ZMP
TMEM200C (2 of 2)
Ensembl ID:
Description:
transmembrane protein 200C [Source:HGNC Symbol;Acc:37208]
Human Orthologue:
TMEM200C
Human Description:
transmembrane protein 200C [Source:HGNC Symbol;Acc:37208]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44552 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33064 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44552
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 |
---|---|---|---|---|---|
ENSDART00000128028 | Nonsense | 206 | 374 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 58959593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 58017225 |
GRCz11 | 2 | 58639060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAAAACACGACGCCGAGAAACTCAGGAAAGCAGCGGCGCCTGTCGTG[C/A]GCCAGAAACAGCTTTGGGTGAGTTACTCTTTACATCATTAAAGGGGTCAT
Long Flanking Sequence:
GTGGTGGTGAAGGGTAAAGTGCAGCTGTGCTCGGGTTCGGGGCTGGTGGCGGCGCTGGGCGTGCTGATCCTGCTGGTGGGTGTGGCCATGGCCGTGCTGGGATACTGGCCTGTTGAAAACACACACGCCACAGCGGGCTTCACGCATAATAACGAGTCCAGCTTTAACTCCTCGTCTCCCGTCGCACACTCACTCGGGTTCTTCCAGAGTCTGTTTGGTGGATACCTGCAGTCGGACAACCTGAAAGTGCTGGGGCCGCTGGTCATGGGCATCGGCATCTTCCTCTTCATCTGCGCCAATGCAGTTCTGCATGAGGACCGAGACAAGAAAACGAAGATAATTAACCTGCGGGACATTTACTCCACCGTCATCGACATCCACAGCCTGCGCAGCAAAGATTGCATCCCGTTCAATGGCCTCATCAGCCACATGCAGTCTAAGAGTGGCGAGGGAAAAAACACGACGCCGAGAAACTCAGGAAAGCAGCGGCGCCTGTCGTG[C/A]GCCAGAAACAGCTTTGGGTGAGTTACTCTTTACATCATTAAAGGGGTCATGAAATGAGAAATCAAAATATCCTTCGTTGTTTCTCATATTAGAGCTCGTATTGTCAAGAAAATGTCCTGTAGGTTTCAGAACTCAACACCTTGTGGTTCCTCTGAAATCAGCTCATGTTGAAGCAGATCTGACCAAACCACAGCTTCTGGAATGTTCTGCTCTATGATGTAATAGGGAGGATAAGCTCCGCCTCCAATAAAGTGATCAAAGGTTTATAGTGTAAAACATTCTGTTAGGGCGTACTCACACTATGCTATCCGAACCGTGCCCAGGCCCGTTTCCCGGATCGTTTGAGAAGTGTGAGTGCGCTGAATCAGGCTCTGGCATGGTTCACTTGGCCGGCCCTGGCCCGGTTGGAAGAGGTGGGCCTGAGCGAGGTTCACTTGGGAATTGGCGCGGTACGCTTGTAGTCTGAGTGCAAAACGCGCCAAAGCCCAAAACTGAAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33064
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 |
---|---|---|---|---|---|
ENSDART00000128028 | Nonsense | 346 | 374 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 58966572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 58024204 |
GRCz11 | 2 | 58632081 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCAGCCGGAGCCCGTGGGGAGACGCCCGCGCGCAGGTTCAGCTGCCCT[C/T]GACTGGAGCGCTGCAGCAGCAGGAGATACAACAAACTAGCAGAGCTGAGC
Long Flanking Sequence:
AATTTAGAGTTTACTAAGACGGTACACTGTAATTAAATGAGCTGTAGTCTGTTACTGTAGATTTTATTAGGTCAATGATGTCAATTTCCATGTCCTGTAGGAAACACAGCCTGTGTGCCAAACGGCAGTCCTTCAGCGACACCATCTACAGCATCTCTGGAGGCGGGCAGGAGGCGCAGTGGGAAACACACTCCATCGTCAGCTCGTCTCTGAACGCCTTCACGCTCCCCGTCATCAAACTGAACAACTGCGAGATGCAGGAGGCCGAGGCGTCTCGGAGGAGGAGCTGCGGAGGAGCCCTGGAGACCCGCGCTCAGGTGTCCCGCACACACATCTCACGCTCACAGGACTCCCAGCTGGAGAAACGACCCACCGCTGCTGGGTCACTGCTGTCTCAGCTGGAGAAACGACCCGCCGCCGGGTCACTCCTGTCTCTGAACACACTGCCGGACGCAGCCGGAGCCCGTGGGGAGACGCCCGCGCGCAGGTTCAGCTGCCCT[C/T]GACTGGAGCGCTGCAGCAGCAGGAGATACAACAAACTAGCAGAGCTGAGCGGAGACTCACTGGAGACACCTGACCCTGACACACACACNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCAGAATCTACAGCCTCAGTTAACCACAGGAGCCGAGAGACGTTTCCCATCATGCTCCACATGTAACAAGCAGAGGTGAAGGTCACACAGGACAGCAGAGGTCAGAGGTCACCGCAGGAATAATGATGATGATGAAGGCTGAAGCAGTGTTAGATGATGATGTTAGATGCGGAGAGCAGACACACACGCACATACAGCAGCGCTCCGTCAGTCGGTCAGTCAGTCATCTTCTTAACTTTACTTATTTGAACGTCAAAAAAACCCTCAAATTCTAAAAAAATAAACAAAATCTCCATTTCTGAAGAACAATATT
Associated Phenotype:
Not determined