ZMP
marveld2b
Ensembl ID:
ZFIN ID:
Description:
MARVEL domain containing 2b [Source:RefSeq peptide;Acc:NP_001119878]
Human Orthologue:
MARVELD2
Human Description:
MARVEL domain containing 2 [Source:HGNC Symbol;Acc:26401]
Mouse Orthologue:
Marveld2
Mouse Description:
MARVEL (membrane-associating) domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2446166]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7564 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa20419 | Nonsense | Available for shipment | Available now |
| sa40430 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20420 | Nonsense | Available for shipment | Available now |
| sa40431 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25297 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17575 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7564
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 > C
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088175 | Missense | 188 | 572 | 1 | 6 |
| ENSDART00000137178 | Missense | 188 | 572 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27851178)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25606476 |
| GRCz11 | 5 | 26206629 |
KASP Assay ID:
554-4014.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGACGCTCTTTGCAGACGGCTATGACTTACAGTGAGAAGGTGGARGAG[T/C]ACAATCAGCGCTATGCCTACATGAAGTCCTGGGCYGGACTCTTGCGTATT
Long Flanking Sequence:
ATCAGGTGCCCATCGGCTCTATGCCGTGGGGTCAGCAACCTCCTTACCCCCTTGGTGGTGGAGTAGCAGCATCCAGTTTTGAGAGTTTACCACCACCTCCGCTACCTGAAAATCCCCCTGTTGGACCAGAATTCTACCCGAGTGATGTTGAAGACCAAGTGGATGATGCCATGGACATCAAACCCATCCGACGCTTCATTCCTGACTCTGTGAAGAACTTCTTCAGGGCCAGTGTCAACCGAGGAAGCAAAAAATTGACTTTTCCTCTACCACCACCACCAATAGATGGAAACACCACCAGCCAAGGCGTCCCGTGTTCCCCTCCACACTCTCGGGCACCATCGCCAACAGCTCCCAGCTCTTACCTAGACCCTTATGGAGGATCTGGGGGCAGCTACACTTCAAGGAAGGAGCAGGCAATGTTATTAGGGGAGCCACTGGAATCAGTTTCTGGACGCTCTTTGCAGACGGCTATGACTTACAGTGAGAAGGTGGAGGAG[T/C]ACAATCAGCGCTATGCCTACATGAAGTCCTGGGCCGGACTCTTGCGTATTTTAGGATGCGTGGAGTTGCTTTTGGGTGCTGCTGTTTTTGCCTGCGTCTGTGCATATGTTCACAAGGATAATGAGTGGTTTAATATGTATGGTTACTCAATGCATCAGGTGTATGGGGGAGCATCAATGGGTGGGATGTATGGAGGATATGGGTCTTCATACTCAGGACCTTTGACACCCTTTGTCCTTGTGGTTGCTGGAGTGGCTTGGATAGTGACTGTCATTATATTAATCTTAGGAATAACCATGTATTATCGTACCATTCTACTCGACTCCAGCTGGTGGCCAATCACAGAGTGTGTGGTAAATGTGGCATTAGGATTGCTCTACTTGGCAGCTGCAATTGTGTACGTGCGAGACACACTTCGTGGAGGTCTCTGCTATTATCAACAATTCACTGTTGGGCCCAATGCAGGATTTTGTCGGACTGAAGCTGGACAGAACGCTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20419
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 |
|---|---|---|---|---|---|
| ENSDART00000088175 | Nonsense | 202 | 572 | 1 | 6 |
| ENSDART00000137178 | Nonsense | 202 | 572 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27851221)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25606519 |
| GRCz11 | 5 | 26206672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGAGTACAATCAGCGCTATGCCTACATGAAGTCCTGGGCCGGACTCT[T/A]GCGTATTTTAGGATGCGTGGAGTTGCTTTTGGGTGCTGCTGTTTTTGCCT
Long Flanking Sequence:
