Busch Lab

ZMP

jkamp

Ensembl ID:
ENSDARG00000028581
ZFIN ID:
ZDB-GENE-040718-382
Description:
JNK1/MAPK8-associated membrane protein [Source:RefSeq peptide;Acc:NP_956776]
Human Orthologue:
JKAMP
Human Description:
JNK1/MAPK8-associated membrane protein [Source:HGNC Symbol;Acc:20184]
Mouse Orthologues:
4931417E11Rik, Jkamp
Mouse Descriptions:
JNK1/MAPK8-associated membrane protein Gene [Source:MGI Symbol;Acc:MGI:1915057]
RIKEN cDNA 4931417E11 gene Gene [Source:MGI Symbol;Acc:MGI:1913990]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9309 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44868 Nonsense Mutation detected in F1 DNA Not yet available
sa32134 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9309
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039438 Essential Splice Site 151 309 4 7
ENSDART00000146786 Essential Splice Site 159 219 3 4

The following transcripts of ENSDARG00000028581 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 14322588)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14439688
GRCz11 17 14447621
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGACTACGTCACCACGTTGCACTGCACACAGGAGGCTGTGTTTCCTCW[G/T]TGAGTGGCTTTTATARCGATATATGKATRTGATTTGAGGCATCAGTTATA
Long Flanking Sequence:
GAAGATTTATGGCTCACTGAAGGAGTTTTTATTTTGAAATATGTATTGTAATCGAAATCTACACACACAGATTGATAAAGTGCAATAAAAGCAGCACATAAAAGCATATTTTGTTTCTGTTTCATTATACTGAAAACAATTTGTGAAAAGCCAAAAGAACTAAATCTCAAAATTAGTTTTTGCCTTTCAGTAAAACTGGTATGACTGAGGAAATTCTGTCGTGTAGATGGGATTTTCCAATATTGTGGCAAAACTTTTCAGACTAACCTGTGTTCTTTTAATGTCATCAACAGTTCTAGTGCCCTTTTCCAGCACATTACGGCCCTGTTTGAATGCACAGTTGCTGCTGTAGTGACTCTGCTGCTCAATGATCCTGTCGGCCAGCTGTATATTCGTTCCTGTGAGGTGAAGATGCTTTCAGACTGGTACACCATGCTGTATAACCCCAGCCCAGACTACGTCACCACGTTGCACTGCACACAGGAGGCTGTGTTTCCTCT[G/T]TGAGTGGCTTTTATAGCGATATATGTATGTGATTTGAGGCATCAGTTATATTTGTTGGTTTCTAGGCTTTACACTATTGACACATTGTTGCATTGTTTAACACAGTTGCATTGGATTGATAATGCCATATATTTTTTATTATAACATTTTAAAACTTATGAAACAAAAAATACAGTTCCTTAAAACCCTATAATTTGGTCTTACTACATTAGGAATGGACCACGCTTGAATGGCGAACTTCTTTTCTGTTAGCTGGACAAAGTAGGTTTTGATCATGATTCTGCTCAACAAAAAACTAACTTGATTTGTGACTTGCTATTTTTTTCCAGATACACCATTGTGTTGATCTACTACGCTTTCTGTCTGGTTTTCATGATGCTTCTACGGCCACTTCTGGTTAAAAAGATTGCATGTGGTTTAGGCAAGACGGATCGTTTCAAGAGCATCTACGCAGCGCTGTATTTCTTTCCCATCCTCACTGTCCTGCAGGCAGTTGGAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44868
Status:
Mutation detected in F1 DNA
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
ENSDART00000039438 Nonsense 213 309 6 7
ENSDART00000146786 None None 219 None 4

