ZMP
si:ch211-117c19.2
Ensembl ID:
ZFIN ID:
Description:
MAM domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001123869]
Human Orthologue:
MAMDC2
Human Description:
MAM domain containing 2 [Source:HGNC Symbol;Acc:23673]
Mouse Orthologue:
Mamdc2
Mouse Description:
MAM domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1918988]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12046 | Essential Splice Site | Available for shipment | Available now |
| sa33721 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40564 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6065 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13995 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12046
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083203 | Essential Splice Site | 11 | 680 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 56445868)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51922138 |
| GRCz11 | 5 | 52568731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTAAAGCTTTATAGTTTGGCTTTATTGATGTGAKGTTCTGTSTCTTC[A/G]GCTGTGGCTCTTGTAGCGCGGTCTCAGACGCAGCTTTTGCGGGGCTCCTG
Long Flanking Sequence:
TGAGCAAGAAGTATGTCATATCTGTCAGACGTTTACATAGCGGTAAACTCCTTACCTAAATAAGATCCATCACCGCTGCCTGTTCTGAAATAGAAACCTCAAGAACCACTCCCTCCTCCTACTGTCTGCCAGACTCAGCATGGAGAGTGAGTTCAGCGGTGTGTGTTCAGTGCGCTGTGCGTCTGCTGCCGTACGCAATCTGCGTTAGCGGAGCGCCGCTCTTCCACTCCAGCATCCCTGCAACTTTTGCCATGAGTTTTCTTCACCCCTTAACGTTTCTGGGTAGGTCATCACTTGATGTAATTGTCTGATTGCATTAATGAAGTTGTTTGCTTGCATGTTTCTGAGCATTTGTGTAAGTTTAATTCCTTCTTCTTCCAAACTGTGCAATTTTTTCGTTGCTGCACATTTGCATCTGCTAACATATTCACTATGAATGCAATGTATGTCTATTTAAAGCTTTATAGTTTGGCTTTATTGATGTGAGGTTCTGTGTCTTC[A/G]GCTGTGGCTCTTGTAGCGCGGTCTCAGACGCAGCTTTTGCGGGGCTCCTGCACATTCGAGGCGGACAGCTGCGGCTACACGTCTGATCCTGCTTATGCTGCCTGGACCATCAACGATGAAGGTATGAGAAACTCTCTTATTATTTGGATCCAGACACTTTTATTAGTAGGCTACTAGTTTCGTTGACATTTATGCCACAAAACTGTCAAACTGAACAAATGTGCTTGAATGGTTCCAAAATAATTCACTGCAGGCATCATACGTGCGTCAGACAGTAGGTGGCGCTATCAACTGTGTAGCCTACATTTGCGATTTAGTTAAAGTTGTATTATGGGCTAGAATCCGATTCCCTCTTCGGAATACTTGAAATTTAACCCCCAAAATATAGGCTACTTATGCTCATGTCAAAGCAGTTTCGTCAATCGAATTGTTTAGTCAGTTGACACGGAGGCGTGGTAGGTAGTGCTGTTGTCTCACAGCAAGAAGGTCACTTTTTCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33721
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083203 | Nonsense | 87 | 680 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 56424775)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51901045 |
| GRCz11 | 5 | 52547638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGTCCGGAGCTGGAGCTCAGAGACTGGAGCTGTGTGCGGCTGGTCTAT[C/T]AGATCTCAGGCTCAGGATCTCTTCAATTGCACTTGCGATCCGAGGAGGAA
Long Flanking Sequence:
