ZMP
mfsd6b
Ensembl ID:
ZFIN ID:
Description:
Major facilitator superfamily domain-containing protein 6-B [Source:UniProtKB/Swiss-Prot;Acc:B0UYT5]
Human Orthologue:
MFSD6
Human Description:
major facilitator superfamily domain containing 6 [Source:HGNC Symbol;Acc:24711]
Mouse Orthologue:
Mfsd6
Mouse Description:
major facilitator superfamily domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:1922925]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21555 | Nonsense | Available for shipment | Available now |
sa10516 | Nonsense | Available for shipment | Available now |
sa41504 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21555
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 |
---|---|---|---|---|---|
ENSDART00000004544 | Nonsense | 131 | 747 | 1 | 6 |
ENSDART00000076815 | Nonsense | 135 | 412 | 3 | 4 |
ENSDART00000135821 | Nonsense | 131 | 747 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42578276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41703446 |
GRCz11 | 9 | 41505233 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTACAAACTATACGCATGCTGGTAATCATACCAGACAGCGAAGATACT[T/A]GACTGAGGATGCATACGCCAATCCTCCACTTTCTCAGCCCATTTTAGCTG
Long Flanking Sequence:
TTAACACTCTGTCCATGGGGCAGGTGGCAAACACTACACCATCAGGTCAAACAGCACCATCTGACACACTCCCCTCTCAATCCTCCCAAAGTATGAACTGCATGGAAAGATGTTGTGCTCGAATAGACAATCGTCTCTTGATTTCCAAGATCTTCTATTTTTTCTTCTACTCTGCATATGGCTCTTTACACCCCTTGCTAGCTGTGTACTACAAGCAGCTGGGAATGACACCTACCCAAAGTGGCCTACTCGTTGGGATCCGTTATTTTATAGAGTTCTGCAGTGCAGTGCACCATTTTGGGGATTTGTGGCAGACCGCTTTAAGAAAGGCAAAGCAGTTTTGCTGTTTTCTGTGCTCTGCTGGGTGGTCTTTAATTGTGGTATTGGCTTCGTCAAGCCTGCAGCTATGAGCTGTGTTAGTGTAGACCCTACTGTTCAGTCACCAGTCAATTTTACAAACTATACGCATGCTGGTAATCATACCAGACAGCGAAGATACT[T/A]GACTGAGGATGCATACGCCAATCCTCCACTTTCTCAGCCCATTTTAGCTGCATACAGACCTCACTCTAGATATATTCGAAGTGCAAATACAAACACCACAAGCGCTCCTTTTAGAAACTCAACAGTGGACATCAGTATGGCATCAAACTTAACAACGATGTCACCCAGTGCCACAAAAGTCCCATTGAAATCTACCTCAACAATGGAAACCCAAGCTATTACTGCCAAAGTCAAACAGTATATCATAATCTTCAATAAGGAGCAAGTAGATACTATATTTCTCCTGATCCTGCTGGTTATTATTATCGGTGAGTTCTTCAGTGCCCCGGCTGTGACCATTGTGGACACGGTCACTCTTCAGTACCTTGGTCAAAACAGAGACCGCTATGGACTCCAGAGGATGTGGGGATCTTTGGGATGGGGTATCGCCATGCTGTCTGTGGGCATTTGGATAGACAATACACACATCACGATCTTCATTCAGGGCTTGGGTTGTGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10516
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004544 | Nonsense | 157 | 747 | 1 | 6 |
ENSDART00000076815 | Nonsense | 161 | 412 | 3 | 4 |
ENSDART00000135821 | Nonsense | 157 | 747 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42578199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41703369 |
GRCz11 | 9 | 41505156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTTTCTCAGCCCATTTTAGCTGCATACAGACCTCACTCTAGATATATT[C/T]GAAGTGCAAATACAAAYACCACAAGCGCTCCTTTTAGAAACTCAACWGTG