The following transcripts of ENSDARG00000028581 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 14319533)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14436633
GRCz11 17 14444566
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAATACCATTGTTTGTATATTTCCCTTTTGTTTATTTTACCAGACTA[T/G]GCGTTTCCGTATATTATTTTGGTCCTATCCTTGGTCACGTTGGCAGTTTA
Long Flanking Sequence:
ACACAAAAGCCACAATATTTTGCATTTCCAAGTGCACATTTTTTAAAAACAAAACTGTTATTGTGTGTGTAAACTACAAAAATATGATTTTGTGAAATGATAACATTCCGGTTTCCCTCACAGTCTAAAGACATGTGGTACAGTTAAATTGGTTAGGCTAAATTGTCCGTAGTGTATTAGTGTGAATGAGTGTGTATAGATGTTTCCCAAAGATGGGTTGCAGCTGGAAGGGCATCCACTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCCACTGTGGAGACCCCAGATTAATGAAGGGATCAAGTCGAAAAGAAAATGAATGAATGAACGAATGAAAAGATAACATCAAGCTTATCTATATCATGTAATTTATAGGCTTAACCAAATAATTAAAAACCAAAACAATGTTAAGCTACATATCCATGTGTACAGCCTTAGTTTTAGCTAATACCATTGTTTGTATATTTCCCTTTTGTTTATTTTACCAGACTA[T/G]GCGTTTCCGTATATTATTTTGGTCCTATCCTTGGTCACGTTGGCAGTTTACATGTCAGCTTCAGAGATACAGGTAAATGCTTTTTTTTTTTTTAATGTTATACTGCTTTTGGTTTTAAATTCAATGCTAATTGTATTAAAACGGTTTGTGAATTATCTCCCACAGTCTTTCAAAAACCTTGTGGCCAAGAAGAAACGGCTCGTCGTTCTCTTTAGCCATTGGCTCCTCCATGCATACGGTATTATTTCTATATCCCGACTGGATAAACTAGGCCAGGATTTGCCTCTGTTGGCTCTGGTGCCTGGACCTGCTCTCTTCTACCTGCTGACGGCCAGATTTACCGAACCAAACCGGATTCTGTCAGAGGGGGGAAATGGACACTGATATCATTACCTTTGCTGGAGAACCGATTCGTCCAAATGTAGAGGAATGGCATTTAGTTTAATGACACCTTTGGGACGAATGCCAAAAAGCCATATTCACAAGATTTCTTTTTTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32134
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039438 Nonsense 268 309 7 7
ENSDART00000146786 None None 219 None 4

The following transcripts of ENSDARG00000028581 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 17 (position 14319277)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14436377
GRCz11 17 14444310
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTTTAGCCATTGGCTCCTCCATGCATACGGTATTATTTCTATATCC[C/T]GACTGGATAAACTAGGCCAGGATTTGCCTCTGTTGGCTCTGGTGCCTGGA
Long Flanking Sequence:
GGATAAGTTGGCGGTTCATTCCACTGTGGAGACCCCAGATTAATGAAGGGATCAAGTCGAAAAGAAAATGAATGAATGAACGAATGAAAAGATAACATCAAGCTTATCTATATCATGTAATTTATAGGCTTAACCAAATAATTAAAAACCAAAACAATGTTAAGCTACATATCCATGTGTACAGCCTTAGTTTTAGCTAATACCATTGTTTGTATATTTCCCTTTTGTTTATTTTACCAGACTATGCGTTTCCGTATATTATTTTGGTCCTATCCTTGGTCACGTTGGCAGTTTACATGTCAGCTTCAGAGATACAGGTAAATGCTTTTTTTTTTTTTAATGTTATACTGCTTTTGGTTTTAAATTCAATGCTAATTGTATTAAAACGGTTTGTGAATTATCTCCCACAGTCTTTCAAAAACCTTGTGGCCAAGAAGAAACGGCTCGTCGTTCTCTTTAGCCATTGGCTCCTCCATGCATACGGTATTATTTCTATATCC[C/T]GACTGGATAAACTAGGCCAGGATTTGCCTCTGTTGGCTCTGGTGCCTGGACCTGCTCTCTTCTACCTGCTGACGGCCAGATTTACCGAACCAAACCGGATTCTGTCAGAGGGGGGAAATGGACACTGATATCATTACCTTTGCTGGAGAACCGATTCGTCCAAATGTAGAGGAATGGCATTTAGTTTAATGACACCTTTGGGACGAATGCCAAAAAGCCATATTCACAAGATTTCTTTTTTGTTTGCTTGTAATGAACCAAGATCAAATGAAATATTCTCATTTCGCTCTTCATTTGTTTACCGTTTTCCTTTAAATCCGAAATGTTTTTGTAAATTTATTGTAGCTTTATTATGTACTATTCATTTAGATACTTGTAACTGTTATCAAACAATAGATCCAACTCAAATACTGACTGTATTGTACAAATTTTACATTTTGCATGTTGTAATTGAAGCAGCAGGTCTGTGAATTTCATTGAAATGTTTTTACCCGCATGTC
Associated Phenotype:
Not determined