ZMP
marveld2a
Ensembl ID:
ZFIN ID:
Description:
LOC558720 protein [Source:UniProtKB/TrEMBL;Acc:Q32PL4]
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 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30929 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24862 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14139 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30929
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 |
|---|---|---|---|---|---|
| ENSDART00000006772 | Nonsense | 275 | 545 | 1 | 6 |
| ENSDART00000132526 | Nonsense | 275 | 545 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 2987034)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 2932671 |
| GRCz11 | 10 | 2959842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCTTGTCTTGGGAATGACCATGTACTATCAGACTATACTTCTAGACT[C/A]AAGTTGGTGGCCTTTAACAGAGTTCGTCATAAACCTTGCTCTTGCACTTC
Long Flanking Sequence:
CCCATCGGTTCCTGGCTCTTACCGCGACCCGTACGGTGGATCCGGAGGCAGCTATAACTCCCGTAAAGAGCGTGAAGCAATGCTTTTAGGAAATCCCGTTGAATCAATCGACGGCCGCACTGCGCACACAGCTTTGACTTACAGCGAAAAGGTAGAGGAGTACAACCAGCGTTACGCATACATGAAGTCTTGGGCTGGACTTTTACGTATTCTCGGGTGCGTCGAGCTGCTTTTGGGGGCAGCCATTTTTGCTTGTGTATGTGCATATATTCATAAAGACAATGAGTGGTATAACACGTTTGGTTACTCGCAGCCTGGTGGCTTCTATGGAGGAGGTTACGGAGGTTATGGAGGCTCTTATGGAAGCGGTTATGGCAATGCCAACTACTCTGGACCAAAGACACCGTTCATCTTGGTGGTAGCAGGATTGGCATGGATCGTGACCATTATCATGCTTGTCTTGGGAATGACCATGTACTATCAGACTATACTTCTAGACT[C/A]AAGTTGGTGGCCTTTAACAGAGTTCGTCATAAACCTTGCTCTTGCACTTCTGTTTTTGGCGGCCGGCTGTGTATATGTGAATGACACCTTACGAGGCGGACTTTGTTACTATCCGGTCTTCAATAATGGCATCAATGGTGCTTTCTGCCGCACCGAAGCAGGACAGACAGCTGCGATAATCTTCCTGTTTTTCACCATGATCGTGTACTTGGTTGGGGCCATAGTGTGTCTGAAACTGTGGCGGCATGAGGCAGCTCGGCGACTACGAGAACGACATGGCCAGGAGGTGAGATTTTTCTACTTTTAATTTATGCATCTTCAGGTCCTCAATTAAACACAAAATCATTTTAGAAATAGATTCTGCATGGTTTCTGACATTTACAATATGCATCACTGTTTTCACTTGAATGGATTCTGAGCTTAGATTTTAACAGCAGATGGTGCTCTAAGCTAGGCTGTTAAAAACTAGTCTGGTGCATGTCTGCTTTTTAAAAACTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24862
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 |
|---|---|---|---|---|---|
| ENSDART00000006772 | Nonsense | 312 | 545 | 1 | 6 |
| ENSDART00000132526 | Nonsense | 312 | 545 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 2986922)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 2932559 |
| GRCz11 | 10 | 2959730 |
KASP Assay ID:
554-7623.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGGCTGTGTATATGTGAATGACACCTTACGAGGCGGACTTTGTTACTA[T/A]CCGGTCTTCAATAATGGCATCAATGGTGCTTTCTGCCGCACCGAAGCAGG
Long Flanking Sequence:
GGCCGCACTGCGCACACAGCTTTGACTTACAGCGAAAAGGTAGAGGAGTACAACCAGCGTTACGCATACATGAAGTCTTGGGCTGGACTTTTACGTATTCTCGGGTGCGTCGAGCTGCTTTTGGGGGCAGCCATTTTTGCTTGTGTATGTGCATATATTCATAAAGACAATGAGTGGTATAACACGTTTGGTTACTCGCAGCCTGGTGGCTTCTATGGAGGAGGTTACGGAGGTTATGGAGGCTCTTATGGAAGCGGTTATGGCAATGCCAACTACTCTGGACCAAAGACACCGTTCATCTTGGTGGTAGCAGGATTGGCATGGATCGTGACCATTATCATGCTTGTCTTGGGAATGACCATGTACTATCAGACTATACTTCTAGACTCAAGTTGGTGGCCTTTAACAGAGTTCGTCATAAACCTTGCTCTTGCACTTCTGTTTTTGGCGGCCGGCTGTGTATATGTGAATGACACCTTACGAGGCGGACTTTGTTACTA[T/A]CCGGTCTTCAATAATGGCATCAATGGTGCTTTCTGCCGCACCGAAGCAGGACAGACAGCTGCGATAATCTTCCTGTTTTTCACCATGATCGTGTACTTGGTTGGGGCCATAGTGTGTCTGAAACTGTGGCGGCATGAGGCAGCTCGGCGACTACGAGAACGACATGGCCAGGAGGTGAGATTTTTCTACTTTTAATTTATGCATCTTCAGGTCCTCAATTAAACACAAAATCATTTTAGAAATAGATTCTGCATGGTTTCTGACATTTACAATATGCATCACTGTTTTCACTTGAATGGATTCTGAGCTTAGATTTTAACAGCAGATGGTGCTCTAAGCTAGGCTGTTAAAAACTAGTCTGGTGCATGTCTGCTTTTTAAAAACTAGCCTAGAGCTCCGTCTGCTGTTAAAAGTAGCTTAGAGCATTGTCTGCTGTTAAAAAAACTAGCCTAGAGCGCTGTCTGCTTTTTAAAAACTAGCCTAGAGCACCATCTGCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14139
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 |
|---|---|---|---|---|---|
| ENSDART00000006772 | Nonsense | 428 | 545 | 3 | 6 |
| ENSDART00000132526 | Nonsense | 428 | 545 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 2983048)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 2928685 |
| GRCz11 | 10 | 2955856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGACACATTCCAGCGGGACACAMTCCTAAACCTGTGATCATGCCGGATTA[T/A]GTTGCGTGAGTACAGTTGTGCAAAAACACAANNNNACTATTACTGTTATA
Long Flanking Sequence:
GAACTACACTGTAAAAAATGCAGGGTTCCACAAAATTCATTTATGTTGTCCCAACACAAATTGATTAAGTTAACTGAACACTTTTAACAAATTTATGTAAATTTAACATAAAACAGTTTAGCTGTCCCAATGAAATCTCAAGAATTGTGTTGTTTCAGCTCATTTTAAATTAGTAGTTTAAACAAGCAAAAAAAAAAATTTTTGGAGTGTCAAAGTGATTCTTGTTTCTCGGTTTCAGCCCACAAATATATGCAAACAATGCAGCACTTCATCAGCAGCTTTAACGAAGTTGGCCAAGGGCTTAGCAAAGAGTCAGTTTGTGACTACACTTGTTATTTAGTGTTTGTCATTCTCTTTGTTCAGGTTGTTGATGGTTCAAGAGAGCCAGTGTCTGTTTTAGCGCCGGTACAGAAAACACACACTGCCGTCTCCAATCCTAAAGTTGTGAAAGGACACATTCCAGCGGGACACACTCCTAAACCTGTGATCATGCCGGATTA[T/A]GTTGCGTGAGTACAGTTGTGCAAAAACACAAGCAAACTATTACTGTTATATGACAATGATAAATATTCACGATTTGATTAATTTATTTACTTCCTCATCATTTGCTTGCGCTCAAGTGTTTATAAACCTTTCTTTTTTTTTTTGTTGAACACAAAGGAAGATATTCTGAAGAATGTTGGAAAAATGCACCCGTTGACATTCTTCAGTTTATCTTCCTTTATGTTCAACAGAAGAAAGAAACTCTTACAGGTTTTGAACAAGTGTAAGACGAGTAAATGAGGGCAGATTTTACATTTTTGAGTGAACTGTCCCTTTAAGTGCGGTGGCTCAGTGGTTAGCACTGTCGCCTCACAGCAAGAAGGTTACTGGTTTCAGTCCTGGCTGGGCCAGTTGGCATTTCTGCGTGGAGTTTGCATGTTTGCATGTGAATTGGATTAATTAAATTGGCCGCAGTTTTTGAGTGTGTGTGTGTGTGAGTGAATGAGAGTGTATGGGTTATT
Associated Phenotype:
Not determined