ZMP
bsg
Ensembl ID:
ZFIN ID:
Description:
basigin [Source:RefSeq peptide;Acc:NP_937785]
Human Orthologue:
BSG
Human Description:
basigin (Ok blood group) [Source:HGNC Symbol;Acc:1116]
Mouse Orthologue:
Bsg
Mouse Description:
basigin Gene [Source:MGI Symbol;Acc:MGI:88208]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7493 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa3178 | Essential Splice Site | F2 line generated | Not yet available |
| sa5689 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa7493
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015951 | Missense | 81 | 404 | 2 | 9 |
| ENSDART00000105392 | None | None | 287 | None | 8 |
| ENSDART00000131131 | None | None | 262 | None | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 19157701)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 18908636 |
| GRCz11 | 22 | 18933614 |
KASP Assay ID:
554-4094.1 (used for ordering genotyping assays)
KASP Sequence:
GCCAGATGAAATCATCACTCAGCTGTTTGATGGTGCAAGAGAGGATCGCG[T/A]TCACATCAACGCCACCTATATTGACCACGCCACCAGCTCGCTCATCCTCA
Long Flanking Sequence:
TTTGTTCTCATTTCATTTTTAAATTAGCTAAGCTTTGATTTTTTTTTTTTTTTTTTTTTTAATGCATGCTTCAGCTCATTGTCTTTTTAAAATGCTTTTAATGTTCTTCAGTTTGGTTTTTATGTCATGATGTCTTGCATCATGATGCTCAATTATTTGTTTCTTATGTATGTCCTTTGTTTTTCATTTCTAACATTTTTCTCTCTTTTTCTCTTCTGCCATTTCTCTTCTTTTTTTTTTGCCTGCCATTCTGCTAATCATTAATCATATCATCTGAATGAACTGTCCACCCTTTATGTAAATCACACTCTCATCAATCGAATGTCCAGCGGGCTTCATAAAATCGCCTTTGTCTCAGATGAAACTCATTGAAGACAATGCAGAGCTGGATTGCGAGGTCATAGGGAATCCCATCCCTGAAGTTCAGTGGTGGTTTATTGAGGGCGAGGAGCCAGATGAAATCATCACTCAGCTGTTTGATGGTGCAAGAGAGGATCGCG[T/A]TCACATCAACGCCACCTATATTGACCACGCCACCAGCTCGCTCATCCTCACCAACCTAACGTTCAACGACACAGGCGTTTATGAGTGCCGTGCCTCAAACGACCCCGACCGCAACGACCTCAGGACCCCGCCAAAAGTCAAGTGGATTCGCTCACAAGCGAACGTTATAGTGTTTGAACGTGAGTTACGTTGTGGAAACGCAGCGTCTCCATTAGTGTAGAAAAGGAAGTCCTGTAGTTTCAGATCCTCAGTCCTTCGTCTTGCCCTCTGCCTTCCTTTTTTCCTTTTGACCAGAGACCAGATTACACTTCTACACTAGCAAGGTTATTTCTTATCAATCGGCTGCCTTATGGGCATGTCACTGCCTAGAGCTTGTGAAATGTAGTTGAACCTCTTAAAGAAATTGCATTGGTCCGTCGATGCCAGGTGTAAATGCCCCGATTTACTTAGTGATAAAAAAAAAAAAAGTGGTGTGATATTTCACAAATCATACATGAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3178
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015951 | Essential Splice Site | 377 | 404 | 6 | 9 |
| ENSDART00000105392 | Essential Splice Site | 260 | 287 | 5 | 8 |
| ENSDART00000131131 | Essential Splice Site | 235 | 262 | 5 | 8 |
| ENSDART00000015951 | Essential Splice Site | 377 | 404 | 6 | 9 |
| ENSDART00000105392 | Essential Splice Site | 260 | 287 | 5 | 8 |
| ENSDART00000131131 | Essential Splice Site | 235 | 262 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 19162989)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 18913924 |
| GRCz11 | 22 | 18938902 |
KASP Assay ID:
554-3076.1 (used for ordering genotyping assays)
KASP Sequence:
ATCATCTTCGTCTACGAGAAGAGAAGAAAGCCTGATGAGATCAATGACGG[T/A]GCGTAACTCTTAACTGTTCGCGCCACAATGATTTCTCACTTACACTTTTC
