ZMP
ighmbp2l
Ensembl ID:
ZFIN ID:
Description:
DNA-binding protein SMUBP-2 [Source:RefSeq peptide;Acc:NP_001038365]
Human Orthologue:
IGHMBP2
Human Description:
immunoglobulin mu binding protein 2 [Source:HGNC Symbol;Acc:5542]
Mouse Orthologue:
Ighmbp2
Mouse Description:
immunoglobulin mu binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:99954]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23288 | Nonsense | Available for shipment | Available now |
sa9011 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6514 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23288
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 |
---|---|---|---|---|---|
ENSDART00000060291 | Nonsense | 89 | 997 | 3 | 15 |
ENSDART00000100674 | None | None | 83 | None | 5 |
ENSDART00000145211 | None | None | 349 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 20310961)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20541184 |
GRCz11 | 18 | 20530250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATAATCGTCTTTTGTATTGTGCTTAAAGGTGATATTATAGGCTTGTA[T/A]CAGGCAGAGGGTCAGGCTCTGCCTACTCAGTTGGGGTCAGGTGTGGTGAC
Long Flanking Sequence:
GTGTGCCACACTACTACAAATTAAACAAAACAAAAAAAAAAAACTTTTACAACATTTTGTATCCTTGGTAACAAAATAGAAGCTGGTTAACAAAGCATGTATGACTTTTGTCTGAAATATCACTGAGATGAAATTCTTCAGTTTTAATAGGTTTCAATGAGGATAGCATGTAGAAGGATTCAATATTATTAAGTATTTTTGTATTGTCAGCGCATGGCAGGAGAATGTGTCTCTCAAGAATCTACAGCACAAAGGAGTGTGTCTGATGAAACTTCAGATCGGAAGCCAGCACACTGGAATGTATGGCAGACTTCTAGTCATTTTTGAACCCAGGAAATGCATAGGGCTCTCAGTTCTACCCAGCAACACTTTTGGACCTGGTGAGACATTGATTTCCTTTGGAGTTTATGATCAATTTATAATTTAGACTTTTTACCCTAGTTCTATCACTACATAATCGTCTTTTGTATTGTGCTTAAAGGTGATATTATAGGCTTGTA[T/A]CAGGCAGAGGGTCAGGCTCTGCCTACTCAGTTGGGGTCAGGTGTGGTGACTCGTGCTACTCAAGCATCTCTGACGGTGGCTTTTGATGACACACAGGATGGTACTAATTTAGACAGAGATGGACTCTACAACCTAATGAAACTGGCAAATGATGTGACCTACAGGCGGCTGTCAAGGTATGTACATTTATCACTTCATGGCTCAAAGACTCAACGTTCCATTTTGGTTTATGCAAAATAGTTTTTATTTAGATAGAAATCATTTTAAATGCAAGTAAAGTGTTTGCTTTAATAAAAAAAATTGGTGGTAAAATATGGGAGAAATAATGCTTCAGTGTCATAACATATTTTGATGTAAAAACTCAACAAAGCAGCTGATGTGTTTTGTACTTATTAAAACGTGCACAAATTAGGTGATCATACCCAAGTAAATTACTTATTTATACAAATATCCTAGTTTTTATTATATTAAAATTATATTGGCAAAATCTAATAATTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9011
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 |
---|---|---|---|---|---|
ENSDART00000060291 | Nonsense | 455 | 997 | 9 | 15 |
ENSDART00000100674 | None | None | 83 | None | 5 |
ENSDART00000145211 | None | None | 349 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 20306940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20537163 |
GRCz11 | 18 | 20526229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTACCGTATGAACAGTGCCATCATGCAGTGGGCTTCAGAGCAGATGTA[T/A]CAGGGAAAACTCATTGCACATCCTTCAGTGGAGAAGCACTTGCTTAGGTA
