ZMP
LOC570565
Ensembl ID:
Human Orthologue:
AC009113.1
Human Description:
Putative solute carrier family 22 member ENSG00000182157 [Source:UniProtKB/Swiss-Prot;Acc:A6NKX4]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21094 | Nonsense | Available for shipment | Available now |
sa21095 | Essential Splice Site | Available for shipment | Available now |
sa14703 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21094
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 |
---|---|---|---|---|---|
ENSDART00000112483 | Nonsense | 127 | 610 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 57690643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 56125969 |
GRCz11 | 7 | 56427380 |
KASP Assay ID:
2259-9570.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCACTGGAGGATGGGAGTTTTCCAAACCAGCGGGACTCCAGAACAACT[T/A]GGTGACCGAGGTTAGTTCTCTAAAGTACCTCAAAAACACTACCAAAGTTG
Long Flanking Sequence:
TTTACTATCAGTCCGTCATGTGCGCAAACAGTTCTCATTCAGTCCGTTTTCCAGCTCCGCAGGGTGCAATGTCTGTGAGAAACAGCTGTTTCCGTCGACAAGGACTCTTAACTTGTTAGCTATGGAGTATGAAACTAAAATTTATCCTCAGGTTGGTGGATATGGGCGATACAACAGGATCATCACTCTTTTCAGCTGGTTTCCAAACTTTGCGGTGTCGTTGAATCTTTTCACGGATGTTTTCTTTACTCTCGTTCCCGAGTCTTACCACTGCAAGCCTGACCAGGCGTTACTACCGCCGTCTGCCCTGCTCTCAAACCTTTCCAGGCAGGCGTACCTCAACCTCACCGTGCCCTGGCTTAAGGGCTCTGGATTCAGCCACTGCGAGCTCTACAAGTACCCAGTGAATGTGAGCAACTACACGGACGATGTGGAGCGGGACGTGGTGTCGTGCACTGGAGGATGGGAGTTTTCCAAACCAGCGGGACTCCAGAACAACT[T/A]GGTGACCGAGGTTAGTTCTCTAAAGTACCTCAAAAACACTACCAAAGTTGTATTATTATTAATTAAGGATACATATTATTTCATGTATTTCTTGAATTTGCGTATTACTGATCATAAGGATATATGCAAAAAGGAGCACTGGAGGCAGACCCTCGATGGAGTATTGCAAAAAGCCTCTAACGTTACTTTTCTCTTTAACGTTACTCTAACGTTAAAAGATCAATATTTTACGGTTTTAAGTCAATCTTGCTCTTTAATGATAGCAATAATAATAATAAAACAAAACATATACTTTCACTTTTTTTTTTTGAAAAATAGCTAAGAAACAGAAAGTCTAACTAAAAAGTAGCTTTAGATTGTTTTCCAAGCAATGTTTAGTAACCATAGTAAATTATTTATTTATTTTTAATTTTTATTCGCATAATGTTTTTGTAAAAGAAGCTGTGATATTCCCCATGACTCTCTAATCATTAATCCTCGTGGGATGTGTCCCAAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21095
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112483 | Essential Splice Site | 467 | 610 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 57728068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 56163394 |
GRCz11 | 7 | 56464805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATGCTTAGCATGTTCTTCGGCAGTGAAGTCATGCCCACCATTGTGCGG[T/A]AATCTCCACCGATATGCCCACTCCTACACACAACATCTGATATTTTTTAG
Long Flanking Sequence:
AGAGAAAGAAAACCAAGCTGTAGAATGGCCCAGCCAATCACCTGACTTGAATCCAATAGAAATGATAAAAAAAAGATCAGATTTAACAAACGAGAACAACAGAACCATCAAGATTCTTCAACTCTGTTAAAGTCTATGAAAAACTCCCACCTGAGCAATTCATGTGACTTTATTCTCCATATGAGAGGCGTCTTTAAGCTGTATTAGATTTGTTTTAGATTTGATTTTTATAAATACCTGCTGAAATTTCTAAGTCAAAAGCACCTTTAAAAATATGTTTTCTGAGAAATATCGTGACGTGTTAAACTTGTTTCCCCCACTGTATAATTGGATAGCATTCATCCAGAAGCCCAAAACAAACTGTTTTTCTCCACCGTCTTCTTTCAGATCTGCATGGAGGGCTGGTTCTGGTTCTGTCTGTAGTGGGTCTCCTCTCCTCGCAGGCTTTGGCTATGCTTAGCATGTTCTTCGGCAGTGAAGTCATGCCCACCATTGTGCGG[T/A]AATCTCCACCGATATGCCCACTCCTACACACAACATCTGATATTTTTTAGATTATCAGCCAAAATAAATGAAATCCAATTCTTCTGACTTTTATGAAAGGAATTATGAAATGGATTTTTATTAAAGGATGATGAGTCATGATTTGCACAAAAAAAGAGAAGCTAAACAATTTTTTGACATTGATAAACCATTATAAGTAATCTAACACCAGTCATAATTTATAAAAACCGAGCAGCATGTCGCAGCACCAGGATCATATGACACTGAATTATAAGTGCTGAAAATGCTGCTTTGATATAACTGGAACACAGTATGTTAAAAATATATATTAAAACATGGAACGGAAATTTTGCTGTATTTTTGCCAGTAAATGTAGATTTCACATTTTTGGTAGCACTTTACAATAATGCTCCATTAGTTAATGTTAAATAATGTTCTTACTAACATGGATAATACATTTATTACATTATTTATTTACTTTTAATCCATTTTGTTTAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14703
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112483 | Nonsense | 556 | 610 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 7 (position 57730441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 56165767 |
GRCz11 | 7 | 56467178 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCTTCCTGTCCCGCATGAGCCGAGAYAATCCTCCATTACTGCGCACG[G/T]AGCCCAATGGCCCTGAGTACAACCGCGATAACTACTCGCGCCTCGTCTCC
Long Flanking Sequence:
ATGTAGTCATAAATATTATTTACTGTCATCACGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTCTTAAAACTATTATGCTTAGAAATGTGTAGAAAAAAAATCTGCTCTCTGTTAAACAGAAATCGGAAAAATATACAGGGGGCTAAAATTTAGGAGGAGTAATATTTATAACTTCAGCTGTAGATTTCTCTACATGTATTGAGCTCATTGCTGTGTTTTCCCTTTCAGCGGTGGTACTCTGGGTCTGATCATGTCCGCAGGCTGTATAGGAATGGCGGCGTCCTCTCTTATGGAGTTGCAGAATAACGGTGGGTATTTCCTGCATCACGTCATCTTCGCGTCCTTCGCTGTCCTGTCCGTCCTGTGCATCATGCTGCTGCCCGAGAGCAAACACAAACCCCTGCCCGACTCTCTGAAAGACGGAGAGCGGCAGCGGCGTCCTCCTCTCTTCCTGTCCCGCATGAGCCGAGACAATCCTCCATTACTGCGCACG[G/T]AGCCCAATGGCCCTGAGTACAACCGCGATAACTACTCGCGCCTCGTCTCCGCCACCAAGAAGATGCTCAGTAAAGACACACTCCCATACAAGATCTCCAGCTCAACACAAGCTCCTCTACTCTCCAGCAATGGTGCTGCTCCAGACGCACAAGAGGACTCGTCATAGCATTTTGTTGTTTATTTTGGATATGATCATCTCACGACATGACCAGTTTGGTCACTCCGTCTTTTCCCAGGGAATATGTGGTATTGATGCTTTAAACTGGTAGTGACGTGTATTCTGTATGCATCGGGAAGCCCTGCTCTACGCACAGATGTTGCTGGGAGACTCTGTGCTCAGTCTCTATCTGATTGCTGAATGCTTTAGCGTCGTAGCCGCTGACGGTCACCTGAGAGCCATCGCCTGTCCACTTAGCAGCTGCATCTCATGCAACTCATTAGCCAAGTCTTGTGACTAAAGCAAAAGTAGCAGTTTTCCCACATGAAGGCTTGCTTAAAG
Associated Phenotype:
Not determined