ZMP
ambpl
Ensembl ID:
ZFIN ID:
Description:
protein AMBP precursor [Source:RefSeq peptide;Acc:NP_957412]
Human Orthologue:
AMBP
Human Description:
alpha-1-microglobulin/bikunin precursor [Source:HGNC Symbol;Acc:453]
Mouse Orthologue:
Ambp
Mouse Description:
alpha 1 microglobulin/bikunin Gene [Source:MGI Symbol;Acc:MGI:88002]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21678 | Essential Splice Site | Available for shipment | Available now |
| sa41600 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21679 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21678
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:
Founder:
SL6_01_A8
KASP Assay Location:
Unknown
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027026 | Essential Splice Site | 83 | 346 | None | 10 |
The following transcripts of ENSDARG00000004296 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 10769164)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 10845030 |
| GRCz11 | 10 | 10803268 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCCAGCGGGTCACCACAAAGCCTCAGCATGACCCGCATCGGCCTCAGG[T/C]ACAAACACAAACATCAACAGCAAATTAATAATCAATCACAAACACACTCA
Long Flanking Sequence:
ATGAATGAATGAATAGCATAATAATAAATATGAAATAAAACAACTAAAAAATAGGTAAAAGGCTAACTTTATTTAAAAGGCTATGATTTTTGTGTATTAAATGCACTTTATTACTATTCTTTGGCCTGAAAATTACAACAGCTATTATAAAAAAAAGTAAGTAAATAATTGCGCAATATAGTGTTTCACCATATTTTGTTGAGTTTTTATTCTTATTATGAGAAATGAAGATATTTGTGTTTCTATTTTCATAATTATTAGTATCAGGCCAGTGATGTGATTTTTCTAACATGATTTAAGACTCTCATAGCCTTTATTTGTCATGATCTGACCTTTCCACCTTTGTCCTCTTGCAGTTCATGGGGAAATGGTATGATATTGCGGTGGCGTCCACATGTCCTTGGATGAAGCGTCATAAAGGAGACGCAGCCATTGGTTCTCTGGAACTGCAGTCCAGCGGGTCACCACAAAGCCTCAGCATGACCCGCATCGGCCTCAGG[T/C]ACAAACACAAACATCAACAGCAAATTAATAATCAATCACAAACACACTCAAATGGCTCTCAATGCAATTAGAGCTAAAATGTCAATTCAATCCCCATTTCCTCAACCTCTTCATTCTTCTGCTAAACACAAAAGAAGATATTTTGACAAATGTTAGAAACTTGTGGCCATTACCATCTACATTAACTTGATGGCTACTGATTTCCATCAATCTTCAAATTATATTCGTCTTTTGTGTTCAACAGAAGAAAGAAACTCATAAAGTTTAACAAAAAGTGAGGGGTAAATATATGATTATCATGTTTGGGTGAACTTTCCCTTTATTCCCTAGGTAGCCTAAAACCCACTTTTAACTTTGAGTAAAGGAACTTTTCAGTCTTGTAATCTAGGTCTTGTTGGCACCTGTTATTAAAGGAAGTTAATTTTATTTCAATCCCCAGAGACCTTTGTTCATCTGTGCAACACAAATTAAGATATTTTAAATGAAATTCAGGAGCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41600
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
Founder:
SL7_02_C12
KASP Assay Location:
Unknown
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027026 | Essential Splice Site | 148 | 346 | None | 10 |
The following transcripts of ENSDARG00000004296 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 10781650)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 10857516 |
| GRCz11 | 10 | 10815754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAACAAAAACCAGGAGGTGAAAAATCAACATCTGTCAAACTCTACGG[T/C]AAAACATTTGTTTTCTTCTGGATGGCATTTCTTTCTTTCTTTCTTTCTAA