TTACCCCCTTGGTGGTGGAGTAGCAGCATCCAGTTTTGAGAGTTTACCACCACCTCCGCTACCTGAAAATCCCCCTGTTGGACCAGAATTCTACCCGAGTGATGTTGAAGACCAAGTGGATGATGCCATGGACATCAAACCCATCCGACGCTTCATTCCTGACTCTGTGAAGAACTTCTTCAGGGCCAGTGTCAACCGAGGAAGCAAAAAATTGACTTTTCCTCTACCACCACCACCAATAGATGGAAACACCACCAGCCAAGGCGTCCCGTGTTCCCCTCCACACTCTCGGGCACCATCGCCAACAGCTCCCAGCTCTTACCTAGACCCTTATGGAGGATCTGGGGGCAGCTACACTTCAAGGAAGGAGCAGGCAATGTTATTAGGGGAGCCACTGGAATCAGTTTCTGGACGCTCTTTGCAGACGGCTATGACTTACAGTGAGAAGGTGGAGGAGTACAATCAGCGCTATGCCTACATGAAGTCCTGGGCCGGACTCT[T/A]GCGTATTTTAGGATGCGTGGAGTTGCTTTTGGGTGCTGCTGTTTTTGCCTGCGTCTGTGCATATGTTCACAAGGATAATGAGTGGTTTAATATGTATGGTTACTCAATGCATCAGGTGTATGGGGGAGCATCAATGGGTGGGATGTATGGAGGATATGGGTCTTCATACTCAGGACCTTTGACACCCTTTGTCCTTGTGGTTGCTGGAGTGGCTTGGATAGTGACTGTCATTATATTAATCTTAGGAATAACCATGTATTATCGTACCATTCTACTCGACTCCAGCTGGTGGCCAATCACAGAGTGTGTGGTAAATGTGGCATTAGGATTGCTCTACTTGGCAGCTGCAATTGTGTACGTGCGAGACACACTTCGTGGAGGTCTCTGCTATTATCAACAATTCACTGTTGGGCCCAATGCAGGATTTTGTCGGACTGAAGCTGGACAGAACGCTGCCATCATTTTTCTCTTTGTAAACATGCTGTTGTATCTTGTTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40430
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 |
|---|---|---|---|---|---|
| ENSDART00000088175 | Nonsense | 390 | 572 | 1 | 6 |
| ENSDART00000137178 | Nonsense | 390 | 572 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27851784)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25607082 |
| GRCz11 | 5 | 26207235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGATGTGGAGACATGAAGCTGCTAGGATGCGCAGAGAGAGATTGGAA[C/T]AAGATGTAAAGTTCAAATCAATAATTCTCTGAAACTAATAAGAGTAGAGC
Long Flanking Sequence:
ATGTTCACAAGGATAATGAGTGGTTTAATATGTATGGTTACTCAATGCATCAGGTGTATGGGGGAGCATCAATGGGTGGGATGTATGGAGGATATGGGTCTTCATACTCAGGACCTTTGACACCCTTTGTCCTTGTGGTTGCTGGAGTGGCTTGGATAGTGACTGTCATTATATTAATCTTAGGAATAACCATGTATTATCGTACCATTCTACTCGACTCCAGCTGGTGGCCAATCACAGAGTGTGTGGTAAATGTGGCATTAGGATTGCTCTACTTGGCAGCTGCAATTGTGTACGTGCGAGACACACTTCGTGGAGGTCTCTGCTATTATCAACAATTCACTGTTGGGCCCAATGCAGGATTTTGTCGGACTGAAGCTGGACAGAACGCTGCCATCATTTTTCTCTTTGTAAACATGCTGTTGTATCTTGTTGGAGCCATCGTCTGTCTAAAGATGTGGAGACATGAAGCTGCTAGGATGCGCAGAGAGAGATTGGAA[C/T]AAGATGTAAAGTTCAAATCAATAATTCTCTGAAACTAATAAGAGTAGAGCCATGTCTAATTTGTTTGTTTTCCCTTTCATATTCATATTTAGATGAAGTCAGATGGGCTTCCACTCAACATGGTAAGCAGTTTAATTTTAATGTTAAAAGAGCAGTTTCACTATTTTAAACTGTTGTTGTAAGATGTAATTTGTAATCTTAGATTGGTGCCGGCTCAAGTGTCTCAGTGCCCATCCAAAGTGCTCCAGTAATGACCAAGCTAGAGACTTTTGATGGCATGCCTGATCATCCAGCTATGATGGAACCGGAGATTTTGAGGGGTCACATCCCTGCTGGCCACATCCCCAAACCTTTGGTCATTGCAGATTATGTGGCGTGAGTTTCAAAGAATACTTATATGAATTATTATCTATGAATTTAAGACATTTTACTCAAAATATGCACCACGTCATTCTTTTTTTATTCCCCTCACCCCTTTTCTAATGACTATTTGTGTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20420
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 |
|---|---|---|---|---|---|
| ENSDART00000088175 | Nonsense | 461 | 572 | 4 | 6 |
| ENSDART00000137178 | Nonsense | 461 | 572 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27852509)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25607807 |
