ZMP
zgc:55347
Ensembl ID:
ZFIN ID:
Description:
immunoglobulin-binding protein 1 [Source:RefSeq peptide;Acc:NP_998687]
Human Orthologues:
AC011195.1, IGBP1
Human Descriptions:
HCG1642624, isoform CRA_aUncharacterized protein [Source:UniProtKB/TrEMBL;Acc:C9JKU5]
immunoglobulin (CD79A) binding protein 1 [Source:HGNC Symbol;Acc:5461]
immunoglobulin (CD79A) binding protein 1 [Source:HGNC Symbol;Acc:5461]
Mouse Orthologues:
Igbp1, Igbp1b
Mouse Descriptions:
immunoglobulin (CD79A) binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1346500]
immunoglobulin (CD79A) binding protein 1b Gene [Source:MGI Symbol;Acc:MGI:1354380]
immunoglobulin (CD79A) binding protein 1b Gene [Source:MGI Symbol;Acc:MGI:1354380]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20473 | Nonsense | Available for shipment | Available now |
| sa14903 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20473
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 |
|---|---|---|---|---|---|
| ENSDART00000006899 | Nonsense | 133 | 355 | 2 | 6 |
The following transcripts of ENSDARG00000002184 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 38132111)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35931795 |
| GRCz11 | 5 | 36531948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGTTTACTTCATAGACTTCCTCAAGAGGTGCAAGGACTATGACATATG[T/A]AGTTTTCAGCTGCCCAAAGACTGCGAGAACACAGCAGACACTCCAACTGA
Long Flanking Sequence:
TACACAGAAGAATTGACCGAAGACGTGGTGGTGGTCATCTTCTTTGGTTTCATTATTTATTTACACATAAGTAGGGCCAGAATTTAGCGCAAAACGTCTGTACGTTAGATTTATGCGGAGTTTGGTAGTATCATAACTAAAAACTTAATATGTGAAATAAAATTTTAACTTTTATGTAATGTTTACTATGCAATTTCAATTAAATCCACTTTAGTAAACAAAGCAAGTCTCTCATATAATAAATCTACTAAAAGACCCAATGCCAAGAGGTTGTCAATAAAAGCACTTGATTTGTTTAAGATGTCTTTCTCTTCTTCCTGCAGCCGTAATGAGGCGCTGGAGGAAATCTCTACTACAGATCTGAAGTATCTGCTGTTGCCGGCTCTGCTGGGCGCTCTCACCATGAAACAGGTGAACCCCAACAAGCGACTGGAGTACGTGCAGGCGGCCCGTGTTTACTTCATAGACTTCCTCAAGAGGTGCAAGGACTATGACATATG[T/A]AGTTTTCAGCTGCCCAAAGACTGCGAGAACACAGCAGACACTCCAACTGAGGAGCAGAGCAGTCCAGCAGTCCCAATGCCAATGTCTCAGCCAGACCTCATCGCCATGGCAACACAGAGACAAGCCAAAATTGAGAGGTGGGTTGGTAGAATTGGGTAGCATGTTTGTTTTTGACCAATAATAATAAAAAAAAAAACAGTAAAGGGAAATGTACAATTTAAATGACCTAAATACTTTTTAAGAAATAATTTAGATCATTTCTTAAAATATTTATCTAAAAATGTAAATATATTATTGTGATGCAAAAGGAACTTGAATTTAGGCATGGTTTAGATTCTGACGGTACAAAAATATCACAATTTAGGATTTCACGGTTTTGCATATATATTCTTATATATTCTTTTTAATATATTCTTTTTAAATGTCTGGGTAAAAACAACAACTTTTTCCTCTTTGAACACAAAATATTTAATTTGAAGAAAGATTTATAATATTTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14903
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 |
|---|---|---|---|---|---|
| ENSDART00000006899 | Nonsense | 172 | 355 | 2 | 6 |
The following transcripts of ENSDARG00000002184 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 38132226)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35931910 |
| GRCz11 | 5 | 36532063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCAGTCCCAATGCCAATGTCTCAGCCAGACCTCATCGCCATGGYAACA[C/T]AGAGACAAGCCAAAATTGAGAGGTGGGTTGGTAGRATTGGGTAGCATGTT
Long Flanking Sequence:
CGGAGTTTGGTAGTATCATAACTAAAAACTTAATATGTGAAATAAAATTTTAACTTTTATGTAATGTTTACTATGCAATTTCAATTAAATCCACTTTAGTAAACAAAGCAAGTCTCTCATATAATAAATCTACTAAAAGACCCAATGCCAAGAGGTTGTCAATAAAAGCACTTGATTTGTTTAAGATGTCTTTCTCTTCTTCCTGCAGCCGTAATGAGGCGCTGGAGGAAATCTCTACTACAGATCTGAAGTATCTGCTGTTGCCGGCTCTGCTGGGCGCTCTCACCATGAAACAGGTGAACCCCAACAAGCGACTGGAGTACGTGCAGGCGGCCCGTGTTTACTTCATAGACTTCCTCAAGAGGTGCAAGGACTATGACATATGTAGTTTTCAGCTGCCCAAAGACTGCGAGAACACAGCAGACACTCCAACTGAGGAGCAGAGCAGTCCAGCAGTCCCAATGCCAATGTCTCAGCCAGACCTCATCGCCATGGCAACA[C/T]AGAGACAAGCCAAAATTGAGAGGTGGGTTGGTAGAATTGGGTAGCATGTTTGTTTTTGACCAATAATAATAAAAAAAAAAACAGTAAAGGGAAATGTACAATTTAAATGACCTAAATACTTTTTAAGAAATAATTTAGATCATTTCTTAAAATATTTATCTAAAAATGTAAATATATTATTGTGATGCAAAAGGAACTTGAATTTAGGCATGGTTTAGATTCTGACGGTACAAAAATATCACAATTTAGGATTTCACGGTTTTGCATATATATTCTTATATATTCTTTTTAATATATTCTTTTTAAATGTCTGGGTAAAAACAACAACTTTTTCCTCTTTGAACACAAAATATTTAATTTGAAGAAAGATTTATAATATTTTGGACACTCAGGCTAAATCATTCAACTAAATCATTGACTTCTGCTGTCTTTATACATTTTAAAAACACTAATCTCTTTAAAACTTTACATTAACTTTAAGAGTAGGGATGTATGATATA
Associated Phenotype:
Not determined