ZMP
tmem57a
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 57a [Source:RefSeq peptide;Acc:NP_956613]
Human Orthologue:
TMEM57
Human Description:
transmembrane protein 57 [Source:HGNC Symbol;Acc:25572]
Mouse Orthologue:
Tmem57
Mouse Description:
transmembrane protein 57 Gene [Source:MGI Symbol;Acc:MGI:1913396]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23542 | Nonsense | Available for shipment | Available now |
sa36859 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1411 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23542
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 |
---|---|---|---|---|---|
ENSDART00000009149 | Nonsense | 71 | 664 | 2 | 11 |
The following transcripts of ENSDARG00000005625 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 29788128)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 29718150 |
GRCz11 | 19 | 29305373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGGCCTTTTTGGCTTTTCATCAGGAGTGTTTATGATTCCTTTAGATA[T/A]CAGGGACTGGTGAGTGTTTCATTGCTCAACTTGAGATTACACAACCGAGT
Long Flanking Sequence:
TTGAAAGCAGAGTCCTCTGTAGAATAGTATTTTTTGCACTTTTATGCATAGACATATATGGAATTGAATTGTAATTATTGCTGAAATAATTGTAAATTATGTTCATTTATTAAAATAATTAAAATGTGAAGTACTGATACTTCACAAATAAATACAAACCCTCCCCCGAAAATGCATATGCAGTAATTATGAATGACTGGAAAAGTCATTGAAATTGTTTAGTAAAATGTTACCCCCTTGTTATCTGTTTTATCTGTTTAGATGACAGAATATTTGCAGAAGCTTTATCAAATTTTTGGAAGCGTTCAAAAAAAAAGTTGTAACATTTTCTGAAACGTTTAACTCTATTAATGATTTTTCTCTTGCAGTACCTTCCTGTACCTGAAGTTCCTGGTCGTTTGGGCGCTGGTTCTGCTGGCTGATTTTGTGTTGGAGTTCAGGTTCGAGTACTTGTGGCCTTTTTGGCTTTTCATCAGGAGTGTTTATGATTCCTTTAGATA[T/A]CAGGGACTGGTGAGTGTTTCATTGCTCAACTTGAGATTACACAACCGAGTGACTTATGACTTTTTAATTTCATCACAGCACTTGTTATCTTCTTCCACAGGCATTCTCTGTGTTCTTTGTGTGTGTCGCATTCACATCAGACATCATCTGCCTCCTGTTCATCCCTAAACAATGGTTGTTCTTCGCTGCCAGCACTTATGTCTGGGTACAGTACGTGTGGCATACAGGTAGGTCAACATTACTCAAGTCCATCCAATCTCACATAGCCTGAGCTTCAGACTCACAACAGAAGTTCTGGAGTACTTTTTTGCTTCTGTTGGCTGATTGACATGTACAACAACCAATCACAGTTCATTTAGAGGTTTTAAATTTTAAAGTTGATGTCCTTGCAATAACACACTAACCTGTAAACTATTGGACTCCTTTTATTGAGGCCTTAAATGGATAGTTCACCAAAATAATGAAAAGTGCCTCATCATTTACTTTCCCCACATGTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36859
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 |
---|---|---|---|---|---|
ENSDART00000009149 | Nonsense | 264 | 664 | 6 | 11 |
The following transcripts of ENSDARG00000005625 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 29801676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 29731698 |
GRCz11 | 19 | 29318921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAACTGGAATACAAAGAGAAGGGCAAAGATAGTGCAAAAGACAAAAAG[C/T]AACAGCAGCACAGCATAGGAATAAACAACAACATCCTACAGACTGTAGAT
Long Flanking Sequence:
