ZMP
zgc:152984
Ensembl ID:
ZFIN ID:
Description:
protein LAP2 [Source:RefSeq peptide;Acc:NP_001180472]
Human Orthologue:
ERBB2IP
Human Description:
erbb2 interacting protein [Source:HGNC Symbol;Acc:15842]
Mouse Orthologue:
Erbb2ip
Mouse Description:
Erbb2 interacting protein Gene [Source:MGI Symbol;Acc:MGI:1890169]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9217 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2551 | Nonsense | F2 line generated | Not yet available |
sa31770 | Essential Splice Site, Missense | Available for shipment | Available now |
sa21689 | Nonsense | Available for shipment | Available now |
sa13728 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9217
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016888 | Nonsense | 29 | 636 | 2 | 18 |
ENSDART00000087680 | None | None | 590 | None | 18 |
ENSDART00000123935 | Nonsense | 29 | 1349 | 2 | 25 |
ENSDART00000129441 | Nonsense | 29 | 1384 | 1 | 25 |
The following transcripts of ENSDARG00000044281 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 15540566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15553873 |
GRCz11 | 10 | 15511992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTGCCGCTGCCTGCGGGGCGAGGAGGAGACYGTCACCACACTGGACTA[C/A]TCGCACTGCAGCCTGGAGCAGGTCCCTAAAGAGATCTTCAGCTTCGAGAA
Long Flanking Sequence:
TTTAACTTTTTTTATTTTGACAGACTGTGATGAAGACTTTTATGTCTATATGATATAACCATTGTTTTTCTCAAATAAAATAGTGAAATGCTGTCAGGTTAGCTCTGGAGATGAGTTCATATAGTGAAATGACAAACACTGAGAACACACAACATCACACACATGTAACAAACAGTAACTTGTAGTACATTTCCATAAATAAAAAGCATCTTATACTCCAGAAATGCAGGAATTAAACCCAATTACTAATCTTAAACCGCTCATTCCCTTCACCCTTGTGTAACTAAGCTGTAAACCAAGCTTGTTTTGACAGCGCTATCCCATATCCCAGTGTTCTTGTGTTTGAATTATTAATGCGGACGTGCTGCTGATCGTGTTCTTCTTCTCTCCTCCAGTGCCTGAGCTGCGGTGAGGATGAGTAGCAAGCGGAGTCTGTTTGTGCGGTTGGTGCCGTGCCGCTGCCTGCGGGGCGAGGAGGAGACCGTCACCACACTGGACTA[C/A]TCGCACTGCAGCCTGGAGCAGGTCCCTAAAGAGATCTTCAGCTTCGAGAAGACCCTGGAGGAGCTCTACCTCGACGCCAACCAGATCGAGGAGCTGCCCAAAGTACCACTCGCACACCCAACAATGCATGCTTAGGCAGTGGAACATTTCCCTTTCAGCATTTGCATCAAATGAAATTTTGTACACACAATTCAGAAATTTAAAATAAATTAACTCCAGGCTATCAGATAACTTCAGTGCAGATCAGATATTGATCTAAATGTGCCTCATTGGCTATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTAATTATTATTATTATTTTTTATTTATTAAGTTGCTTTTATTTAACAAGTAAGTAGTTGTTTTCTTGACCAGAACCCAAAAAGACAATAAAAGGGGTCTCAAACCGGATGTACCCGCTTGGGACATATGACAGTTGAAAGTAACGCACACCAGACGTTCACATTCGCATGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2551
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016888 | Nonsense | 529 | 636 | 16 | 18 |
ENSDART00000087680 | Nonsense | 513 | 590 | 17 | 18 |
ENSDART00000123935 | Nonsense | 529 | 1349 | 16 | 25 |
ENSDART00000129441 | Nonsense | 530 | 1384 | 15 | 25 |
The following transcripts of ENSDARG00000044281 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 15604023)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15617330 |
GRCz11 | 10 | 15575449 |
KASP Assay ID:
554-2907.1 (used for ordering genotyping assays)
KASP Sequence:
ATGAGGCTGGAAAAGAGCCCAGGGTCAGCGAGAGGAACCATATCGGAGTG[C/T]AGGACGTTGGAGTGAAGGTTGGAGTTTAAAAACACTTCCAAATTCATGGC
Long Flanking Sequence:
TGCGCTTTTATGCTGCTTCTGGTAATTAGCAGGCTTGAGGATACACATTCTTAAGATTATTTATGTCCTTGCAGTATTTTACAAGTTTATTTTCAGCTTGAAATAATAGACTTAATTGTGGCTAAAGCTGGTTTTGTTTACCTGCATAAATAAAACTCCGCAGGTTTGCTGACTCAATTGAAACCTAAACATTCATTCAAGTGCCTTGTAAAATATTGTAGAAGTGTATCTTTATTGTACCCCATTAAGTAACGTCTTACACAGTGCATTCAAGCCAGTCTATTTGTCTTGATAGAAGTACACATACTCACATACTTTAACTGTGTCTGTATTTGTATTTGTAGGAAGGCAATCTAAAGCGATACCCCACACCATACCCTGACGAACTAAAGAACATGGTGAAAACGGCTCAGTCCGTGGCTCATAGACTCAAAGAGGATGAGTCCGGGGATGAGGCTGGAAAAGAGCCCAGGGTCAGCGAGAGGAACCATATCGGAGTG[C/T]AGGACGTTGGAGTGAAGGTTGGAGTTTAAAAACACTTCCAAATTCATGGCTGAAATATTTTGATATGTACATTGATATGTTGGATGTGTGAAAAGTGTTTAAAGCGAATCTGACTGCAGATGTTAGAATAAACTTGCATTTTCTGTTTCAGGTGATTGAAAGTCCTTGCACCAATGGTAAACCCGCTGAAATGGATCCTAAAGCAGCAATGAACAGCAATCACAATTACGAACCGATAGATTCAGTAGACAACCACAGCATTGAGAGGATCCCTCTCAAGACCTCAGACAACATGAGAACTATGGTGAACCACGATGACACGCTTGAGGTACTGTATCATTGTTTAAAGAGCTCCTATTTTGCTTTATAAAAGCTCACATTTTGGTTTTGGGGGTCTCCAACAACAGGCTGATATGTGTGCAAGTTCAAAAAACACTTTTTGTTTTATAATATGCATTTATTTTTACCTAATTATCCCAACGACTCTCATATGATTCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31770
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016888 | Essential Splice Site | 593 | 636 | None | 18 |
ENSDART00000087680 | Missense | 578 | 590 | 18 | 18 |
ENSDART00000123935 | Essential Splice Site | 593 | 1349 | None | 25 |
ENSDART00000129441 | Essential Splice Site | 594 | 1384 | None | 25 |
The following transcripts of ENSDARG00000044281 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 15604353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15617660 |
GRCz11 | 10 | 15575779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTCAGACAACATGAGAACTATGGTGAACCACGATGACACGCTTGAGG[T/C]ACTGTATCATTGTTTAAAGAGCTCCTATTTTGCTTTATAAAAGCTCACAT
Long Flanking Sequence:
ATTTGTATTTGTAGGAAGGCAATCTAAAGCGATACCCCACACCATACCCTGACGAACTAAAGAACATGGTGAAAACGGCTCAGTCCGTGGCTCATAGACTCAAAGAGGATGAGTCCGGGGATGAGGCTGGAAAAGAGCCCAGGGTCAGCGAGAGGAACCATATCGGAGTGCAGGACGTTGGAGTGAAGGTTGGAGTTTAAAAACACTTCCAAATTCATGGCTGAAATATTTTGATATGTACATTGATATGTTGGATGTGTGAAAAGTGTTTAAAGCGAATCTGACTGCAGATGTTAGAATAAACTTGCATTTTCTGTTTCAGGTGATTGAAAGTCCTTGCACCAATGGTAAACCCGCTGAAATGGATCCTAAAGCAGCAATGAACAGCAATCACAATTACGAACCGATAGATTCAGTAGACAACCACAGCATTGAGAGGATCCCTCTCAAGACCTCAGACAACATGAGAACTATGGTGAACCACGATGACACGCTTGAGG[T/C]ACTGTATCATTGTTTAAAGAGCTCCTATTTTGCTTTATAAAAGCTCACATTTTGGTTTTGGGGGTCTCCAACAACAGGCTGATATGTGTGCAAGTTCAAAAAACACTTTTTGTTTTATAATATGCATTTATTTTTACCTAATTATCCCAACGACTCTCATATGATTCGGTCAGTGATTCATTTGTTCCCAAACCCCTCCTTAGCTTGAAGCTAATCTGCGCTGATTGATCCCATGACTCAGTTTGTTGTGATTGGTCTTTCAGTGCAGGATGGAGAGAAATGCCCACCACGCCATCAGATGTGTAACTACACGGCTAAGTAGCACACAGAGTATGTGAGAGCCCAAAGCAGGAATGCATTAAAGCAATGCAGTTAACACCAGCATTACTCTATTGTTAACGCTGAAAATTGACTGTGCTGCGTGTGTATCAGAGATGGGAAGTAACGAAGTGCAAATACTATGTTTCTGTACTTAAACAGATTTTTCTGGTATTAGTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21689
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 |
---|---|---|---|---|---|
ENSDART00000016888 | None | None | 636 | None | 18 |
ENSDART00000087680 | None | None | 590 | None | 18 |
ENSDART00000123935 | Nonsense | 965 | 1349 | 20 | 25 |
ENSDART00000129441 | Nonsense | 971 | 1384 | 19 | 25 |