Long Flanking Sequence:
AACAGCACTACCTACTGCACCACTGTGTTGCCCCTTATGTAAACAAAATAGGTGATATATATTGCGCCACCAAAAATGATTAAGGTCATGTCCATGGATAAGCCGATATATTGATTATTGCAACAGGCCAATGGACAATTCAGTTAACCGTATTTTGAATGACTCAAGGTTAACTAGATCTTTTACAAAAGCATATGAACAGCATCATTGATTTATTTTGCAGACGTGGGACCTGTAAGTCCATCAGTGGAGAATATCAGCTGACCAAAACACCTGGAAGATTCCACTACCACAGTGCCAGTGTGTACAACACCACAGCTGTCAGATTGCGCTTCATTCATTTCACTGTTGTTTCACTGTATGTGTGTCTTTCAACCTGTAGAGTGGAATTCTGATGTGGACGCCTACGTAGTGCATACTAACTATAATGAGTACGCTCTGGTGGTGATGTTAAAACAAAAACCAGGAGGTGAAAAATCAACATCTGTCAAACTCTACGG[T/C]AAAACATTTGTTTTCTTCTGGATGGCATTTCTTTCTTTCTTTCTTTCTAATTAGTAATTTAAGTAGGAAAGCAATGAAATGAAAGTTTTGTAAGACTTTTTAAATTGTTTCAATAAATGAATTATTCAGATAAAAAAAAAAAAACAGACAATAAAATAACCAGTAAAATTCAAGACAGACAATAAAATGTTTTGTTTACAGTGAACGAATCAATGAAGCTGATTTTATTTATATTTATGCCTTTATTTACAAAACAGTAGCTAGACAGAAAGTTGAGTGGGAGAGATAGCGGGAATAAGATCGGTAAAGTTTCACAAGCTGGGAGTCAAATTTAGGTCGCCCGAATAGTTTAATGCACTATGCAACTTCTACTAGGCTAGAATCCCTGACGATTGACTCTTTATACCAGCATTGCCATGACAGGACATGAGCACTATTGCAAGCAGCAGGAACAAATATACTAAACAATGTCTTGTCAACATGTTATTTGGGCAGACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21679
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:
Founder:
SL6_04_B10, SL6_04_F10
KASP Assay Location:
Project idt6, Plate 2, Well A12
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027026 | Essential Splice Site | 181 | 346 | 5 | 10 |
The following transcripts of ENSDARG00000004296 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 10782838)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 10858704 |
| GRCz11 | 10 | 10816942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAGAACAAGGAATGAGTGAAGACACTATCATAATTAAAAAGAACAAAG[G/A]TATCCTCACAAAAACATTCATTCATTAATTCATTTTCTTTTTTAGCTTTG
Long Flanking Sequence:
AAGTCATTTGATTGGCTGACATGCTAGGAACCACTTCTTACACTGCATCCAAAATGGCCGACATACAAAAATAAAAATAAAATGTAAAAATTTTCGAATTTTTTTAACCCAAAAGATGTAGGAAATCACAGAAAATAATTATTTGGGTCTCAGAAGGATATCCACAGTCAAATATTGAGCTAATTTGGATTTAAACAGCAAGAGGAAGAGTAAAACCTGCACAATGTAGACTTGCAACATGGCACAGGCATTTTTCAGCTCATATTTTTGATCGATTTTTCTCTCTGGGCCAAAATCTGAAAATGACATTATCAGACAATCATTTTTAGTAGGCGAAAATTTAGTGCATTGTTTTTGTGCTTGTCATCAATAAGTAACTTGTTGTGCTCCCCCTGCAGGACGTACTATGGAACTGCGGCCCACACTTATTGAAGACTTCAAGACTCTGGTGGCAGAACAAGGAATGAGTGAAGACACTATCATAATTAAAAAGAACAAAG[G/A]TATCCTCACAAAAACATTCATTCATTAATTCATTTTCTTTTTTAGCTTTGTCCCTTTATAAATCAGGGGTGGCAACAGTGGAATGAACCGCCAACTTATCCAGCACGTTTTACGCAGCGGATGCCCTTCCAGCTGCAACCCATCACTGGGAAACACTCATACACTGTGATTCACACACATACACTGCAGACAATTTAGCTCACCCAATTCACCTATAGCGCATGTATTTAGACTCCCATGTATCCAACACAAACATGAGAATATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCGAGGTTTGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCCACTGTTTCATCATCACAAAAACAAACTGTAATTCCCACTATGTGCCATTATTTCAACATTCATGTCTTTTTCTCCTTCTTCATGTCATCAGGTGAATGTGTTCCAGGTGAAGAGACCACACCAGAGCCACAGATTCAGGTCAAGGCTTTATGAT
Associated Phenotype:
Not determined