Long Flanking Sequence:
CAATCCTCCCAAAGTATGAACTGCATGGAAAGATGTTGTGCTCGAATAGACAATCGTCTCTTGATTTCCAAGATCTTCTATTTTTTCTTCTACTCTGCATATGGCTCTTTACACCCCTTGCTAGCTGTGTACTACAAGCAGCTGGGAATGACACCTACCCAAAGTGGCCTACTCGTTGGGATCCGTTATTTTATAGAGTTCTGCAGTGCAGTGCACCATTTTGGGGATTTGTGGCAGACCGCTTTAAGAAAGGCAAAGCAGTTTTGCTGTTTTCTGTGCTCTGCTGGGTGGTCTTTAATTGTGGTATTGGCTTCGTCAAGCCTGCAGCTATGAGCTGTGTTAGTGTAGACCCTACTGTTCAGTCACCAGTCAATTTTACAAACTATACGCATGCTGGTAATCATACCAGACAGCGAAGATACTTGACTGAGGATGCATACGCCAATCCTCCACTTTCTCAGCCCATTTTAGCTGCATACAGACCTCACTCTAGATATATT[C/T]GAAGTGCAAATACAAACACCACAAGCGCTCCTTTTAGAAACTCAACAGTGGACATCAGTATGGCATCAAACTTAACAACGATGTCACCCAGTGCCACAAAAGTCCCATTGAAATCTACCTCAACAATGGAAACCCAAGCTATTACTGCCAAAGTCAAACAGTATATCATAATCTTCAATAAGGAGCAAGTAGATACTATATTTCTCCTGATCCTGCTGGTTATTATTATCGGTGAGTTCTTCAGTGCCCCGGCTGTGACCATTGTGGACACGGTCACTCTTCAGTACCTTGGTCAAAACAGAGACCGCTATGGACTCCAGAGGATGTGGGGATCTTTGGGATGGGGTATCGCCATGCTGTCTGTGGGCATTTGGATAGACAATACACACATCACGATCTTCATTCAGGGCTTGGGTTGTGTCCTGCCTGACTACAAGAACTACCAAATTGCGTTTATAGTTTTTGGGGTGCTGATGACCTCGGCGCTGATTGTGGCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41504
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004544 | Nonsense | 181 | 747 | 1 | 6 |
ENSDART00000076815 | Nonsense | 185 | 412 | 3 | 4 |
ENSDART00000135821 | Nonsense | 181 | 747 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42578126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41703296 |
GRCz11 | 9 | 41505083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCGCTCCTTTTAGAAACTCAACAGTGGACATCAGTATGGCATCAAACT[T/G]AACAACGATGTCACCCAGTGCCACAAAAGTCCCATTGAAATCTACCTCAA
Long Flanking Sequence:
TCTTCTATTTTTTCTTCTACTCTGCATATGGCTCTTTACACCCCTTGCTAGCTGTGTACTACAAGCAGCTGGGAATGACACCTACCCAAAGTGGCCTACTCGTTGGGATCCGTTATTTTATAGAGTTCTGCAGTGCAGTGCACCATTTTGGGGATTTGTGGCAGACCGCTTTAAGAAAGGCAAAGCAGTTTTGCTGTTTTCTGTGCTCTGCTGGGTGGTCTTTAATTGTGGTATTGGCTTCGTCAAGCCTGCAGCTATGAGCTGTGTTAGTGTAGACCCTACTGTTCAGTCACCAGTCAATTTTACAAACTATACGCATGCTGGTAATCATACCAGACAGCGAAGATACTTGACTGAGGATGCATACGCCAATCCTCCACTTTCTCAGCCCATTTTAGCTGCATACAGACCTCACTCTAGATATATTCGAAGTGCAAATACAAACACCACAAGCGCTCCTTTTAGAAACTCAACAGTGGACATCAGTATGGCATCAAACT[T/G]AACAACGATGTCACCCAGTGCCACAAAAGTCCCATTGAAATCTACCTCAACAATGGAAACCCAAGCTATTACTGCCAAAGTCAAACAGTATATCATAATCTTCAATAAGGAGCAAGTAGATACTATATTTCTCCTGATCCTGCTGGTTATTATTATCGGTGAGTTCTTCAGTGCCCCGGCTGTGACCATTGTGGACACGGTCACTCTTCAGTACCTTGGTCAAAACAGAGACCGCTATGGACTCCAGAGGATGTGGGGATCTTTGGGATGGGGTATCGCCATGCTGTCTGTGGGCATTTGGATAGACAATACACACATCACGATCTTCATTCAGGGCTTGGGTTGTGTCCTGCCTGACTACAAGAACTACCAAATTGCGTTTATAGTTTTTGGGGTGCTGATGACCTCGGCGCTGATTGTGGCCACACAGTTCCACTTTGACAACAGGGCTTATCAATCAGATGAAGAAGAGGACAAGAAGGAGGATGTGGAAATACCTC
Associated Phenotype:
Not determined