ZMP
adam19b
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A5WW95]
Human Orthologue:
ADAM19
Human Description:
ADAM metallopeptidase domain 19 [Source:HGNC Symbol;Acc:197]
Mouse Orthologue:
Adam19
Mouse Description:
a disintegrin and metallopeptidase domain 19 (meltrin beta) Gene [Source:MGI Symbol;Acc:MGI:105377]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42343 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30976 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38979 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42343
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 |
---|---|---|---|---|---|
ENSDART00000097214 | Nonsense | 114 | 870 | 4 | 21 |
ENSDART00000132913 | None | None | 131 | None | 4 |
ENSDART00000143179 | None | None | 186 | None | 4 |
ENSDART00000097214 | Nonsense | 114 | 870 | 4 | 21 |
ENSDART00000132913 | None | None | 131 | None | 4 |
ENSDART00000143179 | None | None | 186 | None | 4 |
The following transcripts of ENSDARG00000067545 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 6537906)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6265293 |
GRCz11 | 14 | 6572020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGCGTGTCTGTGTTTTTCATAGGGAGCTGTTCTCCTCGGAATAT[C/T]AAGAAATATGGTACGATACAAATGGAAATCGGCAGTTTTCCAGACCTTCC
Long Flanking Sequence:
CGAGACACTGCGCCGGGTGTATGATTGGGCCCATTTAGCGCTTAGTGATTTTTGTTTTAGTCTTTAAGCAGAAAGAGGAGCAAACTGTCCAAGTAGCATAAACAGACTGTTCTCAAACTGTGCTCACATTAACGGTATCTCCGGTTTCAAAGCAATCTTCCACTTCAGATGAATATTTAATGAGCTCAATGCCATTAAAGGAAAGAGACTTCACACTGTCAGCCATTTTCTGTGTTTCTGTGAAATTCTCAACCCGTAAAGCTTCTCAGTTCCTTCTCTCCAACAAACTACATCTGATAGGAATCAAATCTTGATTCATGTGCGACTCCAGAGAAGGAATGGAAAGAAGTTGGGAAATGTTTATGTTTTTCCTTCATGCAAGTGATGGAAGTTGTCTGGTTATGTACCAGCTGTGCTCTGATTAAACATATAGCTGGGTCATTTCGTCATTGTGTGTGCGTGTCTGTGTTTTTCATAGGGAGCTGTTCTCCTCGGAATAT[C/T]AAGAAATATGGTACGATACAAATGGAAATCGGCAGTTTTCCAGACCTTCCATCAGGGTAAGTGCTGGAAGTGTTCACTTCTTTATAAAACTTGAACAGTTCATTTTGTCAACGTAGTCTTGATCCCCTTTAGATATTATGTTCACTTTAAAGGGATAGTTCAATTTTCACGAATTTCATGCACGAATGAATCGAAGATCACGCACGAATGAAATAAATTTCTCATGCAAATGAAGCGAATTTTACATGCAAATTTTAAGCAAATTCAAGCCACAAATTTCAAGTGAATTTCCCACCCGAATGAAACAAATTTCACGTGCAAATGAAGCAATTTCACACACAAATGAAGTGAATGAATGAAGCAAATTTCCCATGTGAATGAAGAAAATTCAAAGCAAATTTTTTGAAGAGAATGAATGAAGTGAATTTTTTACGCGAATGAAGTAAATTTTAATCGAATTAATCGAATTTCACGCTAAGTTTTCAAGCAATTTTTTCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30976
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 |
---|---|---|---|---|---|
ENSDART00000097214 | Nonsense | 114 | 870 | 4 | 21 |
ENSDART00000132913 | None | None | 131 | None | 4 |
ENSDART00000143179 | None | None | 186 | None | 4 |
ENSDART00000097214 | Nonsense | 114 | 870 | 4 | 21 |
ENSDART00000132913 | None | None | 131 | None | 4 |
ENSDART00000143179 | None | None | 186 | None | 4 |
The following transcripts of ENSDARG00000067545 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 6537906)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6265293 |