Long Flanking Sequence:
AACTACTATAATAATGATAATAGGCTATTCATATTAACCTATATTTTACTGAATTGTGAGATAATCATACAATGGTTGGGGAAACACTGAAAATAATGCAAGTTGTTCTATTAGTCAAGTTGTGGTGTTCTTTAAATTACTGAATTTCTGAAAATATTTACAGTATAATTATGATTACAGTTTTCTCCAGTCTTTAATTGCACCCCCTTGATCACACAGACCCCCATCTTTAATGGCACTGATGATAAGTATGAGATCAAGAGCACCCCCAACAAGACCACACTGTATGTCAAAGACCTGGACATCAACGAGGACATGGGCTTCTACCAGTGTCAAGGCACCAGTGAGGTTGGCACTGGTACAGACGACATCCAGCTGCGTGTGCGGAGTCAGCTGGCCGCTCTCTGGCCTTTCCTCGGGATCGTGGCTGAGGTCATCATCCTCATCACCATCATCTTCGTCTACGAGAAGAGAAGAAAGCCTGATGAGATCAATGACGG[T/A]GCGTAACTCTTAACTGTTCGCGCCACAATGATTTCTCACTTACACTTTTCGTCATCGTACAATGACCAGTGAATGTAATTCTTTAATTTTTGTTTTTGTTGATGACCTCGTAATGGTGCAAGATCCTATTTCAGTTTGAGTTGGTATGTTTCTTTTATTTGCCTGTAGTTTGTGGCTGTGCTCTATTTTTATGATTTTTATTGTTTATTTCTCTGTTCGCTGCTGCTTTTCCGTTGTGGTAAGTGTTCAAAAACTGCATGTCAGACTGAAGTGGATTTGCTGCGACGTAGGGCTGCACAATATATTGTAATGAAATCGCAAAAGTGGTGTTTTTCATACACATCTTGTCAGGAAAGAGTTCTCTGATTGATATTTAGTCTCTTTCAATGGGTAAAGGGTCCACAATGTCTTTTAATAGCTTTCTTTAACTTTAAAATAATAATAATAATAATAATGCTATGCCGTTATCTCTGCTTGGAACACTGACATTTTTTTTAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5689
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015951 | Essential Splice Site | 377 | 404 | 6 | 9 |
| ENSDART00000105392 | Essential Splice Site | 260 | 287 | 5 | 8 |
| ENSDART00000131131 | Essential Splice Site | 235 | 262 | 5 | 8 |
| ENSDART00000015951 | Essential Splice Site | 377 | 404 | 6 | 9 |
| ENSDART00000105392 | Essential Splice Site | 260 | 287 | 5 | 8 |
| ENSDART00000131131 | Essential Splice Site | 235 | 262 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 19162989)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 18913924 |
| GRCz11 | 22 | 18938902 |
KASP Assay ID:
554-3076.1 (used for ordering genotyping assays)
KASP Sequence:
ATCATCTTCGTCTACGAGAAGAGAAGAAAGCCTGATGAGATCAATGACGG[T/A]GCGTAACTCTTAACTGTTCGCGCCACAATGATTTCTCACTTACACTTTTC
Long Flanking Sequence:
AACTACTATAATAATGATAATAGGCTATTCATATTAACCTATATTTTACTGAATTGTGAGATAATCATACAATGGTTGGGGAAACACTGAAAATAATGCAAGTTGTTCTATTAGTCAAGTTGTGGTGTTCTTTAAATTACTGAATTTCTGAAAATATTTACAGTATAATTATGATTACAGTTTTCTCCAGTCTTTAATTGCACCCCCTTGATCACACAGACCCCCATCTTTAATGGCACTGATGATAAGTATGAGATCAAGAGCACCCCCAACAAGACCACACTGTATGTCAAAGACCTGGACATCAACGAGGACATGGGCTTCTACCAGTGTCAAGGCACCAGTGAGGTTGGCACTGGTACAGACGACATCCAGCTGCGTGTGCGGAGTCAGCTGGCCGCTCTCTGGCCTTTCCTCGGGATCGTGGCTGAGGTCATCATCCTCATCACCATCATCTTCGTCTACGAGAAGAGAAGAAAGCCTGATGAGATCAATGACGG[T/A]GCGTAACTCTTAACTGTTCGCGCCACAATGATTTCTCACTTACACTTTTCGTCATCGTACAATGACCAGTGAATGTAATTCTTTAATTTTTGTTTTTGTTGATGACCTCGTAATGGTGCAAGATCCTATTTCAGTTTGAGTTGGTATGTTTCTTTTATTTGCCTGTAGTTTGTGGCTGTGCTCTATTTTTATGATTTTTATTGTTTATTTCTCTGTTCGCTGCTGCTTTTCCGTTGTGGTAAGTGTTCAAAAACTGCATGTCAGACTGAAGTGGATTTGCTGCGACGTAGGGCTGCACAATATATTGTAATGAAATCGCAAAAGTGGTGTTTTTCATACACATCTTGTCAGGAAAGAGTTCTCTGATTGATATTTAGTCTCTTTCAATGGGTAAAGGGTCCACAATGTCTTTTAATAGCTTTCTTTAACTTTAAAATAATAATAATAATAATAATGCTATGCCGTTATCTCTGCTTGGAACACTGACATTTTTTTTAACA
Associated Phenotype:
Not determined