ZMP
LOC100149932
Ensembl ID:
Human Orthologue:
CD22
Human Description:
CD22 molecule [Source:HGNC Symbol;Acc:1643]
Mouse Orthologue:
Cd22
Mouse Description:
CD22 antigen Gene [Source:MGI Symbol;Acc:MGI:88322]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1988 | Nonsense | F2 line generated | Not yet available |
| sa39719 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1988
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000133590 | Nonsense | 28 | 412 | 2 | 7 |
| ENSDART00000147771 | Nonsense | 24 | 379 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 57393423)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 56128527 |
| GRCz10 | 1 | 56385078 |
| GRCz11 | 1 | 56843614 |
| GRCz11 | 1 | 57100165 |
KASP Assay ID:
554-2894.1 (used for ordering genotyping assays)
KASP Sequence:
GACAAAAACTACAATGATATCTGTTTTTCAGKGGTTTCTRGTGCTGAYTG[G/A]GYTGTGAATTACAAATCTTTACACAWCTGTGCACTGAAGAACTCATCAGT
Long Flanking Sequence:
GTTTGTGCTCGTGCAAACATTAGTAATTAGAAGTTAATAGAGATAATTCAAGAAAAGCAACCCTGTTTTTTTAATGTATGCTCGCCTTTCATGAAATGCTATGTATACTTGATGAGCCACTTGATTGAAACATGCACTTTTTAAATGAAAACTTCAAGTTAAGCCAAAGAGTGACAATTATGTTTAACGTAACACAATCATGTTAAATGAAAAGTAACCACAATGGCAATAATTTAACATGAATTGTTTATGTAAATTATATTTTTTGGTCTGATTATTTAATTATCTTTAATTGTGTTCTGTGTTCAGAAGTGGTCAATCCTGCAGTTATCGCTTTTGGTAGCGTTGCGTGACGTTATATGTTTGTCTGAACAGCTGTTAACAAAATAAAAAAGTGTTTATATGCATCCAGCCTCCATTTTGTTTTTGTACAGAATATATTGATATTCAGACAAAAACTACAATGATATCTGTTTTTCAGGGGTTTCTGGTGCTGACTG[G/A]GTTGTGAATTACAAATCTTTACACATCTGTGCACTGAAGAACTCATCAGTGATAATCAGCTGCACTTATAAATACCCTAATGGACATCAGATCATGAAAGTGTACTGGACCAAAAACCCTGTAAAGGATGTAGAGCCTCCAGATCTGTCTGAGGACCCTGAATACAGTCAGAGGCTTCAGTATCTGGGAGATAAAAAGCAGAACTGCACCATCAGACTGAGTCATGTGACAAAGAAAGTTGAACATGAGTACTGTTTTAGATTTACTACTGATAAAGATGGGAAATGGCTTGGCTCTCCAGGAGTGATTCTCTCTGTCACAGGTGACTCTCCTGAGGTTTCTCTCTTCTTGTGGTCATTATGTAGAATAATAATCAGTGTATGAGAGCAGCACTAGATATAATGTGTGTGTTGTGTTCAGATCTTCAGCTGGAGTCTCCTGAGAGAGTGACAGAGGGAGATTCAGTCCGTCTGACATGTAAAAGCAGCTGTAAACTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39719
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 |
|---|---|---|---|---|---|
| ENSDART00000133590 | Essential Splice Site | 301 | 412 | 4 | 7 |
| ENSDART00000147771 | Essential Splice Site | 297 | 379 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 1 (position 57394417)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 56129521 |
| GRCz10 | 1 | 56386072 |
| GRCz11 | 1 | 56844608 |
| GRCz11 | 1 | 57101159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGACCATGGAGTGAAATACTCTGATCCTGTGACTTTAGATGTTCAGTG[T/C]GAGTAAATGATGGTTCAGTAACTGATATATTAAATCCTCTAAGTCTGGAT
Long Flanking Sequence:
ACTGACTGACACACCAACATTCATCTGGTACAGAAACTCACACACATTGACTAATATTGGAGATGAACTCAACATCAGCTCAGTCAGAAGAGAAGACGCAGGCAGATATAGATGTGCTGTACATGGACACACACTCACATCACCTGACGTCTATCTCAATGTCACCTGTGAGTCCAGATTTATTTTCATTATATAGTTTTATTATTATTATAGGATTTACACATTTTATTTTTATGTGCTTTAGATCCTCCAAAGAGCGTCTCAGTGTCCATCAGTGGGTCTGCTGTAATAATGTCTGGAGATTCAGTGGCTCTGAGCTGCAGCAGTGACTCAAACCCTCCTGCAGAAATCAACTGGTTTAAAGGAGAAACATCAGTAAGATCTGGAAGAATCTTCAGCATCTCCAAGATCAGCTCTGATGACAGTGGAGAATACAAGTGTAGAGCCAGAAATGACCATGGAGTGAAATACTCTGATCCTGTGACTTTAGATGTTCAGTG[T/C]GAGTAAATGATGGTTCAGTAACTGATATATTAAATCCTCTAAGTCTGGATTTTAATGCCATGTTTGATGTAATTGATATGAGTGTTTTTTTAGTTTTTTTTTTTTTTTCTGTTTCAGACGCACCCAAGAACATCTCAGTGTCCATCAGTGGATCTGCTGTGATAATGTCTGGAGATTCAGTGACTCTGAGCTGCAGCAGTGACTCAAACCCTCCAGCAGATTTTAGCTGGTTTAAAGGAGAAACATCTGTAAGATCTGGAAGAATCTTCAGCATCTCAAATATCAGCTCTGATGACAGTGGAGAATACAAGTGTAGAGCCAGAAATGAACATGGAGAGAAAAACTCTGATCCTGTGACTTTAGATGTCCAGTGTGAGTTTTTGATTATTCAATTACTGAAACATTACCTCCTATAAATATTAATGTTGTGGATGTTATTAAGTAGATATGAGTGTTTTTTCTTTCTAGACCCACCCAAGAGCATCTCAGTGTCCGTCACT
Associated Phenotype:
Not determined