| GRCz11 | 5 | 26207960 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGTAAATGTAAATGTGTTCTGTAATATTTTTCTCCTAACAGGAAATA[T/A]CCAACAATCCGCACTGATGAGGAGAGGGAGCGCTACAAAGCTGTGTTTAA
Long Flanking Sequence:
CAGTGCCCATCCAAAGTGCTCCAGTAATGACCAAGCTAGAGACTTTTGATGGCATGCCTGATCATCCAGCTATGATGGAACCGGAGATTTTGAGGGGTCACATCCCTGCTGGCCACATCCCCAAACCTTTGGTCATTGCAGATTATGTGGCGTGAGTTTCAAAGAATACTTATATGAATTATTATCTATGAATTTAAGACATTTTACTCAAAATATGCACCACGTCATTCTTTTTTTATTCCCCTCACCCCTTTTCTAATGACTATTTGTGTACTAACTGTACCCAAAAAAATAAAAAATAAAATAAATAAATACTAATACTTTCCTTCTTAGACTTTACAGACCTGAAACTTGCCTATAACACGTATTCATTGTTGCTCTTAGTTGTGTAAATTGCTTCCTTGTCCTCATTTGTAAGTCGCTTTGGATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAAATGTGTTCTGTAATATTTTTCTCCTAACAGGAAATA[T/A]CCAACAATCCGCACTGATGAGGAGAGGGAGCGCTACAAAGCTGTGTTTAACGATCAATACGCTGAGTATAAAGAACTGCACGCCGAGGTTCAGGTTTTAACACAGAAGTTTGAGGAAATGGATAATCTGATGAGGAATCTACCACAACGACCTTCCAGCCAGATGGTAATGATTTGTAAAACAGTGCATTCTTTCATAATTATCTTACATGCGGTTTTTATGAGCATGTCTAAACTGAGAGACTATATTTGAAATATTTGAACTTTTAAAATAAAGATGACAGAGATAATTAAAATGGTATTTTCTTATAATCCCCGCAGGGTCTTTAAAGGGCCATGACACCCCCCACTTTCGGTTAAAGTCTACTTCAGAATTTTTTAAAAAGATGCATAATTAATGGGCGTGGAGCTCCATGAGCATAGGGCAGGAGTGGGCGTGGCCAGCAGGGGAGAAGGGGAGCGAACAACTGTTGTTGGCAGTTAGTTTACAAAATGAGACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40431
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 |
|---|---|---|---|---|---|
| ENSDART00000088175 | Nonsense | 494 | 572 | 4 | 6 |
| ENSDART00000137178 | Nonsense | 494 | 572 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27852607)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25607905 |
| GRCz11 | 5 | 26208058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACGATCAATACGCTGAGTATAAAGAACTGCACGCCGAGGTTCAGGTTT[T/A]AACACAGAAGTTTGAGGAAATGGATAATCTGATGAGGAATCTACCACAAC
Long Flanking Sequence:
CACATCCCTGCTGGCCACATCCCCAAACCTTTGGTCATTGCAGATTATGTGGCGTGAGTTTCAAAGAATACTTATATGAATTATTATCTATGAATTTAAGACATTTTACTCAAAATATGCACCACGTCATTCTTTTTTTATTCCCCTCACCCCTTTTCTAATGACTATTTGTGTACTAACTGTACCCAAAAAAATAAAAAATAAAATAAATAAATACTAATACTTTCCTTCTTAGACTTTACAGACCTGAAACTTGCCTATAACACGTATTCATTGTTGCTCTTAGTTGTGTAAATTGCTTCCTTGTCCTCATTTGTAAGTCGCTTTGGATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAAATGTGTTCTGTAATATTTTTCTCCTAACAGGAAATATCCAACAATCCGCACTGATGAGGAGAGGGAGCGCTACAAAGCTGTGTTTAACGATCAATACGCTGAGTATAAAGAACTGCACGCCGAGGTTCAGGTTT[T/A]AACACAGAAGTTTGAGGAAATGGATAATCTGATGAGGAATCTACCACAACGACCTTCCAGCCAGATGGTAATGATTTGTAAAACAGTGCATTCTTTCATAATTATCTTACATGCGGTTTTTATGAGCATGTCTAAACTGAGAGACTATATTTGAAATATTTGAACTTTTAAAATAAAGATGACAGAGATAATTAAAATGGTATTTTCTTATAATCCCCGCAGGGTCTTTAAAGGGCCATGACACCCCCCACTTTCGGTTAAAGTCTACTTCAGAATTTTTTAAAAAGATGCATAATTAATGGGCGTGGAGCTCCATGAGCATAGGGCAGGAGTGGGCGTGGCCAGCAGGGGAGAAGGGGAGCGAACAACTGTTGTTGGCAGTTAGTTTACAAAATGAGACACAAACCGTGAGGAGACGCGTGAGTTTATTGTTTACAAAGTTAAAATGCAAAGAAATGAACAGTAATTTAATGCCCTGCTACATTTTTTATTTGTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25297
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088175 | Essential Splice Site | 516 | 572 | 4 | 6 |