ATAAAACAACAAATACATATATACTTTTCTAAATTTAGGTGAAACTGTGAGTTTTAATGCTGATTTGTAAAGATGTCTATAGTAATGCAATAGGTCAACTGTATTAATCTGTATGTATAAGGGGCATGAAGTGGGTGGGTGGGTTGGGACTAGAGAGTGGAGGTGTGTATTTCAGAGTGTTGTTAGGTAGTCAACTACCTGTCAATAAACTTTTGGCAAAGAAAAATCCTATTCTGAAGGTTTTAAATTGCTGGGGTCAAATTAACCCCAGTGGATAAAACATGTTATCAGATTTTAGGGTAACAGGAGTGTTGAAGTGTTTTATATTCAGTTTTTATACTTGTGACATAATTCATGCATGTGTTTTCATCAGTGTTTAAATATTTCTTTCAGGTCGCTTCATCACAGCAGAATCCTTGTCCTTTGGAGAAAAAGAGAAGCATGTGCTAGTAAGTCCGGAGCTGGAGCTCAGAGACTGGAGCTGTGTGCGGCTGGTCTAT[C/T]AGATCTCAGGCTCAGGATCTCTTCAATTGCACTTGCGATCCGAGGAGGAAAACTTTGACTACATGTTATGGAGTGCAGAGAAACCCTCAGACAGTTGGCTCATCGCAAGTGTGGACCTTCGTAACATTTCTGGAACTTACCAGGTATCATTTCAATGCAAAACAGGGAAACAAGGCCGCTGTGTAAGCTATATAATGTAGTCAGCACTATTTATAGTCTTCTGGAGGATTGTTAGTTTAAAGGGGGTTTAAATGGAGCAGAGTTGAAGAAAAGAGGGCTTTGTAAAGTATGCCTCTCTGTCGATTAGACAAACACTTTTACTCTGCTAATAGTGATGTTTTGTTTCTGGGCATTACTTTTGGAAAGATAGACTAAGTGTAATACATGGCCTTTGTAAACAGATGGATAGTGATTGACTTTGTTTAATAACAAGTGTTATGAATTATGATTGGAAATAAAGGGGATCTATTATGCTAGTTTTGACTGGCAGCGTATGATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40564
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 |
|---|---|---|---|---|---|
| ENSDART00000083203 | Nonsense | 336 | 680 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 56403722)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51879992 |
| GRCz11 | 5 | 52526585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATCACTCATGTTTCAGAGCCAGAGATTGACCCGTCTGTTGCAAACTG[T/A]GACTTTGAGGAGGGCCTGTGTCAGTATTATCAGGAACAGACTGGAGGCTC
Long Flanking Sequence:
AAATTCTATGCATGTTTCAGAATAATGTACCTAACAAAATAGCTGGAATAGAAAATAGTTCATGAATTCAAATAATCAATGTTTTAGTCATTAATTATTGAGTTTGTTAAAGACATTTGCAGTTTAAGTCTACATAAATGAAGCTGCTTATAAATTCAAGACATTTTTACCATTTGATTTTGCAAAAAAAAAAAAATTATGTTGATCCACCATTTTAACAACAAAAATATTTAAAGCTAACTATTCTTTGAAACAGAAAGACAGCCTGTTGTTCTTAAAGAGGCTGACACCGCAACCCACAATTACCAGTAAACTGCTGTTTAATGGGGAATTTTTTTGCTGTTGTCCTGTTATGTAGTAACTACATTGACATTTCCTTTAGTCAGCACTTCACATACATTTCACAAAAAGTCTGTCCATGTGGGAGATGTTCATGTTGTGTGTTTGTTTCATATCACTCATGTTTCAGAGCCAGAGATTGACCCGTCTGTTGCAAACTG[T/A]GACTTTGAGGAGGGCCTGTGTCAGTATTATCAGGAACAGACTGGAGGCTCGCTGTGGAACAAAGTCTCTGTCAAACCGAATGTTTACCGCATTGGAGATCACACCACAGGCACTGGTGCGCAAATCTGTCTTTTGATATTTCTGATTATTTTGATATATTTATATCTTTTCAACCATCCTCCAAGTTACGTTGCTAGCTGGACATAATTGTGTACAAACCTGATTAACATTTGTTATGGTTTAAATCATACTTGTATACTATTTATTGATGCAAATATTAGAAAATACATGGTTCTAAATGGTAGTCTAAATGGGTGTGCAAACTCGGTCCTCCAACTCACCTGAGCATGCCAATCAGTGTCTTCAAGATCACTAGAAATGTTTTGATTAGAGTTGGAGCTAAACTGTGTAGGAAACTGGCCCTCCAGGAACAAGTTTGCCCACCCCTGTACTAAATTTATGTTGTTTTGCTTTGTGACAATAATCAAAGTAATGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6065
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083203 | Nonsense | 538 | 680 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 56390239)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51866509 |
| GRCz11 | 5 | 52513102 |
KASP Assay ID:
554-3846.1 (used for ordering genotyping assays)
KASP Sequence:
AAAAAGGACATTGGCTAAGGATTCGAGGACAGACGCCCACATCTTACACC[G/T]GACCCAAGGGGGACCACACCTTAGGGGTAGGTGAGTCAGATTTATACTTC
Long Flanking Sequence:
ATCCTTTGGTTACCTATCGGATCATTGGAAGATGGGTGTTGCTAACAAAAGAAGGTAGATTGATGAATGGACAAAAGCAGGGTAAAACAACACACACCCCTCCCGAAAGGCATTCCATATGACCAGAAGTAAAGAAAAGTCATTTCGTGGGGGAAGGGAAAGCTAGGATATTTGATAAAATATTATGAGGCTAAATAATATTTAACAAAAATATGAAGTGTACATAAACATCATTTATAACAATTTCTAAAAACTCATATTAAAATAGAAGATTAGCACATTTGAATTTCAGAGTGACTTTAAACTTTCAGACTTTTCCTAATTGGTGAACACTACTATTTCAAAACAGGTCACTTTTTTCTGTTCTCTTTTTAGGACCCTTGAATCCACCTCCTGGACACTGTAACTTTGAAACTGGTGACTGTGGCTACACCCAGAAAAAGAAAGCTAAAAAAGGACATTGGCTAAGGATTCGAGGACAGACGCCCACATCTTACACC[G/T]GACCCAAGGGGGACCACACCTTAGGGGTAGGTGAGTCAGATTTATACTTCAGCTTAGAATGCTTTTATCTCTGATTTCTTGAGACAGAGCACACTAAGTTTCTCCTACTCTGACTTCAAGGTTACTTCATGTACATTGAGGCCTCCCACATGTTACCTAAGCAGTCAGCCCAGCTGATGTCCACTGAGCTGAGGGGCTCATCCATCCCGCAGTGTCTGATCTTCTTTTACCACATGTATGGCTCGGGCACAGGGACCCTGAGCATCCTGCTGCGTAAGGGGGACAAGGAAAGACTGCTTTGGTCTAGGCAAGGAGAACAGAGCGTGTCCTGGATGAAGGCCATGGTGGATTATGAGTGTTACACAAGGCACTGGGTTAGTGACATGTTCTTGCTGCTCTTTGAAAAGTATCTTTTGCAACACTTATATTACAGCAACCATTTGATCACTGAAACCATTGCATTTCTGATGTCCCAGGAAAATGACTTTATTATGTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13995
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083203 | Nonsense | 554 | 680 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 56390101)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 51866371 |
| GRCz11 | 5 | 52512964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AKYACACTAAGTTTCTCCTAYTCTGACTTCAAGGTTACTTCATGTACATT[G/T]AGGCCTCCCAYATGTTACCTAAGCAGTCAGCCCAGCTGATGTCCACTGAG
Long Flanking Sequence:
GTCATTTCGTGGGGGAAGGGAAAGCTAGGATATTTGATAAAATATTATGAGGCTAAATAATATTTAACAAAAATATGAAGTGTACATAAACATCATTTATAACAATTTCTAAAAACTCATATTAAAATAGAAGATTAGCACATTTGAATTTCAGAGTGACTTTAAACTTTCAGACTTTTCCTAATTGGTGAACACTACTATTTCAAAACAGGTCACTTTTTTCTGTTCTCTTTTTAGGACCCTTGAATCCACCTCCTGGACACTGTAACTTTGAAACTGGTGACTGTGGCTACACCCAGAAAAAGAAAGCTAAAAAAGGACATTGGCTAAGGATTCGAGGACAGACGCCCACATCTTACACCGGACCCAAGGGGGACCACACCTTAGGGGTAGGTGAGTCAGATTTATACTTCAGCTTAGAATGCTTTTATCTCTGATTTCTTGAGACAGAGCACACTAAGTTTCTCCTACTCTGACTTCAAGGTTACTTCATGTACATT[G/T]AGGCCTCCCACATGTTACCTAAGCAGTCAGCCCAGCTGATGTCCACTGAGCTGAGGGGCTCATCCATCCCGCAGTGTCTGATCTTCTTTTACCACATGTATGGCTCGGGCACAGGGACCCTGAGCATCCTGCTGCGTAAGGGGGACAAGGAAAGACTGCTTTGGTCTAGGCAAGGAGAACAGAGCGTGTCCTGGATGAAGGCCATGGTGGATTATGAGTGTTACACAAGGCACTGGGTTAGTGACATGTTCTTGCTGCTCTTTGAAAAGTATCTTTTGCAACACTTATATTACAGCAACCATTTGATCACTGAAACCATTGCATTTCTGATGTCCCAGGAAAATGACTTTATTATGTTTTTTGTTTGTAAAATGTACTTTAAGGTTTAATGTCTGGTTTATTGTTTGCAGGTTATATTTGAAGCCACCAGAGGATCGTCAATAAGGAGTGACATTGCGATTGATGATGTTGTGTTTAAAAAGGGACCTTGCAAAGGCAAG
Associated Phenotype:
Not determined