GRCz11 | 14 | 6572020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGCGTGTCTGTGTTTTTCATAGGGAGCTGTTCTCCTCGGAATAT[C/T]AAGAAATATGGTACGATACAAATGGAAATCGGCAGTTTTCCAGACCTTCC
Long Flanking Sequence:
CGAGACACTGCGCCGGGTGTATGATTGGGCCCATTTAGCGCTTAGTGATTTTTGTTTTAGTCTTTAAGCAGAAAGAGGAGCAAACTGTCCAAGTAGCATAAACAGACTGTTCTCAAACTGTGCTCACATTAACGGTATCTCCGGTTTCAAAGCAATCTTCCACTTCAGATGAATATTTAATGAGCTCAATGCCATTAAAGGAAAGAGACTTCACACTGTCAGCCATTTTCTGTGTTTCTGTGAAATTCTCAACCCGTAAAGCTTCTCAGTTCCTTCTCTCCAACAAACTACATCTGATAGGAATCAAATCTTGATTCATGTGCGACTCCAGAGAAGGAATGGAAAGAAGTTGGGAAATGTTTATGTTTTTCCTTCATGCAAGTGATGGAAGTTGTCTGGTTATGTACCAGCTGTGCTCTGATTAAACATATAGCTGGGTCATTTCGTCATTGTGTGTGCGTGTCTGTGTTTTTCATAGGGAGCTGTTCTCCTCGGAATAT[C/T]AAGAAATATGGTACGATACAAATGGAAATCGGCAGTTTTCCAGACCTTCCATCAGGGTAAGTGCTGGAAGTGTTCACTTCTTTATAAAACTTGAACAGTTCATTTTGTCAACGTAGTCTTGATCCCCTTTAGATATTATGTTCACTTTAAAGGGATAGTTCAATTTTCACGAATTTCATGCACGAATGAATCGAAGATCACGCACGAATGAAATAAATTTCTCATGCAAATGAAGCGAATTTTACATGCAAATTTTAAGCAAATTCAAGCCACAAATTTCAAGTGAATTTCCCACCCGAATGAAACAAATTTCACGTGCAAATGAAGCAATTTCACACACAAATGAAGTGAATGAATGAAGCAAATTTCCCATGTGAATGAAGAAAATTCAAAGCAAATTTTTTGAAGAGAATGAATGAAGTGAATTTTTTACGCGAATGAAGTAAATTTTAATCGAATTAATCGAATTTCACGCTAAGTTTTCAAGCAATTTTTTCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38979
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 |
---|---|---|---|---|---|
ENSDART00000097214 | Nonsense | 731 | 870 | 19 | 21 |
ENSDART00000132913 | None | None | 131 | None | 4 |
ENSDART00000143179 | None | None | 186 | None | 4 |
The following transcripts of ENSDARG00000067545 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 6568593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6295980 |
GRCz11 | 14 | 6602707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTTTTTGACTGATGTTTTTGTCTTATCTTATGTGCAGGCAGCTTTTA[T/A]CTTGTGCTGGTTCTCCTCAGCTTGTCTTTTCTTCTGGCGTTGGCTGTGCT
Long Flanking Sequence:
CTTGCACAATTAACCGAATTTGCCTAATTAACCTAGTTAAGCTTTTAAATGGCACTTTAAGCTGAATACTAGTGTCTTGAAAAATATCTACTCAAATATTATGTTCTGTCATCATGACAAAGATAAAATAAATCAATTATTAGAAACTAATTATTAAAACTATTATGTTTAGAAATTATTTGAAAAAAAAATCTATCCGTTAAATAGAAATTGGACAAAAAAATATACAGGGGGGCTTATAATTCTGACTTCAACTGCATGTTGTTGTTGTTGTTTTTTTGTCCTGCAGCTTTGCAATAATAACCACAACTGTCACTGTCACTCCGGTTGGGCTCCACCATTTTGTGGGACATCGGGTCCAGGAGGCAGTTTGGACAGCGGGCCTGTGATCTCACAGAGTACGTCAGCTGATTACCTCAATATTTTATTGAACCCTATCTACGATGAGTTATGTTTTTTGACTGATGTTTTTGTCTTATCTTATGTGCAGGCAGCTTTTA[T/A]CTTGTGCTGGTTCTCCTCAGCTTGTCTTTTCTTCTGGCGTTGGCTGTGCTTGGTGTCTGTTGGTGCCGCTGTAAACAGAGGTTTCTCTCCACCAAAAGCCCAGCTCTTCCTAAAACACAAACATGCATCAAGTAACAGAGTTTATAACTTAATTTGGGGGAAATAAGTATTGAAAACATCTCCACTTTTCTCAGAAAACATATTTCTAAAGGTGCTGTTGACTTGAAATTTTGGTAACAACCAAAACCGGATGTTGGTAACAACCAAACAAATCCATATAAGCAAAGAAGACAAATCTAATTAGTTTACAAATGATTTGACGTGTAAAAAAAAAGAATTGACACAAGGGACAATTATTGAACACATGAAGAAAGGGAGGTGTAGAAAGGCACTGAAAGCCCAGACAGCAGCTGAAATCTCTCAGTAATTCTTCAGTGACCCTCTGCCCTTCCTCGGTGTAAATGAATATTAGCTGCCTGCTTCAATCCTGCATCTACATT
Associated Phenotype:
Not determined