ZMP
si:dkey-17e16.14
Ensembl ID:
ZFIN ID:
Human Orthologue:
TMEM151A
Human Description:
transmembrane protein 151A [Source:HGNC Symbol;Acc:28497]
Mouse Orthologue:
Tmem151a
Mouse Description:
transmembrane protein 151A Gene [Source:MGI Symbol;Acc:MGI:2147713]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44969 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39330 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37318 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44969
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 |
---|---|---|---|---|---|
ENSDART00000110705 | Nonsense | 144 | 486 | 1 | 3 |
ENSDART00000145091 | Nonsense | 198 | 598 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 21 (position 25024529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25607866 |
GRCz11 | 21 | 25644471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCATCAGCTACCATTACGTGCGGCGTACCAGACAGGTCACGCGCTAC[C/T]GAAATGGAGATGCCTATACAACAACGCAGGTGTACCATGAAAGGGTCAAC
Long Flanking Sequence:
TTCAATTTCCTGTCCATCTGTACAACCCTCTGTCCCCCTTTCTTCCTATATTTCCTCCCTATTCCCACCTACAGCAGCGTCCCCTCAAGCAGTCCCTGAGTGGCTCGCTGTGCCGAGAGTCCCACTGGAAGTGCCTGCTGCTCACCTTGCTCATGTATGGCTGCTTTGGCACACTAGGCTGGTGCTCTCTTTACCGCATCACAGTAATGGCTTCTGATGACCAAGGCCCTGCATACTTCTACGGGGACCGAGCCAGACTCTACCATGACAGCCCGTGTTCTAACGGCTACGTCTATATACCTGTAGCATTCCTGGCCATGCTGTACATCGTATACTTGGTGGAGTGCTGGCACTGCTACTCTAAAACAGCTAACCTTGCTAAGGTGGAGATCACAGAGGTTTATGACAGGATACAGCGGTTACAACAAGCCACTCCCTGCATCTGGTGGAAAGCCATCAGCTACCATTACGTGCGGCGTACCAGACAGGTCACGCGCTAC[C/T]GAAATGGAGATGCCTATACAACAACGCAGGTGTACCATGAAAGGGTCAACACGCACGCATCGAGCTCTGAGTTTGATTACTCAAGACTTGGGGTTAAAGATGTTTCAAAGGAGCTGCAGGGTCTGCTGGAGCATCCCGTCACCCGTTTGCGCTTTACCAAGTGTTTCAGCTTTGCCAGCGCCCGTGCTGAGACTGCCTACCTCACGCAACGAGCACGCTTCTTTGGAGACAACGAAGGTCTGGATGACTATATGGAAGCACGAGAGGGTATGCACTTAAAAAATGTTGACTTTCGAGAACATATGCTAGCATTCCCTGACCCTTTACACCCACCCTGGTACACCCGTCGTTGGGTATACTGGTTGGCCTCAACTTTCCTGCTATCGTGGCCTCTTCGTGTAATTGCAGAGTATCGCACAGCATATGTCCACTACCACGTAGAGAAACTGTTTGGTGAGAATGAGGATGCAAATGACAATGATAATACAGAGACAGGGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39330
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 |
---|---|---|---|---|---|
ENSDART00000110705 | Nonsense | 252 | 486 | 1 | 3 |
ENSDART00000145091 | Nonsense | 306 | 598 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 21 (position 25024854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25608191 |
GRCz11 | 21 | 25644796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAAAAAATGTTGACTTTCGAGAACATATGCTAGCATTCCCTGACCCTT[T/A]ACACCCACCCTGGTACACCCGTCGTTGGGTATACTGGTTGGCCTCAACTT
Long Flanking Sequence:
CATCGTATACTTGGTGGAGTGCTGGCACTGCTACTCTAAAACAGCTAACCTTGCTAAGGTGGAGATCACAGAGGTTTATGACAGGATACAGCGGTTACAACAAGCCACTCCCTGCATCTGGTGGAAAGCCATCAGCTACCATTACGTGCGGCGTACCAGACAGGTCACGCGCTACCGAAATGGAGATGCCTATACAACAACGCAGGTGTACCATGAAAGGGTCAACACGCACGCATCGAGCTCTGAGTTTGATTACTCAAGACTTGGGGTTAAAGATGTTTCAAAGGAGCTGCAGGGTCTGCTGGAGCATCCCGTCACCCGTTTGCGCTTTACCAAGTGTTTCAGCTTTGCCAGCGCCCGTGCTGAGACTGCCTACCTCACGCAACGAGCACGCTTCTTTGGAGACAACGAAGGTCTGGATGACTATATGGAAGCACGAGAGGGTATGCACTTAAAAAATGTTGACTTTCGAGAACATATGCTAGCATTCCCTGACCCTT[T/A]ACACCCACCCTGGTACACCCGTCGTTGGGTATACTGGTTGGCCTCAACTTTCCTGCTATCGTGGCCTCTTCGTGTAATTGCAGAGTATCGCACAGCATATGTCCACTACCACGTAGAGAAACTGTTTGGTGAGAATGAGGATGCAAATGACAATGATAATACAGAGACAGGGAACTACTGTACAGGCTTTGAACATGGCACCGGAGGTCCCACCCTTCGAGTCATATCACGGGTCAACACGGTGGATATGACCGAACTGGAATGGCACATTCGTTGTAACCAGCATATGGTGCCTAGTTACTCAGAGGCCTTGCTTATGGATTTGGACATGAACACAAATACACCGTTAACAGTTGCAATGGCTGCACGAATGCGACGCAATTCTAGCTACCTACTACAGAGCTGCCCCAGGTGCCGGCGATCAACAAGCAGCTCCTCTCTCCCTTCATGGGTTAGAGGGAATGTGGCTGCAGGGACAAACTCATTCCCAATTAGGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37318
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110705 | Nonsense | 445 | 486 | 3 | 3 |
ENSDART00000145091 | Nonsense | 548 | 598 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 21 (position 25025579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25608916 |
GRCz11 | 21 | 25645521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGGGGTGTGTTAGAGAGTGAAGGGCTAGAAGATGAAGATGTAGAGGAG[A/T]GAAGCCAGGAACAAGTGGAGGAGAGAGAAAATGTAGAGACCAGGGAGGAC
Long Flanking Sequence:
TATCACGGGTCAACACGGTGGATATGACCGAACTGGAATGGCACATTCGTTGTAACCAGCATATGGTGCCTAGTTACTCAGAGGCCTTGCTTATGGATTTGGACATGAACACAAATACACCGTTAACAGTTGCAATGGCTGCACGAATGCGACGCAATTCTAGCTACCTACTACAGAGCTGCCCCAGGTGCCGGCGATCAACAAGCAGCTCCTCTCTCCCTTCATGGGTTAGAGGGAATGTGGCTGCAGGGACAAACTCATTCCCAATTAGGCCTGGTGGCAGGCTGTCCCTTAGTCGCAGCGGTTTCTCTCTCGGCCGCTTGCATACCACAAGAAGCCGCCACCCTTGCCTGTTCCACTCAAGAAGCCTTGGAGGTGGGATGGGTAGCCGGATGGAAGAAGGGGGTGGGGGTTTCCTTGGTCTTGGGTTTAGAGTGCCAGATGAGGAAAGGAGGGGTGTGTTAGAGAGTGAAGGGCTAGAAGATGAAGATGTAGAGGAG[A/T]GAAGCCAGGAACAAGTGGAGGAGAGAGAAAATGTAGAGACCAGGGAGGACAATAGAGACAGGCCACCCACCTACCAAGATGCTCTGTACCTTCCGGTTTTAATCATTCATGGGGAAGAGAGCTGTCATGGGGGGCATGGGATTGACACAGGATAAAAGAAGAAGTGTGATTTAAAGAAGAATATTTGAAGTGACTTTTGAAAAGCAGAGGCAGACTACCATCAGGGTACAGACAATAGACTGGCAGATTGTGAAGTCAGGAAAGAGATGGGAGTTTTGAACTGAATCAAGATTCAAAAGTTGAACCCAAAGTGTCTCTTGTGTAACACACCTAAAAAAATTTGTTCATGAATGTATGGAACAGGACTATTCAATCTTGCACCTAGGGGGTCAATGTCCTGCTGAGTGTAGCTCCATCAGCTCAAACACAATAGTCTGGAAGTTTCTACAAACCTGTGAAAGGAAAGTGTGCAACCTTTAGCCAAACAAAAGCATAAATGA
Associated Phenotype:
Not determined