| ENSDART00000137178 | Essential Splice Site | 516 | 572 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27852675)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25607973 |
| GRCz11 | 5 | 26208126 |
KASP Assay ID:
554-7489.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGGATAATCTGATGAGGAATCTACCACAACGACCTTCCAGCCAGATG[G/A]TAATGATTTGTAAAACAGTGCATTCTTTCATAATTATCTTACATGCGGTT
Long Flanking Sequence:
TACTTATATGAATTATTATCTATGAATTTAAGACATTTTACTCAAAATATGCACCACGTCATTCTTTTTTTATTCCCCTCACCCCTTTTCTAATGACTATTTGTGTACTAACTGTACCCAAAAAAATAAAAAATAAAATAAATAAATACTAATACTTTCCTTCTTAGACTTTACAGACCTGAAACTTGCCTATAACACGTATTCATTGTTGCTCTTAGTTGTGTAAATTGCTTCCTTGTCCTCATTTGTAAGTCGCTTTGGATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAAATGTGTTCTGTAATATTTTTCTCCTAACAGGAAATATCCAACAATCCGCACTGATGAGGAGAGGGAGCGCTACAAAGCTGTGTTTAACGATCAATACGCTGAGTATAAAGAACTGCACGCCGAGGTTCAGGTTTTAACACAGAAGTTTGAGGAAATGGATAATCTGATGAGGAATCTACCACAACGACCTTCCAGCCAGATG[G/A]TAATGATTTGTAAAACAGTGCATTCTTTCATAATTATCTTACATGCGGTTTTTATGAGCATGTCTAAACTGAGAGACTATATTTGAAATATTTGAACTTTTAAAATAAAGATGACAGAGATAATTAAAATGGTATTTTCTTATAATCCCCGCAGGGTCTTTAAAGGGCCATGACACCCCCCACTTTCGGTTAAAGTCTACTTCAGAATTTTTTAAAAAGATGCATAATTAATGGGCGTGGAGCTCCATGAGCATAGGGCAGGAGTGGGCGTGGCCAGCAGGGGAGAAGGGGAGCGAACAACTGTTGTTGGCAGTTAGTTTACAAAATGAGACACAAACCGTGAGGAGACGCGTGAGTTTATTGTTTACAAAGTTAAAATGCAAAGAAATGAACAGTAATTTAATGCCCTGCTACATTTTTTATTTGTAATTTCATATGCACATAACCACAATTTATATCATTATAAAGATAAGTGTGTTCATGTAAACACTATAAATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17575
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088175 | Nonsense | 561 | 572 | 6 | 6 |
| ENSDART00000137178 | Nonsense | 561 | 572 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 27855009)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25610307 |
| GRCz11 | 5 | 26210460 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATACCTGAAGAACAAACTTGCTYACATAAAGCAGAAAATTCAGGAGTA[T/G]GACAAAAYCATGGACTGGAATGATGGTTACAGCTAGATGGAACCCYAATA
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGCTATGTATGTATGTGTATACATGCAGTTAATTGATCAACAATAATTGATCCTCAGAAGTTGTAATACCCCCCCCCCACACACACACACACACACACACATATATATATATATATATATATATATATGCTGCTAGTTTGACTTGCCAATCCCTTAATCATCTCCTTGTTGCTTTTCTACATTCTTTAGTCATTGCAAAAGAAAGACATGTTATCTGTCTACACTGAGTGCTGTAAACAGTTGAAACTGAAAAACTGGAAATGTTAGGGGGTTGTAAAAGCAGCTATTGATGTGTTAGCATACTTCCTGTGTGTGTGAATGCGCACCAAAGATAATTTTACCTCTTTCTGTTTTTAGGACCCAACTTACCAGGAAAAAAGGGAGAGATGTGAATACCTGAAGAACAAACTTGCTCACATAAAGCAGAAAATTCAGGAGTA[T/G]GACAAAATCATGGACTGGAATGATGGTTACAGCTAGATGGAACCCCAATATACTTTTAAAAATCATGTTAAACTTTACAGATGTTCCAAGAAAGAAAGTGACATGCCTGAAAGTTACGTGTTTGGTTTGGGCTTTGTTGGTAGCAAAATCATATTAAATGCAGTAAATAATGAAGAACATTTTAAAGCCTCAAATTTAAATAGTTTTAACATTCGAATAAATGTTACTTACTAAAATATTGGCGTAAATATTAAGTTAAAGTTTCAATCACATATATATATATATGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTACGACTTCTGAGGATCAATAATTGTTGATCAATTAACTGCGTATACCCTCAGTATATTCAACGGTTTTCCTGATTAGACTTCAGTAATTGTTTGTATTCGCGTCCCCTTTAACTTTATACCAAATGTTTCTTTTTACTCGCATCTTGTTGCAATTGGTGCATTT
Associated Phenotype:
Not determined