The following transcripts of ENSDARG00000044281 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 15611419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15624726 |
GRCz11 | 10 | 15582845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCAAACCTCCGGTAAGCAGCACTCGCTACCCTGCCGGCCCCCCACCA[C/T]AGTATAACATCCAATATGCCAGCAGCACTGTGCCCAAAGATAACCTGTGG
Long Flanking Sequence:
CCATGTCGAGCAACAACAATGCCAGGCTGTCACTCGAGAACCTTGAGAATGGCAATCAGCTTCAGAAAACCCAGTCTGGGGAGAATTTCAATAGCAGAACGGATCAAGTTCCCTTGCGGTATGAGTCTGTGAGGACAGTCTCAACGGGTGTAAACGCATTAAGCGATATGAGTCTTTCTCGTAGCACGGAGGAGCTGTCGCCAGAGAAGAAATGTCCACCAGCCCCAGTGGTGAAATCTCAGAGTATTGCTAATATGGATGGTGGAGGTATGAAGCTGTACTCCATTGAGGGAGAAAGCCCCCCATATGAAGTGGCTTGTGCAAGCAGAACCTCTGTAGCTGGGGCTCAGGGCCAGAGCATTGTCCGCTCCAAATCTGCCTCCTTGCTCAATGACCAGCATATGCAGATCTACCCTGGTTCTTCAGCTTCATCTTCTGACTTGCTGTCCAGCTCCAAACCTCCGGTAAGCAGCACTCGCTACCCTGCCGGCCCCCCACCA[C/T]AGTATAACATCCAATATGCCAGCAGCACTGTGCCCAAAGATAACCTGTGGAGCCAACGTACGCCTGTACCTCCTGACCAGCCTTACATGCCACCACAGCACTCCCTCGCCAACACCAACTTTTCCAACCGCAACAATGCCCCTCCATACCCCCAGCCTCAACAGCGTGGACCGCCCAAGACCCCAGACATGTGGGCCAAGGAAAGAATGCTCCCCCAAGTTGGTCAGCGTGGCACCTTACAAAGACAGGGTAGCGGATCCTCTGGCAACCCCATGTGCATGCCAGATCCACGCCGCATGCCAGGAATGGAAGGAGACTACATGACCTACCGGGACATTCATGCAGCAGGTCGGGGGCCACTGCAGATGAGCCAGGCTCTTCACAGACCTTTGTCTGCTCGCACATACAGCATGGATGGACCCAATGCTCCCAGACCACAGAGTGCCCGGCCCCCACCTCACGAGGTTCCAGAGAGGACCATGTCTGTTAGTGACTTCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13728
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 |
---|---|---|---|---|---|
ENSDART00000016888 | None | None | 636 | None | 18 |
ENSDART00000087680 | None | None | 590 | None | 18 |
ENSDART00000123935 | Nonsense | 1019 | 1349 | 20 | 25 |
ENSDART00000129441 | Nonsense | 1025 | 1384 | 19 | 25 |
The following transcripts of ENSDARG00000044281 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 15611581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 15624888 |
GRCz11 | 10 | 15583007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACCAACTTTTCCAACCGCAACAATGCCCCTCCATACCCCCAGYCTCAA[C/T]AGCGTGGACCGCCCAAGACCCCAGACATGTGGGCCAAGGAAAGAATGCTC
Long Flanking Sequence:
GCGATATGAGTCTTTCTCGTAGCACGGAGGAGCTGTCGCCAGAGAAGAAATGTCCACCAGCCCCAGTGGTGAAATCTCAGAGTATTGCTAATATGGATGGTGGAGGTATGAAGCTGTACTCCATTGAGGGAGAAAGCCCCCCATATGAAGTGGCTTGTGCAAGCAGAACCTCTGTAGCTGGGGCTCAGGGCCAGAGCATTGTCCGCTCCAAATCTGCCTCCTTGCTCAATGACCAGCATATGCAGATCTACCCTGGTTCTTCAGCTTCATCTTCTGACTTGCTGTCCAGCTCCAAACCTCCGGTAAGCAGCACTCGCTACCCTGCCGGCCCCCCACCACAGTATAACATCCAATATGCCAGCAGCACTGTGCCCAAAGATAACCTGTGGAGCCAACGTACGCCTGTACCTCCTGACCAGCCTTACATGCCACCACAGCACTCCCTCGCCAACACCAACTTTTCCAACCGCAACAATGCCCCTCCATACCCCCAGCCTCAA[C/T]AGCGTGGACCGCCCAAGACCCCAGACATGTGGGCCAAGGAAAGAATGCTCCCCCAAGTTGGTCAGCGTGGCACCTTACAAAGACAGGGTAGCGGATCCTCTGGCAACCCCATGTGCATGCCAGATCCACGCCGCATGCCAGGAATGGAAGGAGACTACATGACCTACCGGGACATTCATGCAGCAGGTCGGGGGCCACTGCAGATGAGCCAGGCTCTTCACAGACCTTTGTCTGCTCGCACATACAGCATGGATGGACCCAATGCTCCCAGACCACAGAGTGCCCGGCCCCCACCTCACGAGGTTCCAGAGAGGACCATGTCTGTTAGTGACTTCATCTACCAGCAGGGCAGCCCCAGCAAGAGGTCCAACATGAGGGTAAAGTCCGAGCACTCGTTGCTGGATGGGCCAGTTGGAGGAGGTGGCCGAGTTCCAGCTGACTGGAGGGATCAGGTCATGAGACACATTGAAGCCAAGAAGATGGAGAAGGTATGTTCGTTC
Associated Phenotype:
Not determined