AGCATCATAAACCAAATACATTGTAGCCATGAAAACCCAGCCCTGCTTGATTAACATTGTTCATTCATCACACTGGTAAAGAAAGGTCAACTTTAGTCCACTGCATTTGAAGGATACTTTTCTACACTGCACATGCCACACAGTTTGCCTAATGTTTGTTATTTGCCCTTTCCACGCATTCACAAAATTTCCATATTTTGCACATTATACATCCTGCAGAAACTATTATCTGTCATATTATATAGTACTACATAGCCAATAGATTTGCATTAAACTTTCCAACTTCTAATTTAATTTCTAGACACACAAGTCAAACAGCATTTAACTCATAACCTTAAAATCTGTCTCTCCTTTATTTGGCAGCCACCTCAAAAGGCATGTCTGAAGCAGACTCTGTGTTAGTGGCTCAGAACGGCACTGCAATCAACAAGAAACTGCCCATCTCTCTGCCTGAACTGGAATACAAAGAGAAGGGCAAAGATAGTGCAAAAGACAAAAAG[C/T]AACAGCAGCACAGCATAGGAATAAACAACAACATCCTACAGACTGTAGATGCTAAACTACAAGACATTGAGTACATGGAGAACCACCTAAACGCTAAAAGACTCAACAACGAGCTCGGCGGCAGTGCCGAAAACCTGTTTCTGAAAGAGGAAGTGGGTGCCGGAGGAGGCTCTGCGCCCTCCAAACATTACAAAAACTCCTCGCCACGCAGCCACAACTCAACCAATGGCAGCGTACCATCATCTTCATCCAACAGAAGCGATAAAAAGCAGAAGTGCACAGGGAAAAACCTTGCGCCACATCGAGATTTGATGGAGAACTGTATACCTAATAACCAGCTCAGTAAGCCTGATGCATTAGTTCGGTAAGACTCCTCGTGCAGAAGTTGGGATTTGGCTGCTGGAGTGTGTGTTCAGTCTGTTTATTTTTGTTTTGTGTGCGTTTGTCAGGCTTGAGCAGGATATTAAGAAGCTGAAGGCTGACCTGCAGGCGAGCAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1411
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 |
---|---|---|---|---|---|
ENSDART00000009149 | Nonsense | 652 | 664 | 11 | 11 |
The following transcripts of ENSDARG00000005625 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 29816139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 29746161 |
GRCz11 | 19 | 29333384 |
KASP Assay ID:
554-1332.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGACCCCACATTACTCCTCCAAGTTCATGGACACCAGTCCTTCCAGCT[T/A]GGACCCCAATGCCTCCGTCTACCAGCCGCTCAAKAAGTGAATGTCCACAC
Long Flanking Sequence:
TATAGAGGGAGAGGTGAAGAGGTAGGGGTGGATGGGGGGATTCTTCAAATCGAAGTTGACTGTAAAAACCCTTTATAGCGAGTTAGGAATGGCCTGATCGGTGGATCATACATGCTAATGCAGAACCAGCCGTGTTCAATCATAATCGCATGATCCTCTCGAAATTAGTTTATGAATAAACTCTTATTTTTGCTGCATAGGTCAACATTGTGATTAACACATTATAAAAGCTTCTTCAATCACAAGAGAATTTGATACGGGCAGAAGCCTGCCCATCTCTAATGTTAACATATAATACATCTCTCACAAAGCTTTCCTCTTTTTTAACCTCCTCACAGGTCAGATTCTGCAGAAGGAGCAGGAGATAAAAGAGCTGAAGCAGAAGATCGCAGAGGTCATGGCAGTCATGCCAAGCATCACCTACTCGGCGGAGACCAACAACATGACCCCTGTGACCCCACATTACTCCTCCAAGTTCATGGACACCAGTCCTTCCAGCT[T/A]GGACCCCAATGCCTCCGTCTACCAGCCGCTCAAGAAGTGAATGTCCACACACATCGTCCAGTTTGCTGTTTGATTTGTACTAAAGTTCAGTATGCAAACCAATGGGATGGGGTAGTATTTTTGTTTGATTTACCCCTCCTCTGTTAGTATGACTCTTCTTTGTTGTGGATGATTAGAGAAGGAGAATAAAATAAGGGGGAAAAGGGATGACGATTTGACCAGAACTGCCCTTTTTGTCTTTAAGGTTATTTTTGAAAAAAAAACAAGTTTTCGATAACGGCACTTAAGCCACTTGTGGTTCTCTTGTCATCCTACGTTCATTTTGTGAGGTCTTTATTAAGATCTTTTATTAGTACCTCCTCCATCTTTGTGTTGAACAGTTTTATGTGCCAGACAATGGTGGCATGACTTTCTTTTTTTACTTCCCTGGTGTAAACGTACCATCTTTAAGTTTATTGAATGTAAAAAAAAAAAAAAAGAAAAGGGAAAAGGAGATGAGA
Associated Phenotype:
Not determined