCTCAAGCAATTTTGGAAAAGTTTGGGGTCCGTTCTGTGAATGTGATGACTTCAGCTGCCCTCGCTCTAAAGGACAACTGTGCTCAGGTGAAGCTGCAAACACACATAATTTTTTGTGCTTACATATACAACTCCAAATCAGAAAAAGTTAGACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40042
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025358 | Essential Splice Site | 596 | 820 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 19522232)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 19485267 |
| GRCz11 | 3 | 19635007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGTGATGACTTCAGCTGCCCTCGCTCTAAAGGACAACTGTGCTCAGG[T/C]GAAGCTGCAAACACACATAATTTTTTGTGCTTACATATACAACTCCAAAT
Long Flanking Sequence:
TTTCTCCATCCTCTACTGTTTTACCATGTGAATTGACCTTTAACTTCTTTTTCTCACTCTCCATGAAAGGTTTCGTTCAGCATTGAGGCCAAACTTCACGGCTGCCCCAAACAGAAGAGTCAGACTTTTACAGTGAAGCCAATTGGTTTTAAAGACGCTCTTCAGGTCACTGTGGACTTTGCTTGCGATTGTACCTGTCAGCAGAACTCGGTGCCTGCCAGCCCATACTGTCATGAAGGCAATGGGACGCTGGAGTGCGGCACGTGCCTGTGCGACCCGGGCCGACTGGGCTCCCGATGCGAGTGCAGTGAGAGCGAATATAAACCCACTCAACAGGACAGCTGTAGCCCCAGTCCAGAGGCACGGACCTGTAGTGGACGTGGAGACTGTGTGTGCGGCCAGTGTGCCTGCCGCTCAAGCAATTTTGGAAAAGTTTGGGGTCCGTTCTGTGAATGTGATGACTTCAGCTGCCCTCGCTCTAAAGGACAACTGTGCTCAGG[T/C]GAAGCTGCAAACACACATAATTTTTTGTGCTTACATATACAACTCCAAATCAGAAAAAGTTAGACAGTTTAGAAAACGCAAATAAAAAAGTAGTGCTTTCAAAAGTTACTTTGATTTTGTTCATTGCAGACAATACAACAAACATTATTTAATGTGTTCCTCGTGATTTTTTTTTATAATAAACACATATTTAAATTTTGATTCTCGCAACACATTTAAAAAAAACATTTTAAACATGAAAACATTTACGACTTTGTATTATTGCTGTTTTATTTCACAACATTTAAAAGACGTCTAGGGACTGACACCAAGTGATGAAGTGTTTCAGGTAAAGTTTTGTCCCAATTTTCCCTGCAAACAAGTCTGAAGTTGGCCAACAGAACAGGGTCTTTGTTTTTTTTTTTTTTTTGTTTTTTTGTTTTTTACACATTCTCTATTGAAGACAGGTTGGGACTGCAGGCAGGCCAGTTAAGTACCTGTATCCTCTGTCTTTTATTTTT
Associated Phenotype:
Not determined