Busch Lab

ZMP

NP_001037811.1

Ensembl ID:
ENSDARG00000094671
Description:
thyrotropin releasing hormone receptor 2 [Source:RefSeq peptide;Acc:NP_001037811]
Mouse Orthologue:
Trhr2
Mouse Description:
thyrotropin releasing hormone receptor 2 Gene [Source:MGI Symbol;Acc:MGI:2177284]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa36617 Nonsense Mutation detected in F1 DNA Not yet available
sa10321 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa36617
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000142980 Nonsense 453 497 3 3

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 16832951)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17184717
GRCz11 18 17173783
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGACGTGGACATGAGCAAGATTAATGATAATGGGAAAATAATGGAG[G/T]AAAGCGGTAATAGTGCTCAGGATATTATCGCTGACATGAGCAACACACAG
Long Flanking Sequence:
CCTACAGGACCCTGGTCCTCATCAACTCCTTCGTCAGCACGCCATACCTGGATTCCTGGTTCATTCTCTTCTGCAGGACCTGCATTTACGCTAACAGCGCCATCAACCCTGTCGTTTACAATCTGATGTCCCAGAAGTTTCGCTCGGCCTTCCGCGGACTGTACCGCTGCCGTAGGGAAGATTTGCACCAAAGGACACTCTCAATGCTCCAGAGCGGATACAGCCTAGGAAGAGACCCGCGAATCTGCAGCAACGGCACCAGAGACACTCCTAAGAAAGTCGGTTCAGTCACTCCAGAGCAGAAACAAAACAAGGGCTTTGAGAACAAGGTGGAAAATACAGACAGACAGATTAGCGACGGTGTTGAAAATGAGATTAATCCGAGCATCAAGAAAAATGCATGCGCAAATTGTGACATAGATGAATCGAAAACCTCAGAGATGCCTACAGTGGAGGACGTGGACATGAGCAAGATTAATGATAATGGGAAAATAATGGAG[G/T]AAAGCGGTAATAGTGCTCAGGATATTATCGCTGACATGAGCAACACACAGCAGACACAACGAGTGTCCGGTGAATTCACATCTACTCTGGGGGAAGCAGAACAGAATGATGCAGAGCTCAGTCACAGTGTTTTATAGATCACTCCACTACTGTATATATTACGTTGAAGTGGCGGGGTTGAGCCTGGTTGTTCATTTATAAGCCAGATCTTGAAATTGGAAACTTGTATGTACTCACAGGCATCATTCTCTCTCTCCAGTGAAGGTGACGAAACACTCTCTTCTCGTGATTTGCAAGTGGAACCATTTGGCTGTTAGCACCAGCATCACATGCCTCCTCACTTGGGATGCTTGATGTGTTCAAAGCATAATATTGTGGTTATTCAGACAAAACATTTTAAACTATAATTTTGCTCTCCTATTGCTGCTGCATAGTAATGTAGGTGTATAAGTACTATTCTATATCTAAATGTATGATATAAACTTCTAATTAATATCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10321
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000142980 Nonsense 473 497 3 3

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 16833011)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 17184777
GRCz11 18 17173843
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGTGCTCAGGATATTATCGCTGACATGAGCAACACACAGCAGACACAA[C/T]GAGTGTCCGGTGAATTCACATCTWCTCTGGGRGWAGCAGAACAGAATGAT
Long Flanking Sequence:
TCATTCTCTTCTGCAGGACCTGCATTTACGCTAACAGCGCCATCAACCCTGTCGTTTACAATCTGATGTCCCAGAAGTTTCGCTCGGCCTTCCGCGGACTGTACCGCTGCCGTAGGGAAGATTTGCACCAAAGGACACTCTCAATGCTCCAGAGCGGATACAGCCTAGGAAGAGACCCGCGAATCTGCAGCAACGGCACCAGAGACACTCCTAAGAAAGTCGGTTCAGTCACTCCAGAGCAGAAACAAAACAAGGGCTTTGAGAACAAGGTGGAAAATACAGACAGACAGATTAGCGACGGTGTTGAAAATGAGATTAATCCGAGCATCAAGAAAAATGCATGCGCAAATTGTGACATAGATGAATCGAAAACCTCAGAGATGCCTACAGTGGAGGACGTGGACATGAGCAAGATTAATGATAATGGGAAAATAATGGAGGAAAGCGGTAATAGTGCTCAGGATATTATCGCTGACATGAGCAACACACAGCAGACACAA[C/T]GAGTGTCCGGTGAATTCACATCTACTCTGGGGGAAGCAGAACAGAATGATGCAGAGCTCAGTCACAGTGTTTTATAGATCACTCCACTACTGTATATATTACGTTGAAGTGGCGGGGTTGAGCCTGGTTGTTCATTTATAAGCCAGATCTTGAAATTGGAAACTTGTATGTACTCACAGGCATCATTCTCTCTCTCCAGTGAAGGTGACGAAACACTCTCTTCTCGTGATTTGCAAGTGGAACCATTTGGCTGTTAGCACCAGCATCACATGCCTCCTCACTTGGGATGCTTGATGTGTTCAAAGCATAATATTGTGGTTATTCAGACAAAACATTTTAAACTATAATTTTGCTCTCCTATTGCTGCTGCATAGTAATGTAGGTGTATAAGTACTATTCTATATCTAAATGTATGATATAAACTTCTAATTAATATCAAGGGCGAAATCAAGGTTCGGGTCCCGACTGGACAAGGAGGCCTGAATGTGTGGAGTTTGCAT
Associated Phenotype:
Not determined