Long Flanking Sequence:
TGAACATTTTAATTTCAGGGTGTAACTTTAACCACCGTAGAGCCTTACTCGTCAGGCTAAAATGACTGGGCAGTTATTTTATTGGACTGGTCTGTGTAAAGATTTTTGTTCAATGAGTTTGTCATTGCATGAATTTTTTGGTTTTAGACAGCTTTTTTTTTTGTACGTTTTTTTTTTTTTTTTTCCATAATTGTTTTCAATTGTTTTTGTTTAAACCTTAAAACATGGTAAAAGGTAATATGAACAAATAAATAATCATGGGGTACCTTTAAGATTTTTATTCAGTGTGTTTTTCATTGCATGGATATTTAGGTTTGTGATGAGAAATGCTTTGCATATTTAAGTGTTATTTATGTCTTTCACAGTGCTGCATCTAAAGGCCTGTCTGTCAGTTTAATGGAGAGGCTGATCAAGAAATATGGAGACTCGGTGGTTCGAATGCTGACCACACAGTACCGTATGAACAGTGCCATCATGCAGTGGGCTTCAGAGCAGATGTA[T/A]CAGGGAAAACTCATTGCACATCCTTCAGTGGAGAAGCACTTGCTTAGGTATGTAAAAAAGTGTTTTTGTTAATGTTTAATGATTTAGGTAATTCAGGCAATTCTGTAATTAGTGGACATTTTCAGAAGATTTTCAGTTTTTATTTGAAATGTAAAAATTGCAACATTATGAAAACGTTTGTCACTTTTATGACTTTTATCAATTTAAAGCATCCTTGGAGAATAAAAAATGTATACATATATACACATGAATACATTAGTGGTGTAACGGATCACAGATCTCATCATTTAGATCACACTATGTTTTTTTTTAATCATGGATCAGACTATTTTTCAGATCAGCAAAAAAAGGGAGGAGACAGATATTATTTGCTTTTTACTTATACAAAATTATTACTGCAAAAAGCATTGGGTTTAACAAACATAACTTGGAACATGTAATTTAATAAAAATTAAAATCAAAAAGAGAAACAGCTGAAAAAAAGGAAAATATTCAATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6514
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 |
---|---|---|---|---|---|
ENSDART00000060291 | Nonsense | 920 | 997 | 14 | 15 |
ENSDART00000100674 | None | None | 83 | 4 | 5 |
ENSDART00000145211 | Nonsense | 272 | 349 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 20299596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 20529819 |
GRCz11 | 18 | 20518885 |
KASP Assay ID:
554-5195.1 (used for ordering genotyping assays)
KASP Sequence:
GTGAARTGCAAAGCCAGTGTSCTGACGCTAGGACAACTCTGCATTTACTG[T/A]AACAGACAGTACTGYTTGAGTCACCATATACCCGAGGTACAACTTTTTAT
Long Flanking Sequence:
GCCCTATACACAACTCCTTAACTTTTCGAATTTTGATTGTAATGCAATAATGTGCACCTTTTTTAAGCTTATTTAAACAAAAAATATTGTGAAAAGCTCTATAGAAATAAACTTGTATTGAATTGAATTGAATATAGTTGAATGAGTATATAATATTAAAGCAATCCAATCAAATGTGCTTTTGACAACCTCTGGAAGTGCTCAGAAGTTTATGGCGGTTAAGACTGTTTAAACATGGATTTATTGACATCATCCACTAGTGAAAAAATACATATTAATATCGGGTTTACAAGGCCACTGTCTTATACATCATGATCAATATGTATTTCTTTCATAGGAACTTCAAAGATAAAAGCAGGAGCCACAGATATTGCTGCGGCTGCCAATGGAGATGATGATTTTGATGCTCTCATCAATGCTGTGGTTAAAGCAGAAAGTGTGTGTGGTTTTGTGAAATGCAAAGCCAGTGTGCTGACGCTAGGACAACTCTGCATTTACTG[T/A]AACAGACAGTACTGCTTGAGTCACCATATACCCGAGGTACAACTTTTTATTAAAAGGGTGATCATATTATGGGGGAAAAAAAAATATTTTCAGATATTTTAGAGTGTGTTCAGTGTAACATTATAATAGGCTGTAAATTAAAAAACTCAACTTTGTTCCCTATTGAAATAAAAAAAAATTGACAGAAGTTTTAGTTTTGTTTAATAATCAGTAATGTTGTTCTATTAGGTTACTTAATATAGGACATTATAATGTGCACTCTTCTTTTTACATTTTATTTTACATTCATGGGAAATGTACAGTAATGAATGTAGAATAAAACAAAAAGGTGGCTGTTCTTGTGAATTTGACTTATAATGTTCTTTATAGATTTTCTTAATCAGAAATCAGGAAAATCTTAAGATGATGTTGCATGGATGAAGCTGGATACATGCTTTTATACAAGTCAACAAACATCTGAACAATTGATTTAGCAAATAATTTTGAACAGTTCCGGCATT
Associated Phenotype:
Not determined